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高度保守的甲型流感病毒序列作为基于T细胞表位的疫苗靶点,以应对病毒变异性。

Highly conserved influenza A sequences as T cell epitopes-based vaccine targets to address the viral variability.

作者信息

Tan Paul Thiamjoo, Khan Asif M, August J Thomas

机构信息

Department of Pharmacology and Molecular Sciences, Johns Hopkins University, School of Medicine, Baltimore, USA.

出版信息

Hum Vaccin. 2011 Apr;7(4):402-9. doi: 10.4161/hv.7.4.13845. Epub 2011 Apr 1.

Abstract

Vaccines are the only proven effective method for prevention of human infectious diseases. Almost all traditional vaccines require activating immunological memory B cells to secrete neutralizing antibodies against invading pathogens. The complication with influenza viruses is the high viral mutation rate that results in immune escape through modification of the B cell epitopes. Studies of T-cell immunity to influenza infection provide an alternative vaccine strategy based on highly conserved T-cell epitopes. In this review, we discuss the importance of T cell-mediated immunity in influenza infection and the need for a targeted vaccine approach focused on highly conserved T-cell epitopes to mitigate immune escape. We propose 15 highly conserved pan-influenza sequences as possible T cell epitopes-based vaccine targets for broad protection and lasting immunity against variant influenza strains.

摘要

疫苗是预防人类传染病唯一经证实有效的方法。几乎所有传统疫苗都需要激活免疫记忆B细胞以分泌针对入侵病原体的中和抗体。流感病毒的复杂之处在于其高病毒突变率,这会通过B细胞表位的修饰导致免疫逃逸。对流感感染的T细胞免疫研究提供了一种基于高度保守T细胞表位的替代疫苗策略。在本综述中,我们讨论了T细胞介导的免疫在流感感染中的重要性,以及需要一种针对高度保守T细胞表位的靶向疫苗方法以减轻免疫逃逸。我们提出15个高度保守的泛流感序列作为基于T细胞表位的可能疫苗靶点,以实现对变异流感毒株的广泛保护和持久免疫。

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