IntroductionRenal transplant patients (RTPs) receiving immunomodulatory therapy are at increased risk of severe complications from COVID-19 and other infections. This study aimed to identify immune and proteomic biomarkers associated with COVID-19 in RTPs to improve disease characterization and support future diagnostic and therapeutic strategies.MethodsPeripheral blood samples from RTPs with COVID-19 infection, uninfected RTPs, and healthy controls were analyzed using cytokine gene expression profiling and label-free global quantitative proteomics.
Differential cytokine expression and proteomic alterations were evaluated across study groups and according to disease severity and recovery status.ResultsCytokine levels differed significantly between healthy controls and COVID-19-affected RTPs (p = 0.04), whereas no significant difference was observed between healthy controls and uninfected RTPs (p = 0.92). Within the RTP-COVID group, cytokine expression varied according to disease severity (p = 0.04) but not between acute and recovery phases (p = 0.39).
Proteomic profiling identified eighteen altered protein targets. Eight proteins (SERPINF2, SAA1, HP, PLG, SERPINA3, CFHR1, HRG, and C4A) were associated with RTP-COVID and may represent candidate biomarkers of COVID-19 risk in RTPs.
Frontiers in Immunology published a clinical update in Infectious Disease on 12 Jun 2026.
The item focuses on Predictive biomarkers of COVID-19 impact in renal transplant patients: an exploratory proteomic and cytokine analysis.
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