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四价脑膜炎球菌血清型 A、C、W-135 和 Y 破伤风类毒素结合疫苗在先前接种过四价多糖疫苗的受试者中具有免疫原性,且临床安全性可接受。

The tetravalent meningococcal serogroups A, C, W-135, and Y tetanus toxoid conjugate vaccine is immunogenic with a clinically acceptable safety profile in subjects previously vaccinated with a tetravalent polysaccharide vaccine.

机构信息

Center for Infectious Diseases Research, American University of Beirut, PO Box 11-0236, Riad El Solh, Beirut 1107 2020, Lebanon.

出版信息

Int J Infect Dis. 2012 Aug;16(8):e608-15. doi: 10.1016/j.ijid.2012.04.006. Epub 2012 Jun 14.

DOI:10.1016/j.ijid.2012.04.006
PMID:22704725
Abstract

OBJECTIVES

The immunogenicity and safety of the tetravalent meningococcal serogroups A, C, W-135, and Y tetanus toxoid conjugate vaccine (MenACWY-TT) were evaluated in subjects previously vaccinated with a tetravalent meningococcal polysaccharide vaccine and in subjects without previous meningococcal vaccination.

METHODS

In this phase II, open, controlled study (NCT00661557), healthy subjects aged 4.5-34 years received one dose of MenACWY-TT at month 0. Subjects in the MPS group (n=192) had received polysaccharide vaccine in a study conducted 30-42 months earlier; age-matched subjects in the noMPS control group (n=79) had received no meningococcal vaccination within the past 10 years. Serum bactericidal activity using rabbit complement (rSBA) was measured at month 0 and month 1.

RESULTS

At month 1, ≥97.0% of subjects had rSBA titers ≥1:128. Post-vaccination rSBA geometric mean titers (GMTs) were ≥3.9-fold higher than pre-vaccination in both treatment groups. Exploratory analyses showed no statistically significant differences between groups in percentages of subjects with rSBA titers ≥1:8 and ≥1:128, but significantly lower rSBA GMTs and vaccine response rates for each serogroup in the MPS versus the noMPS group. MenACWY-TT had an acceptable safety profile in both groups.

CONCLUSIONS

These results suggest that MenACWY-TT could be used in vaccination programs irrespective of the pre-vaccination status with polysaccharide vaccine.

摘要

目的

评估已接种过四价脑膜炎奈瑟菌多糖疫苗和未接种过脑膜炎奈瑟菌疫苗的受试者中,四价脑膜炎奈瑟菌血清型 A、C、W-135 和 Y 破伤风类毒素结合疫苗(MenACWY-TT)的免疫原性和安全性。

方法

在这项 II 期、开放性、对照研究(NCT00661557)中,4.5-34 岁的健康受试者在 0 月时接种一剂 MenACWY-TT。MPS 组(n=192)受试者在 30-42 个月前参加了一项多糖疫苗研究;年龄匹配的 noMPS 对照组(n=79)受试者在过去 10 年内未接种过脑膜炎奈瑟菌疫苗。在 0 月和 1 月时测量血清杀菌活性(rSBA)。

结果

在 1 月时,≥97.0%的受试者 rSBA 滴度≥1:128。在两个治疗组中,接种后 rSBA 几何平均滴度(GMT)均比接种前升高≥3.9 倍。探索性分析显示,两组在 rSBA 滴度≥1:8 和≥1:128 的受试者百分比方面无统计学显著差异,但 MPS 组与 noMPS 组相比,每个血清型组的 rSBA GMT 和疫苗反应率均显著较低。MenACWY-TT 在两组中的安全性状况均可接受。

结论

这些结果表明,MenACWY-TT 可用于疫苗接种计划,而不论多糖疫苗的接种情况如何。

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