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Comparative immune profiling of acute respiratory distress syndrome patients with or without SARS-CoV-2 infection. | LitMetric

AI Article Synopsis

  • Acute respiratory distress syndrome (ARDS) is a common complication in severe COVID-19 cases that often leads to ICU admission.
  • Researchers studied three groups of patients to compare the immune responses associated with COVID-19 ARDS and found a unique immune cell signature in those patients.
  • This specific immune profile could lead to personalized treatment approaches for COVID-19-related ARDS, improving overall patient care in the ICU.

Article Abstract

Acute respiratory distress syndrome (ARDS) is the main complication of coronavirus disease 2019 (COVID-19), requiring admission to the intensive care unit (ICU). Despite extensive immune profiling of COVID-19 patients, to what extent COVID-19-associated ARDS differs from other causes of ARDS remains unknown. To address this question, here, we build 3 cohorts of patients categorized in COVID-19ARDS, COVID-19ARDS, and COVID-19ARDS, and compare, by high-dimensional mass cytometry, their immune landscape. A cell signature associating S100A9/calprotectin-producing CD169 monocytes, plasmablasts, and Th1 cells is found in COVID-19ARDS, unlike COVID-19ARDS patients. Moreover, this signature is essentially shared with COVID-19ARDS patients, suggesting that severe COVID-19 patients, whether or not they experience ARDS, display similar immune profiles. We show an increase in CD14HLA-DR and CD14CD16 monocytes correlating to the occurrence of adverse events during the ICU stay. We demonstrate that COVID-19-associated ARDS displays a specific immune profile and may benefit from personalized therapy in addition to standard ARDS management.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8101789PMC
http://dx.doi.org/10.1016/j.xcrm.2021.100291DOI Listing

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