Selected article for: "cell activation and specific antigen"

Author: Youngs, Jonathan; Provine, Nicholas M.; Lim, Nicholas; Sharpe, Hannah R.; Amini, Ali; Chen, Yi-Ling; Luo, Jian; Edmans, Matthew D.; Zacharopoulou, Panagiota; Chen, Wentao; Sampson, Oliver; Paton, Robert; Hurt, William J.; Duncan, David A.; McNaughton, Anna L.; Miao, Vincent N.; Leaver, Susannah; Wyncoll, Duncan L. A.; Ball, Jonathan; Hopkins, Philip; Skelly, Donal T.; Barnes, Eleanor; Dunachie, Susanna; Ogg, Graham; Lambe, Teresa; Pavord, Ian; Shalek, Alex K.; Thompson, Craig P.; Xue, Luzheng; Macallan, Derek C.; Goulder, Philip; Klenerman, Paul; Bicanic, Tihana
Title: Identification of immune correlates of fatal outcomes in critically ill COVID-19 patients
  • Cord-id: pl8l4lof
  • Document date: 2021_9_16
  • ID: pl8l4lof
    Snippet: Prior studies have demonstrated that immunologic dysfunction underpins severe illness in COVID-19 patients, but have lacked an in-depth analysis of the immunologic drivers of death in the most critically ill patients. We performed immunophenotyping of viral antigen-specific and unconventional T cell responses, neutralizing antibodies, and serum proteins in critically ill patients with SARS-CoV-2 infection, using influenza infection, SARS-CoV-2-convalescent health care workers, and healthy adults
    Document: Prior studies have demonstrated that immunologic dysfunction underpins severe illness in COVID-19 patients, but have lacked an in-depth analysis of the immunologic drivers of death in the most critically ill patients. We performed immunophenotyping of viral antigen-specific and unconventional T cell responses, neutralizing antibodies, and serum proteins in critically ill patients with SARS-CoV-2 infection, using influenza infection, SARS-CoV-2-convalescent health care workers, and healthy adults as controls. We identify mucosal-associated invariant T (MAIT) cell activation as an independent and significant predictor of death in COVID-19 (HR = 5.92, 95% CI = 2.49–14.1). MAIT cell activation correlates with several other mortality-associated immunologic measures including broad activation of CD8(+) T cells and non-Vδ2 γδT cells, and elevated levels of cytokines and chemokines, including GM-CSF, CXCL10, CCL2, and IL-6. MAIT cell activation is also a predictor of disease severity in influenza (ECMO/death HR = 4.43, 95% CI = 1.08–18.2). Single-cell RNA-sequencing reveals a shift from focused IFNα-driven signals in COVID-19 ICU patients who survive to broad pro-inflammatory responses in fatal COVID-19 –a feature not observed in severe influenza. We conclude that fatal COVID-19 infection is driven by uncoordinated inflammatory responses that drive a hierarchy of T cell activation, elements of which can serve as prognostic indicators and potential targets for immune intervention.

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