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A conserved immune trajectory of recovery in hospitalized COVID-19 patients.
Burnett, Cassandra E; Okholm, Trine Line Hauge; Tenvooren, Iliana; Marquez, Diana M; Tamaki, Stanley; Sandoval, Priscila Munoz; Calfee, Carolyn S; Hendrickson, Carolyn M; Kangelaris, Kirsten N; Langelier, Charles R; Krummel, Matthew F; Woodruff, Prescott G; Erle, David J; Ansel, K Mark; Spitzer, Matthew H.
Afiliación
  • Burnett CE; Departments of Otolaryngology-Head and Neck Cancer, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Okholm TLH; Department of Immunology & Immunology and Sandler Asthma Basic Research Center, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Tenvooren I; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA 94158, USA.
  • Marquez DM; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
  • Tamaki S; Parker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
  • Sandoval PM; These authors contributed equally.
  • Calfee CS; Department of Immunology & Immunology and Sandler Asthma Basic Research Center, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Hendrickson CM; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA 94158, USA.
  • Kangelaris KN; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
  • Langelier CR; Parker Institute for Cancer Immunotherapy, San Francisco, CA 94129, USA.
  • Krummel MF; These authors contributed equally.
  • Woodruff PG; Departments of Otolaryngology-Head and Neck Cancer, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Erle DJ; Department of Immunology & Immunology and Sandler Asthma Basic Research Center, University of California, San Francisco, San Francisco, CA 94143, USA.
  • Ansel KM; Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA 94158, USA.
  • Spitzer MH; Chan Zuckerberg Biohub, San Francisco, CA 94158, USA.
bioRxiv ; 2022 Mar 16.
Article en En | MEDLINE | ID: mdl-35313585
Many studies have provided insights into the immune response to COVID-19; however, little is known about the immunological changes and immune signaling occurring during COVID-19 resolution. Individual heterogeneity and variable disease resolution timelines obscure unifying immune characteristics. Here, we collected and profiled >200 longitudinal peripheral blood samples from patients hospitalized with COVID-19, with other respiratory infections, and healthy individuals, using mass cytometry to measure immune cells and signaling states at single cell resolution. COVID-19 patients showed a unique immune composition and an early, coordinated and elevated immune cell signaling profile, which correlated with early hospital discharge. Intra-patient time course analysis tied to clinically relevant events of recovery revealed a conserved set of immunological processes that accompany, and are unique to, disease resolution and discharge. This immunological process, together with additional changes in CD4 regulatory T cells and basophils, accompanies recovery from respiratory failure and is associated with better clinical outcomes at the time of admission. Our work elucidates the biological timeline of immune recovery from COVID-19 and provides insights into the fundamental processes of COVID-19 resolution in hospitalized patients.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
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