Abstract: A method for preparing purified yeast is disclosed, where the squalene source is a yeast that hyperproduces squalene. The squalene is useful for pharmaceutical purposes. For instance, it can be used to prepare an oil-in-water emulsion, and the emulsion is particularly suitable for use as an immmological adjuvant.

Abstract: An aerobic treatment system is disclosed herein in which an aerobic holding treatment tank, having an inlet adapted to receive wastewater and an outlet adapted to discharge treated wastewater therefrom, is in communication with an aeration pump having an inlet nozzle in communication with the aerobic holding treatment tank for providing a source of air to the contents of the aerobic holding treatment tank. The aerobic treatment system may further include a generation pump disposed below ground level and in fluid communication with the aerobic holding treatment tank. The generation pump is provided in fluid communication with a high pressure pump in fluid access with an evaporator fan and misting nozzle. The system may further include electronics to connect to grid power, backup electronics for connection to auxiliary power sources, and at least one solar collector for providing a source of electricity.

Abstract: A method for preparing purified yeast is disclosed, where the squalene source is a yeast that hyper-produces squalene. The squalene is useful for pharmaceutical purposes. For instance, it can be used to prepare an oil-in-water emulsion, and the emulsion is particularly suitable for use as an immunological adjuvant.

Abstract: An aerobic treatment system is disclosed herein in which an aerobic holding treatment tank, having an inlet adapted to receive wastewater and an outlet adapted to discharge treated wastewater therefrom, is in communication with an aeration pump having an inlet nozzle in communication with the aerobic holding treatment tank for providing a source of air to the contents of the aerobic holding treatment tank. The aerobic treatment system may further include a generation pump disposed below ground level and in fluid communication with the aerobic holding treatment tank. The generation pump is provided in fluid communication with a high pressure pump in fluid access with an evaporator fan and misting nozzle. The system may further include electronics to connect to grid power, backup electronics for connection to auxiliary power sources, and at least one solar collector for providing a source of electricity.

Abstract: An immunological composition comprising influenza virus haemagglutinin and matrix proteins. These may be from influenza viruses grown in call culture rather than eggs. The matrix protein may be a fragment of a full-length viral matrix protein e.g., a matrix M1 fragment with a molecular weight of less than 20 kDa. The composition may be a subunit vaccine comprising purified surface glycoproteins.

Abstract: Saccharide conjugate vaccines which use diphtheria toxoid or tetanus toxoid as a carrier protein can confer protection against lethal challenge by diphtheria toxin or tetanus toxin. Thus, in addition to protecting against the bacteria whose saccharides have been attached to the carrier, such conjugate vaccines can also be used to protect against diphtheria and tetanus, so the diphtheria toxoid and tetanus toxoid components of current complex combination vaccines may be superfluous. Therefore the antigenic complexity of these vaccines can be reduced without reducing their breadth of protection, and removing these superfluous components creates space in the vaccine for adding immunogens for protecting against further pathogens. The same effect is not seen with a CRM197 carrier, but this observation makes this carrier more attractive for conjugate vaccines which are given concomitantly with infant combination vaccines that contain Dt and Tt.

Abstract: An improved method for the detection of parvovirus B19 in a sample is provided, the improvement consisting of detecting a parvovirus B19 non-structural protein in said sample.

Abstract: A method for preparing purified yeast is disclosed, where the squalene source is a yeast that hyper-produces squalene. The squalene is useful for pharmaceutical purposes. For instance, it can be used to prepare an oil-in-water emulsion, and the emulsion is particularly suitable for use as an immunological adjuvant.

Abstract: An immunogenic composition comprising influenza virus haemagglutinin and matrix proteins. These may be from influenza viruses grown in cell culture rather than eggs. The matrix protein may be a fragment of a full-length viral matrix protein e.g. a matrix M1 fragment with a molecular weight of less than 2 OkDa. The composition may be a subunit vaccine comprising purified surface glycoproteins.

Abstract: Vaccine containing a first vaccine, adjuvated with an oil-in-water emulsion comprising 5% squalene, 0.5% polysorbate 80 and 0.5% sorbitan trioleate in aqueous citrate buffer pH 6.5, and a nonadjuvated second vaccine as combination partners for the simultaneous, separate or phased application for immunization against viral, bacterial or parasitic infectious diseases.

Abstract: The present invention relates to the combination of antigens directed against bacteria and viruses, their uses and the preparation of medicaments in order to confer protection against infectious diseases. In particular, the invention relates to a combination vaccine comprising at least one antigen of Clostridium tetani, at least one antigen from Corynebacterium diphtheriae, and at least one antigen from the TBE-flavivirus suitable to confer seroprotection against diseases and medical conditions caused by these pathogenic organisms.

Abstract: Structural phosphoprotein (pp28) of human cytomegalovirus (HCMV), the preparation and use thereof Expression of an SmaI fragment, which is about 1.0 kb in size, on the left-hand end of the HindIII R fragment makes it possible to synthesize, by genetic manipulation, a structural phosphoprotein of HCMV. This phosphoprotein, or immunogenic parts thereof, can be used as diagnostic aid or vaccine.

Abstract: Vaccine containing a first vaccine, adjuvated with an oil-in-water emulsion comprising 5% squalene, 0.5% polysorbate 80 and 0.5% sorbitan trioleate in aqueous citrate buffer pH 6.5, and a nonadjuvated second vaccine as combination partners for the simultaneous, separate or phased application for immunization against viral, bacterial or parasitic infectious diseases.

Abstract: The present invention relates to a hybrid protein comprising the Pseudomonas aeruginosa outer membrane protein I (OprI) which is fused with its amino terminal end to the carboxy-terminal end of a carboxy-terminal portion of the Pseudomonas aeruginosa outer membrane protein F (OprF), as well as to monoclonal or polyclonal antibodies against this hybrid protein. Both, the hybrid protein and the antibodies directed to the hybrid protein confer protection against an infection by Pseudomonas aeruginosa to laboratory animals or man.

Abstract: The invention pertains to the field of recombinant DNA technology and concerns a method for the production of a protein heterologous to yeast in a homogenous form with the aid of Saccharomyces cerevisiae strain HT393 or a derivative thereof carrying a hybrid vector containing the genes for said protein.

Abstract: Recombinant yeast expression vectors with the features indicated in the patent claims are described. These recombinant yeast expression vectors can be used for the preparation of HBeAg in yeast host organisms. Appropriate expression systems, transformed host organisms, diagnostic aids and medicinal agents are additionally described.

Abstract: Antibodies which are specific for Saccharomyces cerevisiae, Saccharomyces bayanus, Saccharomyces paradoxus and Saccharomyces pastorianus, and epitopes to which such antibodies bind are described. Diagnostic agents and assays for detecting Saccharomyces sensu strictu and epitopes of Saccharomyces sensu strictu also are described.

Abstract: Antibodies which are specific for Saccharomyces cerevisiae, Saccharomyces bayanus, Saccharomyces paradoxus and Saccharomyces pastorianus, and epitopes to which such antibodies bind are described. Diagnostic agents and assays for detecting Saccharomyces sensu strictu and epitopes of Saccharomyces sensu strictu also are described.

Abstract: A live attenuated influenza vaccine contains a H1 subtype influenza A strain. Its hemagglutinin is more closely related to SEQ ID NO: 1 than to SEQ ID NO: 3.