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在非洲人中,脑膜炎球菌 A 结合疫苗的免疫原性和安全性。

Immunogenicity and safety of a meningococcal A conjugate vaccine in Africans.

机构信息

Centre pour le Développement des Vaccins, Bamako, Mali.

出版信息

N Engl J Med. 2011 Jun 16;364(24):2293-304. doi: 10.1056/NEJMoa1003812.

Abstract

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.).

摘要

背景

A 群脑膜炎球菌是非洲脑膜炎流行的主要来源。需要一种价格低廉、高度免疫原性的脑膜炎球菌 A 结合疫苗。

方法

我们在非洲进行了两项研究,以评估一种新型的 MenA 结合疫苗(PsA-TT)。在研究 A 中,601 名 12 至 23 个月大的儿童被随机分配接受 PsA-TT、四价多糖参考疫苗(PsACWY)或对照疫苗(流感嗜血杆菌 b 型结合疫苗[Hib-TT])。10 个月后,这些儿童在每组内再次进行随机分组,接受 PsA-TT 的全剂量、PsACWY 的五分之一剂量或 Hib-TT 的全剂量,最初的 589 名参与者接受了加强剂量。在研究 B 中,900 名 2 至 29 岁的受试者被随机分配接受 PsA-TT 或 PsACWY。评估了安全性和反应原性,并通过测量具有兔补体的血清杀菌抗体(SBA)的活性和进行 IgG 组 A 特异性酶联免疫吸附试验来评估免疫原性。

结果

在研究 A 中,PsA-TT 组 96.0%的受试者和 PsACWY 组 63.7%的受试者的 SBA 滴度至少是基线的 4 倍;在研究 B 中,PsA-TT 组 78.2%的受试者和 PsACWY 组 46.2%的受试者的 SBA 滴度至少是基线的 4 倍。研究 A 和研究 B 中 PsA-TT 组的几何平均 SBA 滴度分别比 PsACWY 组高 16 倍和 3 倍(P<0.001)。在研究 A 中,PsA-TT 组在第 40 周的抗体滴度高于 PsACWY 组,并且在接受多糖加强疫苗后具有明显的免疫记忆。疫苗组之间的安全性概况相似,尽管 PsA-TT 组接种部位的压痛和硬结发生率高于 PsACWY 组。不良事件与研究地区特定年龄的发病率一致;没有报告与疫苗相关的严重不良事件。

结论

PsA-TT 疫苗引发的 A 群抗体反应强于 PsACWY 疫苗。(由脑膜炎疫苗项目通过比尔和梅琳达盖茨基金会的一项赠款资助;对照试验。COM 编号,ISRCTN78147026 和 ISRCTN87739946。)

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