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兽用具有改良 NS1 蛋白的减毒流感 A 病毒疫苗。

Live attenuated influenza A virus vaccines with modified NS1 proteins for veterinary use.

机构信息

Centro de Investigación en Sanidad Animal (CISA), Centro Nacional Instituto de Investigación y Tecnología Agraria y Alimentaria (INIA, CSIC), Madrid, Spain.

Department of Molecular and Cell Biology, Centro Nacional de Biotecnología (CNB-CSIC), Campus Universidad Autónoma de Madrid, Madrid, Spain.

出版信息

Front Cell Infect Microbiol. 2022 Jul 22;12:954811. doi: 10.3389/fcimb.2022.954811. eCollection 2022.

Abstract

Influenza A viruses (IAV) spread rapidly and can infect a broad range of avian or mammalian species, having a tremendous impact in human and animal health and the global economy. IAV have evolved to develop efficient mechanisms to counteract innate immune responses, the first host mechanism that restricts IAV infection and replication. One key player in this fight against host-induced innate immune responses is the IAV non-structural 1 (NS1) protein that modulates antiviral responses and virus pathogenicity during infection. In the last decades, the implementation of reverse genetics approaches has allowed to modify the viral genome to design recombinant IAV, providing researchers a powerful platform to develop effective vaccine strategies. Among them, different levels of truncation or deletion of the NS1 protein of multiple IAV strains has resulted in attenuated viruses able to induce robust innate and adaptive immune responses, and high levels of protection against wild-type (WT) forms of IAV in multiple animal species and humans. Moreover, this strategy allows the development of novel assays to distinguish between vaccinated and/or infected animals, also known as Differentiating Infected from Vaccinated Animals (DIVA) strategy. In this review, we briefly discuss the potential of NS1 deficient or truncated IAV as safe, immunogenic and protective live-attenuated influenza vaccines (LAIV) to prevent disease caused by this important animal and human pathogen.

摘要

甲型流感病毒(IAV)传播迅速,可感染多种禽类或哺乳动物,对人类和动物健康以及全球经济造成巨大影响。IAV 已经进化出有效的机制来对抗先天免疫反应,先天免疫反应是限制 IAV 感染和复制的第一道宿主机制。在这场对抗宿主诱导的先天免疫反应的斗争中,IAV 的非结构蛋白 1(NS1)是一个关键角色,它可以调节感染过程中的抗病毒反应和病毒致病性。在过去的几十年中,反向遗传学方法的实施使得可以修饰病毒基因组来设计重组 IAV,为研究人员提供了一个开发有效疫苗策略的强大平台。其中,对多种 IAV 株的 NS1 蛋白进行不同程度的截断或缺失,导致减毒病毒能够诱导强烈的先天和适应性免疫反应,并在多种动物和人类中对野生型(WT)IAV 形成高水平的保护。此外,该策略还允许开发新的检测方法来区分接种和/或感染的动物,这种方法也被称为区分感染和接种动物(DIVA)策略。在这篇综述中,我们简要讨论了 NS1 缺失或截断的 IAV 作为安全、免疫原性和保护性的减毒活流感疫苗(LAIV)的潜力,以预防这种重要的动物和人类病原体引起的疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89a0/9354547/39dafafae494/fcimb-12-954811-g001.jpg

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