Marked T cell activation, senescence, exhaustion and skewing towards TH17 in patients with COVID-19 pneumonia

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paper: De Biasi S., Meschiari, M., Gibellini, L., Bellinazzi, C., Borella, R., Fidanza, L., Gozzi, L., Iannone, A., Lo T. D., Mattioli, M., Paolini, A., Menozzi, M., Milić, J., Franceschi, G., Fantini, R., Tonelli, R., Sita, M., Sarti, M., Trenti, T., Brugioni, L., Cicchetti, L., Facchinetti, F., Pietrangelo, A., Clini, E., Girardis, M., Guaraldi, G., Mussini, C. and Cossarizza, A. (2020). Marked T cell activation, senescence, exhaustion and skewing towards TH17 in patients with COVID-19 pneumonia. Nat Commun https://doi.org/10.1038/s41467-020-17292-4
contributor: Andrea Cossarizza
contributor_organization: Università degli studi di Modena e Reggio Emilia
contributor_email: andrea.cossarizza@unimore.it

 

    • description: Detailed investigation of T cells and cytokine production in patients affected by COVID-19 pneumonia.
    • exact_source:
    • tissue: PBMC
    • immune_exposure: COVID-19
    • cohort: ADULTS RANGE 35–94 YEARS
    • comparison: patients with COVID-19 pneumonia vs healthy donors
    • repository_id: https://flowrepository.org/id/FR-FCM- Z2N5; https://flowrepository.org/id/FR-FCM-Z2N4.
    • platform:
    • response_components:
    • response_behavior:

 

PMID
32632085
authors
De Biasi, Sara et al
abstract
The immune system of patients infected by SARS-CoV-2 is severely impaired. Detailed investigation of T cells and cytokine production in patients affected by COVID-19 pneumonia are urgently required. Here we show that, compared with healthy controls, COVID-19 patients’ T cell compartment displays several alterations involving naïve, central memory, effector memory and terminally differentiated cells, as well as regulatory T cells and PD1(+)CD57(+) exhausted T cells. Significant alterations exist also in several lineage-specifying transcription factors and chemokine receptors. Terminally differentiated T cells from patients proliferate less than those from healthy controls, whereas their mitochondria functionality is similar in CD4(+) T cells from both groups. Patients display significant increases of proinflammatory or anti-inflammatory cytokines, including T helper type-1 and type-2 cytokines, chemokines and galectins; their lymphocytes produce more tumor necrosis factor (TNF), interferon-γ, interleukin (IL)-2 and IL-17, with the last observation implying that blocking IL-17 could provide a novel therapeutic strategy for COVID-19.
status
review complete
curator
reviewer
journal
Nat Commun
date review completed
year of publication
2020
In Dashboard
Yes