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干细胞旁分泌效应在ALI/ARDS治疗中的研究进展
引用本文:朱峰,文辉才,郭光华.干细胞旁分泌效应在ALI/ARDS治疗中的研究进展[J].中国病理生理杂志,2012,28(4):755-759.
作者姓名:朱峰  文辉才  郭光华
作者单位:1. 南昌大学第一附属医院重症医学科, 江西 南昌 330006;
2. 南昌大学第一附属医院整形科, 江西 南昌 330006;
3. 南昌大学第一附属医院烧伤科, 江西 南昌 330006
基金项目:国家自然科学基金资助项目,江西省科技厅支撑计划
摘    要:急性肺损伤(acute lung injury,ALI)以及它的严重形式——急性呼吸窘迫综合征(acute respiratorydistress syndrome,ARDS)是危重病人发病和死亡的重要原因之一,最近2个世纪以来,死亡率仍在36%~44%左右。ALI/ARDS的病因众多,发病机制十分复杂,涉及的环节多,受损的靶细胞多,主要涉及的环节有:炎症反应失控、细胞损伤与修复、细胞凋

关 键 词:干细胞  急性肺损伤  呼吸窘迫综合征  急性  
收稿时间:2011-11-10

Paracrine effect of stem cells on treatment of acute lung injury/acute respiratory distress syndrome
ZHU Feng , WEN Hui-cai , GUO Guang-hua.Paracrine effect of stem cells on treatment of acute lung injury/acute respiratory distress syndrome[J].Chinese Journal of Pathophysiology,2012,28(4):755-759.
Authors:ZHU Feng  WEN Hui-cai  GUO Guang-hua
Institution:1. Department of Critical Care Medicine, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China;
2. Department of Plastic Surgery, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China;
3. Department of Burning, The First Affiliated Hospital of Nanchang University, Nanchang 330006, China
Abstract:Acute lung injury(ALI) and acute respiratory distress syndrome(ARDS) represent the leading cause of morbidity and mortality in critical patients.Despite improvements in supportive care and mechanical ventilation,recent data indicate that the mortality of ALI/ARDS is still high.Cell-based therapy with stem cells is an attractive new therapeutic approach.Stem cells have the capacity to secrete multiple paracrine factors that can regulate inflammation,improve alveolar fluid clearance,regulate endothelial and epithelial permeability,enhance tissue repair via chemotaxis and inhibit bacterial growth.This review focuses on the recent studies,which support the potential therapeutic use of stem cells in ALI/ARDS with an emphasis on the role of paracrine soluble factors.
Keywords:Stem cells  Acute lung injury  Respiratory distress syndrome  acute
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