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In vitro Interleukin-7 treatment partially rescues MAIT cell dysfunction caused by SARS-CoV-2 infection.
- Source :
-
Scientific reports [Sci Rep] 2021 Jul 08; Vol. 11 (1), pp. 14090. Date of Electronic Publication: 2021 Jul 08. - Publication Year :
- 2021
-
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.
- Subjects :
- Cells, Cultured
Female
Granzymes metabolism
Humans
Male
Mucosal-Associated Invariant T Cells metabolism
Perforin metabolism
Tumor Necrosis Factor-alpha metabolism
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
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 11
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 34238985
- Full Text :
- https://doi.org/10.1038/s41598-021-93536-7