表位
病毒学
埃利斯波特
生物
糖蛋白
T细胞
严重急性呼吸综合征
表位定位
冠状病毒
抗原
免疫学
免疫系统
医学
分子生物学
2019年冠状病毒病(COVID-19)
疾病
内科学
传染病(医学专业)
作者
Xiaojuan Liu,Yuzhong Li,Hongjian Xiao,Yanwei Bi,Yue Gong,Zhengrong Hu,Yaxin Zeng,Ming Sun,Zhanlong He,Shan Lu,Qihan Li,Wei Cun
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2021-05-12
卷期号:206 (11): 2527-2535
被引量:2
标识
DOI:10.4049/jimmunol.2000922
摘要
The T cell response is an important detection index in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine development. The present study was undertaken to determine the T cell epitopes in the spike (S) protein of SARS-CoV-2 that dominate the T cell responses in SARS-CoV-2-infected patients. PBMCs from rhesus macaques vaccinated with a DNA vaccine encoding the full-length S protein were isolated, and an ELISPOT assay was used to identify the recognized T cell epitopes among a total of 158 18-mer and 10-aa-overlapping peptides spanning the full-length S protein. Six multipeptide-based epitopes located in the S1 region, with four of the six located in the receptor-binding domain, were defined as the most frequently recognized epitopes in macaques. The conservation of the epitopes across species was also verified, and peptide mixtures for T cell response detection were established. Six newly defined T cell epitopes were found in the current study, which may provide a novel potential target for T cell response detection and the diagnosis and vaccine design of SARS-CoV-2 based on multipeptide subunit-based epitopes.
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