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A regulatory T cell signature distinguishes the immune landscape of COVID-19 patients from those with other respiratory infections.
Vick, Sarah C; Frutoso, Marie; Mair, Florian; Konecny, Andrew J; Greene, Evan; Wolf, Caitlin R; Logue, Jennifer K; Franko, Nicholas M; Boonyaratanakornkit, Jim; Gottardo, Raphael; Schiffer, Joshua T; Chu, Helen Y; Prlic, Martin; Lund, Jennifer M.
Afiliación
  • Vick SC; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Frutoso M; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Mair F; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Konecny AJ; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Greene E; Department of Immunology, University of Washington, Seattle, WA 98195, USA.
  • Wolf CR; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Logue JK; Department of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Franko NM; Department of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Boonyaratanakornkit J; Department of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Gottardo R; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Schiffer JT; Department of Medicine, University of Washington, Seattle, WA 98195, USA.
  • Chu HY; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Prlic M; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
  • Lund JM; Department of Medicine, University of Washington, Seattle, WA 98195, USA.
Sci Adv ; 7(46): eabj0274, 2021 Nov 12.
Article en En | MEDLINE | ID: mdl-34757794
Despite recent studies of immunity to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), little is known about how the immune response against SARS-CoV-2 differs from other respiratory infections. We compare the immune signature from hospitalized SARS-CoV-2­infected patients to patients hospitalized prepandemic with influenza or respiratory syncytial virus (RSV). Our in-depth profiling indicates that the immune landscape in SARS-CoV-2 patients is largely similar to flu or RSV patients. Unique to patients infected with SARS-CoV-2 who had the most critical clinical disease were changes in the regulatory T cell (Treg) compartment. A Treg signature including increased frequency, activation status, and migration markers was correlated COVID-19 severity. These findings are relevant as Tregs are considered for therapy to combat the severe inflammation seen in COVID-19 patients. Likewise, having defined the overlapping immune landscapes in SARS-CoV-2, existing knowledge of flu and RSV infections could be leveraged to identify common treatment strategies.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Sci Adv Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Sci Adv Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos