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CD8+ T-cell immune escape by SARS-CoV-2 variants of concern
Arnaud John Kombe Kombe1, Fleury Augustin Nsole Biteghe2, Zélia Nelly Ndoutoume3
1Department of Obstetrics and Gynecology, The First Affiliated Hospital of University of Science and Technology of China (USTC), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
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.
Insights
New SARS-CoV-2 variants of concern (VOCs) resist immunity due to mutations. This review details how VOCs evade cellular immunity, specifically impacting CD8+ T-cell responses against COVID-19.
Area of Science:
- Virology
- Immunology
- Infectious Diseases
Background:
- The COVID-19 pandemic persists despite available countermeasures like vaccines and antivirals.
- Emergence of SARS-CoV-2 variants of concern (VOCs) poses a significant challenge due to immune evasion.
- VOCs exhibit mutations conferring resistance to natural and vaccine-induced immune responses, increasing infectivity and fatality.
Purpose of the Study:
- To review the mechanisms by which SARS-CoV-2 VOCs adapt within host cells.
- To elucidate the evasion strategies of VOCs from anti-COVID-19 cellular immunity.
- To focus on the impact of specific viral mutations on CD8+ T-cell immunity.
Main Methods:
- Literature review of studies on SARS-CoV-2 variants and immune evasion.
- Analysis of viral genomic mutations in VOCs.
- Examination of cellular immune responses, particularly CD8+ T-cells, in the context of VOC infection.
Main Results:
- VOCs possess mutations enabling escape from humoral and cellular immunity.
- Specific mutations within SARS-CoV-2 VOCs are identified as key factors in immune evasion.
- The review highlights the under-elaboration of VOC evasion from cellular immunity compared to humoral immunity.
Conclusions:
- SARS-CoV-2 VOCs adapt to evade host cellular immunity through specific mutations.
- Understanding these evasion mechanisms is crucial for developing effective COVID-19 control strategies.
- Further research is needed to fully characterize the impact of viral mutations on T-cell mediated immunity.
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