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Sci Rep ; 11(1): 14090, 2021 07 08.
Article in English | MEDLINE | ID: covidwho-1303787

ABSTRACT

MAIT cells have been shown to be activated upon several viral infections in a TCR-independent manner by responding to inflammatory cytokines secreted by antigen-presenting cells. Recently, a few studies have shown a similar activation of MAIT cells in response to severe acute respiratory coronavirus 2 (SARS-CoV-2) infection. In this study, we investigate the effect of SARS-CoV-2 infection on the frequency and phenotype of MAIT cells by flow cytometry, and we test in vitro stimulation conditions on the capacity to enhance or rescue the antiviral function of MAIT cells from patients with coronavirus disease 2019 (COVID-19). Our study, in agreement with recently published studies, confirmed the decline in MAIT cell frequency of hospitalized donors in comparison to healthy donors. MAIT cells of COVID-19 patients also had lower expression levels of TNF-alpha, perforin and granzyme B upon stimulation with IL-12 + IL-18. 24 h' incubation with IL-7 successfully restored perforin expression levels in COVID-19 patients. Combined, our findings support the growing evidence that SARS-CoV-2 is dysregulating MAIT cells and that IL-7 treatment might improve their function, rendering them more effective in protecting the body against the virus.


Subject(s)
COVID-19/prevention & control , COVID-19/virology , Interleukin-7/pharmacology , Mucosal-Associated Invariant T Cells/physiology , Mucosal-Associated Invariant T Cells/virology , SARS-CoV-2/pathogenicity , Cells, Cultured , Female , Granzymes/metabolism , Humans , Male , Mucosal-Associated Invariant T Cells/metabolism , Perforin/metabolism , Tumor Necrosis Factor-alpha/metabolism
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