Immunogenicity and Safety of a Meningococcal A Conjugate Vaccine in Africans

被引:132
|
作者
Sow, Samba O. [1 ]
Okoko, Brown J. [2 ]
Diallo, Aldiouma [3 ]
Viviani, Simonetta [4 ]
Borrow, Ray [5 ]
Carlone, George [6 ]
Tapia, Milagritos [1 ]
Akinsola, Adebayo K. [2 ]
Arduin, Pascal [3 ]
Findlow, Helen [5 ]
Elie, Cheryl [6 ]
Haidara, Fadima Cheick [1 ]
Adegbola, Richard A. [2 ]
Diop, Doudou [3 ]
Parulekar, Varsha [7 ]
Chaumont, Julie [4 ]
Martellet, Lionel [4 ]
Diallo, Fatoumata [1 ]
Idoko, Olubukola T. [2 ]
Tang, Yuxiao [4 ]
Plikaytis, Brian D. [6 ]
Kulkarni, Prasad S. [8 ]
Marchetti, Elisa [4 ]
LaForce, F. Marc [4 ]
Preziosi, Marie-Pierre [9 ]
机构
[1] Ctr Dev Vaccins, Bamako, Mali
[2] MRC Labs, Basse, Gambia
[3] Inst Rech Dev, Dakar, Senegal
[4] Program Appropriate Technol Hlth, Meningitis Vaccine Project, Ferney Voltaire, France
[5] Hlth Protect Agcy NW, Vaccine Evaluat Unit, Manchester, Lancs, England
[6] Ctr Dis Control & Prevent, Atlanta, GA USA
[7] DiagnoSearch Life Sci, Bombay, Maharashtra, India
[8] Serum Inst India, Pune, Maharashtra, India
[9] WHO, Initiat Vaccine Res, Meningitis Vaccine Project, CH-1211 Geneva 27, Switzerland
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2011年 / 364卷 / 24期
关键词
NEISSERIA-MENINGITIDIS GROUP; POLYSACCHARIDE VACCINE; EPIDEMIC MENINGITIS; SEROGROUP-A; ANTIBODY; MEMORY; TRIAL; BELT; RISK; QUADRIVALENT;
D O I
10.1056/NEJMoa1003812
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Group A meningococci are the source of major epidemics of meningitis in Africa. An affordable, highly immunogenic meningococcal A conjugate vaccine is needed. Methods We conducted two studies in Africa to evaluate a new MenA conjugate vaccine (PsA-TT). In study A, 601 children, 12 to 23 months of age, were randomly assigned to receive PsA-TT, a quadrivalent polysaccharide reference vaccine (PsACWY), or a control vaccine (Haemophilus influenzae type b conjugate vaccine [Hib-TT]). Ten months later, these children underwent another round of randomization within each group to receive a full dose of PsA-TT, a one-fifth dose of PsACWY, or a full dose of Hib-TT, with 589 of the original participants receiving a booster dose. In study B, 900 subjects between 2 and 29 years of age were randomly assigned to receive PsA-TT or PsACWY. Safety and reactogenicity were evaluated, and immunogenicity was assessed by measuring the activity of group A serum bactericidal antibody (SBA) with rabbit complement and performing an IgG group A-specific enzyme-linked immunosorbent assay. Results In study A, 96.0% of the subjects in the PsA-TT group and 63.7% of those in the PsACWY group had SBA titers that were at least four times as high as those at baseline; in study B, 78.2% of the subjects in the PsA-TT group and 46.2% of those in the PsACWY group had SBA titers that were at least four times as high as those at baseline. The geometric mean SBA titers in the PsA-TT groups in studies A and B were greater by factors of 16 and 3, respectively, than they were in the PsACWY groups (P<0.001). In study A, the PsA-TT group had higher antibody titers at week 40 than the PsACWY group and had obvious immunologic memory after receiving a polysaccharide booster vaccine. Safety profiles were similar across vaccine groups, although PsA-TT recipients were more likely than PsACWY recipients to have tenderness and induration at the vaccination site. Adverse events were consistent with age-specific morbidity in the study areas; no serious vaccine-related adverse events were reported. Conclusions The PsA-TT vaccine elicited a stronger response to group A antibody than the PsACWY vaccine. (Funded by the Meningitis Vaccine Project through a grant from the Bill and Melinda Gates Foundation; Controlled-Trials.com numbers, ISRCTN78147026 and ISRCTN87739946.)
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页码:2293 / 2304
页数:12
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