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10.1084/jem.20200872

http://scihub22266oqcxt.onion/10.1084/jem.20200872
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32886755!7472174!32886755
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suck abstract from ncbi


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pmid32886755      J+Exp+Med 2020 ; 217 (12): ä
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  • Phenotypical and functional alteration of unconventional T cells in severe COVID-19 patients #MMPMID32886755
  • Jouan Y; Guillon A; Gonzalez L; Perez Y; Boisseau C; Ehrmann S; Ferreira M; Daix T; Jeannet R; Francois B; Dequin PF; Si-Tahar M; Baranek T; Paget C
  • J Exp Med 2020[Dec]; 217 (12): ä PMID32886755show ga
  • COVID-19 includes lung infection ranging from mild pneumonia to life-threatening acute respiratory distress syndrome (ARDS). Dysregulated host immune response in the lung is a key feature in ARDS pathophysiology. However, cellular actors involved in COVID-19-driven ARDS are poorly understood. Here, in blood and airways of severe COVID-19 patients, we serially analyzed unconventional T cells, a heterogeneous class of T lymphocytes (MAIT, gammadeltaT, and iNKT cells) with potent antimicrobial and regulatory functions. Circulating unconventional T cells of COVID-19 patients presented with a profound and persistent phenotypic alteration. In the airways, highly activated unconventional T cells were detected, suggesting a potential contribution in the regulation of local inflammation. Finally, expression of the CD69 activation marker on blood iNKT and MAIT cells of COVID-19 patients on admission was predictive of clinical course and disease severity. Thus, COVID-19 patients present with an altered unconventional T cell biology, and further investigations will be required to precisely assess their functions during SARS-CoV-2-driven ARDS.
  • |*Phenotype[MESH]
  • |Aged[MESH]
  • |Antigens, CD/blood[MESH]
  • |Antigens, Differentiation, T-Lymphocyte/blood[MESH]
  • |Betacoronavirus/*genetics[MESH]
  • |COVID-19[MESH]
  • |Cells, Cultured[MESH]
  • |Coronavirus Infections/*immunology/virology[MESH]
  • |Cytokines/metabolism[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Inflammation/immunology/metabolism[MESH]
  • |Lectins, C-Type/blood[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Mucosal-Associated Invariant T Cells/immunology/*metabolism[MESH]
  • |Natural Killer T-Cells/immunology/*metabolism[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*immunology/virology[MESH]
  • |Prognosis[MESH]
  • |Prospective Studies[MESH]
  • |Receptors, Antigen, T-Cell, gamma-delta/*metabolism[MESH]
  • |Respiratory Distress Syndrome/*immunology/virology[MESH]
  • |SARS-CoV-2[MESH]


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