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Clin Transl Immunology. 2020 Dec 14;9(12):e1224. doi: 10.1002/cti2.1224. eCollection 2020.

Innate lymphoid cell composition associates with COVID-19 disease severity.

Clinical & translational immunology

Marina García, Efthymia Kokkinou, Anna Carrasco García, Tiphaine Parrot, Laura M Palma Medina, Kimia T Maleki, Wanda Christ, Renata Varnaitė, Iva Filipovic, Hans-Gustaf Ljunggren, Niklas K Björkström, Elin Folkesson, Olav Rooyackers, Lars I Eriksson, Anders Sönnerborg, Soo Aleman, Kristoffer Strålin, Sara Gredmark-Russ, Jonas Klingström, Jenny Mjösberg,

Affiliations

  1. Department of Medicine Huddinge Center for Infectious Medicine Karolinska Institutet Karolinska University Hospital Stockholm Sweden.
  2. Department of Infectious Diseases Karolinska University Hospital Stockholm Sweden.
  3. Department of Medicine Solna Division of Infectious Diseases Karolinska Institutet Stockholm Sweden.
  4. Department of Clinical Science, Technology and Intervention Division of Anesthesiology and Intensive Care Karolinska Institutet Huddinge Sweden.
  5. Function Perioperative Medicine and Intensive Care Karolinska University Hospital Stockholm Sweden.
  6. Department of Physiology and Pharmacology Section for Anesthesiology and Intensive Care Karolinska Institutet Stockholm Sweden.
  7. Division of Infectious Diseases and Dermatology Department of Medicine Huddinge Karolinska Institutet Stockholm Sweden.

PMID: 33343897 PMCID: PMC7734472 DOI: 10.1002/cti2.1224

Abstract

OBJECTIVES: The role of innate lymphoid cells (ILCs) in coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is unknown. Understanding the immune response in COVID-19 could contribute to unravel the pathogenesis and identification of treatment targets. Here, we describe the phenotypic landscape of circulating ILCs in COVID-19 patients and identified ILC phenotypes correlated to serum biomarkers, clinical markers and laboratory parameters relevant in COVID-19.

METHODS: Blood samples collected from moderately (

RESULTS: Innate lymphoid cells were largely depleted from the circulation of COVID-19 patients compared with healthy controls. Remaining circulating ILCs revealed decreased frequencies of ILC2 in severe COVID-19, with a concomitant decrease of ILC precursors (ILCp) in all patients, compared with controls. ILC2 and ILCp showed an activated phenotype with increased CD69 expression, whereas expression levels of the chemokine receptors CXCR3 and CCR4 were significantly altered in ILC2 and ILCp, and ILC1, respectively. The activated ILC profile of COVID-19 patients was associated with soluble inflammatory markers, while frequencies of ILC subsets were correlated with laboratory parameters that reflect the disease severity.

CONCLUSION: This study provides insights into the potential role of ILCs in immune responses against SARS-CoV-2, particularly linked to the severity of COVID-19.

© 2020 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc.

Keywords: COVID‐19; SARS‐CoV‐2; coronavirus; immune response; innate lymphoid cells; respiratory viral infection

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. HGL is a member of the boar

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