ABSTRACT Sepsis remains a leading cause of global mortality, characterized by uncontrolled inflammation and multi‐organ dysfunction. Galectin‐3 (Gal‐3) is a damage‐associated molecular pattern (DAMP) protein that amplifies inflammatory cascades during sepsis and represents a potential therapeutic target. We conducted an integrated translational investigation combining clinical observation (87 septic patients, 27 healthy volunteers) with preclinical Gal‐3 removal using an anti‐Gal‐3 apheresis column in two sepsis models: a rat cecal ligation and puncture (CLP) model ( n = 48) and a porcine lipopolysaccharide (LPS)‐induced model ( n = 31). Mechanistic assessments included serum testing, multi‐omics profiling, invasive hemodynamic monitoring, and histopathology. Patients with sepsis exhibited markedly elevated Gal‐3 levels ( p < 0.001), and survivors showed progressive Gal‐3 decline compared with non‐survivors ( p < 0.01). Gal‐3 removal significantly improved survival in rats (57.1% vs. 25.0%, p = 0.003) and pigs (68.8% vs. 26.7%, p = 0.004). Treatment attenuated neutrophil activation and tissue infiltration, preserved endothelial barrier integrity, and modulated pro‐survival and hypoxia‐response signaling pathways, accompanied by reduced vasopressor requirements and pulmonary edema. Collectively, these findings demonstrate that Gal‐3 removal improves survival and reduces organ damage in preclinical sepsis models in association with coordinated neutrophil modulation and endothelial barrier preservation, highlighting Gal‐3 as a promising therapeutic target in sepsis.
Sun et al. (Sun,) studied this question.