US2012027800A1PendingUtilityA1
Neisserial vaccine compositions comprising a combination of antigens
Assignee: BERTHET FRANCOIS-XAVIER JACQUESPriority: Aug 2, 2002Filed: Sep 29, 2011Published: Feb 2, 2012
Est. expiryAug 2, 2022(expired)· nominal 20-yr term from priority
Inventors:Francois-Xavier BerthetRalph Leon BiemansPhilippe DenoelChristiane FeronCarine GorajJan PoolmanVincent Weynants
A61P 37/00A61P 37/02A61P 31/00A61P 37/04A61P 31/04A61P 43/00C07K 14/22A61K 2039/55572A61K 2039/55577A61K 2039/55505A61K 39/1045A61K 39/102A61K 39/095A61K 2039/70A61K 2039/521A61K 2039/55516A61P 11/00A61K 39/02C12N 15/00Y02A50/30
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Claims
Abstract
The present invention relates to immunogenic compositions and vaccines for the treatment and prevention of Neisserial disease. Immunogenic compositions of the invention contain combinations of antigens selected from at least two different classes of antigens including adhesins, autotransporter proteins, toxins, iron acquisitions proteins and membrane-associated protein (preferably integral outer membrane protein)s. Such combinations of antigens are able to target the immune response against different aspects of the neisserial life cycle, resulting in a more effective immune response.
Claims
exact text as granted — not AI-modified1 .- 12 . (canceled)
13 . An immunogenic composition comprising at least one Neisserial autotransporter antigen, at least one Neisserial Fe acquisition protein antigen, and at least one Neisserial outer membrane protein antigen wherein each of the at least one Neisserial autotransporter antigen, the at least one Neisserial Fe acquisition protein antigen, and the at least one Neisseral outer membrane protein antigen is isolated and wherein said immunogenic composition comprises both a subunit composition and an outer membrane vesicle composition wherein the outer membrane vesicle composition comprises a concentration of LPS immunotype L3 that is achievable using 0.02-0.4% deoxychoate extraction.
14 . The immunogenic composition of claim 13 wherein all of the Neisserial protein antigens are derived from N. meningitidis.
15 . The immunogenic composition of claim 13 further comprising one or more bacterial capsular polysaccharides or oligosaccharides.
16 . The immunogenic composition of claim 15 wherein the capsular polysaccharides or oligosaccharides are derived from bacteria selected from the group consisting of: Neisseria meningitidis serogroup A, C, Y and W-135.
17 . The immunogenic composition of claim 13 further comprising an adjuvant.
18 . The immunogenic composition of claim 17 , wherein the adjuvant comprises aluminum salts.
19 . The immunogenic composition of claim 18 , wherein said aluminum salt is aluminum hydroxide gel.
20 . The immunogenic composition of claim 13 , wherein the outer membrane protein antigen is GNA1870.
21 . The immunogenic composition of claim 13 , wherein the Neisseral autotransporter antigen is NadA.
22 . The immunogenic composition of claim 13 , wherein the Neisseral Fe acquisition protein antigen is transferrin binding protein related protein.Join the waitlist — get patent alerts
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