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Autologous umbilical cord blood mononuclear cells + pulmonary surfactant is an investigational combination cell therapy being developed for the prevention and treatment of bronchopulmonary dysplasia (BPD) in preterm infants. The therapy involves the intratracheal administration of the patient's own umbilical cord blood mononuclear cells (CBMNC) in conjunction with pulmonary surfactant (PS). CBMNCs are believed to exert therapeutic effects through the secretion of paracrine factors that reduce inflammation and promote lung tissue repair, while the pulmonary surfactant provides immediate structural stability to the alveoli, reducing the risk of collapse and further injury in ventilated neonates. This approach is currently being evaluated in Phase 1 clinical trials (e.g., NCT03855202) led by investigator Yang Jie.
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