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一种新西兰流行株B群脑膜炎球菌外膜囊泡疫苗在婴儿中的免疫原性和耐受性

Immunogenicity and tolerability in infants of a New Zealand epidemic strain meningococcal B outer membrane vesicle vaccine.

作者信息

Wong Sharon H, Lennon Diana R, Jackson Catherine M, Stewart Joanna M, Reid Stewart, Ypma Ellen, O'Hallahan Jane M, Oster Philipp, Mulholland Kim, Martin Diana R

机构信息

The University of Auckland, Auckland, New Zealand.

出版信息

Pediatr Infect Dis J. 2009 May;28(5):385-90. doi: 10.1097/INF.0b013e318195205e.

DOI:10.1097/INF.0b013e318195205e
PMID:19384263
Abstract

BACKGROUND

An outer membrane vesicle meningococcal vaccine (MeNZB), was developed for the New Zealand epidemic strain of Neisseria meningitidis B:4:P1.7-2,4.

METHODS

A phase II, randomized, observer blind, controlled study evaluating the safety, reactogenicity, and immunogenicity of MeNZB administered with routine New Zealand immunizations at 6 weeks, 3 months, and 5 months of age (n = 375). Group 1 (n = 250) received 25 mug MeNZB and routine immunizations with a fourth MeNZB dose given at 10 months (n = 51). Group 2 (n = 125) received routine immunizations only. Sero-response was a > or =4-fold rise in vaccine strain serum bactericidal antibody titer compared with baseline or a titer of at least 1:8 for baselines <1:4. Reactogenicity was monitored for 7 days after vaccination.

RESULTS

Sero-response in Group 1 was achieved in 53% (95% Confidence interval [CI]: 46-59, n = 239) and 69% (95% CI: 54-80, n = 45) with geometric mean antibody titers of 9 (95% CI: 7-10) and 22 (95% CI: 12-39) after the third and fourth doses, respectively. No negative interference by MeNZB on routine immunizations was detected. There were no serious adverse events judged to be vaccine related.

CONCLUSIONS

In this group of New Zealand infants, 4 MeNZB doses were required to demonstrate titers comparable with those achieved after 3 doses in older children. MeNZB was safe when used concomitantly with routine New Zealand immunizations to 5 months of age.

摘要

背景

一种外膜囊泡脑膜炎球菌疫苗(MeNZB)是针对新西兰流行的B群脑膜炎奈瑟菌菌株B:4:P1.7-2,4研发的。

方法

一项II期随机、观察者盲法、对照研究,评估在6周、3个月和5个月龄时与新西兰常规免疫联合接种MeNZB的安全性、反应原性和免疫原性(n = 375)。第1组(n = 250)接受25μg MeNZB和常规免疫,在10个月时给予第四剂MeNZB(n = 51)。第2组(n = 125)仅接受常规免疫。血清反应定义为疫苗株血清杀菌抗体滴度较基线升高≥4倍,或基线<1:4时滴度至少为1:8。接种疫苗后监测7天的反应原性。

结果

第1组中,第三剂和第四剂后血清反应分别在53%(95%置信区间[CI]:46 - 59,n = 239)和69%(95%CI:54 - 80,n = 45)的受试者中实现,几何平均抗体滴度分别为9(95%CI:7 - 10)和22(95%CI:12 - 39)。未检测到MeNZB对常规免疫有负面干扰。未判定有与疫苗相关的严重不良事件。

结论

在这组新西兰婴儿中,需要4剂MeNZB才能达到与大龄儿童3剂接种后相当的滴度。MeNZB与新西兰5个月龄前的常规免疫联合使用时是安全的。

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