4.7 Article

Antibody to genome-derived neisserial antigen 2132, a Neisseria meningitidis candidate vaccine, confers protection against bacteremia in the absence of complement-mediated bactericidal activity

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 188, Issue 11, Pages 1730-1740

Publisher

UNIV CHICAGO PRESS
DOI: 10.1086/379375

Keywords

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Funding

  1. NHLBI NIH HHS [T32-HL007951] Funding Source: Medline
  2. NIAID NIH HHS [R01 AI45642, AI46464] Funding Source: Medline
  3. NATIONAL HEART, LUNG, AND BLOOD INSTITUTE [T32HL007951] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI046464, R01AI045642] Funding Source: NIH RePORTER

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Genome-derived neisserial antigen 2132 (GNA2132) is a novel vaccine candidate that was identified during the Neisseria meningitidis group B strain MC58 genome-sequencing project. To assess the vaccine potential of GNA2132, we prepared antisera from mice immunized with recombinant GNA2132 (gene from strain NZ394/98). Anti-GNA2132 antibody bound to the surface of live bacteria from all 7 capsular group B or C strains tested and elicited deposition of human Ob on the bacterial surface. However, with human or infant-rat Complement, anti-GNA2132 had no detectable bactericidal activity (titer, <1:4) against the nominal strain, NZ394/98, and was bactericidal against only 2 of the other 6 strains tested. These differences between strains were unrelated to GNA2132 amino acid sequence or level of protein expression. Despite lack of bactericidal activity, anti-GNA2132 antiserum passively protected infant rats against meningococcal bacteremia after challenge with all 5 resistant strains. GNA2132 is thus a promising vaccine candidate for prevention of disease caused by N. meningitidis.

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