Identification of Potential SARS-CoV-2 CD8+ T Cell Escape Mutants

被引:5
|
作者
Ahmed, Syed Faraz [1 ,2 ]
Sohail, Muhammad Saqib [2 ]
Quadeer, Ahmed Abdul [2 ]
McKay, Matthew R. [1 ,2 ,3 ,4 ]
机构
[1] Univ Melbourne, Dept Elect & Elect Engn, Parkville, Vic 3010, Australia
[2] Hong Kong Univ Sci & Technol, Dept Elect & Comp Engn, Hong Kong, Peoples R China
[3] Univ Melbourne, Peter Doherty Inst Infect & Immun, Dept Microbiol & Immunol, Melbourne, Vic 3000, Australia
[4] Hong Kong Univ Sci & Technol, Dept Chem & Biol Engn, Hong Kong, Peoples R China
关键词
SARS-CoV-2; COVID-19; CD8(+) T cell epitopes; immunoprevalent; immune escape; mutations; variants of concern; VARIANTS;
D O I
10.3390/vaccines10040542
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Memory SARS-CoV-2-specific CD8(+) T cell responses induced upon infection or COVID-19 vaccination have been important for protecting against severe COVID-19 disease while being largely robust against variants of concern (VOCs) observed so far. However, T cell immunity may be weakened by genetic mutations in future SARS-CoV-2 variants that lead to widespread T cell escape. The capacity for SARS-CoV-2 mutations to escape memory T cell responses requires comprehensive experimental investigation, though this is prohibited by the large number of SARS-CoV-2 mutations that have been observed. To guide targeted experimental studies, here we provide a screened list of potential SARS-CoV-2 T cell escape mutants. These mutants are identified as candidates for T cell escape as they lie within CD8(+) T cell epitopes that are commonly targeted in individuals and are predicted to abrogate HLA-peptide binding.
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页数:7
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