Review of thymosin β4's renal biology and disease-modifying potential in chronic kidney disease (CKD). Covers evidence from transgenic and knockout models showing endogenous TB4 is required for normal renal function; pharmacological TB4 protects in AKI, diabetic nephropathy, and glomerular disease. Discusses anti-fibrotic mechanisms (Ac-SDKP generation, TGF-β/NF-κB suppression) and anti-inflammatory/epithelial repair activities. Positions TB4 as a novel therapeutic direction for CKD—a condition affecting 800 million people worldwide with limited disease-modifying options beyond renin-angiotensin blockade.
Vasilopoulou, Elisavet; Riley, Paul R; Long, David A