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用M2e5x病毒样颗粒进行鼻内接种可诱导体液免疫和细胞免疫反应,从而对异亚型流感病毒产生交叉保护。

Intranasal vaccination with M2e5x virus-like particles induces humoral and cellular immune responses conferring cross-protection against heterosubtypic influenza viruses.

作者信息

Lee Young-Tae, Ko Eun-Ju, Lee Youri, Kim Ki-Hye, Kim Min-Chul, Lee Yu-Na, Kang Sang-Moo

机构信息

Center for Inflammation, Immunity & Infection, Institute for Biomedical Sciences, Georgia State University, Atlanta, Georgia, United States of America.

Animal and Plant Quarantine Agency, Gimcheon, Gyeongsangbukdo, Republic of Korea.

出版信息

PLoS One. 2018 Jan 11;13(1):e0190868. doi: 10.1371/journal.pone.0190868. eCollection 2018.

Abstract

Current influenza vaccines do not provide broad cross-protection. Here, we report that intranasal vaccination with virus-like particles containing the highly conserved multiple ectodomains of matrix protein 2 (M2e5x VLP) of influenza virus induces broad cross-protection by M2-specific humoral and cellular immune responses. M2e5x VLP intranasal vaccination prevented severe weight loss, attenuated inflammatory cytokines and cellular infiltrates, and lowered viral loads, and induced germinal center phenotypic B and plasma cells. In addition, depletion studies demonstrate the protective roles of CD4 and CD8 T cells induced by M2e5x VLP intranasal vaccination. Thus, this study provides evidence that mucosal delivery of M2e5x VLP vaccine provides cross-protection by inducing humoral and cellular immune responses.

摘要

目前的流感疫苗不能提供广泛的交叉保护。在此,我们报告称,用含有流感病毒基质蛋白2高度保守的多个胞外域(M2e5x VLP)的病毒样颗粒进行鼻内接种,可通过M2特异性体液免疫和细胞免疫反应诱导广泛的交叉保护。M2e5x VLP鼻内接种可防止严重体重减轻,减轻炎性细胞因子和细胞浸润,并降低病毒载量,还可诱导生发中心表型的B细胞和浆细胞。此外,耗竭研究证明了M2e5x VLP鼻内接种诱导的CD4和CD8 T细胞的保护作用。因此,本研究提供了证据,表明M2e5x VLP疫苗的黏膜递送通过诱导体液免疫和细胞免疫反应提供交叉保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b7cf/5764335/a1586d5fd8fc/pone.0190868.g001.jpg

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