BIFIDOBACTERIUM LONGUM ABLE TO BENEFICIALLY MODULATE IMMUNE RESPONSE TO RESPIRATORY VIRUS INFECTION
Bifidobacterium longum strains and cell wall fractions isolated from Bifidobacterium longum strains are useful in the prophylaxis or treatment of a respiratory viral infection in a subject. They are also useful in the prophylaxis of a secondary bacterial infection associated with a respiratory viral infection in a subject, especially a subject who is susceptible to respiratory infections.
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This application is a continuation of U.S. Application No. 16/489,132, filed on Aug. 27, 2019, which is the U.S. national phase entry under 35 U.S.C. § 371 of International Application No. PCT/EP2018/054918, filed on Feb. 28, 2018, which are incorporated by reference herein in their entireties, PCT/EP2018/054918 claiming benefit of priority to European Application Nos. 17158557.3, 17158567.2, 17158559.9, 17158560.7, 17158561.5, and 17158564.9, each filed on Feb. 28, 2017, and to European Application No. 17175221.5, filed on Jun. 9, 2017.
SEQUENCE LISTINGThis application contains a sequence listing, submitted electronically in XML format under the file name 00175-0008-01000.xml, which is incorporated by reference herein in its entirety. The XML copy of the sequence listing was created on Dec. 2, 2022, and is 7,349 bytes in size.
FIELD OF THE INVENTIONThe invention relates to Bifidobacteria which are one of several predominant culturable bacteria present in human colonic microflora.
BACKGROUND OF THE INVENTIONBifidobacteria are considered to be probiotics as they are living organisms which exert healthy effects beyond basic nutrition when ingested in sufficient numbers. A high level of ingested bifidobacteria must reach their site of action in order to exert a probiotic effect. A minimum level of approximately 106-107 viable bifidobacteria per gram intestinal contents has been suggested (Bouhnik, Y., Lait 1993). There are reports in the literature which show that in vivo studies completed in adults and in infants indicate that some strains of bifidobacteria are capable of surviving passage through the gastrointestinal tract. Significant differences have been observed between the abilities of different bifidobacteria strains to tolerate acid and bile salts, indicating that survival is an important criterion for the selection of potential probiotic strains.
Ingestion of bifidobacteria can improve gastrointestinal transit and may prevent or assist in the treatment of illnesses which may be caused by deficient or compromised microflora such as gastrointestinal tract (GIT) infections, constipation, irritable bowel syndrome (IBS), inflammatory bowel disease (IBD) - Crohn’s disease and ulcerative colitis, food allergies, antibiotic-induced diarrhoea, cardiovascular disease, and certain cancers (e.g. colorectal cancer).
Viral infections are a major cause of morbidity and mortality. Influenza virus, rhinovirus (common cold) and respiratory syncytial virus (RSV) are highly infectious viruses that usually are successfully cleared by an appropriate host immune response in healthy individuals. However much of the issue with these infections is not the initial virus but rather the secondary infections that often accompany it e.g. bacterial infections causing pneumonia, infection of sinus tissue etc. Susceptible individuals such as those suffering from COPD or Asthma or Obesity respond very poorly to viral infections and subsequent secondary infections are serious and can be life threatening to such individuals.
These virus-induced exacerbations of these conditions are associated with substantial healthcare costs and significant suffering. Development of new and effective therapies for these exacerbations would be beneficial as there is a major unmet clinical need. Administration of corticosteroids to patients affected by influenza virus, especially pandemic avian influenza virus, although relatively common, remains controversial. Routine steroid use is not be ideal for influenza virus infection as it does not reduce the viral burden and also inhibits the clearance of secondary bacterial infections afterwards (Yang et al, 2015).
In the early stages of infection, influenza, rhinovirus and RSV replication occurs in lung epithelial cells, leading to activation of viral sensors and the release of antiviral Type I and Type III interferons (IFN’s) as well as chemokines and cytokines. These pro-inflammatory mediators help to clear the primary infection but Type I IFN’s can also cause subsequent damage (immunopathology). IFN Type I responses, such as increases in IFN-α and IFN-β molecules, have been shown to directly correlate with increased morbidity and mortality in models of influenza infection (Davidson et al, 2014). Over-production of antiviral Type I IFN’s and the related IP-10 chemokine inhibit the appropriate immune response to clear secondary infections (Nakamura et al, 2011; Shahangian et al, 2009; Li et al, 2012) such as caused by bacterial agents such as Streptococcus pneumonia, Moraxella catarrhalis, and Haemophilus influenzae and even Staphylococcus aureus (Hewitt et al, 2016). These secondary infections cause excessive cell death within the lungs. In susceptible individuals, this leads to lung tissue injury and reduced lung function which causes serious complications and mortality in some cases e.g. in COPD patients. Importantly the pro-inflammatory activation occurs only to Type I IFN responses which cause the recruitment of neutrophils and not to Type III IFN responses (Galani et al, 2017).
However, Type III IFN’s such as IFN lambda (IFN-λ) can limit viral replication without inducing pro-inflammatory responses or immunopathology (Davidson et al, 2016; Galani et al, 2017).
Therefore, therapeutic agents that can limit the Type I IFN responses and accompanying pro-inflammatory and tissue damaging response to viral infection, while maintaining appropriate Type III responses and anti-viral defence, would be a significant advancement in the management of respiratory viral infections. This reduction of immunopathology is critical for host survival and resolution of disease.
Other innate sensors or immune mediators can also play an important role in early anti-viral defence Surfactant protein D (SP-D) can stop the influenza virus from entering epithelial cells which is part of the early phase of the infection. (Thiel et al, 1989; Sastry et al, 1993). Again, therapeutic agents that can induce this innate sensor which can bind to the virus and stop it from infecting the bronchial epithelial cells would be a significant advancement in the treatment of viruses such as influenza, rhinovirus and RSV. In addition, inhibition of tumor necrosis factor-alpha (TNF-α), an important inflammatory cytokine has a significant effect on the extent of lung immunopathology and inhibited inflammatory cellular infiltration and cytokine responses. TNF-α, has been shown to correlate with morbidity and mortality in macaques monkeys and humans infected with highly virulent influenza viruses. A decrease in influenza virus replication and an increased survival of influenza virus-infected mice was observed when the TNF-α was suppressed (Shi et al, 2013). Inhibition of this inflammatory cytokine with etanercept provides protection against lethal H1N1 influenza infection in mice (Shi et al, 2013).
Therapeutic agents which can induce Type III IFN-λ and/or SP-D would have a role to play in early clearance of the primary viral infection while reducing the likelihood of secondary bacterial infections and would be a significant advancement in the management of ARDS, asthma, obesity and COPD.
STATEMENTS OF INVENTIONThe invention provides a cell wall fraction isolated from a strain of Bifidobacterium longum.
The invention also provides a cell wall fraction isolated from a Bifidobacterium longum strain for use in the prophylaxis or treatment of a respiratory viral infection in a subject.
The invention further provides a cell wall fraction isolated from a Bifidobacterium longum strain for use in the prophylaxis of a secondary bacterial infection associated with a respiratory viral infection in a subject
The cell wall fraction may attenuate the IP-10 response to a virus. This is important because IP-10 is secreted by several cell types in response to IFN-γ. These cell types include monocytes and endothelial cells. IP-10 has been attributed to several roles, including chemoattraction for monocytes/macrophages, T cells, NK cells, and dendritic cells, and promotion of T cell adhesion to endothelial cells and is a marker of viral induced host system activation
The cell wall fraction may enhance the type III interferon response to the virus such as the interferon lambda response to the virus.
The cell wall fraction may supress the interferon type I response to the virus such as the interferon alpha response to the virus, and/or the interferon beta response to the virus.
The cell wall fraction may enhance the surfactant protein D response to the virus.
In some cases the virus is a respiratory virus. The virus may be selected from influenza virus, rhinovirus, and respiratory syncytial virus.
In some cases the molecular weight of the cell wall fraction is greater than 100 kDa.
In some cases the cell wall fraction is less than 0.45 µm in size.
The fraction may be isolated by opening the Bifidobacterium longum and separating the cell wall fraction from a cytoplasmic fraction.
The opening of the Bifidobacterium longum may comprise at least one of:-
- treating with a chelating agent;
- treating with an enzyme; and
- applying shear force.
In one case the chelating agent is a calcium chelating agent such as ethylenediaminetetraacetic acid (EDTA).
In some cases the enzyme is a glycoside hydrolase such as lysozyme. Alternatively or additionally the enzyme is a muralytic enzyme such as mutanolysin.
In some cases the shear force is applied by sonication. Alternatively or additionally the shear force is applied by pressure such as by a French press.
The separation in some cases comprises centrifugation.
After separation the cell wall fraction may be filtered to provide a fraction with a size of less than 0.45 µm.
The invention also provides a formulation which comprises a cell wall fraction as defined. The formulation may further comprise a prebiotic material and/or an ingestable carrier such as a pharmaceutically acceptable carrier such as a capsule, tablet or powder or the ingestable carrier is a food product such as acidified milk, yoghurt, frozen yoghurt, milk powder, milk concentrate, ice-cream, cheese spreads, dressings or beverages.
The formulation may further comprise a protein and/or peptide, in particular proteins and/or peptides that are rich in glutamine/glutamate, a lipid, a carbohydrate, a vitamin, mineral and/or trace element.
The formulation may further comprise an adjuvant, a drug entity, and/or a biological compound.
The formulation may be adapted for administration to the lung or to the nose. The formulation may comprise a nasal spray. In some cases the formulation has a viscosity of from 1 cps to 2000 cps.
In some cases a nasal application of the cell wall fraction may be preferable to a nasal application of whole cells in a viable from due to bacterial load.
The respiratory virus may be selected from influenza virus, rhinovirus, and respiratory syncytial virus.
In some cases the subject has been diagnosed with an inflammatory lung disease.
In some cases the subject has increased susceptibility to a respiratory infection. For example, the subject may be obese, the subject may be an acute respiratory distress syndrome (ARDS) patient, the subject may be an asthma patient, and/or the subject may be a chronic obstructive pulmonary disease (COPD) patient.
In one case the subject is a child less than 5 years of age.
In another case the subject is an elderly person greater than 60 years of age.
The invention also provides a process for isolating a cell wall fraction of a Bifidobacterium longum comprising the steps of:-
- opening the Bifidobacterium longum to form a cell wall fraction and a cytoplasmic fraction; and
- separating the cell wall fraction from the cytoplasmic fraction.
In one case the opening of the Bifidobacterium longum comprises at least one of:-
- treating with a chelating agent;
- treating with an enzyme; and
- applying a shear force
The chelating agent may be a calcium chelating agent such as ethylenediaminetetraacetic acid (EDTA). The enzyme may be a glycoside hydrolase such as lysozyme and/or the enzyme may be a muralytic enzyme such as mutanolysin.
In some cases the shear force is applied by sonication and/or the shear force is applied by pressure such as by a French press. The separation may comprise centrifugation.
According to the invention there is provided a Bifidobacterium longum strain for use in the prophylaxis or treatment of a respiratory viral infection in a subject.
Also provided is Bifidobacterium longum strain for use in the prophylaxis of a secondary bacterial infection associated with a respiratory viral infection in a subject
The Bifidobacterium longum may attenuate the IP-10 response to a virus.
The Bifidobacterium longum may enhance the type III interferon response to a virus such as the interferon lambda response to a virus.
The Bifidobacterium longum may suppress the interferon type I response to a virus such as the interferon alpha response to a virus and/or the interferon beta response to a virus.
The Bifidobacterium longum strain may enhance the surfactant protein D response to a virus.
In some embodiments the respiratory virus is selected from influenza virus, rhinovirus, and respiratory syncytial virus.
The subject may have been diagnosed with an inflammatory lung disease. In some cases the subject has increased susceptibility to a respiratory infection. For example, the subject may be obese and/or the subject is an acute respiratory distress syndrome (ARDS) patient, and/or the subject is an asthma patient and/or the subject is a chronic obstructive pulmonary disease (COPD) patient. In one case the subject is a child less than 5 years of age. In another case the subject is an elderly person greater than 60 years of age.
In one embodiment the Bifidobacterium longum is strain NCIMB 41003.
In one embodiment the Bifidobacterium longum is strain NCIMB 41715.
In one embodiment the Bifidobacterium longum is strain NCIMB 41713.
In one embodiment the Bifidobacterium longum is strain NCIMB 42020.
In some embodiments the Bifidobacterium longum is not strain NCIMB 41003.
In some embodiments the Bifidobacterium longum is not strain NCIMB 42020.
The invention also provides a formulation comprising a strain of Bifidobacterium longum wherein the Bifidobacterium longum attenuates the IP-10 response to a respiratory virus and wherein the formulation is adapted for administration to the lung or to the nose. In one case, the formulation is a nasal spray.
The formulation may further comprise a prebiotic material, a carrier, an adjuvant, a drug entity and/or a biological compound.
The formulation in some cases has a viscosity of from 1cps to 2000cps.
The invention also provides Bifidobacterium longum strain AH0103 having the accession number NCIMB 41713. The strain may be in the form of a biologically pure culture. Also provided is an isolated strain of Bifidobacterium longum NCIMB 41713. The strain may be in the form of viable cells and/or non-viable cells.
In some cases the strain is in the form of a bacterial broth or a freeze-dried powder.
Also provided is a formulation which comprises a Bifidobacterium strain as defined above. The formulation may further comprise another probiotic material, a prebiotic material and/or an ingestable carrier such as a pharmaceutically acceptable carrier such as a capsule, tablet or powder, or the ingestable carrier is a food product such as acidified milk, yoghurt, frozen yoghurt, milk powder, milk concentrate, ice cream, cheese spread, dressing or beverage.
The formulation may further comprise a protein and/or peptide, in particular proteins and/or peptides that are rich in glutamine/glutamate, a lipid, a carbohydrate, a vitamin, mineral and/or trace element.
In some cases the Bifidobacterium strain is present in the formulation in an amount of more than 106 cfu per gram of the formulation.
The formulation in some cases further comprises an adjuvant, a drug entity, and/or a biological compound.
The invention also provides a Bifidobacterium strain as defined or a formulation as defined for use in foodstuffs.
The invention further provides a Bifidobacterium strain as defined or a formulation as defined for use as a medicament.
The Bifidobacterium strain or formulation may be for use in the prophylaxis and/or treatment of undesirable inflammatory activity.
Also provided is a Bifidobacterium strain as defined or an active derivative or fragment or mutant or variant thereof for use in the prophylaxis and/or treatment of undesirable inflammatory activity.
According to the invention there is provided Bifidobacterium longum NCIMB 41003 for use in the prophylaxis or treatment of a viral infection in a subject.
In one case the strain attenuates the IP-10 response to a virus.
In one case the strain enhances the type III interferon response to the virus.
In one case the strain suppresses the interferon alpha response to the virus.
In one case the strain suppresses the interferon beta response to the virus.
The invention also provides Bifidobacterium longum NCIMB 41003 for use in the prophylaxis or treatment of a viral infection, wherein the strain:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
In one embodiment the strain is administered in a formulation which is suitable for administration to the lung or the nose.
In one case the subject is an acute respiratory distress syndrome (ARDS) patient.
In another case the subject is an asthma patient.
Ina further case the subject is a chronic obstructive pulmonary disease (COPD) patient.
The invention also provides a method for prophylaxis or treatment of a viral infection comprising the step of administering Bifidobacterium longum NCIMB 41003.
The invention provides an isolated strain of Bifidobacterium longum NCIMB 41713.
The invention also provides a mutant or variant of an isolated strain of Bifidobacterium longum NCIMB 41713.
The isolated strain may be in the form of viable cells.
The isolated strain may be in the form of non-viable cells.
The invention also provides a formulation comprising an isolated strain of Bifidobacterium longum NCIMB 41713.
The formulation may comprise an ingestible carrier. The ingestible carrier may be a pharmaceutically acceptable carrier such as a capsule, tablet or powder. The ingestible carrier may be a food product such as acidified milk, yoghurt, frozen yoghurt, milk powder, milk concentrate, cheese spreads, dressings or beverages.
In one embodiment the strain attenuates the IP-10 response to a virus.
In one embodiment the strain enhances the type III interferon response to the virus.
In one embodiment the strain suppresses the interferon alpha response to the virus.
In one embodiment the strain suppresses the interferon beta response to the virus.
In one case the strain:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
The strain may be present at more than 106 cfu per gram of ingestible carrier.
The invention further provides a composition comprising an isolated strain of Bifidobacterium longum NCIMB 41713 and a pharmaceutically acceptable carrier.
The invention also provides for the use of a Bifidobacterium longum strain NCIMB 41713 as a probiotic strain.
In one embodiment the formulation is adapted for administration to the lung or to the nose.
It will be appreciated that the specific strain of the invention may be administered to animals (including humans) in an orally ingestible form in a conventional preparation such as capsules, microcapsules, tablets, granules, powder, troches, pills, suppositories, suspensions and syrups. Suitable formulations may be prepared by methods commonly employed using conventional organic and inorganic additives. The amount of active ingredient in the medical composition may be at a level that will exercise the desired therapeutic effect.
The formulation may also include a bacterial component, a drug entity or a biological compound.
In addition, a vaccine comprising the strains of the invention may be prepared using any suitable known method and may include a pharmaceutically acceptable carrier or adjuvant.
The invention also provides a Bifidobacterium strain of the invention or a formulation of the invention for use in the prophylaxis or treatment of a viral infection in a subject.
In one case the subject is an acute respiratory distress syndrome (ARDS) patient.
In another case the subject is an asthma patient.
In a further case the subject is a chronic obstructive pulmonary disease (COPD) patient.
The invention also provides a cell wall fraction isolated from Bifidobacterium longum NCIMB 41713 wherein the cell wall fraction attenuates the IP-10 response to a virus.
In one case the fraction enhances the type III interferon response to the virus.
In one case the fraction suppresses the interferon alpha response to the virus.
In one case the fraction suppresses the interferon beta response to the virus.
Also provided is a cell wall fraction isolated from Bifidobacterium longum NCIMB 41713, wherein the cell wall fraction:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
In one case the molecular weight of the cell wall fraction is greater than 100 kDa.
In one case the cell wall fraction is less than 0.45 µm in size.
Also provided is a cell wall fraction isolated from Bifidobacterium longum NCIMB 41713, the cell wall fraction having a molecular weight of greater than 100 kDa and being less than 0.45 µm in size.
The invention also provides a method for prophylaxis or treatment of a viral infection in a subject comprising the step of administering a cell wall fraction isolated from Bifidobacterium longum NCIMB 41713.
In one case the cell wall fraction attenuates the IP-10 response to a virus.
In one case the fraction enhances the type III interferon response to the virus.
In one case the fraction suppresses the interferon alpha response to the virus.
In one case the fraction suppresses the interferon beta response to the virus.
Also provided is a method for the prophylaxis or treatment of a viral infection in a subject comprising administering a cell wall fraction isolated from Bifidobacterium longum NCIMB 41713, wherein the fraction:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
In one case the molecular weight of the cell wall fraction is greater than 100 kDa.
In one case the cell wall fraction is less than 0.45 µm in size.
In one case the cell wall fraction is administered in a formulation which is suitable for administration to the lung or the nose.
In one case the subject is an acute respiratory distress syndrome (ARDS) patient.
In one case the subject is an asthma patient.
In one case the subject is a chronic obstructive pulmonary disease (COPD) patient.
The invention provides an isolated strain of Bifidobacterium longum NCIMB 42020 (AH0106).
The invention also provides a mutant or variant of an isolated strain of Bifidobacterium longum NCIMB 42020.
The isolated strain may be in the form of viable cells.
The isolated strain may be in the form of non-viable cells.
The invention also provides a formulation comprising an isolated strain of Bifidobacterium longum NCIMB 42020.
The formulation may comprise an ingestible carrier. The ingestible carrier may be a pharmaceutically acceptable carrier such as a capsule, tablet or powder. The ingestible carrier may be a food product such as acidified milk, yoghurt, frozen yoghurt, milk powder, milk concentrate, cheese spreads, dressings or beverages.
In one embodiment the strain attenuates the IP-10 response to a virus.
In one embodiment the strain enhances the type III interferon response to the virus.
In one embodiment the strain suppresses the interferon alpha response to the virus.
In one embodiment the strain suppresses the interferon beta response to the virus.
In one case the strain:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
The strain may be present at more than 106 cfu per gram of ingestible carrier.
The invention further provides a composition comprising an isolated strain of Bifidobacterium longum NCIMB 42020 and a pharmaceutically acceptable carrier.
The invention also provides for the use of a Bifidobacterium longum strain NCIMB 42020 as a probiotic strain.
In one embodiment the formulation is adapted for administration to the lung or to the nose.
It will be appreciated that the specific strain of the invention may be administered to animals (including humans) in an orally ingestible form in a conventional preparation such as capsules, microcapsules, tablets, granules, powder, troches, pills, suppositories, suspensions and syrups. Suitable formulations may be prepared by methods commonly employed using conventional organic and inorganic additives. The amount of active ingredient in the medical composition may be at a level that will exercise the desired therapeutic effect.
The formulation may also include a bacterial component, a drug entity or a biological compound.
In addition, a vaccine comprising the strains of the invention may be prepared using any suitable known method and may include a pharmaceutically acceptable carrier or adjuvant.
The invention also provides a Bifidobacterium strain of the invention or a formulation of the invention for use in the prophylaxis or treatment of a viral infection in a subject.
In one case the subject is an acute respiratory distress syndrome (ARDS) patient.
In another case the subject is an asthma patient.
In a further case the subject is a chronic obstructive pulmonary disease (COPD) patient.
The invention provides an isolated strain of Bifidobacterium longum NCIMB 42020 (AH0106).
The invention also provides a mutant or variant of an isolated strain of Bifidobacterium longum NCIMB 42020.
The isolated strain may be in the form of viable cells.
The isolated strain may be in the form of non-viable cells.
The invention also provides a formulation comprising an isolated strain of Bifidobacterium longum NCIMB 42020.
The formulation may comprise an ingestible carrier. The ingestible carrier may be a pharmaceutically acceptable carrier such as a capsule, tablet or powder. The ingestible carrier may be a food product such as acidified milk, yoghurt, frozen yoghurt, milk powder, milk concentrate, cheese spreads, dressings or beverages.
In one embodiment the strain attenuates the IP-10 response to a virus.
In one embodiment the strain enhances the type III interferon response to the virus.
In one embodiment the strain suppresses the interferon alpha response to the virus.
In one embodiment the strain suppresses the interferon beta response to the virus.
In one case the strain:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
The strain may be present at more than 106 cfu per gram of ingestible carrier.
The invention further provides a composition comprising an isolated strain of Bifidobacterium longum NCIMB 42020 and a pharmaceutically acceptable carrier.
The invention also provides for the use of a Bifidobacterium longum strain NCIMB 42020 as a probiotic strain.
In one embodiment the formulation is adapted for administration to the lung or to the nose.
It will be appreciated that the specific strain of the invention may be administered to animals (including humans) in an orally ingestible form in a conventional preparation such as capsules, microcapsules, tablets, granules, powder, troches, pills, suppositories, suspensions and syrups. Suitable formulations may be prepared by methods commonly employed using conventional organic and inorganic additives. The amount of active ingredient in the medical composition may be at a level that will exercise the desired therapeutic effect.
The formulation may also include a bacterial component, a drug entity or a biological compound.
In addition, a vaccine comprising the strains of the invention may be prepared using any suitable known method and may include a pharmaceutically acceptable carrier or adjuvant.
The invention also provides a Bifidobacterium strain of the invention or a formulation of the invention for use in the prophylaxis or treatment of a viral infection in a subject.
In one case the subject is an acute respiratory distress syndrome (ARDS) patient.
In another case the subject is an asthma patient.
In a further case the subject is a chronic obstructive pulmonary disease (COPD) patient.
The invention also provides a cell wall fraction isolated from Bifidobacterium longum NCIMB 42020 wherein the cell wall fraction attenuates the IP-10 response to a virus.
In one case the fraction enhances the type III interferon response to the virus.
In one case the fraction suppresses the interferon alpha response to the virus.
In one case the fraction suppresses the interferon beta response to the virus.
The invention further provides a cell wall fraction isolated from Bifidobacterium longum NCIMB 42020, wherein the cell wall fraction:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
In one case the molecular weight of the cell wall fraction is greater than 100 kDa.
In one case the cell wall fraction is less than 0.45 µm in size.
In one case the cell wall fraction has a molecular weight of greater than 100 kDa and is less than 0.45 µm in size.
The invention further provides a method for prophylaxis or treatment of a viral infection in a subject comprising the step of administering a cell wall fraction isolated from Bifidobacterium longum NCIMB 42020.
In one case the cell wall fraction attenuates the IP-10 response to a virus.
In one case the fraction enhances the type III interferon response to the virus.
In one case the fraction suppresses the interferon alpha response to the virus.
In one case the fraction suppresses the interferon beta response to the virus.
Also provided is a method for the prophylaxis or treatment of a viral infection in a subject comprising administering a cell wall fraction isolated from Bifidobacterium longum NCIMB 42020, wherein the fraction:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
In one case the molecular weight of the cell wall fraction is greater than 100 kDa.
In one case the cell wall fraction is less than 0.45 µm in size.
In one case the cell wall fraction is administered in a formulation which is suitable for administration to the lung or the nose.
In one case the subject is an acute respiratory distress syndrome (ARDS) patient.
In one case the subject is an asthma patient.
In one case the subject is a chronic obstructive pulmonary disease (COPD) patient.
The invention also provides a cell wall fraction isolated from Bifidobacterium longum NCIMB 42020 wherein the cell wall fraction attenuates the IP-10 response to a virus.
In one case the fraction enhances the type III interferon response to the virus.
In one case the fraction suppresses the interferon alpha response to the virus.
In one case the fraction suppresses the interferon beta response to the virus.
The invention further provides a cell wall fraction isolated from Bifidobacterium longum NCIMB 42020, wherein the cell wall fraction:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
In one case the molecular weight of the cell wall fraction is greater than 100 kDa.
In one case the cell wall fraction is less than 0.45 µm in size.
In one case the cell wall fraction has a molecular weight of greater than 100 kDa and is less than 0.45 µm in size.
The invention further provides a method for prophylaxis or treatment of a viral infection in a subject comprising the step of administering a cell wall fraction isolated from Bifidobacterium longum NCIMB 42020.
In one case the cell wall fraction attenuates the IP-10 response to a virus.
In one case the fraction enhances the type III interferon response to the virus.
In one case the fraction suppresses the interferon alpha response to the virus.
In one case the fraction suppresses the interferon beta response to the virus.
Also provided is a method for the prophylaxis or treatment of a viral infection in a subject comprising administering a cell wall fraction isolated from Bifidobacterium longum NCIMB 42020, wherein the fraction:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
In one case the molecular weight of the cell wall fraction is greater than 100 kDa.
In one case the cell wall fraction is less than 0.45 µm in size.
In one case the cell wall fraction is administered in a formulation which is suitable for administration to the lung or the nose.
In one case the subject is an acute respiratory distress syndrome (ARDS) patient.
In one case the subject is an asthma patient.
In one case the subject is a chronic obstructive pulmonary disease (COPD) patient.
According to the invention there is provided cell wall fraction isolated from Bifidobacterium longum NCIMB 41003 wherein the cell wall fraction attenuates the IP-10 response to a virus.
In one case the fraction enhances the type III interferon response to the virus.
In one case the fraction suppresses the interferon alpha response to the virus.
In one case the fraction suppresses the interferon beta response to the virus.
The invention also provides a cell wall fraction isolated from Bifidobacterium longum NCIMB 41003, wherein the cell wall fraction:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
In one case the molecular weight of the cell wall fraction is greater than 100 kDa.
In one case the cell wall fraction is less than 0.45 µm in size.
Also provided is a cell wall fraction isolated from Bifidobacterium longum NCIMB 41003, the cell wall fraction having a molecular weight of greater than 100 kDa and being less than 0.45 µm in size.
The invention also provides a method for prophylaxis or treatment of a viral infection in a subject comprising the step of administering a cell wall fraction isolated from Bifidobacterium longum NCIMB 41003.
In one case the cell wall fraction attenuates the IP-10 response to a virus.
In one case the fraction enhances the type III interferon response to the virus.
In one case the fraction suppresses the interferon alpha response to the virus.
In one case the fraction suppresses the interferon beta response to the virus.
The invention further provides a method for the prophylaxis or treatment of a viral infection in a subject comprising administering a cell wall fraction isolated from Bifidobacterium longum NCIMB 41003, wherein the fraction:-
- attenuates the IP-10 response to the virus;
- enhances the type III interferon response to the virus;
- suppresses the interferon alpha response to the virus; and
- suppresses the interferon beta response to the virus.
The molecular weight of the cell wall fraction may be greater than 100 kDa.
The cell wall fraction may be less than 0.45 µm in size.
In some embodiments the cell wall fraction is administered in a formulation which is suitable for administration to the lung or the nose.
In one case the subject is an acute respiratory distress syndrome (ARDS) patient.
In another case the subject is an asthma patient.
In a further case the subject is a chronic obstructive pulmonary disease (COPD) patient.
The invention provides a use of the strain of Bifidobacterium longum AH1362 deposited with the NCIMB under accession number NCIMB 41715.
The strain was isolated from a faecal sample from a placebo-fed healthy adult volunteer.
The strain may be in the form of viable cells. The strain may be in the form of non-viable cells. The general use of probiotic bacteria is in the form of viable cells. However, use can also be extended to non-viable cells such as killed cultures, mixtures of viable and non-viable cultures or compositions containing beneficial factors expressed by the probiotic bacteria. This could include thermally killed micro-organisms or micro-organisms killed by exposure to altered pH or subjection to pressure or gamma irradiation. With non-viable cells product preparation is simpler, cells may be incorporated easily into pharmaceuticals and storage requirements are much less limited than viable cells. Lactobacillus casei YIT 9018 offers an example of the effective use of heat killed cells as a method for the treatment and/or prevention of tumour growth as described in U.S. Pat. No. US4,347,240.
The invention also provides a use of a formulation which comprises a strain NCIMB 41715. The formulation may further comprise a probiotic material. The formulation may further comprise a prebiotic material. The formulation may further comprise a carrier. The carrier may be an ingestible carrier may a pharmaceutically acceptable carrier such as a capsule, tablet or powder. The ingestible carrier may be a food product such as acidified milk, yoghurt, frozen yoghurt, milk powder, milk concentrate, cheese spreads, dressings or beverages. Some examples include a fermented food product such as a fermented milk product. The formulation may further comprise a protein and/or peptide, in particular proteins and/or peptides that are rich in glutamine/glutamate, a lipid, a carbohydrate, a vitamin, mineral and/or trace element. The Bifidobacterium strain may be present in an amount of more than 106 cfu per gram of the formulation. The formulation may further comprise an adjuvant. The formulation may further comprise a bacterial component. The formulation may further comprise a drug entity. The formulation may further comprise a biological compound. In all cases the formulation comprises a strain as described herein and may include a carrier or other agent. Such a carrier or other agent in some cases, do not occur in nature. The formulation may in some cases be used for immunisation and vaccination protocols.
The invention also provides a freeze-dried composition comprising a strain NCIMB 41715 or a formulation of strain NCIMB 41715.
It will be appreciated that the strain NCIMB 41715 may be administered to animals (including humans) in an orally ingestible form in a conventional preparation such as capsules, microcapsules, tablets, granules, powder, troches, pills, suppositories, suspensions and syrups. Suitable formulations may be prepared by methods commonly employed using conventional organic and inorganic additives. The amount of active ingredient in the medical composition may be at a level that will exercise the desired therapeutic effect.
The formulation may also include a bacterial component, a drug entity or a biological compound. In some cases the medicament is in a form suitable for inhalation.
The invention further provides a strain or a formulation as described herein for use in the prophylaxis or treatment of a viral infection in a subject.
In some cases, the subject may be an acute respiratory distress syndrome (ARDS) patient, an asthma patient, or a chronic obstructive pulmonary disease (COPD) patient.
The invention also provides a cell wall fraction isolated from Bifidobacterium longum NCIMB 41715 wherein the cell wall fraction attenuates the IP-10 response to a virus.
Also provided is a method for prophylaxis or treatment of a viral infection in a subject comprising the step of administering a cell wall fraction isolated from Bifidobacterium longum NCIMB 41715. The cell wall fraction may attenuate the IP-10 response to a virus. In some cases the cell wall fraction is administered in a formulation which is suitable for administration to the lung or the nose. In some cases the subject is an acute respiratory distress syndrome (ARDS) patient, an asthma patient, or a chronic obstructive pulmonary disease (COPD) patient.
We have discovered that a component of a particular bacterial strain promotes anti-viral defence and inhibits damaging pro-inflammatory responses and are particularly useful in the prevention and/or treatment of virus induced ARDS, or viral-induced exacerbations in asthma and COPD patients.
The invention also includes mutants and variants of the deposited strains. Throughout the specification the terms mutant, variant and genetically modified mutant include a strain whose genetic and/or phenotypic properties are altered compared to the parent strain. Naturally occurring variant includes the spontaneous alterations of targeted properties selectively isolated. Deliberate alteration of parent strain properties is accomplished by conventional (in vitro) genetic manipulation technologies, such as gene disruption, conjugative transfer, etc. Genetic modification includes introduction of exogenous and/or endogenous DNA sequences into the genome of a strain, for example by insertion into the genome of the bacterial strain by vectors, including plasmid DNA, or bacteriophages.
Natural or induced mutations include at least single base alterations such as deletion, insertion, transversion or other DNA modifications which may result in alteration of the amino acid sequence encoded by the DNA sequence.
The terms mutant, variant and genetically modified mutant also include a strain that has undergone genetic alterations that accumulate in a genome at a rate which is consistent in nature for all micro-organisms and/or genetic alterations which occur through spontaneous mutation and/or acquisition of genes and/or loss of genes which is not achieved by deliberate (in vitro) manipulation of the genome but is achieved through the natural selection of variants and/or mutants that provide a selective advantage to support the survival of the bacterium when exposed to environmental pressures such as antibiotics. A mutant can be created by the deliberate (in vitro) insertion of specific genes into the genome which do not fundamentally alter the biochemical functionality of the organism but whose products can be used for identification or selection of the bacterium, for example antibiotic resistance.
A person skilled in the art would appreciate that mutant or variant strains of can be identified by DNA sequence homology analysis with the parent strain. Strains of having a close sequence identity with the parent strain without demonstrable phenotypic or measurable functional differences are considered to be mutant or variant strains. A strain with a sequence identity (homology) of 99.5% or more with the parent DNA sequence may be considered to be a mutant or variant. Sequence homology may be determined using on-line homology algorithm “BLAST” program, publicly available at http://www.ncbi.nlm.nih,gov/BLAST/.
The invention will be more clearly understood from the following description thereof given by way of example only.
The invention will be more clearly understood from the following description thereof, given by way of example only, with reference to the accompanying figures in which:-
A deposit of Bifidobacterium longum strain AH0103 was made at the National Collections of Industrial and Marine Bacteria Limited (NCIMB) Ferguson Building, Craibstone Estate, Bucksburn, Aberdeen, AB21 9YA, Scotland, UK on May 10, 2010 and accorded the accession number NCIMB 41713.
A deposit of Bifidobacterium longum strain AH0106 was made at the National Collections of Industrial and Marine Bacteria Limited (NCIMB) Ferguson Building, Craibstone Estate, Bucksburn, Aberdeen, AB21 9YA, Scotland, UK on 2nd August 2012 and accorded the accession number NCIMB 42020.
A deposit of Bifidobacterium longum AH1362 was made at the National Collections of Industrial and Marine Bacteria Limited (NCIMB) Ferguson Building, Craibstone Estate, Bucksburn, Aberdeen, AB21 9YA, Scotland, UK on May 6, 2010 and accorded the accession number NCIMB 41715. This strain is described in WO2017/097987A, the entire contents of which are incorporated herein by reference.
The strain Bifidobacterium longum 35624 was deposited at the National Collections of Industrial and Marine Bacteria Limited (NCIMB) Ferguson Building, Craibstone Estate, Bucksburn, Aberdeen, AB21 9YA, Scotland, UK on Jan. 13, 1999 under accession number NCIMB 41003. This strain is described in WO00/42168A, the entire contents of which are incorporated herein by reference.
We have discovered that Bifidobacterium longum strains and cell wall fractions isolated from Bifidobacterium longum strains are useful in the prophylaxis or treatment of a respiratory viral infection in a subject. The strains and cell wall fractions are useful in the prophylaxis of a secondary bacterial infection associated with a respiratory viral infection in a subject. The strains and cell wall fractions are particularly useful in subjects which have increased susceptibility to a respiratory infection.
In the case of viral infections, we have identified a cell wall fraction that is a non-viable component of B. longum strains that is surprisingly effective in reducing viral infections, associated secondary bacterial infections and associated inflammatory processes, using a targeted and immune balancing method of action not identified before. We have demonstrated that this fraction can be isolated from more than one related B. longum strain but is not present in other bifidobacteria. In addition we have demonstrated that, in a further surprising result, the related viable stains from which this fraction can be isolated can be used in a similar way to the isolated cell wall fraction to modulate host immune response to virus in the respiratory system in a targeted fashion, especially upon delivery to the nose. This effect of both fraction and strain is both preventative and therapeutic.
We have discovered that a cell wall fraction of NCIMB 41003 (35624® strain) promotes anti-viral defence and inhibits damaging pro-inflammatory responses and is particularly useful in the prevention and/or treatment of virus induced ARDS, or viral-induced exacerbations and also virus induced bacterial superinfections in asthma and COPD patients or obese individuals.
It is now well established that the commensal microbiota is required for optimal host development and for ongoing immune homeostasis, which involves inter-dependent interactions between microbes and immunity. This requires discriminative responses to commensals in comparison to pathogens to ensure tolerance and protective immunity respectively. A characteristic feature of mucosal tolerance is the induction and expansion of Foxp3+ T regulatory cells which limit excessive pro-inflammatory responses. The 35624® strain has been shown to reduce pro-inflammatory responses to infection within the gastrointestinal tract in mice and protects against inflammatory diseases in humans via the induction of regulatory immune responses (O’Mahony L. et al. 2005; O′Mahony C. et al., 2008; Konieczna P. et al. 2012; Groeger D. et al., 2013).
We have now identified a novel cell wall fraction from B. longum 35624 strain which has potent anti-viral properties not associated with the strains EPS and with a different effect in human disease progression linked to suppression of viral replication and secondary pro-inflammatory responses.
Example 1: Cell Wall Pellet Generation Bacterial Harvesting/WashingMethod:
- 1. The equivalent of 250 ml of original bacterial biomass (total cell count=1.5 X 1011) is harvested by centrifugation (14000 rpm, 4° C., 20 min; rotor JA-20 (Avanti J-26 x P Beckman Coulter). The bacterial pellet is washed with sterile PBS and the supernatant is discarded and washed again (repeat two more times).
- 2. For viable and non-viable lyophilised bacteria (0.5 g of 3.0 X 1011 powder or total cell count=1.5 X 1011) was resuspended in 50 mls and harvested by centrifugation (14000 rpm, 4° C., 20 min; rotor JA-20 (Avanti J-26 x P Beckman Coulter). The bacterial pellet is washed with sterile PBS and the supernatant is discarded and washed again (repeat two more times).
- 3. Finally the pellet is resuspended in 50ml of sterile PBS and the bacterial solution divided into two 25 ml aliquots
The aim of this procedure was for the generation of a cell wall fraction from the whole bacteria and the elimination of the cytoplasmic fraction and other components. This involves one or more steps selected from:
- treatment with a chelating agent optionally in conjunction with freeze thaw procedure to prevent DNAse or protease activity when using enzymatic treatment to aid lysis.
- Enzymatic treatment with a glycoside hydrolase and/ or N-acetylmuramidase.
- Application of shear force such as ultra-sonication or application of high pressure such as using a French press.
- Separation of the cell wall fraction from the cytoplasmic fraction by using centrifugation
- Filtration of the cell wall fraction.
Materials:
- EDTA (0.5 M Fluka) is chelator for removal of metal ions (calcium or magnesium) to prevent DNAse or protease activity when using enzymes for cell wall lysis.
- Lysozyme (Sigma 10 mg/ml) *endotoxin free is a glycoside hydrolase that catalyses the hydrolysis of 1, 4-beta-linkages between N-acetylmuramic acid and N-acetyl-D-glucosamine residues. This hydrolysis compromises the integrity of bacterial cell walls causing lysis of the bacteria.
- Mutanolysin (10 KU Sigma diluted in 1 ml H2O) is an N-acetylmuramidase., which is an muralytic enzyme that cleaves the β-N-acetylmuramyl-(1→4)-N-acetylglucosamine linkage of the bacterial cell wall. This cleavage compromises the integrity of bacterial cell walls causing lysis of the bacteria.
- Glass beads 90-150 µM particle size (VWR) used in conjunction with sonication to aid lysis.
Method:
- 1. Add 250 µl EDTA (0.5 M stock Fluka) to each of the 25 ml aliquots therefore having a final concentration of 5 mM EDTA.
- 2. Freeze the aliquots by placing the 2 aliquots in liquid nitrogen till frozen then thaw the aliquots in water; repeat this procedure twice.
- 3. Each 25 ml of bacterial aliquot is incubated with 250 µl Lysozyme (10 mg/ml) and 250 µl Mutanolysin (2.5 KU) for 1 hour at 37° C. with an occasional mild vortex. From this step shear force is used either by a sonicator or a French press to disrupt the bacterial cell
- A half teaspoon of autoclaved glass beads 90-150 µM particle size (VMR) were added to the bacterial aliquots just before sonication.
- Sonicate 25 ml of resuspended bacterial material at a time, then put on ice and sonicate the other aliquot using the Sonicator (VibraCell SONICS) with the 50 ml probe. (Settings Tune =50, Frequency =60). This procedure is repeated four times for 10 minutes on ice.
- Following sonication, the glass beads, unbroken cells and cell debris are removed by centrifugation at 1000 rpm for 10 minutes at 4° C.
- Alternatively, the Bacterial cells are disrupted by pressure of 1500 psi on the high setting (20,000 psi equivalent) using a French press (Thermo Electron Corporation FA-078A). This procedure is repeated three times on ice.
- Application of a shear force using the French press results in a clearing of the turbid bacterial cells after the third run. Following French press disruption, the unbroken cells and cell debris are removed by centrifugation at 1000 rpm for 10 minutes at 4° C. and the supernatant containing the cell wall material and cytoplasmic fractions is retained.
- 4. Following application of a shear force (sonication or high pressure) a supernatant containing the cell wall material and cytoplasmic fractions was retained. This supernatant is centrifuged for 20 min at 14000 rpm at 4° C. to separate the cell wall material from the cytoplasmic material. The supernatant is discarded.
- 5. The pellet containing the cell wall material is re-suspended in 5 ml of PBS per 250 ml of original bacterial biomass. The pellet of cell wall material was centrifuged at 1000 rpm for 10 minutes to remove black residue in the pellet. The pellet containing the cell wall material was stored at -80° C.
- Avanti J-E Centrifuge Beckman Coulter
- Rotors: JA-20
- VibraCell SONICS, Sonics and Materials
- Probe 435-09
- French Press FA-078A
- Cell FA-032 (40 K Standard) (Standard FRENCH Pressure 40,000 psi Cell with 35ml capacity, pressure up to 40,000 psi)
Materials:
- Polyvinylidene difluoride (PVDF) membrane filters (0.45 µm pore size, Millipore, Bedford, MA)
- 100 kDa MWCO UF device (Millipore).
1. The resuspended bacterial Pellet containing cell wall material (5 ml) is thawed and filtered through polyvinylidene difluoride (PVDF) membrane filters (0.45 µm pore size, Millipore, Bedford, MA; rinsed thoroughly with PBS before use). The material that comes through the membrane filter is free of intact bacteria and is a cell wall material having a size of <0.45 µm. 4 ml of cell wall material is produced by this 0.45 µm filter step. From the original 250 mls of bacterial culture, 4 ml of the suspended cell wall material remains.
2. The <0.45 µm cell wall material is then ultrafiltered.
- a. Rinse UF device first with 15 ml PBS, spin at 3500 x g at 4° C.
- b. Take the <0.45 µm bacterial Pellet extracts, load ~4 ml into the 100 kDa MWCO UF device.
- c. When the >100 kDa upper solution gets lower in volume, diafilter with PBS.
- d. The material that comes thru the 100 kDa filter will be retained and stored at -80° C.
- e. The retentate should be resuspended in the same volume of PBS as was added to the ultrafiltration device (4 ml). This material is termed the >100 kDa bacterial Pellet. The final dry weight of the cell wall fraction thus produced is 120 mg in 4 mls of retentate which equates to a final concentration is 30 mg of cell wall fraction per 1 ml.
- f. This cell wall fraction was concentrated for in vitro and in vivo tests for more enhanced solubility. To make more concentrated material than 30 mg/ml such as 300 mg/ml (10X) or 150 mg/ml (5X) >100 kDa bacterial Pellet solutions the cell wall fraction is just resuspended in 10 times or 5 times less volume than the starting material.
The excessive immune response by monocytes and dendritic cells to viral infection causes pro-inflammatory responses in the lung. To determine if the cell wall fraction 30 mg/ml from 35624 as produced in Example 1, has a beneficial anti-viral effect, human CD14+ monocytes from peripheral blood, isolated cells were exposed to rhinovirus (RV) and the IP-10 response to RV was monitored. Peripheral blood mononuclear cells (PBMCs) were isolated from healthy donors using density gradient centrifugation. Peripheral blood mononuclear cells (PBMCs) were isolated from healthy donors using density gradient centrifugation. Human peripheral blood monocytes were isolated using CD14 positive isolation with the MACS system (Miltenyi Biotec, 130-050-201). Cells were cultured in cRPMI media (RPMI (Life Technologies, 21875-091) +10% fetal bovine serum (Sigma catalog F4135) and 1% penicillin/streptomycin (Sigma catalog P0781). Monocytes were stimulated with Human rhinovirus 16 (HRV16) (virapure) (multiplicity of infection (MOI) 25:1) for 6 h, 24 h and 48 h time points in cRPMI at 37° C., 5 % CO2 following pre-treatment with (1 h) with bacterial fractions or just HRV16 alone. Surprising, of the cytokines screened the IP-10 response to RV was attenuated by B. longum 35624 cell wall pellet fraction (
For monocyte-derived dendritic cells generation: Peripheral blood mononuclear cells (PBMCs) were isolated from healthy donors using density gradient centrifugation. Human peripheral blood monocytes were isolated using CD14 positive isolation with the MACS system (Miltenyi Biotec, 130-050-201). Cells were cultured in cRPMI media (Life Technologies, 21875-091) with interleukin 4 1000 U/ml (Novartis) and granulocyte macrophage colony stimulating factor (PeproTech, 300-03) 1000 U/ml for 6 days in order to differentiate them into monocyte-derived dendritic cells (MDDCs). MDDCs were pre-treated with cell wall fractions from B. longum 35624 before being exposed to (HRV16) and the IP-10 response to HRV16 was monitored. MDDCs were stimulated with HRV16 (MOI) 25:1) for 6 h, 24 h and 48 h time points in cRPMI at 37° C., 5 % CO2 following pre-treatment (1 h) with cell fractions from B. longum 35624 (30 mg/ml) or just HRV16 alone.
In agreement with the HRV16 stimulated monocytes results above of the 15 cytokines screened, the IP-10 (
MDDCs were stimulated with HRV16 (MOI) 25:1) for 24 h in cRPMI at 37° C., 5 % CO2 following pre-treatment (1 h) with different cell wall fractions (30 mg/ml) (Bif P) or just HRV16 alone. (Bif P, , , These cell wall fractions were heated to 80° C. (Bif P HT), or nuclease treated Bif P nuclease) or filtered through a 0.45 µm cut off Bif 0.45 µM or size exclusion filtered (Bif 0.45 µM HT, Bif 0.45 µM <3 kDa, Bif 0.45 µM 3-30 kDa, Bif 0.45 µM >100 kDa). The IP-10 suppression activity remained following heat treatment at 80° C., demonstrating that the activity was not DNA or RNA mediated (nuclease digestion did not alter the effect) and was associated with a >100 kDa fraction following filtration at 0.45 µm to remove all intact cells (
A particular class of DC’s, plasmacytoid dendritic cells (pDCs), are prominent cells of antiviral immunity in that they are the biggest producers of IFN-α and they exhibit pro-inflammatory or tolerogenic functions depending on the environment to which they are exposed. pDCs have recently been shown to be detrimental in asthma, particularly after viral infection (Chairakaki et al 2017). Human pDCs were isolated from peripheral blood and the IFN-α response to RV was monitored. Human Plasmacytoid Dendritic Cells (pDCs) were isolated using the Diamond Plasmacytoid Dendritic Cell Isolation Kit II (Miltenyi Biotec) and cultured with IL-3 100 ng/ml (PeproTech). pDCs were stimulated with HRV16 (MOI) 25:1) for 24 h in cRPMI at 37° C., 5 % CO2 following pre-treatment (1 h) with cell wall fractions from B. longum 35624 (75 mg/ml) or just HRV16 alone. IFN-α secretion was examined by Quantitine ELISA (R&D systems). Interestingly, the IFN-α response to RV was attenuated by the cell wall pellet fraction (
Cell wall fraction from another Bifidobacteria, Bifidobacteria breve (Bif UCC2003) was also tested using the methodology described in example 2 and did not show similar significant effects. The Bif UCC2003 fraction reduced IP-10 production following viral stimulation but not to the same extent as the B. longum 35624 cell wall fraction during a 24 hours assay (
Bronchial epithelial cells are one of the main cell types in which viral replication occurs. In these cells it is important to support anti-viral defence mechanisms as an early host defence against disease. It is important to limit immune cell over-activation to prevent tissue damage. We cultured human bronchial epithelial in air-liquid interface (ALI) cultures and examined the influence of the cell wall fraction from 35624 on viral replication and cytokine secretion.
Primary human bronchial epithelial cells (Lonza) were cultured as monolayers in Bronchial Epithelial Cell Growth Medium (BEGM (Lonza) containing Bronchial Epithelial Basal Medium plus all the bullet-kit singlequots at 37° C. in a humidified atmosphere at 5% CO2. Medium was changed every second day. Cells were seeded at a density of 75,000 cells in a 6.5-mm-diameter polyester membrane with a pore size of 0.4 mm (Corning Costar,) in BEGM medium. Once confluent, the medium in the apical compartment was removed and the medium in the basal compartment was substituted with ALI medium (Dulbecco modified Eagle medium [Gibco-BRL, Invitrogen] mixed 1:1 with BEGM supplemented with all-trans retinoic acid (ATRA) 50 nM to allow the cells to differentiate as air liquid interface (ALI) cultures.
ALI culture cells were exposed to cell wall fractions from B. longum 35624 30 mg/ml apically for 4 hours. The apical surface was washed twice with PBS all remaining liquid removed. The ALI culture cells were allowed to settle for 2 hours and then were stimulated with HRV16 (Virapur) (MOI 30:1) apically for 2 hours. The apical surface was washed twice with PBS all remaining liquid removed and left for 24 hours. Epithelial cell viral titer was quantified using a PCRmax qPCR kit for HRV16, according to manufacturer’s instructions. Supernatant IFN-λ1 and IP-10 levels were quantified using a Bio-Plex kit (Bio-Rad) as per the manufacturer’s instructions.
The cell wall fraction reduced viral replication in bronchial epithelial cells over a 48 hour period, while having a minimal impact on IP-10 chemokine secretion (
Once dendritic cells become activated, they induce T-cell activation and polarization. This activation can be beneficial or detrimental to the host depending on the type of signal that has been received from the dendritic cell. We co-incubated dendritic cells and autologous T cells following dendritic cell exposure to RV or exposure to RV with the cell wall pellet fraction from B. longum 35624. MDDCs were stimulated for 9 hours with HRV16 (MOI 25:1) and /or bacterial fractions and then washed and co-cultured with CD4+ or CD8 T cells from autologous donor at a ratio of 1:10 in AIM-V media (Life Technologies, 12055091). After 5 days cells were removed from culture from some of the wells and stained for CD4, CD25, Foxp3, T-bet and Ror-γt expression using flow cytometry (eBioscience, San Diego). Cytokine concentrations in the supernatant were measured using the BioPlex assay (Biororad). The cell wall pellet fraction did not alter the induction of CD25+Foxp3+ regulatory T cells as these cells are independently induced by the presence of the rhinovirus. The B. longum 35624 cell wall fraction (
In addition, the cell wall fraction supported T-bet+ TH1 lymphocyte development and IFN-γ secretion, and reduced GATA-3+ TH2 lymphocyte polarization. Th2 polarizing cytokines IL-4 and IL-5 were also decreased (
We tested the efficacy of the cell wall fraction in pre-clinical models. RV murine models are not considered to be good surrogates of human infection as mice do not have ICAM which is the receptor for major group rhinoviruses to enter the cell therefore we utilized a lethal influenza model in mice, which is considered a better model (Bartlett et al 2015). The H1N1 influenza strain A/PR8/34 (100 PFU/50 ul) was used to infect mice. The B. longum 35624 cell wall fraction (150 mg/ml) was administered intranasally at -2 hours, +1 day, +3 days and +5 days following viral infection (
-2 h, day 1, 3 and 5 Administration of vehicle control (Group 1) and B. longum 35624 cell wall fraction (Group 2) per nasal (in 50 µl volume).
Day 0 Administration of a dose of lethal influenza (PR8) per nasal (Group 1 - 3).
Day 0-10 Monitoring of animals for morbidity (weight, temperature and clinical score, Group 1 -2).
Day 3, 5 and 10: 5 animals per group are sacrificed for terminal bleed, organ removal and analysis on each day. Day 3 (Group 1 and 2), day 5 (Group 1-3) and day 10 (Group 1 and 2). Day 3, 5 and 10: Isolation of BAL fluid for the measurement of cytokines and markers of lung damage. Collection of the lung tissue for the quantification of viral titre in the lung by quantitative PCR (half of all lung lobes).
Measurement of Viral Titre in Lung TissueLung lobes isolated were prepared for the quantification of viral load in lung tissue by quantitative PCR. RNA was prepared with TRI Reagent (Molecular Research Center) and then treated with DNase (Invitrogen) to avoid genomic DNA contamination before RNA was converted to cDNA by reverse transcription using SuperScript III (Invitrogen). cDNA was quantified by real-time PCR (iCycler; Bio-Rad) using SYBR Green (Stratagene) and samples were normalized with GAPDH expression levels. Primers sequences (forward and reverse, respectively) used were influenza PR8 M protein, 5′- GGACTGCAGCGTAGACGCTT-3′ (SEQ ID No. 1) and 5′CATCCTGTATATGAGGCCCAT-3′ (SEQ ID No. 2).
Groups 3):
- 1. Treatment with vehicle control.
- 2. Treatment with B. longum 35624 cell wall fraction.
- 3. Untreated control Group (Influenza infection only).
- Number of mice per group (Group 1 and 2) = 15
- Number of mice per group (Group 3) = 5
This exact experiment was repeated with multiple doses of B. longum 35624 cell wall fraction Groups (1-7) for the dose response experiment:
- 1. Treatment with vehicle control.
- 2. Treatment with B. longum 35624 cell wall fraction (150 mg/ml).
- 3. Treatment with B. longum 35624 cell wall fraction (⅒ diluted).
- 4. Treatment with B. longum 35624 cell wall fraction (1/30 diluted
- 5. Treatment with B. longum 35624 cell wall fraction (1/1′00 diluted).
- 6. Treatment with B. longum 35624 cell wall fraction (⅒′00 diluted).
- 7. Untreated control Group (Influenza infection only).
Administration of the B. longum 35624 cell wall fraction protected the mice. Morbidity and Mortality due to influenza infection was reduced (
The concentrations of mouse IL-1β, IL-2, IL-4, IL-5, IL-6, IL-9, IL-10, IL-12p70, IL-12/IL-23p40, IL-13, IL-15, IL-16, IL-17A, IL-17A/F, IL-17C, IL-17E, IL-17F, IL-21, IL-22, IL-23, IL-30, IL-31, IL-33, IP-10, MIP3α, MIP-2, MIP-1β, MIP-1α, MCP-1, KC/GRO, TNF-α, VEGF, EPO, GM-CSF, IFN-γ in both serum and BAL fluid were measured using a commercial U-PLEX Biomarker Group 1 Mouse 35-Plex (MesoScale Discovery) platform following the manufacturers’ instructions; mouse IL-28 (IFN-λ ⅔), mouse G-CSF, mouse TRAIL, mouse AREG were detected using ELISA kits (RayBiotech, Inc,); Oncostatin M and mouse surfactant protein D (SPD) were measured using Quantikine kits from R&D Systems following the manufacturer’s instructions. Mouse IFN-α was measured in serum and BAL fluid by mouse IFN alpha platinum ELISA (ThermoFisher Scientific) Serum and BAL fluid levels of mouse interferon-β (IFN-β) were measured using VeriKine Mouse Interferon Beta HS ELISA Kits (PBL Assay Science).
The early immune response contributed to the enhanced viral clearance seen in the cell wall treated animals. By day 5 post-infection, this potent immune response was gone in the cell wall treated animals (
While current antiviral therapy is effective in preventing infection, no current therapy can prevent or treat influenza-induced pulmonary immune pathology (cell damage). We tested the efficacy of the cell wall fraction to influence two markers of lung epithelial cell damage (lactate dehydrogenase (LDH), albumin).
Lung Damage AssessmentVascular leakage in BAL fluid was assessed using a mouse albumin ELISA Quantitation Set (Bethyl Laboratories, Inc., Montgomery, TX). To measure lung injury, lactose dehydrogenase (LDH) activity was measured using the LDH assay (Sigma-Aldrich). This assay was performed in a 96-well plate for 30 min according to the manufacturer’s instructions and analysed using the MicroTek plate reader (Bio-Rad, Hercules, CA).
Mice which had been administered the cell wall fraction displayed significant reductions in markers for lung epithelial cell damage, but this was not shown in the vehicle control animals. (
We tested the efficacy of the cell wall fraction in pre-clinical superinfection models (
2 h, day 1, 3 and 5 Administration of vehicle control (Group 1) and B. longum 35624 cell wall fraction (150 mg/ml) (Group 2) per nasal (in 50 µl volume).
Day 0 Administration of a dose of lethal influenza (PR8) (100 PFU/50 µl) per nasal (Group 1 - 3).
Day 7 Administration of a dose of Streptococcus pneumonia D39 (105 CFU/50 µl) per nasal (Group 1 - 3).
Day 0-15 Monitoring of animals for morbidity (weight, temperature and clinical score, Group 1 -4).
Day 8: 5 animals per group are sacrificed for lung removal. Collection of the lung tissue for the quantification of Streptococcus pneumonia counts
- Groups 1 - Vehicle + Influenza +Streptococcus pneumonia
- Groups 2 - B. longum 35624 cell wall fraction + Influenza +Streptococcus pneumonia
- Group 3 - Influenza + Streptococcus pneumonia (no treatment)
- Group 4 - Vehicle + Streptococcus pneumonia (No Influenza
The H1N1 influenza PR8 strain was used to infect mice followed by a secondary bacterial infection with Streptococcus pneumonia D39 at day 8. The B. longum 35624 cell wall fraction was administered intranasally at -2 hours, +1 day, +3 days and +5 days following viral infection. Again, administration of the cell wall fraction from the 35624 strain protected the mice.
Measurement of Bacteria Colonization in Lung TissueLung tissues were harvested, homogenized in 2 ml saline (gentle medimachine homogenization) and 25 ul of serial dilutions (10e-2, 10e-3, 10e-4 and 10e-5 dilutions) were plated on TSA plate (Tryptic soy agar, aseptic plates, BD-Brunschwig Tryptic soy agar, aseptic plates. Chemie Brunschwig AG, Basel, Switzerland. Catalogue number 254051). Following overnight incubation colonies were counted on plates with separate colonies detectable and CFU per ml solution were calculated.
Lung counts of Streptococcus pneumonia were reduced to the same levels as mice which who were not infected with influenza (
Groups 4):
- 1. Treatment with vehicle control. Administration at -2 hr, day 1, day 3).
- 2. Treatment with B. longum 35624 cell wall fraction (150 mg/ml) Administration at -2 hr, day 1, day 3).
- 3. Treatment with B. longum 35624 cell wall fraction (150 mg/ml) Administration on day 1, day 3.
- 4. Untreated control Group (Influenza infection only).
We tested the efficacy of the cell wall fraction therapeutically in the H1N1 influenza PR8 strain infection model. The B. longum 35624 cell wall fraction was administered intranasal, +1 day, +3 days following viral infection (
In summary, as illustrated in examples 2-8, we have shown that in cells that first experience viral infection (bronchial epithelia), where an enhanced Type III interferon response to stop viral replication is beneficial, addition of the cell wall fraction from 35624 causes this desired response. In other cells that are part of the later host immune system response (monocytes, DC’s) the cell wall fraction blocks the excessive Type 1 interferon response that can lead to cell damage and secondary infection. This targeted effect has benefit in infections caused by influenza, the common cold (rhino virus) and RSV, viral exacerbation of chronic respiratory diseases such as asthma, COPD and ARDs in both children and adults and in obese individuals.
Cascade ResponseThe cascade of abnormal response to viral infection is illustrated in
The cascade of cell wall fraction mediated response to viral infection is illustrated in
The main antiviral response is controlled by IFNs. The most well-defined type I IFNs are IFN-α and IFN-β. Most cell types produce IFN-β, whereas haematopoietic cells, particularly plasmacytoid dendritic cells, are the predominant producers of IFN-α (Ivashkiv and Donlin 2014). As mentioned previously, the Interferon type I responses, such as IFN-α and IFN-β has been shown to directly correlate with increased morbidity and mortality in models of influenza infection (Davidson et al, 2014). Type 1 IFNs can stimulate the production of IP-10 (also called CXCL-10) a chemokine which binds to CXCR3 where its primary function is a chemoattractant for Th1 cells. Lambda IFNs (IFNls, type III IFNs or IL-28 and IL-29) constitute a newer class of interferons that share homology, expression patterns, and antiviral functions with type I IFNs (Lazear et al., 2015b; Wack et al., 2015). They induce downstream signalling that appears remarkably similar to that of type I IFNs, driving the expression of ISGs and the induction of antiviral responses (Durbin et al, 2013; Mendoza et al, 2017). However, type III interferons play an important role in limiting pro-inflammatory responses or immunopathology.
IP-10 is elevated in the lungs on infection with influenzas virus (Ichikawa et al, 2013). Indeed, blocking IP-10 using monoclonal antibodies ameliorates virus induced lung injury (Wang et al, 2013). IP-10 is elevated in the lungs of ARDS patients and it has been shown to be an important factor in the ARDS pathology (Ichikawa et al, 2013).
SP-D has an important role in innate host defence against influenza by binding to mannose-rich glycans on the HA/NA glycoproteins of the virus (Hartshorn et al, 1997; Reading et al, 1997; Hartshorn et al, 2000). SP-D mediates a range of antiviral activities in vitro, including neutralization of virus infectivity and inhibition of the enzymatic activity of the viral NA, and SP-D-deficient mice were more susceptible to infection with highly glycosylated influenza viruses. (Hartshorn et al, 1997; Reading et al, 1997; Tecle et al, 2007; LeVine et al, 2001; Vigerust et al, 2007; Hawgood et al, 2004). SP-D enhances phagocytosis and pulmonary clearance of RSV (LeVine et al, 2004).
Secondary bacterial infections are a major issue following viral infection. Virus-bacterial co-infection is well recognized with influenza, rhinovirus and RSV. The major bacterial infections in the respiratory tract include Streptococcus pneumoniae, Moraxella catarrhalis, and Haemophilus influenzae but Staphylococcus aureus has been also shown to cause serious infections post viral infection (Hewitt et al, 2016). Secondary bacterial infections occur most frequently at 5-10 days after primary viral infections, thus suggesting that a transient immunosuppression (the primary response) maybe responsible for the bacterial outgrowth. A mechanism proposed for a synergism between influenza and S. pneumoniae suggests that the antiviral type 1 IFN (IFN-α/β) response elicited by the primary influenza virus infection enhances the susceptibility of the host to secondary bacterial challenge via suppression of antibacterial immunity (Nakamura et al, 2011; Shahangian et al, 2009; Li et al, 2012). In contrast type III interferons such as IFN-λ can limit viral replication without inhibiting the clearance of the secondary bacterial infections which happens after IFN-a/β induction. It has been shown that the impact of attenuating IFN-λ signalling directly before bacterial challenge with an IFNLR1 Fc protein significantly increased bacterial burden in the lung compared with controls in animals (Rich et al, 2017). Furthermore, deficiency of SP-D was associated with enhanced colonisation and infection with S. pneumoniae of the upper and lower respiratory tract and earlier onset and longer persistence of bacteraemia. SP-D was shown to binds and agglutinates Streptococcus pneumoniae in vitro (a secondary bacterial infection agent that is a key problem in secondary exacerbations in asthma and COPD patients) (Jounblat et al, 2005).
The different conditions that are acutely affected by the dysregulated or aberrant immune response to viral infection are summarized as follows; Acute respiratory distress syndrome (ARDS), Asthma including childhood asthma, COPD, Obesity.
Acute respiratory distress syndrome (ARDS) affects a large number of people worldwide and is associated with a very high mortality rate (30-50%). Respiratory viral infections (e.g. influenza) are associated with ARDS.
Asthma is a chronic inflammatory disorder of the airways, usually associated with airway hyper-responsiveness and variable airflow.
Asthma is a chronic inflammatory disorder of the airways, usually associated with airway hyper-responsiveness and variable airflow obstruction that is often reversible spontaneously or during treatment (WHO, 2007). Approximately 80 to 85 % of asthma exacerbations in children, adolescents, and less frequently adults are associated with viral upper respiratory tract viral infections, and rhinovirus (RV) accounts for ~60-70 % of these virus-associated exacerbations. Viral infections are closely linked to wheezing illnesses in children of all ages. RSV is the main causative agent of bronchiolitis or croup, whereas rhinovirus (RV) is most commonly detected in wheezing children thereafter. Severe respiratory illness induced by either of these viruses is associated with subsequent development of asthma, and the risk is greatest for young children who wheeze with RV infections (Jartti and Gern, 2017).
Obesity is associated with dysregulated immune and inflammatory responses. The effect of obesity on the occurrence of asthma seems to be more prominent in women and non-allergic individuals, while there is a dose response effect of increasing body mass index (BMI) on asthma incidence. It is becoming increasingly evident that obesity is associated with a unique asthma phenotype that is characterized by more severe disease with variable response to conventional asthma therapies. In addition, obesity was identified as a risk factor for severe influenza during the 2009 influenza A(H1N1) pandemic and obese individuals have an impaired antiviral defence against respiratory viruses (Almond et al, 2013). Evidence suggests that it is not the virus itself but the nature of the immune response to RV that drives this damaging response (Steinke et al, 2016).
COPD is the third leading cause of death in the USA. In fact, COPD is the only major cause of death whose incidence is on the increase and is expected to be the third leading cause of death in the developed world by 2030 (exceeded only by heart disease and stroke). It results from inflammation induced damage of the airways causing chronic bronchitis and/or emphysema. A wider spectrum of viruses can induce exacerbations in COPD patients, but again it seems that it is not the virus, but the immune response to the virus that results in worsening of symptoms (Zhou et al, 2015).
Bifidobacterium longum 35624 ( B. longum 35624) has been shown to reduce pro-inflammatory responses to infection within the gastrointestinal tract (O’Mahony C, et al., PLoS Pathogens 2008). It does not automatically follow that the whole strain would have beneficial effects in other human systems. Therefore, in addition to the cell wall fraction, the ability of the whole bacterial strain to modify the immune response to virus infection in vitro in human dendritic cells and bronchial epithelial cells has now been investigated, with surprising results.
Example 9Dendritic cells (DCs) were generated following isolation of human CD14+ monocytes from peripheral blood and culture in GM-CSF and IL-4 for 5 days. DCs were exposed to rhinovirus (RV) and the IP-10 response to RV was monitored. Surprisingly, the IP-10 response to RV was attenuated by B. longum 35624 in a dose-dependent manner (
Not every bacterial strain has this effect. Co-incubation with a Staphylococcus aureus strain did not reduce DC IP-10 secretion in response to HRV (
Bifidobacterium longum strain NCIMB 42020 was isolated from faecal samples from healthy human subjects.
Faecal samples were screened for probiotic bacterial strains. Samples were transferred to a collection tube containing Phosphate Buffered Saline (PBS), supplemented with 0.05% cysteine-HCl). The solutions were then incubated for 10 min. The samples were vortexed and plated on selective agar (De Man, Rogosa and Sharpe (MRS) agar + 10% sucrose + Mupirocin and Congo red + cysteine + Mupirocin). A Congo red agar screen was used to phenotypically screen for EPS expressing bacterial strains. Briefly, 10 ml Modified Rogosa broth media (+ 0.05% cysteine) was inoculated aseptically with a freshly grown colony of the bacterial strain and incubated anaerobically at 37° C. until turbid (about 16 to about 24 hours). The broth cultures were aseptically streaked onto Congo Red Agar plates and incubated anaerobically at 37° C. for 48 hours. It is believed that EPS produced as a by-product of the growth and/or metabolism of certain strains prevents the uptake of the Congo red stain resulting in a cream/white colony morphology. Stains that produce less EPS take up the Congo red stain easily, resulting in a pink/red colony morphology. Strains that do not produce an EPS stain red and look almost transparent in the red agar background.
Isolated colonies were picked from the plates and re-streaked three times to ensure purity. Microscope examination, Gram staining, Catalase testing, Fructose-6-Phosphate Phosphoketolase assessment were used to determine presumptive Bifidobacteria species and isolates were stocked in 40% glycerol and stored at -80° C. 16S intergenic spacer region sequencing (IGS) were used to confirm the identity of the newly isolated strains.
Following isolation of a pure bifidobacteria strain, assigned the designation AH0106, it was subsequently deposited at the NCIMB and given the designation 42020. Microbiological characteristics were assessed and are summarized in Table 1 below. B. longum NCIMB 42020 is a gram positive, catalase negative pleomorphic shaped bacterium which is Fructose-6-Phoshate Phosphoketolase positive, confirming its identity as a bifidobacterium.
16 s-23 s intergenic spacer (IGS) sequencing was performed to identify the species of Bifidobacteria isolated. Briefly, DNA was isolated from NCIMB 42020 using 100 µl of extraction Solution and 25 µl of Tissue Preparation solution (Sigma, XNAT2 Kit). The samples were incubated for 2 hours at room temperature followed by 2 hrs at 95° C. and then 100 µl of Neutralization Solution (Sigma, XNAT2 kit) was added. Genomic DNA solution was quantified using a Nanodrop spectrophotometer and stored at 4° C. PCR was performed using the IGS primers. The primer pairs used were IGS R 5′-CTGGTGCCAAGGCATCCA-3′ (SEQ ID No. 3) and IGS L 5′-GCTGGATCACCTCCTTTCT-3′ (SEQ ID No. 4). The cycling conditions were 94° C. for 4 min (1 cycle), 94° C. for 45 sec, 53° C. for 45 sec, 72° C. for 45 sec (28 cycles). The PCR reaction contained 2 µl (100 ng) of DNA, PCR mix (Sigma, Red Taq), 0.025 nM IGS L and R primer (MWG Biotech, Germany). The PCR reactions were performed on a Biotherma thermocycler. The PCR products (10µl) were ran alongside a molecular weight marker (100 bp Ladder, Roche) on a 2 % agarose EtBr stained gel in TAE, to determine the IGS profile. PCR products of Bifidobacterium (single band) were purified using the Promega Wizard PCR purification kit. The purified PCR products were sequenced using the primer sequences (above) for the intergenic spacer region. Sequence data was then searched against the NCBI nucleotide database to determine the identity of the strain by nucleotide homology. The resultant DNA sequence data was subjected to the NCBI standard nucleotide-to-nucleotide homology BLAST search engine (http://www.ncbi.nlm.nih.gov/BLAST/). The nearest match to the sequence was identified and then the sequences were aligned for comparison using DNASTAR MegAlign software. The sequences can be viewed in the sequence listing (Table 2). Searching the NCIMB database revealed that NCIMB 42020 has a unique IGS (Table 2) sequence with its closest sequence homology to a Bifidobacterium longum.
Table 2 IGS Sequence B. Longum NCIMB 42020 (SEQ ID No. 5)
Peripheral blood mononuclear cells (PBMCs) were isolated from healthy donors using density gradient centrifugation. PBMCs were washed and resuspended in Dulbecco’s Modified Eagle Medium- Glutamax (DMEM) TM (Glutamax (Glutamine substitute) + pyruvate + 4.5 g/l glucose (Gibco catalog 10569-010) 10% fetal bovine serum (Sigma catalog F4135), and 1% penicillin/streptomycin (Sigma catalog P0781). PBMCs were stimulated with different doses of Bifidobacteria longum (Total bacteria:PBMC) high (100:1) and mid (50:1)) for 24 h in supplemented DMEM at 37° C., 5 % CO2.
For monocyte-derived dendritic cells generation: Peripheral blood mononuclear cells (PBMCs) were isolated from healthy donors using density gradient centrifugation. Human peripheral blood monocytes were isolated using CD14 positive isolation with the MACS system (Miltenyi Biotec, 130-050-201). Cells were cultured in cRPMI media (Life Technologies, 21875-091) with interleukin 4 1000 U/ml (Novartis) and granulocyte macrophage colony stimulating factor (PeproTech, 300-03) 1000U/ml for 6 days in order to differentiate them into monocyte-derived dendritic cells (MDDCs). MDDCs were stimulated with different doses of B. longum ((Total bacteria:MDDC) high (100:1) and mid (50:1)) for 24 h in cRPMI at 37° C., 5 % CO2. Cytokine secretion was measured using a commercial cytokine kits (MesoScale Discovery) platform following the manufacturers’ instructions.
AH0106 induced more IL-10, IL-12p40, TNF-α, IL-1β in both PBMCs and MDDCs than all of the other bacterial strains (35624, AH1206, AH1362, 1714, BL1207) which gave similar profiles to each other (
The excessive immune response by dendritic cells to viral infection causes pro-inflammatory responses in the lung. Type 1 IFNs can stimulate the production of IP-10 a chemokine which binds is a chemoattractant for Th1 cells. To determine if a B. longum AH0106 might have a beneficial anti-viral effect, on human monocyte-derived dendritic cells, MDDCs were stimulated with B. longum AH0106 before being exposed to Human rhinovirus 16 (HRV16) and the interferons and IP-10 response to HRV16 was monitored. MDDCs were stimulated with HRV16 (MOI) 25:1) for 24 h in cRPMI at 37° C., 5 % CO2 following pre-treatment (1 h) with multiple doses of B. longum AH0106 (100:1, 50:1, 25:1, 10:1, 1:1) or just HRV16 alone. Cytokine secretion was examined by Bio-Plex multiplex suspension array (Bio-Rad Laboratories) measuring IFN-α, IFN-β, IFN-λ, and IP-10. Surprisingly, the IP-10 response to RV was attenuated by B. longum AH0106 strain in a dose-dependent manner (
To determine if another gram positive bacterial strain might have a beneficial anti-viral effect, on human monocyte-derived dendritic cells, MDDCs stimulated with Staphylococcus aureus were exposed to human rhinovirus 16 (HRV16) and the IP-10 response monitored. Briefly, MDDCs were stimulated with HRV16 (MOI) 25:1) for 24 h in cRPMI at 37° C., 5 % CO2 following pre-treatment (1 h) with multiple doses of Staphylococcus aureus (100:1, 50:1) compared to B. longum AH0106 (100:1) or just HRV16 alone. The Staphylococcus aureus strain did not reduce DC IP-10 secretion in response to HRV16 (
Within the inflamed mucosa, it is not just the virus itself that induces IP-10 and TNF-α secretion, but also other (toll like receptor) TLR ligands can induce its production. Therefore, MDDCs were pretreated with B. longum AH0106 or B. longum 35624 before being exposed to LPS. The IP-10 and TNF- response to LPS a TLR-4 agonist was monitored. Briefly, MDDCs were stimulated with LPS (50 ng/ml) for 24 h in cRPMI at 37° C., 5 % CO2 following pre-treatment (1h) with B. longum AH0106 or 35624 at a dose of (100:1) or just LPS alone. Surprisingly, the IP-10 and TNF-α response to LPS was attenuated by B. longum AH106 whereas there was only a slight reduction in IP-10 response to LPS after exposure to B. longum 35624 (
We tested the efficacy of B. longum AH0106 strain in pre-clinical models designed to show therapeutic benefit. Rhinovirus murine models are not considered to be good surrogates of human infection as mice do not have ICAM, the receptor for major group rhinoviruses to enter the cell. Therefore, we utilized a lethal influenza model in mice, which is considered a better model (Bartlett et al, 2015). The H1N1 influenza strain A/PR8/34 (100 PFU/50 ul) strain was used to infect mice.
The B. longum AH0106 strain, B. longum 35624 strain or placebo was administered intranasally at -2 hours, +1 day, and +3 days following viral infection (
2h, day 1, and 3 administration of vehicle control (Group 1), B. longum AH0106 (Group 2 and B. longum 35624 cell wall fraction (Group 3) per nasal (in 50 µl volume).
Day 0 Administration of a dose of lethal influenza (PR8) per nasal (Group 1 - 3).
Day 0-10 Monitoring of animals for morbidity (weight, temperature and clinical score, Group 1 -3).
Day 5: 5 animals per group are sacrificed for terminal bleed, organ removal and analysis on each day. Day 5 (Group 1-3).
Day 5: Isolation of BAL fluid for the measurement of cytokines and cell infiltrates. Collection of the lung tissue for the quantification of viral titre in the lung by quantitative PCR (half of all lung lobes).
Measurement of Viral Titre in Lung TissueLung lobes isolated were prepared for the quantification of viral load in lung tissue by quantitative PCR. RNA was prepared with TRI Reagent (Molecular Research Center) and then treated with DNase (Invitrogen) to avoid genomic DNA contamination before RNA was converted to cDNA by reverse transcription using SuperScript III (Invitrogen). cDNA was quantified by real-time PCR (iCycler; Bio-Rad) using SYBR Green (Stratagene) and samples were normalized with GAPDH expression levels. Primers sequences (forward and reverse, respectively) used were influenza PR8 M protein, 5′-GGACTGCAGCGTAGACGCTT-3′ (SEQ ID No. 1) and 5′CATCCTGTATATGAGGCCCAT-3′ (SEQ ID No. 2).
Groups 3):
- 1. Treatment with Placebo - cryoprotectant resuspended in PBS.
- 2. Treatment with B. longum AH0106 10^9 total cells.
- 3. Treatment with B. longum 35624 10^9 total cells
- Number of mice per group (Group 1 -3) = 5
- Measurements of Cytokines and Chemokine.
The concentrations of mouse IL-1β, IL-2, IL-4, IL-5, IL-6, IL-9, IL-10, IL-12p70, IL-12/IL-23p40, IL-13, IL-15, IL-16, IL-17A, IL-17A/F, IL-17C, IL-17E, IL-17F, IL-21, IL-22, IL-23, IL-30, IL-31, IL-33, IP-10, MIP3α, MIP-2, MIP-1β, MIP-1α, MCP-1, KC/GRO, TNF-α, VEGF, EPO, GM-CSF, IFN-γ in both serum and BAL fluid were measured using a commercial U-PLEX Biomarker Group 1 Mouse 35-Plex (MesoScale Discovery) platform following the manufacturers’ instructions; mouse IL-28 (IFN-λ ⅔), mouse G-CSF, mouse TRAIL, mouse AREG were detected using ELISA kits (RayBiotech, Inc,); Oncostatin M and mouse surfactant protein D (SPD) were measured using Quantikine kits from R&D Systems following the manufacturer’s instructions. Mouse IFN-α was measured in serum and BAL fluid by mouse IFN alpha platinum ELISA (ThermoFisher scientific) Serum and BAL fluid levels of mouse interferon-β (IFN-β) were measured using VeriKine Mouse Interferon Beta HS ELISA Kits (PBL Assay Science).
Measurement of Cellular Infiltrates Into BALCells were isolated from the BAL fluid and total cell numbers in the bronchoalveolar lavage (BAL) fluid was determined using a Coulter Counter (IG Instrumenten-Gesellschaft AG, Basel, Switzerland). Differential cell counts were performed (200 cell counts/ samples) based upon standard morphological and cytochemical criteria on cytospins stained with Diff-Quik solution (Dade Behring, Siemens Healthcare Diagnostics, Deerfield, IL).
Surprisingly, administration of the B. longum AH0106 protected the mice better than the B. longum 35624 strain. Viral titre was reduced by similar levels in both strains (
Following the procedures outlined in Example 1, pellets of cell wall fraction from strain AH0106 was isolated.
The cell wall fraction (<0.45 µm, >100 kDa) was concentrated for in vitro and in vivo tests for more enhanced solubility. To make more concentrated material than 30 mg/ml such as 300 mg/ml (10X) or 150 mg/ml (5X) >100 kDa bacterial Pellet solutions the cell wall fraction is just resuspended in 10 times or 5 times less volume than the starting material.
Example 17: The Cell Wall Fraction From the AH0106 (Beneficially Blocks Type 1 Interferons And Resultant IP-10 Induction (a Pro-Inflammatory Chemokine) in MDDCSTo determine if a cell wall fraction from B. longum AH0106, as produced in example 16, might have a beneficial anti-viral effect the fraction was incubated on human MDDC’s exposed to HRV16 and type 1 interferon and the cell IP-10 response was monitored. For monocyte-derived dendritic cells generation: Peripheral blood mononuclear cells (PBMCs) were isolated from healthy donors using density gradient centrifugation. Human peripheral blood monocytes were isolated using CD14 positive isolation with the MACS system (Miltenyi Biotec, 130-050-201). Cells were cultured in cRPMI media (Life Technologies, 21875-091) with interleukin 4 1000 U/ml (Novartis) and granulocyte macrophage colony stimulating factor (PeproTech, 300-03) 1000 U/ml for 6 days to differentiate them into MDDCs. Cells were cultured in cRPMI media (RPMI (Life Technologies, 21875-091) +10% fetal bovine serum (Sigma catalog F4135) and 1% penicillin/streptomycin (Sigma catalog P0781).
MDDCs were stimulated with HRV16 (MOI) 25:1) for 24 h in cRPMI at 37° C., 5 % CO2 following pre-treatment (1 h) with a cell wall fraction from B. longum AH0106 (30 mg/ml) or just HRV16 alone. Cytokine secretion was examined by Bio-Plex multiplex suspension array (Bio-Rad Laboratories) (IFN-α, IFN-β, IP-10).
In agreement with the HRV16 stimulated MDDC pretreated with the B. longum AH0106 strain results above, the IP-10 (
Cell wall fraction from another Bifidobacteria, Bifidobacteria breve (Bif UCC2003) was also tested using the methodology described in example 4 and did not show similar significant effects. The Bif UCC2003 fraction reduced IP-10 production following viral stimulation but not to the same extent as the B. longum\ AH0106 cell wall fraction during a 24 hours assay (
Additionally, within the inflamed mucosa, it is not just the virus itself that induces IP-10 secretion; other cytokines can also induce IP-10 production. Cytokines such as IFN-β are produced as part of the primary anti-viral host response. IFN-β in particular is a potent inducer of IP-10. Therefore, we examined the effect of the cell wall fraction on secretion of IP-10 in response to IFN-β (
Within the inflamed mucosa, it is not just the virus itself that induces pro-inflammatory TNF-α secretion, but also other (toll like receptor) TLR ligands can induce its production. Therefore we examined the secretion of TNF-α in response to the TLR ligands Poly:IC (TLR-3) and LPS (TLR-4). MDDCs were pretreated with cells wall B. longum AH0106, B. longum 35624 and Bif UCC2003 before being exposed to LPS, a TLR-4 agonist, and the IP-10 and TNF- response to was monitored. MDDCs were stimulated with either the TLR-4 agonist LPS (50 ng/ml) or the TLR-3 agonist Poly:IC (5 µg/ml) for 24 h in cRPMI at 37° C., 5 % CO2 following pre-treatment (1 h) with cell wall fractions from Bifidobacteria at a dose of (30 mg/ml) or just the TLR agonist alone. TNF-α secretion was examined by Quantikine ELISA (R &D systems). In agreement with the results from the whole B. longum AH0106 strain the TNF-α response to LPS and Poly:IC was attenuated by the cell wall fraction from B. longum AH106 whereas both the cell wall fractions from B. longum 35624 and Bif UCC2003 increases TNF-α at the same dose (
In summary, as illustrated in examples 9 to 19, we have shown there is an enhanced Type III interferon response which beneficial, and addition of the cell wall fraction from AH0106 causes this desired response. In cells that are part of the later host immune system response (DC’s) the cell wall fraction blocks the excessive Type 1 interferon response that can lead to cell damage and secondary infection. This targeted effect has benefit in infections caused by influenza, the common cold (rhino virus) and RSV, viral exacerbation of chronic respiratory diseases such as asthma, COPD and ARDs in both children and adults and in obese individuals.
Example 20: Isolation and Characterisation of Bacteria Isolated From Adult Faeces Isolation of Probiotic BacteriaFresh faeces was obtained from healthy adults and serial dilutions were plated on TPY (trypticase, peptone and yeast extract) and MRS (deMann, Rogosa and Sharpe) media supplemented with 0.05% cysteine and mupirocin. Plates were incubated in anaerobic jars (BBL, Oxoid) using CO2 generating kits (Anaerocult A, Merck) for 2-5 days at 37° C. Gram positive, catalase negative rod-shaped or bifurcated/pleomorphic bacteria isolates were streaked for purity on to complex non-selective media (MRS and TPY). Isolates were routinely cultivated in MRS or TPY medium unless otherwise stated at 37° C. under anaerobic conditions. Presumptive Bifidobacterium were stocked in 40% glycerol and stored at -20° C. and -80° C.
Following isolation of the pure bifidobacteria strain, assigned the designation AH0103, it was subsequently deposited at the NCIMB and given the designation 41713. Microbiological characteristics were assessed and are summarized in Table 1 below. B. longum NCIMB 41713 is a gram positive, catalase negative pleomorphic shaped bacterium which is Fructose-6-Phoshate Phosphoketolase positive confirming its identity as a bifidobacterium.
16 s intergenic spacer (IGS) sequencing was performed to identify the species of bifidobacteria isolated. Briefly, DNA was isolated from AH0103 using 100 µl of Extraction Solution and 25 µl of Tissue Preparation solution (Sigma, XNAT2 Kit). The samples were incubated for 5 minutes at 95° of Neutralization Solution (XNAT2 kit) was added. Genomic DNA solution was quantified using a Nanodrop spectrophotometer and stored at 4° C. PCR was performed using the IGS primers, IGS L: 5′-GCTGGATCACCTCCTTTCT-3′ (SEQ ID No. 4) and IGS R: 5′-CTGGTGCCAAGGCATCCA-3′ (SEQ ID No. 3). The cycling conditions were 94° C. for 3 min (1 cycle), 94° C. for 30 sec, 53° C. for 30 sec, 72° C. for 30 sec (28 cycles). The PCR reaction contained 4 µl (50 ng) of DNA, PCR mix (XNAT2 kit), 0.4 µM IGS L and R primer (MWG Biotech, Germany). The PCR reactions were performed on an Eppendorf thermocycler. The PCR products (10 µl) were ran alongside a molecular weight marker (100 bp Ladder, Roche) on a 2 % agarose EtBr stained gel in TAE, to determine the IGS profile. PCR products of Bifidobacterium (single band) were purified using the Promega Wizard PCR purification kit. The purified PCR products were sequenced using the primer sequences (above) for the intergenic spacer region. Sequence data was then searched against the NCBI nucleotide database to determine the identity of the strain by nucleotide homology. The resultant DNA sequence data was subjected to the NCBI standard nucleotide-to-nucleotide homology BLAST search engine (http://www.ncbi.nlm.nih.gov/BLAST/). The nearest match to the sequence was identified and then the sequences were aligned for comparison using DNASTAR MegAlign software. Searching the NCIMB database revealed that NCIMB 41713 has a unique IGS (SEQ ID No. 6) with its closest sequence homology to a Bifidobacterium longum.
The IGS sequence identified by the BLAST search engine is:
The cell wall fraction (<0.45 µm, >100 kDa) was concentrated for in vitro and in vivo tests for more enhanced solubility. To make more concentrated material than 30 mg/ml such as 300 mg/ml (10X) or 150 mg/ml (5X) >100 kDa bacterial Pellet solutions the cell wall fraction is just resuspended in 10 times or 5 times less volume than the starting material.
Example 22 The Cell Wall Fraction From the NCIMB Strain 41713 (AH0103) (Beneficially Blocks Type 1 Interferons and Resultant IP-10 Induction (a Pro-Inflammatory Chemokine) in Dendritic CellsTo determine if a cell wall fraction from B. longum AH0103, as produced in example 20, might have a beneficial anti-viral effect the fraction was incubated on human DC’s exposed to HRV16 Cytokine secretion was examined by Bio-Plex multiplex suspension array (Bio-Rad Laboratories). First IP-10 was assessed and then subsequently a range of cytokines were assessed (IFN-α, IFN-β, IP-10).
In agreement with the HRV16 stimulated MDDC pretreated with the B. longum AH0106 strain results above, the IP-10 response to HRV16 was attenuated by a cell wall fraction from the B. longum AH0103 strain (
In agreement with the HRV16 stimulated MDDC pretreated with the B. longum AH0106 strain results above, the IFN-α, IFN-β, and IP-10response to HRV16 was attenuated by a cell wall fraction from the B. longum AH0103 strain. (
B. longum NCIMB 41713 promotes anti-viral defence and inhibits damaging pro-inflammatory responses and is useful in the prevention and/or treatment of virus induced ARDS, or viral-induced exacerbations in asthma and COPD patients.
Dendritic cells (DCs) are generated following isolation of human CD14+ monocytes from peripheral blood and culture in GM-CSF and IL-4 for 6 days. DCs are exposed to rhinovirus (HRV 16) and the IP-10 response to RV is monitored. However, the activity was reduced following filtration at 0.45 µM to remove all intact cells (
Within the inflamed mucosa, it is not just the virus itself that induces IP-10 secretion, but also other cytokines can induce its production. Therefore, we examined the secretion of IP-10 in response to interferon-beta, interferon-gamma, and interferon-lambda (
A final B. longum strain NCMIB 41715 (AH1362) was also tested to determine if this type of response was also present
Example 24: Cell Wall Pellet GenerationThe cell wall fraction (<0.45 µm, >100 kDa) was concentrated for in vitro and in vivo tests for more enhanced solubility. To make more concentrated material than 30 mg/ml such as 300 mg/ml (10X) or 150 mg/ml (5X) >100 kDa bacterial Pellet solutions the cell wall fraction is just resuspended in 10 times or 5 times less volume than the starting material.
In this case the Bacterial cells were disrupted by pressure of 1500 psi on the high setting (20,000 psi equivalent) using a French press (Thermo Electron Corporation FA-078A). This procedure is repeated three times on ice.
Example 25B. longum NCIMB 41715 promotes anti-viral defence and inhibits damaging pro-inflammatory responses and is useful in the prevention and/or treatment of virus induced ARDS, or viral-induced exacerbations in asthma and COPD patients.
Dendritic cells (DCs) are generated following isolation of human CD14+ monocytes from peripheral blood and culture in GM-CSF and IL-4 for 6 days. DCs are exposed to rhinovirus (RV) and the IP-10 response to RV is monitored. The IP-10 response to RV is attenuated by B. longum NCIMB 41715 cell wall pellet fraction (
To determine if a cell wall fraction from B. longum AH1362, as produced in example 20, might have a beneficial anti-viral effect the fraction was incubated on human DC’s exposed to HRV16 Cytokine secretion was examined by Bio-Plex multiplex suspension array (Bio-Rad Laboratories). First IP-10 was assessed and then subsequently a range of cytokines were assessed (IFN-α, IFN-β, IP-10).
In agreement with the HRV16 stimulated MDDC’s pre-treated with the B. longum AH0106 or the AH103 strain results above the IFN-α, IFN-β, and IP-10 response to HRV16 was attenuated by a cell wall fraction from the B. longum AH1362 strain. (
In agreement with the HRV16 stimulated MDDC pretreated with the other B. longum strain results above, the IFN-α, IFN-β, and IP-10 response to HRV16 was attenuated by a cell wall fraction from the B. longum AH1362 strain. (
It will be appreciated that the strains of the invention may be administered to animals (including humans) in an orally ingestible form in a conventional preparation such as capsules, microcapsules, tablets, granules, powder, troches, pills, suppositories, suspensions and syrups. Suitable formulations may be prepared by methods commonly employed using conventional organic and inorganic additives. The amount of active ingredient in the medical composition may be at a level that will exercise the desired therapeutic effect.
The formulation may also include a bacterial component, a drug entity or a biological compound.
In addition, a vaccine comprising the strains of the invention may be prepared using any suitable known method and may include a pharmaceutically acceptable carrier or adjuvant.
The human immune system plays a significant role in the aetiology and pathology of a vast range of human diseases. Hyper and hypo-immune responsiveness results in, or is a component of, the majority of disease states. One family of biological entities, termed cytokines, are particularly important to the control of immune processes. Perturbances of these delicate cytokine networks are being increasingly associated with many diseases. These diseases include but are not limited to inflammatory disorders, immunodeficiency, inflammatory bowel disease, irritable bowel syndrome, cancer (particularly those of the gastrointestinal and immune systems), diarrhoeal disease, antibiotic associated diarrhoea, paediatric diarrhoea, appendicitis, autoimmune disorders, multiple sclerosis, Alzheimer’s disease, rheumatoid arthritis, coeliac disease, diabetes mellitus, organ transplantation, bacterial infections, viral infections, fungal infections, periodontal disease, urogenital disease, sexually transmitted disease, HIV infection, HIV replication, HIV associated diarrhoea, surgical associated trauma, surgical-induced metastatic disease, sepsis, weight loss, anorexia, fever control, cachexia, wound healing, ulcers, gut barrier function, allergy, asthma, respiratory disorders, circulatory disorders, coronary heart disease, anaemia, disorders of the blood coagulation system, renal disease, disorders of the central nervous system, hepatic disease, ischaemia, nutritional disorders, osteoporosis, endocrine disorders, epidermal disorders, psoriasis and acne vulgaris. The effects on cytokine production are specific for the probiotic strain-examined. Thus, specific probiotic strains may be selected for normalising an exclusive cytokine imbalance particular for a specific disease type.
The enteric flora is important to the development and proper function of the intestinal immune system. In the absence of an enteric flora, the intestinal immune system is underdeveloped, as demonstrated in germ free animal models, and certain functional parameters are diminished, such as macrophage phagocytic ability and immunoglobulin production. The importance of the gut flora in stimulating non-damaging immune responses is becoming more evident. The increase in incidence and severity of allergies in the western world has been linked with an increase in hygiene and sanitation, concomitant with a decrease in the number and range of infectious challenges encountered by the host. This lack of immune stimulation may allow the host to react to non-pathogenic, but antigenic, agents resulting in allergy or autoimmunity. Deliberate consumption of a series of non-pathogenic immunomodulatory bacteria would provide the host with the necessary and appropriate educational stimuli for proper development and control of immune function.
Inflammation is the term used to describe the local accumulation of fluid, plasma proteins and white blood cells at a site that has sustained physical damage, infection or where there is an ongoing immune response. Control of the inflammatory response is exerted on a number of levels. The controlling factors include cytokines, hormones (e.g. hydrocortisone), prostaglandins, reactive intermediates and leukotrienes. Cytokines are low molecular weight biologically active proteins that are involved in the generation and control of immunological and inflammatory responses, while also regulating development, tissue repair and haematopoiesis. They provide a means of communication between leukocytes themselves and also with other cell types. Most cytokines are pleiotropic and express multiple biologically overlapping activities. Cytokine cascades and networks control the inflammatory response rather than the action of a particular cytokine on a particular cell type. Waning of the inflammatory response results in lower concentrations of the appropriate activating signals and other inflammatory mediators leading to the cessation of the inflammatory response. TNFα is a pivotal pro-inflammatory cytokine as it initiates a cascade of cytokines and biological effects resulting in the inflammatory state. Therefore, agents which inhibit TNFα are currently being used for the treatment of inflammatory diseases, e.g. infliximab.
Pro-inflammatory cytokines are thought to play a major role in the pathogenesis of many inflammatory diseases, including inflammatory bowel disease (IBD). Current therapies for treating IBD are aimed at reducing the levels of these pro-inflammatory cytokines, including IL-8 and TNFα. Such therapies may also play a significant role in the treatment of systemic inflammatory diseases such as rheumatoid arthritis.
The strains of the present invention may have potential application in the treatment of a range of inflammatory diseases, particularly if used in combination with other anti-inflammatory therapies, such as non-steroid anti-inflammatory drugs (NSAIDs) or Infliximab.
The production of multifunctional cytokines across a wide spectrum of tumour types suggests that significant inflammatory responses are ongoing in patients with cancer. It is currently unclear what protective effect this response has against the growth and development of tumour cells in vivo. However, these inflammatory responses could adversely affect the tumour-bearing host. Complex cytokine interactions are involved in the regulation of cytokine production and cell proliferation within tumour and normal tissues. It has long been recognized that weight loss (cachexia) is the single most common cause of death in patients with cancer and initial malnutrition indicates a poor prognosis. For a tumour to grow and spread it must induce the formation of new blood vessels and degrade the extracellular matrix. The inflammatory response may have significant roles to play in the above mechanisms, thus contributing to the decline of the host and progression of the tumour. Due to the anti-inflammatory properties of Bifidobacterium longum these bacterial strains they may reduce the rate of malignant cell transformation. Furthermore, intestinal bacteria can produce, from dietary compounds, substances with genotoxic, carcinogenic and tumour-promoting activity and gut bacteria can activate pro-carcinogens to DNA reactive agents. In general, species of Bifidobacterium have low activities of xenobiotic metabolizing enzymes compared to other populations within the gut such as bacteroides, eubacteria and clostridia. Therefore, increasing the number of Bifidobacterium bacteria in the gut could beneficially modify the levels of these enzymes.
The majority of pathogenic organisms gain entry via mucosal surfaces. Efficient vaccination of these sites protects against invasion by a particular infectious agent. Oral vaccination strategies have concentrated, to date, on the use of attenuated live pathogenic organisms or purified encapsulated antigens. Probiotic bacteria, engineered to produce antigens from an infectious agent, in vivo, may provide an attractive alternative as these bacteria are considered to be safe for human consumption (GRAS status).
Murine studies have demonstrated that consumption of probiotic bacteria expressing foreign antigens can elicit protective immune responses. The gene encoding tetanus toxin fragment C (TTFC) was expressed in Lactococcus lactis and mice were immunized via the oral route. This system was able to induce antibody titers significantly high enough to protect the mice from lethal toxin challenge. In addition to antigen presentation, live bacterial vectors can produce bioactive compounds, such as immunestimulatory cytokines, in vivo. L. lactis secreting bioactive human IL-2 or IL-6 and TTFC induced 10-15 fold higher serum IgG titres in mice immunized intranasally. However, with this particular bacterial strain, the total IgA level was not increased by co-expression with these cytokines. Other bacterial strains, such as Streptococcus gordonii, are also being examined for their usefulness as mucosal vaccines. Recombinant S. gordonii colonizing the murine oral and vaginal cavities induced both mucosal and systemic antibody responses to antigens expressed by this bacterial. Thus, oral immunization using probiotic bacteria as vectors would not only protect the host from infection but may replace the immunological stimuli that the pathogen would normally elicit thus contributing to the immunological education of the host.
PrebioticsThe introduction of probiotic organisms is accomplished by the ingestion of the micro-organism in a suitable carrier. It would be advantageous to provide a medium that would promote the growth of these probiotic strains in the large bowel. The addition of one or more oligosaccharides, polysaccharides, or other prebiotics enhances the growth of lactic acid bacteria in the gastrointestinal tract. Prebiotics refers to any non-viable food component that is specifically fermented in the colon by indigenous bacteria thought to be of positive value, e.g. bifidobacteria, lactobacilli. Types of prebiotics may include those that contain fructose, xylose, soya, galactose, glucose and mannose. The combined administration of a probiotic strain with one or more prebiotic compounds may enhance the growth of the administered probiotic in vivo resulting in a more pronounced health benefit and is termed synbiotic.
Other Active IngredientsIt will be appreciated that the probiotic strains may be administered prophylactically or as a method of treatment either on its own or with other probiotic and/or prebiotic materials as described above. In addition, the bacteria may be used as part of a prophylactic or treatment regime using other active materials such as those used for treating inflammation or other disorders especially those with an immunological involvement. Such combinations may be administered in a single formulation or as separate formulations administered at the same or different times and using the same or different routes of administration.
Pharmaceutical CompositionsA pharmaceutical composition is a composition that comprises or consists of a therapeutically effective amount of a pharmaceutically active agent. It preferably includes a pharmaceutically acceptable carrier, diluent or excipients (including combinations thereof). Acceptable carriers or diluents for therapeutic use are well known in the pharmaceutical art, and are described, for example, in Remington’s Pharmaceutical Sciences. The choice of pharmaceutical carrier, excipient or diluent can be selected with regard to the intended route of administration and standard pharmaceutical practice. The pharmaceutical compositions may comprise as - or in addition to - the carrier, excipient or diluent any suitable binder(s), lubricant(s), suspending agent(s), coating agent(s), solubilising agent(s), propellants(s).
Examples of pharmaceutically acceptable carriers include, for example, water, salt solutions, alcohol, silicone, waxes, petroleum jelly, vegetable oils, polyethylene glycols, propylene glycol, liposomes, sugars, gelatin, lactose, amylose, magnesium stearate, talc, surfactants, silicic acid, viscous paraffin, perfume oil, fatty acid monoglycerides and diglycerides, petroethral fatty acid esters, hydroxymethyl-cellulose, polyvinylpyrrolidone, and the like.
Where appropriate, the pharmaceutical compositions can be administered by any one or more of: inhalation, in the form of a suppository or pessary, topically in the form of a lotion, solution, cream, ointment or dusting powder, by use of a skin patch, orally in the form of tablets containing excipients such as starch or lactose, or in capsules or ovules either alone or in a mixture with excipients, or in the form of elixirs, solutions or suspensions containing flavouring or colouring agents, or they can be injected parenterally, for example intracavemosally, intravenously, intramuscularly or subcutaneously. For parenteral administration, the compositions may be best used in the form of a sterile aqueous solution which may contain other substances, for example enough salts or monosaccharides to make the solution isotonic with blood. For buccal or sublingual administration, the compositions may be administered in the form of tablets or lozenges which can be formulated in a conventional manner.
The strains and/or cell wall fractions in some cases are administered to the mouth, larynx, nasal cavity and/or oropharynx. In some cases the strains and/or cell wall fractions are not swallowed and in some cases are not substantially delivered to the gastrointestinal tract. The formulation may or may not be swallowed.
Intranasal administration can be accomplished using a nasal spray, nasal wash solution or direct application within the nose.
Administration to the lung could be in the form of a dry powder, inhaled using an inhaler device. In some cases the formulation is in the form of an aerosol. The aerosol may be a solution, suspension, spray, mist, vapour, droplets, particles, or a dry powder, for example, using a method dose inhaler including HFA propellant, a metered dose inhaler with non-HFA propellant, a nebulizer, a pressurized can, of a continuous sprayer.
The formulation may be designed to encapsulate, remove and/or inactivate a virus. The formulation alternatively or additionally may deter a virus from further infecting the respiratory tract.
To aid delivery to and maintenance in the respiratory tract such as in the nasal cavity, the formulation may have a desired viscosity of 1 centipoise to 2,000 centipoise, for example, 5 cps to 500 cps, or 5 cps to 300 cps. Any suitable viscosity modifying agent may be used to achieve the desired viscosity. Such agents may be suitable natural or synthetic polymeric materials such as hydroxypropyl methylcellulose.
There may be different composition/formulation requirements dependent on the different delivery systems. By way of example, the pharmaceutical composition of the present invention may be formulated to be delivered using a mini-pump or by a mucosal route, for example, as a nasal spray or aerosol for inhalation or ingestible solution, or parenterally in which the composition is formulated by an injectable form, for delivery, by, for example, an intravenous, intramuscular or subcutaneous route. Alternatively, the formulation may be designed to be delivered by both routes.
The invention is not limited to the embodiment hereinbefore described, which may be varied in detail.
REFERENCESBouhnik, Y., Survie et effets chez l′homme des bacteries ingérées dans les laits fermentés. Lait 1993, 73;241-247.
Yang JW., Fan LC., Miao XY., Mao B., Li MH., Lu HW., Liang S., Xu JF. Corticosteroids for the treatment of human infection with influenza virus: a systematic review and meta-analysis. Clin Microbiol Infect. 2015 Oct;21(10):956-63.
Davidson S., Crotta S., McCabe TM., Wack A. Pathogenic potential of interferon αβ in acute influenza infection. Nat Commun. 2014 May 21;5:3864.
Nakamura S., Davis KM., Weiser JN. Synergistic stimulation of type I interferons during influenza virus coinfection promotes Streptococcus pneumoniae colonization in mice. J Clin Invest 2011;121:3657-65.
Shahangian A., Chow EK., Tian X. et al. Type I IFNs mediate development of postinfluenza bacterial pneumonia in mice. J Clin Invest 2009;119:1910-20.
Li W., Moltedo B., Moran TM. Type I interferon induction during influenza virus infection increases susceptibility to secondary Streptococcus pneumoniae infection by negative regulation of gammadelta T cells. J Virol 2012;86:12304-12.
Hewitt R., Fame H., Ritchie A., Luke E., Johnston SL., Mallia P. The role of viral infections in exacerbations of chronic obstructive pulmonary disease and asthma. Ther Adv Respir Dis. 2016 Apr;10(2):158-74. doi: 10.1177/1753465815618113.
Galani IE., Triantafyllia V., Eleminiadou EE., Koltsida O., Stavropoulos A., Manioudaki M., Thanos D., Doyle SE., Kotenko SV., Thanopoulou K., Andreakos E. Interferon-λ Mediates Non-redundant Front-Line Antiviral Protection against Influenza Virus Infection without Compromising Host Fitness. Immunity. 2017 May 16;46(5):875-890.
Davidson S., McCabe TM., Crotta S., Gad HH., Hessel EM., Beinke S., Hartmann R., Wack A. IFN-λ, is a potent anti-influenza therapeutic without the inflammatory side effects of IFN-α treatment. EMBO Mol Med. 2016 Sep 1;8(9):1099-112.
Thiel, S., and Reid K. 1989 -Structures and functions associated with the group of mammalian lectins containing collagen-like sequences. FEBS Lett. 250:78.2.
Sastry, K., and Ezekowitz R.A. 1993. Collectins: pattern recognition molecules involved in first line host defense. Curr. Opin. Immunol. 5:59.
Shi X., Zhou W., Huang H., Zhu H., Zhou P., Zhu H., Ju D. Inhibition of the inflammatory cytokine tumor necrosis factor-alpha with etanercept provides protection against lethal H1N1 influenza infection in mice. Crit. Care, 2013; 17(6);R301.
O′Mahony L., McCarthy J., Kelly P., Hurley G., Luo F., Chen K., O′Sullilvan GC., Kiely B., Collins JK., Shanahan F., Quigley EM. Lactobacillus and Bifidobacterium in irritable bowel syndrome: symptom responses and relationship to cytokine profiles. Gastroenterology. 2005 Mar;128(3):541-51.
O′Mahony C. et al., PLoS Pathogens 2008.
Konieczna P., Groeger D., Ziegler M., Frei R., Ferstl R., Shanahan F., Quigley EM., Kiely B., Akdis CA., O′Mahony L. Bifidobacterium infantis 35624 administration includes Foxp3 T regulatory cells in human peripherial blood: potential role for myeloid and plasmacytoid dendritic cells. Gut. 2012 Mar;61(3):354-66. doi: 10.1136/gutjnl-2011-300936.
Groeger D., O′Mahony L., Murphy EF., Bourke JF., Dinan TG., Kiely B., Shanahan F., Quigley EM. Bifidobacterium infantis 35624 modulates host inflammatory processes beyond the gut. Gut Microbes. 2013 Jul-Aug;4(4):325-39. doi: 10.4161/gmic.25487
Bartlett NW1., Singanayagam A., Johnston SL. Mouse models of rhinovirus infection and airways disease. Methods Mol Biol. 2015;1221:181-8. doi: 10.1007/978-1-4939-1571-2_14.
Ivashkiv LB., and Donlin LT. Regulation of type I interferon responses. Nat Rev Immunol. 2014 Jan; 14(1): 36-49.
Lazear HM., Nice TJ., Diamond MS. Interferon-λ: Immune Functions at Barrier Surfaces and Beyond. Immunity, 2015 Jul 21;43(1): 15-28.
Wack A., Terczyńska-Fyla E., Hartmann R. Guarding the frontiers: the biology of the type III interferons. Nat Immunol. 2015 Aug; 16(8): 802-9.
Durbin RK., Kotenko SV., Durbin JE. Interferon induction and function at the muscol surface. Immunol Rev. 2013 Sep;255(1): 25-39.
Mendoza JL., Schneider WM., Hoffmann HH., Vercauteren K., Jude KM., Xiong A., Moraga I., Horton TM., Glenn JS., de Jong YP., Rice CM., Garcia KC. The IFN-λ-IFN-λR1-IL-10Rβ Complex Reveals Structural Features Underlying Type III IFN Functional Plasticity. Immunity. 2017 Mar 21;46(3): 379-392.
Ichikawa A., Kuba K., Morita M., Chida S., Tezuka H., Hara H., Sasaki T., Ohteki T., Ranieri VM., dos Santos CC., Kawaoka Y., Akira S., Luster AD., Lu B., Penninger JM., Uhlig S., Slutsky AS., Imai Y. CXCL10-CXCR3 enhances the development of neutrophil-mediated fulminant lung injury of viral and nonviral origin. Am J Respir Crit Care Med. 2013 Jan 1;187(1):65-77.
Wei Wang., Penghui Yang., et al. Monoclonal antibody against CXCL-10/IP-10 ameliorates influenza A (H1N1) virus induced acute lung injury. Cell Research (2013) 23:577-580.
Hartshorn KL., White MR., Shepherd V., Reid K., Jensenius JC., Crouch EC. Mechanisms of anti-influenza activity of surfactant proteins A and D: comparison with serum collectins. Am J Physiol 1997; 273: L1156-L1166.
Reading PC., Morey LS., Crouch EC., Anders EM. Collectin-mediated antiviral host defense of the lung: evidence from influenza virus infection of mice. J Virol 1997;71: 8204-8212.
Hartshorn KL., White MR., Voelker DR., Coburn J., Zaner K., Crouch EC. Mechanism of binding of surfactant protein D to influenza A viruses: importance of binding to haemagglutinin to antiviral activity. Biochem J 2000; 351 (Pt 2): 449-458.
Tecle T., White MR., Crouch EC., Hartshorn KL. Inhibition of influenza viral neuraminidase activity by collectins. Arch Virol 2007; 152: 1731-1742.
LeVine AM., Whitsett JA., Hartshorn KL., Crouch EC., Korfhagen TR. SP- D enhances clearance of influenza A virus from the lung in in vivo mouse models. J Immunol 2001; 167:5868-5873.
Vigerust DJ., Ulett KB., Boyd KL., Madsen J., Hawgood S., McCullers JA. N-linked glycosylation attenuates H3N2 influenza viruses. J Virol 2007; 81:8593-8600.
Hawgood S., Brown C., Edmondson J., Stumbaugh A., Allen L., Goerke J. et al. Pulmonary collectins modulate strain-specific influenza a virus infection and host responses. J Virol 2004; 78: 8565-8572.
LeVine AM(1)., Elliott J., Whitsett JA., Srikiatkhachorn A., Crouch E., DeSilva N., Korfhagen T. Surfactant protein-d enhances phagocytosis and pulmonary clearance of respiratory syncytial virus. Am J Respir Cell Mol Biol. 2004 Aug;31(2):193-9.
Rich H., Robinson KE., McHugh KJ., Clay ME., Alcorn JF. The role of interferon lambda during influenza, Staphylococcus aureus super-infection.J Immunol May 1, 2017, 198(1 Supplement) 77.16.
Jounblat R., Clark H., Eggleton P., Hawgood S., Andrew PW., Kadioglu A. The role of surfactant protein D in the colonisation of the respiratory tract and onset of bacteraemia during pneumococcal pneumonia Respir Res. 2005 Oct 28;6:126.
World Health Organisation 2007. Global surveillance, prevention and control of chronic respiratory diseases, a comprehensive approach. (Editors Jean Bousquet and Nikolai Khaltaev).
Jartti T., Gern JE. Role of viral infections in the development and exacerbation of asthma in children. J Allergy Clin Immunol. 2017 Oct;140(4):895-906.
Almond MH1., Edwards MR., Barclay WS., Johnston SL. Obesity and susceptibility to severe outcomes following respiratory viral infection. Thorax. 2013 Jul;68(7):684-6. doi: 10.1136/thoraxjnl-2012-203009.
Steinke JW., Borish L. Immune Responses in Rhinovirus-Induced Asthma Exacerbations. Curr Allergy Asthma Rep. 2016 Nov;16(11):78.
Zhou X., Li Q., Zhou X. Exacerbation of Chronic Obstructive Pulmonary Disease. Cell Biochem Biophys. 2015 Nov;73(2):349-55.
Claims
1-125. (canceled)
126. A method of treating a human subject, the method comprising administering to the subject a formulation comprising an ingestible carrier and a strain of Bifidobacterium longum or cell wall fraction thereof, wherein the Bifidobacterium longum strain has the accession number NCIMB 41003 or NCIMB 42020, and wherein the treatment alters the subject’s immune response to a respiratory virus by enhancing a type III interferon response to the virus and suppressing an interferon type I response to the virus.
127. The method of claim 126, wherein the formulation comprises a cell wall fraction of the Bifidobacterium longum strain, and a molecular weight of the cell wall fraction is greater than 100 kDa.
128. The method of claim 127, wherein the cell wall fraction is less than 0.45 µm in size.
129. The method of claim 126, wherein the treatment attenuates an IP-10 response to the virus in the subject.
130. The method of claim 126, wherein the treatment increases an interferon lambda response to the virus in the subject.
131. The method of claim 126, wherein the treatment suppresses an interferon alpha response or an interferon beta response to the virus in the subject.
132. The method of claim 126, wherein the treatment increases a surfactant protein D response to the virus in the subject.
133. The method of claim 126, wherein the virus is an influenza virus, rhinovirus, or respiratory syncytial virus.
134. The method of claim 126, wherein the subject has been diagnosed with an inflammatory lung disease, acute respiratory distress syndrome, asthma, or chronic obstructive pulmonary disease.
135. The method of claim 126, wherein the subject has increased susceptibility to a respiratory infection, is obese, or is greater than 60 years of age.
136. The method of claim 126, wherein the formulation is administered to the lung or the nose of the subject.
137. The method of claim 126, wherein the formulation is in the form of a nasal spray.
138. A method of treating a human subject, the method comprising administering to the subject a formulation comprising a cell wall fraction isolated from a Bifidobacterium longum strain having the accession number NCIMB 41003 or NCIMB 42020 and an ingestible carrier, wherein the formulation is administered to the lung or nose of the subject as a spray, and wherein the treatment alters the subject’s immune response to a respiratory virus.
139. The method of claim 138, wherein the treatment enhances a type III interferon response to the virus and suppresses an interferon type I response to the virus.
140. The method of claim 138, wherein the treatment attenuates an IP-10 response to the virus, enhances an interferon lambda response to the virus, suppresses an interferon alpha response to the virus, suppresses an interferon beta response to the virus, or enhances a surfactant D protein response to the virus.
141. The method of claim 138, wherein the subject has been diagnosed with an inflammatory lung disease, acute respiratory distress syndrome, asthma, or chronic obstructive pulmonary disease, the subject having increased susceptibility to a respiratory infection.
142. The method of claim 138, wherein the molecular weight of the cell wall fraction is greater than 100 kDa, and wherein the cell wall fraction is less than 0.45 µm in size.
143. A method of treating a human subject, the method comprising administering to the subject a formulation comprising an ingestible carrier and a strain of Bifidobacterium longum or cell wall fraction thereof; wherein the Bifidobacterium longum strain has the accession number NCIMB 41003 or NCIMB 42020; wherein the treatment alters the subject’s immune response to a respiratory virus chosen from an influenza virus, rhinovirus, or respiratory syncytial virus; and wherein the subject has been diagnosed with an inflammatory lung disease, acute respiratory distress syndrome, asthma, or chronic obstructive pulmonary disease, the subject having increased susceptibility to a respiratory infection.
144. The method of claim 143, wherein the ingestible carrier is a capsule, a tablet, a powder, a food product, or a beverage.
145. The method of claim 143, wherein the treatment increases a surfactant protein D response to the virus in the subject.
Type: Application
Filed: Dec 6, 2022
Publication Date: Jul 6, 2023
Applicant: PrecisionBiotics Group Limited (Cork)
Inventors: Barry KIELY (Cork), Liam O'MAHONY (Cork), David GROEGER (Cork)
Application Number: 18/062,221
