Elevated plasma levels of CXCL16 in severe COVID-19 patients

Genome-wide association studies have recently identified 3p21.31, with lead variant pointing to the CXCR6 gene, as the strongest thus far reported susceptibility risk locus for severe manifestation of COVID-19. In order the determine its role, we measured plasma levels of Chemokine (C‐X‐C motif) lig...

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Veröffentlicht in:Cytokine (Philadelphia, Pa.) Pa.), 2022-04, Vol.152, p.155810-155810, Article 155810
Hauptverfasser: Smieszek, Sandra P., Polymeropoulos, Vasilios M., Polymeropoulos, Christos M., Przychodzen, Bartlomiej P., Birznieks, Gunther, Polymeropoulos, Mihael H.
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Sprache:eng
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Zusammenfassung:Genome-wide association studies have recently identified 3p21.31, with lead variant pointing to the CXCR6 gene, as the strongest thus far reported susceptibility risk locus for severe manifestation of COVID-19. In order the determine its role, we measured plasma levels of Chemokine (C‐X‐C motif) ligand 16 (CXCL16) in the plasma of COVID-19 hospitalized patients. CXCL16 interacts with CXCR6 promoting chemotaxis or cell adhesion. The CXCR6/CXCL16 axis mediates homing of T cells to the lungs in disease and hyper-expression is associated with localised cellular injury. To characterize the CXCR6/CXCL16 axis in the pathogenesis of severe COVID-19, plasma concentrations of CXCL16 collected at baseline from 115 hospitalized COVID-19 patients participating in ODYSSEY COVID-19 clinical trial were assessed together with a set of controls. We report elevated levels of CXCL16 in a cohort of COVID-19 hospitalized patients. Specifically, we report significant elevation of CXCL16 plasma levels in association with severity of COVID-19 (as defined by WHO scale) (P-value 
ISSN:1043-4666
1096-0023
1096-0023
DOI:10.1016/j.cyto.2022.155810