These cytokines serve as pivotal molecular switches that initiate the differentiation of nave T cells into effector subtypes Th1 and Th17, respectively (de Alcantara et al
The KidneyIntelX platform utilizes plasma levels of KIM-1, soluble tumor necrosis factor (sTNF) receptor-1, and sTNF receptor-2 to predict diabetic kidney disease progression over 5 years [130] A biomarker panel comprising serum creatinine, osteopontin, tryptase, urea, and estimated glomerular filtration rate (eGFR) achieved an 84.3% accuracy in predicting CKD progression [131] Combining standard markers such as creatinine and cystatin C with sensitive biomarkers such as beta-trace protein (BTP), tissue inhibitor of metalloproteinase-1, TGF-, asymmetric dimethylarginine (ADMA), TNF-, and N-terminal pro-B-type natriuretic peptide (proBNP) have shown improved diagnostic performance for early CKD detection [132] Panels integrating tumor necrosis factor receptor (TNFR)-1, TNFR-2, and KIM-1 have demonstrated superior predictive accuracy for renal function decline The kidney injury test uses urinary markers including cell-free DNA (cfDNA), methylated cfDNA, clusterin, C-X-C motif chemokine ligand 10 (CXCL10), total protein, and creatinine to generate a diagnostic score with high sensitivity and specificity, even when eGFR and proteinuria remain within normal ranges For AKI detection, urinary biomarker panels combining NGAL, KIM-1, cystatin C, and hemojuvelin have shown strong predictive value
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TGF- receptor inhibitors target the CD44 high /Id1 high glioma-initiating cell population in human glioblastoma
This protective action is crucial for preventing initial cellular damage and supporting the recovery of injured tissues
