Behaviors of Human T cells in SARS-CoV-2 Infection: Lessons and Tips
Ali Shams1, Sahar Khosravi1, Aysan Zareiye1
1Department of Immunology, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran.
Abstract:
Cell-mediated immunity (CMI) is crucial in controlling the highly aggressive and progressive SARS-CoV-2 infection. Despite extensive researches on severe COVID-19 infection, the etiology and/or mechanisms of lymphopenia, decreased T cell-mediated responses in patients, cytokine release storms (CRS), and enhanced pro-inflammatory mediators are not fully understood. Several T cell subpopulations, including innate-like lymphocytes (ILLs) and conventional T cells, are involved in COVID-19 infection; however, their contribution to immunity and complications remains to be more elucidated. CD16+ T cells are among the effective players in the development of T helper1 (Th1) responses in COVID-19 infection, while their robust cytolytic properties contribute to lung tissue damage. While CD56-CD16bright NK cells play a protective role, natural killer T (NKT) cells, mucosal-associated invariant T (MAIT) cells, and γδ T cells and their roles in COVID-19 require further investigation. The involvement of the other T cell subsets, such as Th17, along with neutrophils, adds to the complexity of the situation. In this review, we presented and discussed the findings of recent studies on T cell responses and the contribution of each type of immune cells to COVID-19.
Insights
Cell-mediated immunity (CMI) is vital for controlling SARS-CoV-2. This review explores T cell responses and immune cell contributions to COVID-19, clarifying lymphopenia and cytokine release storm mechanisms.
Area of Science:
- Immunology
- Virology
- Infectious Diseases
Background:
- Cell-mediated immunity (CMI) is critical for managing SARS-CoV-2 infection.
- Mechanisms behind lymphopenia, diminished T cell responses, and cytokine release storms (CRS) in severe COVID-19 remain unclear.
- Various T cell subpopulations, including innate-like lymphocytes (ILLs) and conventional T cells, are implicated in COVID-19 pathogenesis.
Purpose of the Study:
- To review and discuss recent findings on T cell responses in COVID-19.
- To elucidate the roles of different immune cell types in COVID-19 immunity and complications.
- To clarify the underlying mechanisms of immune dysregulation during SARS-CoV-2 infection.
Main Methods:
- Literature review of recent studies on T cell responses in COVID-19.
- Analysis of the involvement of various T cell subpopulations (e.g., CD16+ T cells, NK cells, NKT cells, MAIT cells, γδ T cells, Th17 cells).
- Discussion of the contribution of neutrophils and other immune cells to COVID-19 pathogenesis.
Main Results:
- CD16+ T cells contribute to Th1 responses and lung tissue damage.
- CD56-CD16bright NK cells exhibit a protective role.
- The roles of NKT cells, MAIT cells, γδ T cells, Th17 cells, and neutrophils in COVID-19 require further investigation.
Conclusions:
- Understanding T cell dynamics and immune cell interactions is crucial for managing COVID-19.
- Further research is needed to fully elucidate the complex immune responses in SARS-CoV-2 infection.
- Clarifying these mechanisms may lead to improved therapeutic strategies for severe COVID-19.
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