Nature Communications · 2020 · 434 citations · 19 references
Life SciencesImmunologyInfectious DiseasesImmunology Of Infectious DiseasesImmunopathologyInflammationCell-mediated ImmunityCellular Immunity In InfectionCytotoxic T Lymphocyte ResponsesImmune-mediated DiseaseT Cell ActivationT Cell BiologyCd4 Positive T CellsCd8 Positive T CellsCd8 T Cell ActivationCell ActivationSars-cov-2 InfectionT Cell-mediated InflammationT-cell Mediated InflammationT-cell Mediated Responses
COVID-19 is associated with 5.1% mortality. Although the virological, epidemiological, clinical, and management outcome features of COVID-19 patients have been defined rapidly, the inflammatory and immune profiles require definition as they influence pathogenesis and clinical expression of COVID-19. Here we show lymphopenia, selective loss of CD4+ T cells, CD8+ T cells and NK cells, excessive T-cell activation and high expression of T-cell inhibitory molecules are more prominent in severe cases than in those with mild disease. CD8+ T cells in patients with severe disease express high levels of cytotoxic molecules. Histochemical studies of lung tissue from one fatality show sub-anatomical distributions of SARS-CoV-2 RNA and massive infiltration of T cells and macrophages. Thus, aberrant activation and dysregulation of CD8+ T cells occur in patients with severe COVID-19 disease, an effect that might be for pathogenesis of SARS-CoV-2 infection and indicate that immune-based targets for therapeutic interventions constitute a promising treatment for severe COVID-19 patients.
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Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China
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