Multivalent meningococcal serogroup B vaccines: challenges in predicting protection and measuring effectiveness

被引:14
|
作者
Poolman, Jan T. [1 ]
Richmond, Peter [2 ]
机构
[1] Janssen, Bacterial Vaccine Discovery & Early Dev, NL-2333 CK Leiden, Netherlands
[2] Univ Western Australia, Sch Paediat & Child Hlth, Princess Margaret Hosp Children, Wesfarmers Ctr Vaccines & Infect Dis,Telethon Ins, Subiaco, WA 6008, Australia
关键词
immunogenicity; meningococcal antigen typing system; Neisseria meningitidis; outer membrane vesicle vaccines; vaccine; FACTOR-H-BINDING; MEMBRANE-VESICLE VACCINE; BIVALENT RLP2086 VACCINE; SYNERGISTIC BACTERICIDAL ACTIVITY; INVASIVE NEISSERIA-MENINGITIDIS; NEW-ZEALAND EPIDEMIC; PHASE; 1/2; TRIAL; UNITED-STATES; STRAIN COVERAGE; PROTEIN VACCINE;
D O I
10.1586/14760584.2015.1071670
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Vaccines targeting Neisseria meningitidis serogroup B (MenB) have been attempted for 40 years. Monovalent outer membrane vesicle vaccines targeted at epidemic outbreaks have been successfully developed. Newer vaccines aim to induce antibodies to cross-reactive antigens, such as factor H binding protein (rLP2086) or a mix of outer membrane vesicle, factor H binding protein and other minor antigens (4CMenB). The true protective coverage among circulating MenB isolates afforded by these vaccines is unknown. Carefully conducted Phase IV post-implementation evaluations designed to measure specific effectiveness against major circulating MenB clonal lineages are needed to address the critical question of which antigens are linked to protection. Progress with whole-genome sequencing and bio-informatics may allow the composition of antigen mozaics based on two major outer membrane proteins: PorA and FetA.
引用
收藏
页码:1277 / 1287
页数:11
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