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Hepatocyte growth factor-modified mesenchymal stem cells (HGF-MSCs) are an experimental, preclinical and early clinical-stage gene-modified cell therapy. Mesenchymal stem cells (MSCs), derived from sources such as bone marrow or umbilical cord, are genetically engineered (often via lentiviral or adenoviral vectors) to overexpress hepatocyte growth factor (HGF). HGF is a pleiotropic cytokine and growth factor that promotes cell survival, tissue regeneration, and angiogenesis while suppressing inflammation and fibrosis. The genetic modification is designed to enhance the survival, homing, and therapeutic efficacy of the transplanted MSCs in hostile microenvironments. HGF-MSCs have been investigated in preclinical models of acute lung injury, myocardial infarction, liver fibrosis, spinal cord injury, and rheumatoid arthritis-associated interstitial lung disease (RA-ILD). A small clinical study has also evaluated autologous HGF-modified bone marrow MSCs for the treatment of pulmonary silicosis.
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