| Literature DB >> 16125824 |
Daniel M Stein1, John Robbins, Mark A Miller, Feng-Ying C Lin, Rachel Schneerson.
Abstract
As polysialic acid (PSA), the capsule of Group B meningococcus (GBM) and Escherichia coli K1, is a component of mammalian glycopeptides, there is concern that vaccines against PSA could induce immunopathology. Purified PSA is not immunogenic; however, as a component of bacteria or bound to proteins, it induces protective antibodies. In this review, we did not unearth data indicating an association of IgG anti-PSA with immunopathology in experimental animals or humans. We found no increased incidence of autoimmunity from GBM infections in our review of the natural history/sequellae of Neisseria meningitis infections. Accordingly, we propose that clinical trials of PSA conjugate vaccines, be considered.Entities:
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Year: 2005 PMID: 16125824 DOI: 10.1016/j.vaccine.2005.07.084
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641