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M2e-based universal influenza vaccines: a historical overview and new approaches to development

机译:基于M2e的通用流感疫苗:历史回顾和新的开发方法

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摘要

The influenza A virus was isolated for the first time in 1931, and the first attempts to develop a vaccine against the virus began soon afterwards. In addition to causing seasonal epidemics, influenza viruses can cause pandemics at random intervals, which are very hard to predict. Vaccination is the most effective way of preventing the spread of influenza infection. However, seasonal vaccination is ineffective against pandemic influenza viruses because of antigenic differences, and it takes approximately six months from isolation of a new virus to develop an effective vaccine. One of the possible ways to fight the emergence of pandemics may be by using a new type of vaccine, with a long and broad spectrum of action. The extracellular domain of the M2 protein (M2e) of influenza A virus is a conservative region, and an attractive target for a universal influenza vaccine. This review gives a historical overview of the study of M2 protein, and summarizes the latest developments in the preparation of M2e-based universal influenza vaccines.
机译:甲型流感病毒是在1931年首次分离出的,此后不久就开始了开发抗该病毒疫苗的首次尝试。流感病毒除了引起季节性流行外,还可以随机间隔引起大流行,这很难预测。接种疫苗是预防流感感染扩散的最有效方法。但是,由于抗原差异,季节性疫苗接种对大流行性流感病毒无效,并且从分离出新病毒大约需要六个月才能开发出有效的疫苗。应对大流行的可能方法之一可能是使用一种新型的,具有长期广泛作用的疫苗。甲型流感病毒的M2蛋白(M2e)的胞外域是一个保守区域,是通用流感疫苗的有吸引力的靶标。这篇综述对M2蛋白的研究进行了历史回顾,并总结了基于M2e的通用流感疫苗制备的最新进展。

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