ANTI-BAG3 ANTIBODIES FOR THERAPEUTIC USE
The present invention relates to the use of BAGS antibodies as a medicament, in particular for use in the treatment of pancreatic tumours or other pathologies of an immune, inflammatory, neoplastic and/or degenerative nature.
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The present invention relates to the use of Anti-BAG3 antibodies as a medicament, in particular for use in the treatment of pancreatic tumours or other pathologies of an immune, inflammatory, neoplastic and/or degenerative nature.
STATE OF THE ARTBAG3 protein is a 74 kDa cytoplasmic protein which belongs to the family of co-chaperonins that interact with the ATPase domain of the protein HSP70 (Heat Shock Protein) through the structural domain known as the BAG domain (amino acids 110-124). Furthermore, BAG3 protein contains a WW domain (Trp-Trp), a proline-rich region (PXXP), and two conserved motifs IPV (Ile-Pro-Val), which can mediate binding to other proteins. Thanks to the nature of BAG3 protein as an adapter, attributable to the presence of many functional domains, such protein can therefore interact with different proteins.
In humans, bag3 gene expression is constitutive for a few kinds of normal cells, including myocytes, while mutations thereof are associated with diseases of the skeletal and cardiac muscles. Furthermore, BAG3 protein is expressed in many types of primary tumours or tumour cell lines (lymphoid or myeloid leukemias, neuroblastoma, pancreatic cancer, thyroid cancer, breast cancer and prostate cancer, melanoma, osteosarcoma, glioblastoma and tumours of the kidney, colon, and ovary).
In normal cell types, such as leukocytes, epithelial cells and glial cells and cells of the retina, bag3 gene expression can be induced by stressors, such as oxidants, high temperatures, lack of serum, heavy metals, HIV-1 infections, etc. These findings indicate that bag3 gene expression regulation is an important component in the cellular response to stress and is correlated with the presence of elements that respond to the transcription factor HSF1 (Heat Shock Transcription Factor), which is activated in various forms of cellular stress in bag3 gene promoter (Franceschelli S., et al. J Cell Physiol 215 (2008) 575-577).
Moreover, due to the presence of many protein-protein interaction domains in the structure thereof, BAG3 protein influences cell survival in different types of cells, interacting with different molecular partners. (A. Rosati et al. Cell Death Dis. (2011) 2:e141). The first mechanism reported in relation to BAG3 anti-apoptotic activity was identified in osteosarcoma and melanoma cells, where it was observed that BAG3 protein modulates the activation of transcription factor NF-kB and cell survival (Ammirante M. et al., Proc Natl Acad Sci USA 107 (2010) 7497-7502). A different molecular mechanism has been described in glioblastoma cells, where BAG3 protein cooperates in a positive way with HSP70 protein to maintain BAX protein in the cytosol and prevent the translocation thereof into the mitochondria (Festa M. et al., Am J Pathol 178 (2011) 2504-25). Finally, in some tumours, BAG3 has been shown to regulate proteins that modulate cell adhesion.
The presence of cytoplasmic BAG3 protein has also been described in many different cellular systems and has been associated, not only with various tumours, but also in pathologies in general related to cell survival.
Furthermore, patent application n. WO2011/067377 describes soluble BAG3 protein, secreted externally to the cell, as a biochemical marker in serum, which is highly specific for the diagnosis of certain pathological conditions, such as cardiac pathologies and pancreatic tumour. In particular, it has been demonstrated that, in patients suffering from pancreatic adenocarcinoma, the concentration of (extra-cellular) soluble BAG3 is generally greater than 10 ng/ml.
Furthermore, it has recently been reported that BAG3 protein is expressed in 346/346 patients with pancreatic ductal adenocarcinoma (PDAC) and is released by the cells of the pancreatic tumour, but such protein is not expressed in either the surrounding non-neoplastic tissues or in a normal pancreas; likewise, it has been reported that the levels of BAG3 expression are related to patient survival. The results of the study demonstrate that the use of specific siRNA molecules for BAG3 mRNA can silence bag3 gene expression and induce cell death, confirming that BAG3 protein is an important survival factor for pancreatic tumour cells and that the down-regulation thereof, when combined with gentamicin, may contribute to the eradication of the tumor cells (Rosati et al., Am J Pathol. 2012 November; 181 (5):1524-9).
As it is known, conventional chemotherapy treatments for tumour pathologies, as well as treatments of inflammatory and immune diseases with corticosteroids or NSAIDs (non-steroidal anti-inflammatory drugs) pose numerous drawbacks linked to side effects and are not, at present, definitive means of treating such pathologies.
There is therefore an evident need for a new and improved therapeutic treatment which has the advantage of being highly specific and having few or no side effects, as compared with the conventional, commonly known therapies used for the treatment of diseases of an inflammatory, immune, and neoplastic nature described in the present invention.
DESCRIPTION OF THE INVENTIONSurprisingly, it has been demonstrated, for the first time, that the inhibition of soluble (i.e. extra-cellular) BAG3 protein through the use of anti-BAG3 monoclonal antibodies, impairs development of pancreatic tumour cells. Anti-BAG3 antibodies represent a new and improved therapeutic tool for the treatment of pancreatic tumours. Furthermore, it has also been found, surprisingly, that the aforesaid BAG3 protein is involved in the activation of macrophages.
Therefore, treatment with any of the anti-BAG3 antibodies described in patent application n. WO03/055908 able to inhibit, specifically, the activity of soluble BAG3 protein (i.e. extra-cellular) on macrophages, that are considered the target cells, proves particularly effective in the treatment of those pathologies characterised by the activation of macrophages, such as neoplastic diseases and diseases of an inflammatory, immune, or degenerative nature. In fact, these specific antibodies for BAG3 can bind and block, in a highly selective and targeted manner, pathological effects related to BAG3 protein when secreted by cells.
In particular, the use of anti-BAG3 antibodies in this process has the surprising advantage of being more specific for the selected pathological states characterised by the over-expression and release of BAG3 protein, and also less damaging in terms of side effects.
The term “soluble BAG3 protein” is understood as extra-cellular BAG3 protein, i.e. the protein secreted externally to the cell.
One aim of the present invention is therefore the use of anti-BAG3 antibodies as a medicament.
The antibodies useable in accordance with the present invention may be either monoclonal or polyclonal antibodies, and are preferably monoclonal antibodies.
Still more preferably, said monoclonal antibodies may be chosen from the following: murinr antibodies, humanised antibodies, chimeric antibodies, recombinant antibodies, conjugated antibodies, scFv fragments (diabody, triabody and tetrabody), Fab fragments, and fragments F (ab′) 2.
The term “polyclonal antibody” refers to a mixture of antibodies which are genetically different since produced by different plasma cells and which recognise a different epitope of the same antigen.
The term “monoclonal antibody” refers to a set of antibodies which are all identical since produced by cell lines from only one type of immune cell (i.e. a cell clone).
The term “humanized antibody” refers to an antibody of human origin, whose hypervariable region has been replaced by the homologous region of non-human monoclonal antibodies.
The term “chimeric antibody” refers to an antibody containing portions derived from different antibodies.
The term “recombinant antibody” refers to an antibody obtained using recombinant DNA methods.
The term “conjugated antibody” refers to antibodies conjugated with drugs, toxins, radioactive substances or other agents.
The term “scFv fragment” (single chain variable fragment) refers to immunoglobulin fragments only capable of binding with the antigen concerned. ScFv fragments can also be synthesised into dimers (diabodies), trimers (triabodies) and tetramers (tetrabodies) using peptide linkers.
The terms “Fab fragment” (antigen-binding fragment) and “Fab2 fragment” refer to immunoglobulin fragments consisting of a light chain linked to the Fc fragment of the adjacent heavy chain, and such fragments are monovalent antibodies. When the Fab portions are in pairs, the fragment is called Fab2.
The term “hybridoma” refers to a cell producing monoclonal antibodies.
The monoclonal antibodies used in the examples were obtained by immunising mice against four distinct BAG3 protein peptides using any method known to a person skilled in the art. Such peptides were chosen because they are BAG3 protein-specific and are not shared with any other protein, including BAG proteins.
The sequences of the four peptides are included in the BAG3 amino acid sequence (RefSeq: NP—004272; Gene ID 9531) and are selected from the following:
Preferably, said antibodies may be obtained by means of the Multiple Antigene Peptide approach (MAP) (Keah H H et al., J Pept Res (1988); 51: 2. Tam J P; Proc Natl acad Sci USA (1988), 85: 5409. Ota S, et al., Cancer Res (2002), 62: 1471), using the following map constructs:
According to a preferred embodiment of the present invention, said polyclonal anti-BAG3 antibodies are obtained by immunising the animals against one of the four peptides of the sequences SEQ ID NO. 1-4 stated above.
According to a preferred embodiment, the monoclonal anti-BAG3 antibodies of the present invention are obtained by means of a standard procedure (Tassone P., et al., Tissue Antigens 51: 671 (1998)) using the four MAP-BAG3 peptides described above and are produced by at least one of the nine mother clones chosen from the following: AC-1, AC-2, AC-3, AC-4, AC-5, AC-6, AC-7, AC-8, or AC-9 (described in WO03/055908), which contain specific hybridomas for each of the four MAP-BAG3 constructs used.
According to a further embodiment, the antibodies used are monoclonal anti-BAG3 antibodies obtained from at least one of the aforesaid mother clones, and preferably at least one chosen from the following: AC-1, AC-2, AC-3, AC-4, or AC-5. More preferably, said monoclonal antibodies are obtained from at least one mother clone chosen from the following: AC-1, AC-2, and AC-3.
According to a further preferred embodiment, with the standard procedure (Ceran C, Cokol M, Cingöz S, Tasan I, Ozturk M, Yagci T. Novel anti-HER2 monoclonal antibodies: synergy and antagonism with tumor necrosis factor-α.BMC Cancer. 2012 Oct. 4; 12:450) and the immunisation of mice with a BAG3 recombinant protein, the monoclonal anti-BAG3 antibodies envisaged in the present invention are obtained from at least one of the following clones: AC-rb1, AC-rb2, AC-rb3 and AC.rb4, and/or at least one of the following subclones: AC-rb1a, AC-rb1b, AC-rb2a, AC-rb2b, AC-rb3a, AC-rb3b, AC-rb4a, and AC-rb4b. The monoclonal antibodies produced by all these clones and subclones recognise the BAG3 recombinant protein in an ELISA test. (Example 2).
Preferably, said monoclonal anti-BAG3 antibodies are those that recognise epitopes in the BAG3 protein amino acid sequence, which include at least one of the following fragments: 18-33, 385-399, 533-547 or 562-575.
A further aim of the present invention is the use of the aforesaid anti-BAG3 antibodies in the treatment of a particular pathological state which involves the activation of macrophages. Such pathological state can be chosen from: neoplastic diseases, inflammatory diseases, immune diseases, and/or degenerative diseases.
Preferably, such neoplastic diseases may be either pancreatic tumour or bladder tumor, more preferably pancreatic tumour.
Preferably, said inflammatory diseases can be chosen from diseases related to inflammation of the skin, nerves, bones, blood vessels, and connective tissues, and more preferably, psoriasis, arthritis, neuritis, connectivitis.
Preferably, said immune diseases can be chosen from autoimmune diseases such as rheumatic diseases, connective tissue diseases, neuromuscular diseases, endocrine diseases, gastrointestinal diseases, haematologic diseases, skin diseases, and vasculitis, and more preferably, rheumatoid arthritis, multiple sclerosis, connectivitis, lupus erythematosus, endometriosis, and ulcerative colitis. Preferably, said degenerative diseases can be chosen from neurodegenerative diseases and muscular degenerative diseases, and more preferably Alzheimer's disease, Parkinson's disease, and muscular dystrophy.
According to a more preferred embodiment of the invention, the anti-BAG3 antibodies are used in the treatment of neoplastic diseases, inflammatory diseases, immune diseases, and degenerative diseases.
A further aim of the present invention is a pharmaceutical composition comprising the aforesaid anti-BAG3 antibody in association with at least one pharmaceutically acceptable excipient.
A further object of the present invention is the use of said composition as a medicament.
A preferred embodiment of the present invention is the use of the composition in the treatment of neoplastic diseases and diseases of an inflammatory, immune and/or degenerative nature.
The composition of the present invention can be formulated in a form suitable for oral administration or in a form suitable for parenteral or topical administration.
In a preferred embodiment of the present invention, said oral form can be chosen from the following: tablets, capsules, solutions, suspensions, granules, and oily capsules.
In a further preferred embodiment of the present invention, said topical form can be chosen from the following: cream, ointment, ointment, solution, suspension, eye drops, pessary, nebuliser solution, spray, powder, or gel.
In a further preferred embodiment of this invention, said parenteral form can be either an aqueous buffer solution or an oily suspension.
Said parenteral administration include administration by intramuscular, intravenous, intradermal, subcutaneous, intraperitoneal, intranodal, or intrasplenic means.
Nude mice (nu/nu) female BALB/c 6 weeks (Charles Rivers Wilmington, Mass., USA) were caged (3 per cage) with food and water ad libitum and kept in 12 h light/dark cycles in standard, pathogen-free conditions. The research protocol was approved by the Ethics Committee in accordance with Italian Ministry of Health official guidelines. After one week of acclimatisation, the mice were subjected to inoculation of cancer cells. 10 mice were used in total, each one individually identified. The entire experiment was conducted in laminar flow hoods and all surgical procedures were performed in strict compliance with aseptic techniques. The mice were anesthetised with 100 mg/ml of ketamine HCl and 20 mg/ml of xylazine injected intraperitoneally; they were then subjected to laparotomy and the tail of the pancreas was gently exteriorised. MIA-PaCa 2 RFP cells (2.5×106) were resuspended in 40 microlitres of PBS 1× in a 1 ml syringe; using a 25 G needle, the cells were injected into the tail of the pancreas and the injection point was swabbed with sterile cotton. Once homeostasis was ascertained, the tail of the pancreas was repositioned in the abdomen and the wound closed. After two weeks, the mice were randomised into two groups: the first received an intraperitoneal injection of 100 mg/kg of mouse IgG and the second 100 mg/kg of a murine monoclonal anti-BAG3 antibody (AC-rb2). This treatment was performed twice a week in total and the mice were then anesthetised again to check the tumour area using Macro Fluo and LAS V3.7 software, by Leica Mycrosystems Ltd. In each imaging, the tumour mass was determined by quantification of the fluorescent area.
ResultsThe results shown in
Similar results were obtained with the murine monoclonal antibody AC-rb3.
Example 2 ELISA Test on the Antibodies Obtained from the Subclones AC-rb1a, AC-rb1b, AC-rb2a, AC-rb2b, AC-rb3a, AC-rb3b, AC-rb4a and AC-rb4bThe NUNC Maxisorp 96-well microtitre plates were functionalised with BAG3 recombinant protein 1 μg/ml in PBS 1×pH 7 (50 μl/well) and incubated for 18 hours at 4° C. The plates were then washed twice with a buffer wash (PBS 1×+0.05% Tween-20), and then kept in place for one hour at room temperature with 0.5% fish gelatin in PBS 1× (150 μl/well). Subsequently, the plates were buffer-washed twice and the supernatants of the eight subclones were diluted 1/10, 1/100, and 1/1000, in a 0.5% fish gelatin in PBS 1× and then incubated (50 μl/well) in triplicate and incubated at room temperature for 2 hours. The plates were then buffer-washed six times. To develop the signal, murine anti-IgG antibodies (H+L) (Sigma Aldrich) were used, diluted in the same buffer 1/20,000, then added to the plate (50 μl/well) and incubated at 4° C. for 30 minutes. After incubation, the plates were washed six times, then developed with TMB (50 μl/well) (eBioscience), and the reaction was stopped with sulphuric acid 4.5 M (25 μl/well). The plates were then analysed in a spectrophotometer at a wavelength of 450 nm. The results are expressed
as O.D. (optical densitometry).
The results obtained demonstrate that all the antibodies obtained by the subclones tested were able to recognise BAG3 protein.
Claims
1-16. (canceled)
17. A method for treating neoplastic diseases, inflammatory diseases, immune diseases and/or degenerative diseases, comprising administering an anti-BAG3 antibody to a subject in need thereof, wherein BAG3 protein is soluble.
18. The method according to claim 17, wherein said neoplastic disease is pancreatic tumor.
19. The method according to claim 17, wherein said neoplastic disease is bladder tumor.
20. The method according to claim 17, wherein said anti-BAG3 antibody is a polyclonal antibody.
21. The method according to claim 17, wherein said anti-BAG3 antibody is a monoclonal antibody.
22. The method according to claim 21, wherein said monoclonal antibody is a murine antibody, a humanized antibody, a chimeric antibody, a recombinant antibody, a conjugated antibody, an scFv fragment, a Fab fragment or a F(ab′)2 fragment.
23. The method according to claim 22, wherein said scFv fragment is diabody, triabody or tetrabody.
24. The method according to claim 22, wherein said monoclonal antibody is produced by at least one of the nine mother clones selected from the group consisting of: AC-1, AC-2, AC-3, AC-4, AC-5, AC-6, AC-7, AC-8 and AC-9.
25. The method according to claim 24, wherein said monoclonal antibody is produced by at least one of the five mother clones selected from the group consisting of: AC-1, AC-2, AC-3, AC-4, and AC-5.
26. The method according to claim 22, wherein said monoclonal antibody is produced by at least one of the following clones: AC-rb1, AC-rb2, AC-rb3, or AC-rb4, and by at least one of the following subclones: AC-rb1a, AC-rb1b, AC-rb2a, AC-rb2b, AC-rb3a, AC-rb3b, AC-rb4a, or AC-rb4b.
27. A pharmaceutical composition comprising at least one anti-BAG3 antibody and at least one pharmaceutically acceptable excipient, wherein the BAG3 protein is soluble.
28. The pharmaceutical composition according to claim 27, wherein said anti-BAG3 antibody is a monoclonal antibody produced by at least one of the nine mother clones selected from the group consisting of: AC-1, AC-2, AC-3, AC-4, AC-5, AC-6, AC-7, AC-8 and AC-9.
29. The pharmaceutical composition according to claim 27, wherein said anti-BAG3 antibody is a monoclonal antibody produced by at least one of the five mother clones selected from the group consisting of: AC-1, AC-2, AC-3, AC-4, and AC-5.
30. The pharmaceutical composition according to claim 27, wherein said composition is formulated in a form suitable for oral administration, parenteral administration, or topical administration.
31. The pharmaceutical composition according to claim 30, wherein said form suitable for oral administration is selected from the group consisting of tablets, capsules, solutions, suspensions, granules, and oily capsules.
32. The pharmaceutical composition according to claim 30, wherein said parenteral administration is intramuscular, intravenous, intradermal, subcutaneous, intraperitoneal, intranodal, or intrasplenic administration.
33. The pharmaceutical composition according to claim 30, wherein said form suitable for topical administration is cream, salve, ointment, or gel.
34. The pharmaceutical composition according to claim 30, wherein said form suitable for parenteral administration is an aqueous buffer solution or an oily suspension.
Type: Application
Filed: Mar 4, 2014
Publication Date: Nov 19, 2015
Applicant: BIOUNIVERSA S.R.L. (Fisciano (SA))
Inventor: Maria Caterina TURCO (Avellino)
Application Number: 14/651,213
