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用重组流感病毒和 MVA 诱导对 TBEV NS1 蛋白的体液和细胞免疫可提供针对小鼠致死性 TBEV 感染的部分保护。

Induction of humoral and cell-mediated immunity to the NS1 protein of TBEV with recombinant Influenza virus and MVA affords partial protection against lethal TBEV infection in mice.

机构信息

Research Center for Emerging Infections and Zoonoses, University of Veterinary Medicine Hannover, Foundation, Hannover, Germany.

Department of Pathology, University of Veterinary Medicine Hannover, Foundation, Hannover, Germany.

出版信息

Front Immunol. 2023 Jul 7;14:1177324. doi: 10.3389/fimmu.2023.1177324. eCollection 2023.

DOI:10.3389/fimmu.2023.1177324
PMID:37483628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10360051/
Abstract

INTRODUCTION

Tick-borne encephalitis virus (TBEV) is one of the most relevant tick-transmitted neurotropic arboviruses in Europe and Asia and the causative agent of tick-borne encephalitis (TBE). Annually more than 10,000 TBE cases are reported despite having vaccines available. In Europe, the vaccines FSME-IMMUN® and Encepur® based on formaldehyde-inactivated whole viruses are licensed. However, demanding vaccination schedules contribute to sub-optimal vaccination uptake and breakthrough infections have been reported repeatedly. Due to its immunogenic properties as well as its role in viral replication and disease pathogenesis, the non-structural protein 1 (NS1) of flaviviruses has become of interest for non-virion based flavivirus vaccine candidates in recent years.

METHODS

Therefore, immunogenicity and protective efficacy of TBEV NS1 expressed by neuraminidase (NA)-deficient Influenza A virus (IAV) or Modified Vaccinia virus Ankara (MVA) vectors were investigated in this study.

RESULTS

With these recombinant viral vectors TBEV NS1-specific antibody and T cell responses were induced. Upon heterologous prime/boost regimens partial protection against lethal TBEV challenge infection was afforded in mice.

DISCUSSION

This supports the inclusion of NS1 as a vaccine component in next generation TBEV vaccines.

摘要

简介

蜱传脑炎病毒(TBEV)是欧洲和亚洲最重要的蜱传神经嗜性虫媒病毒之一,也是蜱传脑炎(TBE)的病原体。尽管有疫苗可用,但每年仍报告超过 10000 例 TBE 病例。在欧洲,基于甲醛灭活全病毒的 FSME-IMMUN®和 Encepur®疫苗获得许可。然而,苛刻的疫苗接种时间表导致疫苗接种率不理想,并且已经反复报告了突破性感染。由于其免疫原性以及在病毒复制和疾病发病机制中的作用,近年来,黄病毒的非结构蛋白 1(NS1)已成为基于非病毒颗粒的黄病毒疫苗候选物的研究热点。

方法

因此,本研究中研究了由神经氨酸酶(NA)缺陷型流感 A 病毒(IAV)或改良安卡拉痘苗病毒(MVA)载体表达的 TBEV NS1 的免疫原性和保护效力。

结果

用这些重组病毒载体,诱导了 TBEV NS1 特异性抗体和 T 细胞反应。在异源初免/加强方案中,这些重组病毒载体在小鼠中提供了针对致死性 TBEV 挑战感染的部分保护。

讨论

这支持将 NS1 作为下一代 TBEV 疫苗的疫苗成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa63/10360051/5f6331dc25f0/fimmu-14-1177324-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa63/10360051/5f6331dc25f0/fimmu-14-1177324-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa63/10360051/996578634b56/fimmu-14-1177324-g002.jpg
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