US2005031646A1PendingUtilityA1
Vaccine
Est. expiryMar 19, 2019(expired)· nominal 20-yr term from priority
Inventors:Carine CapiauMarguerite DeschampsPierre DesmonsCraig LaferriereJan PoolmanJean-Paul Prieels
A61P 37/04A61P 27/06A61P 27/16A61P 31/04A61P 31/00A61P 11/00A61K 47/646A61K 39/102A61K 39/12A61K 2039/70A61K 2039/6037A61K 2039/55572A61K 39/155A61K 2039/6068A61K 39/092A61K 2039/55505Y10S424/831A61K 39/095A61K 2039/6075A61K 39/385Y02A50/30
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Claims
Abstract
The present invention relates to the field of bacterial polysaccharide antigen vaccines. In particular, the present invention relates to bacterial polysaccharides conjugated to protein D from H influenzae.
Claims
exact text as granted — not AI-modified1 - 18 . (Cancelled).
19 . An immunogenic composition comprising a plurality of polysaccharide conjugate antigens consisting of a polysaccharide antigen derived from a pathogenic bacterium conjugated to protein D from Haemophilus influenzae or a protein D fragment thereof.
20 . The immunogenic composition as claimed in claim 19 wherein the polysaccharide antigens are selected from the group consisting of: Vi polysaccharides from Salmonella typhi , meningococcal polysaccharides, polysaccharides and modified polysaccharides of group B meningococcus, polysaccharides from Staphylococcus aureus , polysaccharides from Streptococcus agalactiae , polysaccharides from Streptococcus pneumoniae , polysaccharides from Mycobacteria, polysaccharide from Cryptococcus neoformans , lipopolysaccharides of non-typeable Haemophilus influenzae , capsular polysaccharide from Haemophilus influenzae b, lipopolysaccharides of Moraxella catharralis , lipopolysaccharides of Shigella sonnei , and lipopeptidophosphogylcan (LPPG) of Trypanosoma cruzi.
21 . The immunogenic composition as claimed in claim 20 comprising Streptococcus pneumoniae polysaccharide antigens from at least four Streptococcus pneumoniae serotypes.
22 . The immunogenic composition of claim 20 additionally comprising at least one Streptococcuspneumoniae protein antigen.
23 . The immunogenic compositions of claim 22 , wherein the protein antigen is an outer surface protein or a secreted protein of Streptococcus pneumoniae or immunologically functional equivalents thereof.
24 . The immunogenic composition of claim 22 , wherein the protein antigen is a toxin, adhesin or lipoprotein of Streptococcus pneumoniae or immunologically functional equivalents thereof.
25 . The immunogenic composition of claim 22 , wherein the protein antigen, or immunologically functional equivalent thereof, is selected from the group consisting of: pneumolysin, PspA or transmembrane deletion variants thereof, PspC or transmembrane deletion variants thereof, PsaA or transmembrane deletion variants thereof, glyceraldehydes-3-phosphate dehydrogenase, and CbpA or transmembrane deletion variants thereof.
26 . The immunogenic composition of claim 20 , wherein the polysaccharide antigens conjugated to protein D are derived from a combination of N. meningitidis serotypes A, C or Y.
27 . An immunogenic composition comprising conjugated capsular polysaccharides of Haemophilus influenzae b, meningococcus C and meningococcus Y, wherein the capsular polysaccharide antigens are conjugated to protein D from H. influenzae , with the proviso that the capsular polysaccharide from Haemophilus influenzae b is conjugated to tetanus toxoid.
28 . An immunogenic composition comprising conjugated capsular polysaccharides of Streptococcus pneumoniae, Haemophilus influenzae b, meningococcus C and meningococcus Y, wherein the capsular polysaccharide antigens are conjugated to protein D from H. influenzae , with the proviso that the capsular polysaccharide from Haemophilus influenzae b is conjugated to tetanus toxoid.
29 . An immunogenic composition as claimed in any of the preceding claims additionally comprising an adjuvant.
30 . An immunogenic composition as claimed in claimed 29 wherein the polysaccharide—protein D conjugate antigens are adsorbed onto aluminum phosphate.
31 . An immunogenic composition as claimed in claim 29 wherein the adjuvant is a preferential inducer of a TH1 response.
32 . An immunogenic composition as claimed in claim 31 , wherein the adjuvant comprises at least one of the following: 3D-MPL, a saponin immunostimulant, or an immunostimulatory CpG oligonucleotide.
33 . An immunogenic composition as claimed in claim 19 for use as a medicament.
34 . A vaccine comprising the immunogenic composition of claim 29 .
35 . A method of producing an immunogenic composition to a plurality of pathogenic bacteria comprising the steps of:
isolating a plurality of polysaccharide antigens from said pathogenic bacteria; activating the polysaccharides; conjugating the polysaccharides to protein D from H. influenzae ; and mixing the conjugated polysaccharides together.
36 . A method of treating a patient suffering from, or susceptible to, infection from a pathogenic bacterium comprising administering an effective amount of an immunogenic composition as claimed in claim 19.Join the waitlist — get patent alerts
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