Frontiers in Immunology (May 2022)

Evaluating the Immune Response in Treatment-Naive Hospitalised Patients With Influenza and COVID-19

  • Jelmer Legebeke,
  • Jelmer Legebeke,
  • Jenny Lord,
  • Rebekah Penrice-Randal,
  • Andres F. Vallejo,
  • Stephen Poole,
  • Stephen Poole,
  • Nathan J. Brendish,
  • Nathan J. Brendish,
  • Xiaofeng Dong,
  • Catherine Hartley,
  • John W. Holloway,
  • John W. Holloway,
  • Jane S. Lucas,
  • Jane S. Lucas,
  • Anthony P. Williams,
  • Gabrielle Wheway,
  • Fabio Strazzeri,
  • Aaron Gardner,
  • James P. R. Schofield,
  • Paul J. Skipp,
  • Paul J. Skipp,
  • Julian A. Hiscox,
  • Julian A. Hiscox,
  • Julian A. Hiscox,
  • Marta E. Polak,
  • Marta E. Polak,
  • Tristan W. Clark,
  • Tristan W. Clark,
  • Diana Baralle,
  • Diana Baralle

DOI
https://doi.org/10.3389/fimmu.2022.853265
Journal volume & issue
Vol. 13

Abstract

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The worldwide COVID-19 pandemic has claimed millions of lives and has had a profound effect on global life. Understanding the body’s immune response to SARS-CoV-2 infection is crucial in improving patient management and prognosis. In this study we compared influenza and SARS-CoV-2 infected patient cohorts to identify distinct blood transcript abundances and cellular composition to better understand the natural immune response associated with COVID-19, compared to another viral infection being influenza, and identify a prognostic signature of COVID-19 patient outcome. Clinical characteristics and peripheral blood were acquired upon hospital admission from two well characterised cohorts, a cohort of 88 patients infected with influenza and a cohort of 80 patients infected with SARS-CoV-2 during the first wave of the pandemic and prior to availability of COVID-19 treatments and vaccines. Gene transcript abundances, enriched pathways and cellular composition were compared between cohorts using RNA-seq. A genetic signature between COVID-19 survivors and non-survivors was assessed as a prognostic predictor of COVID-19 outcome. Contrasting immune responses were detected with an innate response elevated in influenza and an adaptive response elevated in COVID-19. Additionally ribosomal, mitochondrial oxidative stress and interferon signalling pathways differentiated the cohorts. An adaptive immune response was associated with COVID-19 survival, while an inflammatory response predicted death. A prognostic transcript signature, associated with circulating immunoglobulins, nucleosome assembly, cytokine production and T cell activation, was able to stratify COVID-19 patients likely to survive or die. This study provides a unique insight into the immune responses of treatment naïve patients with influenza or COVID-19. The comparison of immune response between COVID-19 survivors and non-survivors enables prognostication of COVID-19 patients and may suggest potential therapeutic strategies to improve survival.

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