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Mechanisms of Dysregulated Humoral and Cellular Immunity by SARS-CoV-2
Nima Taefehshokr1, Sina Taefehshokr2, Bryan Heit1,3
1Department of Microbiology and Immunology, Center for Human Immunology, The University of Western Ontario, London, ON N0M 2N0, Canada.
Insights
Severe acute respiratory syndrome corona virus 2 (SARS-CoV-2) impairs adaptive immunity by depleting T cells and reducing B cell responses. This immune dysfunction correlates with COVID-19 severity and may increase reinfection risk.
Area of Science:
- Immunology
- Virology
- Pathogenesis
Background:
- The COVID-19 pandemic, caused by SARS-CoV-2, has resulted in significant global mortality.
- Adaptive immunity, involving B and T cells, is crucial for viral clearance.
- SARS-CoV-2 employs mechanisms to evade adaptive immune responses.
Purpose of the Study:
- To review the current understanding of B and T cell immune responses in SARS-CoV-2 pathogenesis.
- To explore how SARS-CoV-2 impacts T cell function and antibody production.
- To discuss the implications of immune dysfunction for COVID-19 severity and reinfection.
Main Methods:
- This is a review article, synthesizing existing research on SARS-CoV-2 and immune responses.
- Analysis of studies focusing on T cell depletion, exhaustion, and B cell memory in COVID-19 patients.
- Examination of the correlation between immune cell activity and disease severity.
Main Results:
- SARS-CoV-2 can lead to T cell depletion and exhaustion, particularly in severe cases.
- Neutralizing antibody titers and memory B cell responses may be transient.
- Impaired adaptive immunity is linked to increased COVID-19 severity.
Conclusions:
- SARS-CoV-2 actively counters the adaptive immune system, impacting T cell and B cell functions.
- Dysfunctional immune responses contribute to severe COVID-19 outcomes.
- The short-lived nature of antibody and B cell memory raises concerns about reinfection susceptibility.
Abstract:
The current coronavirus disease 2019 (COVID-19) pandemic, a disease caused by severe acute respiratory syndrome corona virus 2 (SARS-CoV-2), was first identified in December 2019 in China, and has led to thousands of mortalities globally each day. While the innate immune response serves as the first line of defense, viral clearance requires activation of adaptive immunity, which employs B and T cells to provide sanitizing immunity. SARS-CoV-2 has a potent arsenal of mechanisms used to counter this adaptive immune response through processes, such as T cells depletion and T cell exhaustion. These phenomena are most often observed in severe SARS-CoV-2 patients, pointing towards a link between T cell function and disease severity. Moreover, neutralizing antibody titers and memory B cell responses may be short lived in many SARS-CoV-2 patients, potentially exposing these patients to re-infection. In this review, we discuss our current understanding of B and T cells immune responses and activity in SARS-CoV-2 pathogenesis.
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