» Articles » PMID: 36389664

CD8 T-cell Immune Escape by SARS-CoV-2 Variants of Concern

Overview
Journal Front Immunol
Date 2022 Nov 17
PMID 36389664
Authors
Affiliations
Soon will be listed here.
Abstract

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.

Citing Articles

The trend of phylogenetic and epitope variations of SARS-CoV-2 Omicron sub-lineages in Iran.

Shabani M, Nejati A, Yavarian J, Sadeghi K, Zadheidar S, Ahmadi A Front Microbiol. 2025; 15:1531712.

PMID: 39943963 PMC: 11815659. DOI: 10.3389/fmicb.2024.1531712.


The role of inflammatory gene polymorphisms in severe COVID-19: a review.

Yip J, Oo A, Ng Y, Chin K, Tan K, Chu J Virol J. 2024; 21(1):327.

PMID: 39707400 PMC: 11662554. DOI: 10.1186/s12985-024-02597-3.


Features of Highly Homologous T-Cell Receptor Repertoire in the Immune Response to Mutations in Immunogenic Epitopes.

Zornikova K, Dianov D, Ivanova N, Davydova V, Nenasheva T, Fefelova E Int J Mol Sci. 2024; 25(23).

PMID: 39684303 PMC: 11641755. DOI: 10.3390/ijms252312591.


SARS-CoV-2 within-host population expansion, diversification and adaptation in zoo tigers, lions and hyenas.

Bashor L, Gallichotte E, Galvan M, Erbeck K, Croft L, Stache K bioRxiv. 2024; .

PMID: 39484504 PMC: 11527109. DOI: 10.1101/2024.10.24.620075.


The molecular mechanisms of CD8 T cell responses to SARS-CoV-2 infection mediated by TCR-pMHC interactions.

Deng S, Xu Z, Hu J, Yang Y, Zhu F, Liu Z Front Immunol. 2024; 15:1468456.

PMID: 39450171 PMC: 11499136. DOI: 10.3389/fimmu.2024.1468456.


References
1.
Tan Y, Schneider T, Leong M, Aravind L, Zhang D . Novel Immunoglobulin Domain Proteins Provide Insights into Evolution and Pathogenesis of SARS-CoV-2-Related Viruses. mBio. 2020; 11(3). PMC: 7267882. DOI: 10.1128/mBio.00760-20. View

2.
Pereira F . SARS-CoV-2 variants combining spike mutations and the absence of ORF8 may be more transmissible and require close monitoring. Biochem Biophys Res Commun. 2021; 550:8-14. PMC: 7906533. DOI: 10.1016/j.bbrc.2021.02.080. View

3.
Yang X, Yu Y, Xu J, Shu H, Xia J, Liu H . Clinical course and outcomes of critically ill patients with SARS-CoV-2 pneumonia in Wuhan, China: a single-centered, retrospective, observational study. Lancet Respir Med. 2020; 8(5):475-481. PMC: 7102538. DOI: 10.1016/S2213-2600(20)30079-5. View

4.
Wu L, Wang N, Chang Y, Tian X, Na D, Zhang L . Duration of antibody responses after severe acute respiratory syndrome. Emerg Infect Dis. 2008; 13(10):1562-4. PMC: 2851497. DOI: 10.3201/eid1310.070576. View

5.
Chen G, Wu D, Guo W, Cao Y, Huang D, Wang H . Clinical and immunological features of severe and moderate coronavirus disease 2019. J Clin Invest. 2020; 130(5):2620-2629. PMC: 7190990. DOI: 10.1172/JCI137244. View