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基于改良安卡拉痘苗病毒的甲型流感病毒(H5N1)疫苗在随机 1/2a 期临床试验中诱导跨属抗体和 T 细胞反应。

Induction of Cross-Clade Antibody and T-Cell Responses by a Modified Vaccinia Virus Ankara-Based Influenza A(H5N1) Vaccine in a Randomized Phase 1/2a Clinical Trial.

机构信息

Department of Viroscience, Postgraduate School of Molecular Medicine, Erasmus Medical Center, Rotterdam, the Netherlands.

Institute for Infectious Diseases and Zoonoses, Ludwig Maximilian University of Munich, Munich.

出版信息

J Infect Dis. 2018 Jul 13;218(4):614-623. doi: 10.1093/infdis/jiy214.

Abstract

BACKGROUND

High-pathogenicity avian influenza viruses continue to circulate in poultry and wild birds and occasionally infect humans, sometimes with fatal outcomes. Development of vaccines is a priority to prepare for potential pandemics but is complicated by antigenic variation of the surface glycoprotein hemagglutinin. We report the immunological profile induced by human immunization with modified vaccinia virus Ankara (MVA) expressing the hemagglutinin gene of influenza A(H5N1) virus A/Vietnam/1194/04 (rMVA-H5).

METHODS

In a double-blinded phase 1/2a clinical trial, 79 individuals received 1 or 2 injections of rMVA-H5 or vector control. Twenty-seven study subjects received a booster immunization after 1 year. The breadth, magnitude, and properties of vaccine-induced antibody and T-cell responses were characterized.

RESULTS

rMVA-H5 induced broadly reactive antibody responses, demonstrated by protein microarray, hemagglutination inhibition, virus neutralization, and antibody-dependent cellular cytotoxicity assays. Antibodies cross-reacted with antigenically distinct H5 viruses, including the recently emerged subtypes H5N6 and H5N8 and the currently circulating subtype H5N1. In addition, the induction of T cells specific for H5 viruses of 2 different clades was demonstrated.

CONCLUSIONS

rMVA-H5 induced immune responses that cross-reacted with H5 viruses of various clades. These findings validate rMVA-H5 as vaccine candidate against antigenically distinct H5 viruses.

CLINICAL TRIALS REGISTRATION

NTR3401.

摘要

背景

高致病性禽流感病毒继续在禽类和野鸟中传播,偶尔会感染人类,有时导致致命后果。开发疫苗是为潜在的大流行做准备的当务之急,但由于表面糖蛋白血凝素的抗原变异而变得复杂。我们报告了用表达流感 A(H5N1)病毒 A/Vietnam/1194/04(rMVA-H5)血凝素基因的改良安卡拉牛痘病毒(MVA)对人类进行免疫接种所引起的免疫谱。

方法

在一项双盲 1/2a 期临床试验中,79 名个体接受了 1 或 2 次 rMVA-H5 或载体对照的接种。27 名研究对象在 1 年后接受了加强免疫。特征是疫苗诱导的抗体和 T 细胞反应的广度、幅度和特性。

结果

rMVA-H5 诱导了广泛反应的抗体反应,通过蛋白质微阵列、血凝抑制、病毒中和和抗体依赖性细胞毒性测定来证明。抗体与抗原上不同的 H5 病毒发生交叉反应,包括最近出现的 H5N6 和 H5N8 亚型以及目前流行的 H5N1 亚型。此外,还证明了对 2 种不同谱系的 H5 病毒具有特异性的 T 细胞的诱导。

结论

rMVA-H5 诱导了与各种谱系的 H5 病毒发生交叉反应的免疫反应。这些发现验证了 rMVA-H5 作为针对抗原上不同的 H5 病毒的候选疫苗。

临床试验注册

NTR3401。

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