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Dynamic MAIT Cell Recovery after Severe COVID-19 Is Transient with Signs of Heterogeneous Functional Anomalies.
Kammann, Tobias; Gorin, Jean-Baptiste; Parrot, Tiphaine; Gao, Yu; Ponzetta, Andrea; Emgård, Johanna; Maleki, Kimia T; Sekine, Takuya; Rivera-Ballesteros, Olga; Gredmark-Russ, Sara; Rooyackers, Olav; Skagerberg, Magdalena; Eriksson, Lars I; Norrby-Teglund, Anna; Mak, Jeffrey Y W; Fairlie, David P; Björkström, Niklas K; Klingström, Jonas; Ljunggren, Hans-Gustaf; Aleman, Soo; Buggert, Marcus; Strålin, Kristoffer; Sandberg, Johan K.
Afiliación
  • Kammann T; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Gorin JB; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Parrot T; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Gao Y; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Ponzetta A; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Emgård J; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Maleki KT; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Sekine T; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Rivera-Ballesteros O; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Gredmark-Russ S; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Rooyackers O; Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.
  • Skagerberg M; Department of Clinical Interventions and Technology, Karolinska Institutet, Stockholm, Sweden.
  • Eriksson LI; Perioperative Medicine and Intensive Care, Karolinska University Hospital, Stockholm, Sweden.
  • Norrby-Teglund A; Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.
  • Mak JYW; Perioperative Medicine and Intensive Care, Karolinska University Hospital, Stockholm, Sweden.
  • Fairlie DP; Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
  • Björkström NK; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Klingström J; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia.
  • Ljunggren HG; Institute for Molecular Bioscience, The University of Queensland, Brisbane, Queensland, Australia.
  • Aleman S; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Buggert M; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Strålin K; Center for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Sandberg JK; Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.
J Immunol ; 212(3): 389-396, 2024 Feb 01.
Article en En | MEDLINE | ID: mdl-38117799
ABSTRACT
Mucosal-associated invariant T (MAIT) cells are an abundant population of unconventional T cells in humans and play important roles in immune defense against microbial infections. Severe COVID-19 is associated with strong activation of MAIT cells and loss of these cells from circulation. In the present study, we investigated the capacity of MAIT cells to recover after severe COVID-19. In longitudinal paired analysis, MAIT cells initially rebounded numerically and phenotypically in most patients at 4 mo postrelease from the hospital. However, the rebounding MAIT cells displayed signs of persistent activation with elevated expression of CD69, CD38, and HLA-DR. Although MAIT cell function was restored in many patients, a subgroup displayed a predominantly PD-1high functionally impaired MAIT cell pool. This profile was associated with poor expression of IFN-γ and granzyme B in response to IL-12 + L-18 and low levels of polyfunctionality. Unexpectedly, although the overall T cell counts recovered, normalization of the MAIT cell pool failed at 9-mo follow-up, with a clear decline in MAIT cell numbers and a further increase in PD-1 levels. Together, these results indicate an initial transient period of inconsistent recovery of MAIT cells that is not sustained and eventually fails. Persisting MAIT cell impairment in previously hospitalized patients with COVID-19 may have consequences for antimicrobial immunity and inflammation and could potentially contribute to post-COVID-19 health problems.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Células T Invariantes Asociadas a Mucosa / COVID-19 Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Células T Invariantes Asociadas a Mucosa / COVID-19 Límite: Humans Idioma: En Año: 2024 Tipo del documento: Article