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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.
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页码:1277 / 1287
页数:11
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