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CD34(+)骨髓来源单个核细胞自体移植治疗不可重建的严重下肢缺血

Autologous transplantation of CD34(+) bone marrow derived mononuclear cells in management of non-reconstructable critical lower limb ischemia.

作者信息

Ismail Ahmed M, Abdou Said M, Aty Hassan Abdel, Kamhawy Adel H, Elhinedy Mohammed, Elwageh Mohammed, Taha Atef, Ezzat Amal, Salem Hoda A, Youssif Said, Salem Mohamed L

机构信息

Vascular Surgery Unit, Tanta University, Tanta, Egypt.

Clinical Pathology Department, Tanta University, Tanta, Egypt.

出版信息

Cytotechnology. 2016 Aug;68(4):771-81. doi: 10.1007/s10616-014-9828-7. Epub 2014 Dec 16.

Abstract

Patients with a decrease in limb perfusion with a potential threat to limb viability manifested by ischemic rest pain, ischemic ulcers, and/or gangrene are considered to have critical limb ischemia (CLI). Because of this generally poor outcome, there is a strong need for attempting any procedure to save the affected limb. The aim of this work is to evaluate the possibility to use stem cell therapy as a treatment option for patients with chronic critical lower limb ischemia with no distal run off. This study includes 20 patients with chronic critical lower limb ischemia with no distal run off who are unsuitable for vascular or endovascular option. These patients underwent stem cell therapy (SCT) by autologous transplantation of bone marrow derived mononuclear cells. 55 % of patients treated with SCT showed improvement of the rest pain after the first month, 60 % continued improvement of the rest pain after 6 months, 75 % after 1 year and 80 % after 2 years and continued without any deterioration till the third year. Limb salvage rate after STC was 80 % after the first year till the end of the second and third years. SCT can result in angiogenesis in patients with no-option CLI, providing a foundation for the application of this therapy to leg ischemia.

摘要

肢体灌注减少且因缺血性静息痛、缺血性溃疡和/或坏疽而对肢体生存能力构成潜在威胁的患者被认为患有严重肢体缺血(CLI)。由于这种情况通常预后较差,因此迫切需要尝试任何挽救患肢的手术。这项工作的目的是评估将干细胞疗法作为治疗无远端流出道的慢性严重下肢缺血患者的一种治疗选择的可能性。本研究纳入了20例无远端流出道、不适合血管或血管内治疗方案的慢性严重下肢缺血患者。这些患者通过自体移植骨髓来源的单核细胞接受了干细胞治疗(SCT)。接受SCT治疗的患者中,55%在第一个月后静息痛有所改善,60%在6个月后静息痛持续改善,75%在1年后改善,80%在2年后改善,并且直到第三年都没有任何恶化。从第一年到第二年末及第三年末,STC后的肢体挽救率为80%。SCT可在无可选择的CLI患者中诱导血管生成,为将该疗法应用于腿部缺血提供了依据。

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