病毒学
病毒
生物
抗原漂移
血凝素(流感)
原罪
甲型流感病毒
抗原转移
细胞毒性T细胞
接种疫苗
表位
免疫
正粘病毒科
流感疫苗
H5N1基因结构
异源的
抗原
免疫系统
免疫学
基因
医学
体外
传染病(医学专业)
遗传学
2019年冠状病毒病(COVID-19)
疾病
病理
作者
Arwen F. Altenburg,Guus F. Rimmelzwaan,Rory D. de Vries
出处
期刊:Vaccine
[Elsevier BV]
日期:2014-12-09
卷期号:33 (4): 500-506
被引量:143
标识
DOI:10.1016/j.vaccine.2014.11.054
摘要
Since inactivated influenza vaccines mainly confer protective immunity by inducing strain-specific antibodies to the viral hemagglutinin, these vaccines only afford protection against infection with antigenically matching influenza virus strains. Due to the continuous emergence of antigenic drift variants of seasonal influenza viruses and the inevitable future emergence of pandemic influenza viruses, there is considerable interest in the development of influenza vaccines that induce broader protective immunity. It has long been recognized that influenza virus-specific CD8(+) T cells directed to epitopes located in the relatively conserved internal proteins can cross-react with various subtypes of influenza A virus. This implies that these CD8(+) T cells, induced by prior influenza virus infections or vaccinations, could afford heterosubtypic immunity. Furthermore, influenza virus-specific CD4(+) T cells have been shown to be important in protection from infection, either via direct cytotoxic effects or indirectly by providing help to B cells and CD8(+) T cells. In the present paper, we review the induction of virus-specific T cell responses by influenza virus infection and the role of virus-specific CD4(+) and CD8(+) T cells in viral clearance and conferring protection from subsequent infections with homologous or heterologous influenza virus strains. Furthermore, we discuss vector-based vaccination strategies that aim at the induction of a cross-reactive virus-specific T cell response.
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