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西尼罗河病毒疫苗在 50 岁以上健康成年人中的单剂安全性和免疫原性的 II 期、剂量范围研究。

Phase II, dose ranging study of the safety and immunogenicity of single dose West Nile vaccine in healthy adults ≥ 50 years of age.

机构信息

Sanofi Pasteur, USA, 1 Discovery Drive, Swiftwater, PA 18370, USA.

出版信息

Vaccine. 2012 Oct 19;30(47):6656-64. doi: 10.1016/j.vaccine.2012.08.063. Epub 2012 Sep 7.

DOI:10.1016/j.vaccine.2012.08.063
PMID:22959989
Abstract

INTRODUCTION

ChimeriVax-WN02 is a live, attenuated chimeric vaccine for protection against West Nile virus (WNV) produced by insertion of the genes encoding the pre-membrane (prM) and envelope (E) proteins of WNV (strain NY99) into the yellow fever 7D vaccine virus. This Phase II, randomized, double-blind, placebo-controlled, multi-center study in the US assessed the immunogenicity, viremia, and safety of the ChimeriVax-WN02 vaccine.

METHODS

The study included adults in general good health. Subjects aged ≥ 50 years were randomized to one of four treatment groups: ChimeriVax-WN02 4 × 10(3) plaque-forming units (pfu) (n=122), 4 × 10(4)pfu (n=124), 4 × 10(5)pfu (n=113), or placebo (n=120). A subset of subjects was randomized to assess viremia after vaccination at three different dose levels. Subjects were followed for safety up to 6 months after vaccination.

RESULTS

A total of 121 subjects for WN024 × 10(3), 122 for WN02 4 × 10(4), 110 for WN02 4 × 10(5), and 120 for the placebo group completed the study up to the 6-month safety follow-up. Seroconversion, as measured by plaque reduction neutralization test (PRNT), was achieved at Day 28 by 92.1%, 93.2%, and 95.4% of subjects in the WN02 4 × 10(3), the WN02 4 × 10(4), and the WN02 4 × 10(5) groups, respectively. Viremia was transient, detected between Days 2 and 14 but not at Day 28, and in most cases did not reach the quantification threshold. The percentage of subjects reporting at least one event of reactogenicity was similar in the placebo and active vaccine groups and showed no dose relationship.

CONCLUSIONS

The ChimeriVax-WN02 vaccine was highly immunogenic and well tolerated among subjects ≥ 50 years old at all dose levels.

摘要

简介

ChimeriVax-WN02 是一种用于预防西尼罗河病毒(WNV)的活减毒嵌合疫苗,由插入 WNV( strain NY99)的前膜(prM)和包膜(E)蛋白基因的黄热病 7D 疫苗病毒制成。这项在美国进行的 II 期、随机、双盲、安慰剂对照、多中心研究评估了 ChimeriVax-WN02 疫苗的免疫原性、病毒血症和安全性。

方法

该研究纳入了一般健康状况良好的成年人。年龄≥50 岁的受试者被随机分配至四个治疗组之一:ChimeriVax-WN02 4×10(3)蚀斑形成单位(pfu)(n=122)、4×10(4)pfu(n=124)、4×10(5)pfu(n=113)或安慰剂(n=120)。一部分受试者被随机分配以评估在三个不同剂量水平下接种后的病毒血症。在接种后,受试者接受安全性随访至 6 个月。

结果

共有 121 例 WN024×10(3)、122 例 WN02 4×10(4)、110 例 WN02 4×10(5)和 120 例安慰剂组完成了至 6 个月安全性随访的研究。通过蚀斑减少中和试验(PRNT)测量的血清转化率在 WN02 4×10(3)、WN02 4×10(4)和 WN02 4×10(5)组分别在第 28 天达到 92.1%、93.2%和 95.4%。病毒血症短暂,在第 2 天至 14 天之间检测到,但在第 28 天未检测到,并且在大多数情况下未达到定量阈值。报告至少一次不良反应事件的受试者百分比在安慰剂和活性疫苗组中相似,且与剂量无关。

结论

ChimeriVax-WN02 疫苗在所有剂量水平下均高度免疫原性且在 50 岁以上受试者中耐受性良好。

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