Targeting Nonhealing Ulcers of Lower Extremity in Human Through Autologous Bone Marrow-Derived Mesenchymal Stem Cells

医学 间充质干细胞 养生 外科 干细胞 川地34 植入 伤口愈合 骨髓 糖尿病足 下肢静脉性溃疡 病理 内科学 糖尿病 生物 遗传学 内分泌学
作者
Nihar Ranjan Dash,Surjya Narayan Dash,P. Routray,Sribatsha Mohapatra,Prakash Chandra Mohapatra
出处
期刊:Rejuvenation Research [Mary Ann Liebert, Inc.]
卷期号:12 (5): 359-366 被引量:314
标识
DOI:10.1089/rej.2009.0872
摘要

Bone marrow (BM)-derived mesenchymal stem cells (MSCs) represent a promising population for supporting new concepts in cellular therapy. This study was undertaken to assess the efficacy and feasibility of autologous BM-derived MSCs in the treatment of chronic nonhealing ulcers (diabetic foot ulcers and Buerger disease) of the lower extremities. A total of 24 patients with nonhealing ulcers of the lower limb were enrolled and randomized into implant and control groups. In the implant group, the patients received autologous cultured BM-derived MSCs along with standard wound dressing; the control group received only the standard wound dressing regimen, followed up for at least a 12-week period. Wound size, pain-free walking distance, and biochemical parameters were measured before therapy and at every 2-week interval following intervention. The implant group had significant improvement in pain-free walking distance and reduction in ulcer size as compared to those in the control group. In the implant group for Buerger disease, the ulcer area decreased from 5.04 ± 0.70 cm2 to 1.48 ± 0.56 cm2 (p < 0.001), whereas the pain-free walking distance increased from 38.33 ± 17.68 m to 284.44 ± 212.12 m (p < 0.001). In the diabetic foot ulcer group, the ulcer size decreased from 7.26 ± 1.41 cm2 to 2 ± 0.98 cm2 (p < 0.001) at 12 weeks. Mononuclear cells were cultured for a minimum of five passages and characterized by cell-surface markers showing CD90+, CD105+, and CD34−. There was no significant alteration in the biochemical parameters observed during the follow-up period, indicating normal liver and renal function following intervention. Biopsy microsection of implanted tissues showed development of dermal cells (mainly fibroblasts), including mature and immature inflammatory cells. The study indicates that autologous implantation of BM-derived MSCs in nonhealing ulcers accelerates the healing process and improves clinical parameters significantly.

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