Xenogeneic human umbilical cord-derived mesenchymal stem cells reduce mortality in rats with acute respiratory distress syndrome complicated by sepsis

被引:38
|
作者
Lee, Fan-Yen [1 ,2 ]
Chen, Kuan-Hung [2 ,3 ]
Wallace, Christopher Glenn [4 ]
Sung, Pei-Hsun [2 ,5 ]
Sheu, Jiunn-Jye [1 ,2 ]
Chung, Sheng-Ying [2 ,5 ,6 ]
Chen, Yung-Lung [2 ,5 ]
Lu, Hung-I [1 ,2 ]
Ko, Sheung-Fat [2 ]
Sun, Cheuk-Kwan [7 ]
Chiang, Hsin-Ju [2 ,8 ]
Chang, Hsueh-Wen [9 ]
Lee, Mel S. [2 ,10 ]
Yip, Hon-Kan [2 ,5 ,11 ,12 ,13 ,14 ]
机构
[1] Kaohsiung Chang Gung Mem Hosp, Dept Surg, Div Thorac & Cardiovasc Surg, Kaohsiung, Taiwan
[2] Chang Gung Univ, Coll Med, Kaohsiung, Taiwan
[3] Kaohsiung Chang Gung Mem Hosp, Dept Anesthesiol, Kaohsiung, Taiwan
[4] Royal Devon & Exeter Hosp, Dept Plast Surg, Exeter EX2 5DW, Devon, England
[5] Kaohsiung Chang Gung Mem Hosp, Dept Internal Med, Div Cardiol, Kaohsiung, Taiwan
[6] Kaohsiung Chang Gung Mem Hosp, Dept Radiol, Kaohsiung, Taiwan
[7] I Shou Univ, Sch Med Int Students, E Da Hosp, Dept Emergency Med, Kaohsiung, Taiwan
[8] Kaohsiung Chang Gung Mem Hosp, Dept Obstet & Gynecol, Kaohsiung, Taiwan
[9] Natl Sun Yat Sen Univ, Dept Biol Sci, Kaohsiung, Taiwan
[10] Kaohsiung Chang Gung Mem Hosp, Dept Orthoped, Kaohsiung, Taiwan
[11] Kaohsiung Chang Gung Mem Hosp, Inst Translat Res Biomed, Kaohsiung, Taiwan
[12] Kaohsiung Chang Gung Mem Hosp, Ctr Shockwave Med & Tissue Engn, Kaohsiung, Taiwan
[13] Asia Univ, Dept Nursing, Taichung, Taiwan
[14] China Med Univ, China Med Univ Hosp, Dept Med Res, Taichung, Taiwan
关键词
acute respiratory distress syndrome; sepsis syndrome; inflammatory and immune reactions; xenogeneic mesenchymal stem cell; mortality; ISCHEMIA-REPERFUSION INJURY; EXTRACORPOREAL MEMBRANE-OXYGENATION; ACUTE LUNG INJURY; SEPTIC SHOCK; INFLAMMATORY RESPONSE; HOSPITAL MORTALITY; COMBINED THERAPY; ORGAN DAMAGE; T-CELLS; MELATONIN;
D O I
10.18632/oncotarget.17320
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study tested the hypothesis that xenogeneic human umbilical cord-derived mesenchymal stem cell (HUCDMSC) therapy would improve survival rates in rats with acute respiratory distress-syndrome (ARDS, induction by 48 h inhalation of 100% oxygen) and sepsis-syndrome (SS, induction by cecal-ligation and puncture) (ARDS-SS). Adult-male Sprague-Dawley rats were categorized into group 1 (sham-controls), group 2 (ARDS-SS), group 3 [ARDS-SS+ HUCDMSC (1.2 x10(6) cells administered 1 h after SS-induction)], and group 4 [ARDS-SS+ HUCDMSC (1.2 x106 cells administered 24 h after SS-induction)]. The mortality rate was higher in groups 2 and 4 than in groups 1 and 3 (all p<0.0001). The blood pressure after 28 h was lower in groups 2, 3 and 4 (p<0.0001) than in group 1. Albumin levels and percentages of inflammatory cells in broncho-alveolar lavage fluid, and the percentages of inflammatory and immune cells in circulation, were lowest in group 1, highest in group 2, and higher in group 3 than group 4 (all p<0.0001). The percentages of inflammatory cells in ascites and kidney parenchyma showed identical patterns, as did kidney injury scores (all p<0.0001). EarlyHUCDMSC therapy reduced rodent mortality after induced ARDS-SS.
引用
收藏
页码:45626 / 45642
页数:17
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