CD8+ T-cell immune escape by SARS-CoV-2 variants of concern

被引:10
|
作者
Kombe Kombe, Arnaud John [1 ]
Biteghe, Fleury Augustin Nsole [2 ]
Ndoutoume, Zelia Nelly [3 ]
Jin, Tengchuan [1 ,4 ,5 ]
机构
[1] Univ Sci & Technol China, Univ Sci & Technol China USTC, Dept Obstet & Gynecol, Div Life Sci & Med,Affiliated Hosp 1, Hefei, Peoples R China
[2] Cedars Sinai Med Ctr, Dept Radiat Oncol, Los Angeles, CA USA
[3] Chongqing Med Univ, Clin Sch 2, Med Imaging, Chongqing, Peoples R China
[4] Univ Sci & Technol China, Div Life Sci & Med, Lab Struct Immunol, Chinese Acad Sci Key Lab Innate Immun & Chron Dis, Hefei, Peoples R China
[5] Chinese Acad Sci, Chinese Acad Sci CAS Ctr Excellence Mol Cell Sci, Shanghai, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
SARS-CoV-2; cellular immunity; CD8+T-cell epitope; cytotoxic T lymphocytes (CTL); variant of concern (VOC); protein mutation; HLA; immune escape; ACUTE RESPIRATORY SYNDROME; MEMORY; INFECTION; RESPONSES; ANTIGEN; PROTECTION; SELECTION; EPITOPES;
D O I
10.3389/fimmu.2022.962079
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite the efficacy of antiviral drug repositioning, convalescent plasma (CP), and the currently available vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the worldwide coronavirus disease 2019 (COVID-19) pandemic is still challenging because of the ongoing emergence of certain new SARS-CoV-2 strains known as variants of concern (VOCs). Mutations occurring within the viral genome, characterized by these new emerging VOCs, confer on them the ability to efficiently resist and escape natural and vaccine-induced humoral and cellular immune responses. Consequently, these VOCs have enhanced infectivity, increasing their stable spread in a given population with an important fatality rate. While the humoral immune escape process is well documented, the evasion mechanisms of VOCs from cellular immunity are not well elaborated. In this review, we discussed how SARS-CoV-2 VOCs adapt inside host cells and escape anti-COVID-19 cellular immunity, focusing on the effect of specific SARS-CoV-2 mutations in hampering the activation of CD8(+) T-cell immunity.
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页数:19
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