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The CXCL9/10/11-CXCR3 axis as a predictor of COVID-19 progression: a prospective, case-control study
Neslihan Çelik1, Onur Çelik2, Esra Laloğlu3
1Health Sciences University, Erzurum Regional Education and Research Hospital, Department of Infection Diseases and Clinical Microbiology, Erzurum, Turkey.
Insights
Chemokine (CXCL9, CXCL10, CXCL11) and receptor (CXCR3) levels correlate with COVID-19 severity and mortality. Higher levels indicate worse outcomes, aiding in clinical decision-making for patient prognosis.
Area of Science:
- Immunology
- Virology
- Clinical Medicine
Background:
- COVID-19 pathogenesis involves complex immune responses.
- Chemokines and their receptors play a role in inflammatory diseases.
Purpose of the Study:
- To investigate the association between CXCL9, CXCL10, CXCL11, and CXCR3 levels and COVID-19 patient mortality.
- To determine if these markers can predict disease severity.
Main Methods:
- Enzyme-linked immunosorbent assays (ELISAs) were used to measure serum levels of CXCL9, CXCL10, CXCL11, and CXCR3.
- Study included 71 hospitalized COVID-19 patients and 35 healthy controls.
- Patients were categorized by disease severity (mild, moderate, severe) and outcome (survived, deceased).
Main Results:
- Significantly elevated CXCL9, CXCL10, CXCL11, and CXCR3 levels were observed in severe COVID-19 patients compared to non-severe cases.
- These chemokine levels were higher in both COVID-19 patient groups than in healthy controls.
- Deceased patients exhibited higher levels of these chemokines compared to survivors.
Conclusions:
- CXCL9, CXCL10, CXCL11, and CXCR3 levels are significantly associated with COVID-19 disease severity.
- These biomarkers can serve as valuable indicators for predicting patient outcomes and guiding clinical management decisions.
Background:
This study examined the relationship between levels of the chemokines CXCL9, CXCL10, CXCL11, and CXCR3 and mortality in patients with COVID-19..
Methods:
A total of 71 patients hospitalized with COVID-19 and 35 health workers with no symptoms and negative SARS-CoV-2 PCR results were included in the study. CXCL9, CXCL10, CXCL11, and CXCR3 levels were measured in blood samples using enzyme-linked immunosorbent assays. Participants were divided into three groups: healthy individuals, patients with mild to moderate pneumonia, and patients with severe pneumonia. Patients were also divided into sub-groups according to the outcome: dead and survived.
Results:
Serum CXCL9, CXCL10, CXCL11, and CXCR3 levels were significantly higher in patients with severe COVID-19 than in those with non-severe COVID-19; were higher in both patient groups than in the control group; and were higher in patients who died than in those who survived. Lymphocyte counts, and fibrinogen and PaO2/FiO2 levels were significantly lower in patients with severe COVID-19 than in those with moderate disease. Patients with COVID-19 also had elevated neutrophil/lymphocyte ratios, neutrophil counts, and lactate dehydrogenase, C-reactive protein, D-dimer, and ferritin levels.
Conclusions:
This study confirmed that CXCL9, CXCL10, CXCL11, and CXCR3 levels are associated with disease severity in patients with COVID-19. These laboratory parameters can help to estimate disease severity and predict outcomes, and are useful in clinical decision-making.
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