Review of Meningococcal Group B Vaccines

被引:147
作者
Granoff, Dan M. [1 ]
机构
[1] Childrens Hosp, Oakland Res Inst, Ctr Immunobiol & Vaccine Dev, Oakland, CA 94609 USA
基金
美国国家卫生研究院;
关键词
FACTOR-H-BINDING; MENINGITIDIS SEROGROUP-B; MEMBRANE-VESICLE VACCINE; SYNERGISTIC BACTERICIDAL ACTIVITY; NEISSERIA-MENINGITIDIS; UNITED-STATES; CONFERS PROTECTION; CONJUGATE VACCINE; HEXAVALENT PORA; CONFORMATIONAL EPITOPES;
D O I
10.1086/648966
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:S54 / S65
页数:12
相关论文
共 132 条
[1]  
[Anonymous], 2008, 16 INT PATH NEISS C
[2]  
[Anonymous], 1991, NIPH ANN
[3]  
Baker M G, 2001, J Paediatr Child Health, V37, pS13, DOI 10.1046/j.1440-1754.2001.00722.x
[4]   Distribution and genetic variability of three vaccine components in a panel of strains representative of the diversity of serogroup B meningococcus [J].
Bambini, Stefania ;
Muzzi, Alessandro ;
Olcen, Per ;
Rappuoli, Rino ;
Pizza, Mariagrazia ;
Comanducci, Maurizio .
VACCINE, 2009, 27 (21) :2794-2803
[5]   Meningococcal Factor H-Binding Protein Variants Expressed by Epidemic Capsular Group A, W-135, and X Strains from Africa [J].
Beernink, P. T. ;
Caugant, D. A. ;
Welsch, J. A. ;
Koeberling, O. ;
Granoff, D. M. .
JOURNAL OF INFECTIOUS DISEASES, 2009, 199 (09) :1360-1368
[6]   Fine antigenic specificity and cooperative bactericidal activity of monoclonal antibodies directed at the meningococcal vaccine candidate factor H-binding protein [J].
Beernink, Peter T. ;
Welsch, Jo Anne ;
Bar-Lev, Michal ;
Koeberling, Oliver ;
Comanducci, Maurizio ;
Granoff, Dan M. .
INFECTION AND IMMUNITY, 2008, 76 (09) :4232-4240
[7]   Bactericidal antibody responses induced by meningococcal recombinant chimeric factor H-binding protein vaccines [J].
Beernink, Peter T. ;
Granoff, Dan M. .
INFECTION AND IMMUNITY, 2008, 76 (06) :2568-2575
[8]   Prevalence of factor H-binding protein variants and NadA among meningococcal group B isolates from the United States: Implications for the development of a multicomponent group B vaccine [J].
Beernink, Peter T. ;
Welsch, Jo Anne ;
Harrison, Lee H. ;
Leipus, Arunas ;
Kaplan, Sheldon L. ;
Granoff, Dan M. .
JOURNAL OF INFECTIOUS DISEASES, 2007, 195 (10) :1472-1479
[9]   The modular architecture of meningococcal factor H-binding protein [J].
Beernink, Peter T. ;
Granoff, Dan M. .
MICROBIOLOGY-SGM, 2009, 155 :2873-2883
[10]   Genetic diversity and carriage dynamics of Neisseria lactamica in infants [J].
Bennett, JS ;
Griffiths, DT ;
McCarthy, ND ;
Sleeman, KL ;
Jolley, KA ;
Crook, DW ;
Maiden, MCJ .
INFECTION AND IMMUNITY, 2005, 73 (04) :2424-2432