4.7 Review

Review of Meningococcal Group B Vaccines

期刊

CLINICAL INFECTIOUS DISEASES
卷 50, 期 -, 页码 S54-S65

出版社

OXFORD UNIV PRESS INC
DOI: 10.1086/648966

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资金

  1. National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH) [R01 AI046464]
  2. National Center for Research Resources, NIH [C06 RR-16226]
  3. NATIONAL CENTER FOR RESEARCH RESOURCES [C06RR016226, M01RR001271] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI046464, R21AI061533] Funding Source: NIH RePORTER

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No broadly effective vaccines are available for prevention of group B meningococcal disease, which accounts for >50% of all cases. The group B capsule is an autoantigen and is not a suitable vaccine target. Outermembrane vesicle vaccines appear to be safe and effective, but serum bactericidal responses in infants are specific for a porin protein, PorA, which is antigenically variable. To broaden protection, outer-membrane vesicle vaccines have been prepared from >1 strain, from mutants with >1 PorA, or from mutants with genetically detoxified endotoxin and overexpressed desirable antigens, such as factor H binding protein. Also, recombinant protein vaccines such as factor H binding protein, given alone or in combination with other antigens, are in late-stage clinical development and may be effective against the majority of group B strains. Thus, the prospects have never been better for developing vaccines for prevention of meningococcal disease, including that caused by group B strains.

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