TY - JOUR
T1 - Mucosal-associated invariant T (MAIT) cells are highly activated and functionally impaired in COVID-19 patients
AU - Deschler, Sebastian
AU - Kager, Juliane
AU - Erber, Johanna
AU - Fricke, Lisa
AU - Koyumdzhieva, Plamena
AU - Georgieva, Alexandra
AU - Lahmer, Tobias
AU - Wiessner, Johannes R.
AU - Voit, Florian
AU - Schneider, Jochen
AU - Horstmann, Julia
AU - Iakoubov, Roman
AU - Treiber, Matthias
AU - Winter, Christof
AU - Ruland, Jürgen
AU - Busch, Dirk H.
AU - Knolle, Percy A.
AU - Protzer, Ulrike
AU - Spinner, Christoph D.
AU - Schmid, Roland M.
AU - Quante, Michael
AU - Böttcher, Katrin
N1 - Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/2
Y1 - 2021/2
N2 - 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.
AB - 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.
KW - COVID-19
KW - Mucosal-associated invariant T (MAIT) cells
KW - SARS-CoV-2
UR - https://www.scopus.com/pages/publications/85101032112
U2 - 10.3390/v13020241
DO - 10.3390/v13020241
M3 - Article
C2 - 33546489
AN - SCOPUS:85101032112
SN - 1999-4915
VL - 13
JO - Viruses
JF - Viruses
IS - 2
M1 - 241
ER -