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基质蛋白 2 胞外结构域在通用流感疫苗开发中的作用。

The Role of Matrix Protein 2 Ectodomain in the Development of Universal Influenza Vaccines.

机构信息

VIB-UGent Center for Medical Biotechnology, Ghent.

Department of Biomedical Molecular Biology, Ghent University, Belgium.

出版信息

J Infect Dis. 2019 Apr 8;219(Suppl_1):S68-S74. doi: 10.1093/infdis/jiz003.

Abstract

The influenza A virus matrix protein 2 ectodomain (M2e) is a universal influenza A vaccine candidate. Numerous studies in laboratory mice, but very few in natural influenza A virus hosts, have demonstrated that M2e-based vaccines can provide protection against any influenza A virus challenge. M2e-based immunity is largely accomplished by IgG and early stage clinical studies have demonstrated that the vaccine is safe. Yet M2e is considered a difficult target to develop as a vaccine: it does not offer sterilizing immunity and its mode of action relies on Fcγ receptor-mediated effector mechanisms, most likely in concert with alveolar macrophages. In a human challenge study with an H3N2 virus, treatment with a monoclonal M2e-specific human IgG was associated with a faster recovery compared to placebo treatment. If the universal influenza vaccine field incorporates this antigen into next generation vaccines, M2e could prove its merit when the next influenza pandemic strikes.

摘要

甲型流感病毒基质蛋白 2 胞外域(M2e)是一种通用的甲型流感疫苗候选物。大量在实验小鼠中的研究,以及非常少的在自然甲型流感病毒宿主中的研究,已经证明基于 M2e 的疫苗可以提供针对任何甲型流感病毒挑战的保护。基于 M2e 的免疫主要是通过 IgG 实现的,早期的临床研究已经证明该疫苗是安全的。然而,M2e 被认为是一种难以开发的疫苗靶标:它不能提供杀菌性免疫,其作用模式依赖于 Fcγ 受体介导的效应机制,很可能与肺泡巨噬细胞协同作用。在一项针对 H3N2 病毒的人体挑战研究中,与安慰剂治疗相比,用单克隆 M2e 特异性人 IgG 治疗与更快的康复相关。如果通用流感疫苗领域将这种抗原纳入下一代疫苗中,那么当下一次流感大流行来袭时,M2e 可能会证明其价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6207/6452325/3a6149f7f557/jiz00301.jpg

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