间充质干细胞治疗特发性肺纤维化的机遇与挑战OA
Mesenchymal stem cells therapy for idiopathic pulmonary fibrosis:opportunities and challenges
特发性肺纤维化(IPF)是一种退行性疾病,其特征为肺组织不可逆的纤维增生和结缔组织沉积,常见于50岁以上人群.衰老、遗传和环境等因素会触发表观遗传改变,导致肺泡上皮细胞损伤并被异常激活,引起纤维化的发生,被认为是IPF发生的关键.但是,具体病因和发病机制尚不完全明确,且疾病预后不佳,尚无治愈方法.细胞疗法已经成为多种疾病的新兴治疗策略,本文综述间充质干细胞(MSCs)的自我更新、多向分化潜能以及免疫调节能力和成瘤风险较低等特性,提出了MSCs在IPF治疗中的挑战和展望,为治疗IPF提供了新的思路.
Idiopathic pulmonary fibrosis(IPF)is a degenerative disease characterized by irreversible fibrosis and connective tissue deposition in the lung tissue,commonly seen in people over the age of 50.Aging,genet-ic and environmental factors can trigger epigenetic changes,leading to the damage and abnormal activation of alveolar epithelial cells,which in turn cause fibrosis and are considered key to the occurrence of IPF.Howev-er,the specific etiology and pathogenesis are not yet clear,and the prognosis of the disease is poor,with no cure currently available.Cellular therapy has become an emerging treatment strategy for a variety of diseases.Mesenchymal stem cells(MSCs),with their strong self-renewal,multidirectional differentiation potential and immune regulation capabilities,and low tumorigenic risk,are of significant clinical value and can provide a new perspective for the treatment of IPF.This paper discussed the challenges and prospects of MSCs in the treatment of IPF,providing a reference for future research.
王芸;雷泽林
甘肃中医药大学 第一临床医学院,甘肃 兰州 730000甘肃中医药大学 第一临床医学院,甘肃 兰州 730000||兰州大学第一医院 呼吸科,甘肃 兰州 730000
医药卫生
间充质干细胞特发性肺纤维化临床前研究临床研究归巢能力
mesenchymal stem cellsidiopathic pulmonary fibrosispreclinical researchclinical researchhoming capacity
《兰州大学学报(医学版)》 2025 (6)
72-78,7
国家自然科学基金资助项目(8196010043)甘肃省自然科学基金资助项目(23JRRA1593)
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