Predictive Value and Diagnostic Potential of IL-10, IL-17A, IL1-β, IL-6, CXCL, and MCP for Severe COVID-19 and COVID-19 Mortality

Biomedicines. 2024 Jul 10;12(7):1532. doi: 10.3390/biomedicines12071532.

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) necessitates advanced prognostic tools to anticipate disease progression and optimize patient outcomes. This study evaluates the predictive value and diagnostic potential of interleukins interleukin (IL) IL-10, IL-17A, IL1-β, IL-6, chemokine ligand (CXCL), and Monocyte Chemotactic Protein (MCP) for severe coronavirus disease 2019 (COVID-19) and COVID-19 mortality, aiming to correlate cytokine levels with disease severity. Conducted from January 2023 to January 2024, this prospective cohort study involved patients hospitalized with moderate and severe COVID-19 from Romania. This study analyzed statistically significant predictors of severe COVID-19 outcomes. IL-6 and MCP emerged as significant, with hazard ratios (HRs) of 2.35 (95% confidence interval (CI): 1.54-3.59, p = 0.014) and 2.05 (95% CI: 1.22-3.45, p = 0.007), respectively. Compound scores integrating multiple inflammatory markers also demonstrated predictive value; Compound Score 2 had an HR of 2.23 (95% CI: 1.35-3.68, p = 0.002), surpassing most single markers in association with severe disease. Notably, interleukins IL-10 and IL-1β did not show significant associations with disease severity. This study underscores the importance of IL-6 and MCP as robust predictors of severe COVID-19, substantiating their role in clinical assessments to foresee patient deterioration. The utility of compound scores in enhancing predictive accuracy suggests a composite approach may be more effective in clinical settings.

Keywords: COVID-19; SARS-CoV-2; inflammation; respiratory infections.

Grants and funding

This research was performed in the Center for Research and Development of the Morphological and Genetic Studies of Malignant Pathology from the Ovidius University of Constanta, POSCCE 2.2.1. Project ID: 1844, SMIS code: 48750, CEDMOG, contract 627/11.03.2014. This work was supported by the COVIL project, in the framework of the Ovidius University of Constanta biomedical grant competition; contract number 15137/05.10.2022. The article processing charge was paid by “Victor Babes” University of Medicine and Pharmacy, Timisoara, Romania.