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Patients with chronic kidney disease (CKD) are at high risk of severe complications from COVID‐19 and functional monocyte disturbances have been implicated to play a role. Our objective was to analyse the association between kidney function and monocyte modulatory factors, with risk of mortality in patients with COVID‐19. Hospitalized patients with COVID‐19 (n = 110) were included and in‐hospital mortality was analysed with unadjusted and adjusted multiple logistic regression analysis. Plasma levels of monocyte chemoattractant factors (MIP‐1α, MCP‐1, IL‐6) and a monocyte immune modulator (sCD14) were analysed and correlated to kidney function and risk of mortality. Monocyte modulatory factors were also determined in CKD patients without infection (disease controls) and in healthy subjects. Patients who died in hospital were more often in CKD stages 3‐5, with lower estimated glomerular filtration rate (eGFR) and had significantly higher MIP‐1α and IL‐6 levels than survivors. In multiple regression analyses adjusted for age, sex and eGFR, both high MCP‐1 and high MIP‐1α were significantly associated with risk of in‐hospital mortality. Apart from impaired kidney function, also the concentrations of MCP‐1 and MIP‐1α add important prognostic information in hospitalized patients with COVID‐19. These data provide an increased understanding of the impact of monocyte modulators in patients with COVID‐19 and normal or impaired kidney function, and warrant consideration in the pursuit of new effective therapies. [ABSTRACT FROM AUTHOR]

Background: Chronic kidney disease (CKD) is a recognized risk factor for severe complications in COVID-19. Our objective was to analyze the association between kidney function / T and B lymphocyte modulatory factors and risk of mortality in COVID-19 patients.Methods: In-hospital and 30-day mortality were analyzed in COVID-19 patients (n = 110). Plasma levels of selected T and B cell modulators were analyzed and correlated to mortality risk. A subgroup of sex- and eGFR-matched COVID-19 patients was compared to CKD patients without infection and healthy subjects.Results: COVID-19 patients who died in hospital and within 30 days had significantly higher BAFF and sCD25 plasma levels than survivors. In logistic regression models patients with high BAFF, sCD25 and sPD-L1 levels had significantly higher risk of both in-hospital and 30-day mortality while there was no association to eGFR. In the subgroup analysis, a higher level of BAFF, IFN-α, sCD25, sPD-L1 and a lower level of sCD40L was observed in COVID-19 patients compared to the CKD group with corresponding kidney function.Conclusions: We demonstrate that kidney function and concentrations of BAFF, sCD25 and PD-L1, independent of previously recognized risk factors; age, male gender, and leukocytosis are associated with risk of in-hospital and 30-day mortality in patients with COVID-19. These data indicate the significance of adaptive immune system modulators in COVID-19 and motivate further analysis to identify new potential prognostic and therapeutic approaches. [ABSTRACT FROM AUTHOR]