Article ; Online: Mucosal-Associated Invariant T (MAIT) Cells Are Highly Activated and Functionally Impaired in COVID-19 Patients.
2021 Volume 13, Issue 2
Abstract: ... for the pathogenesis of COVID-19, although especially the contribution of innate-like T cells remains poorly understood ... Here, we analysed the phenotype and function of mucosal-associated invariant T (MAIT) cells, innate ... like T cells with potent antimicrobial effector function, in patients with mild and severe COVID-19 ...
Abstract | Coronavirus disease 2019 (COVID-19), caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), comprises mild courses of disease as well as progression to severe disease, characterised by lung and other organ failure. The immune system is considered to play a crucial role for the pathogenesis of COVID-19, although especially the contribution of innate-like T cells remains poorly understood. Here, we analysed the phenotype and function of mucosal-associated invariant T (MAIT) cells, innate-like T cells with potent antimicrobial effector function, in patients with mild and severe COVID-19 by multicolour flow cytometry. Our data indicate that MAIT cells are highly activated in patients with COVID-19, irrespective of the course of disease, and express high levels of proinflammatory cytokines such as IL-17A and TNFα ex vivo. Of note, expression of the activation marker HLA-DR positively correlated with SAPS II score, a measure of disease severity. Upon MAIT cell-specific in vitro stimulation, MAIT cells however failed to upregulate expression of the cytokines IL-17A and TNFα, as well as cytolytic proteins, that is, granzyme B and perforin. Thus, our data point towards an altered cytokine expression profile alongside an impaired antibacterial and antiviral function of MAIT cells in COVID-19 and thereby contribute to the understanding of COVID-19 immunopathogenesis. |
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MeSH term(s) | Adaptive Immunity ; COVID-19/immunology ; COVID-19/physiopathology ; Cytokines/metabolism ; Female ; Granzymes/metabolism ; HLA-DR Antigens ; Humans ; Interleukin-17/metabolism ; Killer Cells, Natural/immunology ; Lymphocyte Activation ; Male ; Mucosal-Associated Invariant T Cells/immunology ; Mucosal-Associated Invariant T Cells/metabolism ; Severity of Illness Index ; T-Lymphocyte Subsets/immunology ; Tumor Necrosis Factor-alpha/metabolism |
Chemical Substances | Cytokines ; HLA-DR Antigens ; IL17A protein, human ; Interleukin-17 ; TNF protein, human ; Tumor Necrosis Factor-alpha ; GZMB protein, human (EC 3.4.21.-) ; Granzymes (EC 3.4.21.-) |
Language | English |
Publishing date | 2021-02-03 |
Publishing country | Switzerland |
Document type | Journal Article ; Research Support, Non-U.S. Gov't |
ZDB-ID | 2516098-9 |
ISSN | 1999-4915 ; 1999-4915 |
ISSN (online) | 1999-4915 |
ISSN | 1999-4915 |
DOI | 10.3390/v13020241 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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