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Nat Commun ; 12(1): 3006, 2021 05 21.
Article in English | MEDLINE | ID: mdl-34021143

ABSTRACT

Coronavirus disease 2019 (COVID-19) can lead to pneumonia and hyperinflammation. Here we show a sensitive method to measure polyclonal T cell activation by downstream effects on responder cells like basophils, plasmacytoid dendritic cells, monocytes and neutrophils in whole blood. We report a clear T cell hyporeactivity in hospitalized COVID-19 patients that is pronounced in ventilated patients, associated with prolonged virus persistence and reversible with clinical recovery. COVID-19-induced T cell hyporeactivity is T cell extrinsic and caused by plasma components, independent of occasional immunosuppressive medication of the patients. Monocytes respond stronger in males than females and IL-2 partially restores T cell activation. Downstream markers of T cell hyporeactivity are also visible in fresh blood samples of ventilated patients. Based on our data we developed a score to predict fatal outcomes and identify patients that may benefit from strategies to overcome T cell hyporeactivity.


Subject(s)
COVID-19/immunology , Inflammation/immunology , Lymphocyte Activation/immunology , Pneumonia/immunology , SARS-CoV-2/immunology , T-Lymphocytes/immunology , Adult , Aged , Basophils/immunology , COVID-19/virology , Cells, Cultured , Dendritic Cells/immunology , Female , Humans , Male , Middle Aged , Monocytes/immunology , Neutrophils/immunology , SARS-CoV-2/physiology , Young Adult
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