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Sbierski-Kind, Julia; Schlickeiser, Stephan; Feldmann, Svenja; Ober, Veronica; Grüner, Eva; Pleimelding, Claire; Gilberg, Leonard; Brand, Isabel; Weigl, Nikolas; Ahmed, Mohamed I. M.; Ibarra, Gerardo; Ruzicka, Michael ORCID logoORCID: https://orcid.org/0000-0002-2451-1070; Benesch, Christopher; Pernpruner, Anna; Valdinoci, Elisabeth; Hoelscher, Michael ORCID logoORCID: https://orcid.org/0000-0002-7642-1835; Adorjan, Kristina ORCID logoORCID: https://orcid.org/0000-0001-7501-9556; Stubbe, Hans Christian ORCID logoORCID: https://orcid.org/0000-0002-7873-996X; Pritsch, Michael; Seybold, Ulrich ORCID logoORCID: https://orcid.org/0000-0001-9830-8350 und Roider, Julia ORCID logoORCID: https://orcid.org/0000-0002-1347-2838 (2024): Persistent immune abnormalities discriminate post-COVID syndrome from convalescence. In: Infection, Bd. 52: S. 1087-1097 [PDF, 1MB]

Abstract

Background : Innate lymphoid cells (ILCs) are key organizers of tissue immune responses and regulate tissue development, repair, and pathology. Persistent clinical sequelae beyond 12 weeks following acute COVID-19 disease, named post-COVID syndrome (PCS), are increasingly recognized in convalescent individuals. ILCs have been associated with the severity of COVID-19 symptoms but their role in the development of PCS remains poorly defined.

Methods and results : Here, we used multiparametric immune phenotyping, finding expanded circulating ILC precursors (ILCPs) and concurrent decreased group 2 innate lymphoid cells (ILC2s) in PCS patients compared to well-matched convalescent control groups at > 3 months after infection or healthy controls. Patients with PCS showed elevated expression of chemokines and cytokines associated with trafficking of immune cells (CCL19/MIP-3b, FLT3-ligand), endothelial inflammation and repair (CXCL1, EGF, RANTES, IL-1RA, PDGF-AA).

Conclusion : These results define immunological parameters associated with PCS and might help find biomarkers and disease-relevant therapeutic strategies.

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