EBioMedicine (Jul 2022)

The host response in different aetiologies of community-acquired pneumonia

  • Alex R. Schuurman,
  • Tom D.Y. Reijnders,
  • Tjitske S.R. van Engelen,
  • Valentine Léopold,
  • Justin de Brabander,
  • Christine van Linge,
  • Michiel Schinkel,
  • Liza Pereverzeva,
  • Bastiaan W. Haak,
  • Xanthe Brands,
  • Maadrika M.N.P. Kanglie,
  • Inge A.H. van den Berk,
  • Renée A. Douma,
  • Daniël R. Faber,
  • Prabath W.B. Nanayakkara,
  • Jaap Stoker,
  • Jan M. Prins,
  • Brendon P. Scicluna,
  • W. Joost Wiersinga,
  • Tom van der Poll

Journal volume & issue
Vol. 81
p. 104082

Abstract

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Summary: Background: Community-acquired pneumonia (CAP) can be caused by a variety of pathogens, of which Streptococcus pneumoniae, Influenza and currently SARS-CoV-2 are the most common. We sought to identify shared and pathogen-specific host response features by directly comparing different aetiologies of CAP. Methods: We measured 72 plasma biomarkers in a cohort of 265 patients hospitalized for CAP, all sampled within 48 hours of admission, and 28 age-and sex matched non-infectious controls. We stratified the biomarkers into several pathophysiological domains- antiviral response, vascular response and function, coagulation, systemic inflammation, and immune checkpoint markers. We directly compared CAP caused by SARS-CoV-2 (COVID-19, n=39), Streptococcus pneumoniae (CAP-strep, n=27), Influenza (CAP-flu, n=22) and other or unknown pathogens (CAP-other, n=177). We adjusted the comparisons for age, sex and disease severity scores. Findings: Biomarkers reflective of a stronger cell-mediated antiviral response clearly separated COVID-19 from other CAPs (most notably granzyme B). Biomarkers reflecting activation and function of the vasculature showed endothelial barrier integrity was least affected in COVID-19, while glycocalyx degradation and angiogenesis were enhanced relative to other CAPs. Notably, markers of coagulation activation, including D-dimer, were not different between the CAP groups. Ferritin was most increased in COVID-19, while other systemic inflammation biomarkers such as IL-6 and procalcitonin were highest in CAP-strep. Immune checkpoint markers showed distinctive patterns in viral and non-viral CAP, with highly elevated levels of Galectin-9 in COVID-19. Interpretation: Our investigation provides insight into shared and distinct pathophysiological mechanisms in different aetiologies of CAP, which may help guide new pathogen-specific therapeutic strategies. Funding: This study was financially supported by the Dutch Research Council, the European Commission and the Netherlands Organization for Health Research and Development.

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