急性缺血性脑卒中患者頸動脈內輸血循環自體 CD34 +細胞的長期療效--一項隨機、開放標籤、對照 II 期臨床試驗。

IF 7.1 2区 医学 Q1 CELL & TISSUE ENGINEERING
Hung-Sheng Lin, Pei-Hsun Sung, Shu-Hua Huang, Wei-Che Lin, John Y Chiang, Ming-Chun Ma, Yi-Ling Chen, Kuan-Hung Chen, Fan-Yen Lee, Sheung-Fat Ko, Hon-Kan Yip
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引用次数: 0

摘要

背景:这项II期随机对照试验检验了在急性缺血性脑卒中(IS)后14±7天内对患者进行颈动脉内给予(ICAA)自体CD34 +细胞是否安全,并进一步改善短期和长期预后:2018年1月至2022年3月期间,28名连续患者被平均随机分配到细胞治疗组(CD34 +细胞/3.0 × 107/患者)或对照组(接受最佳药物治疗)。在导管室通过 ICAA 将 CD34 + 细胞输注到细胞治疗患者的同侧脑梗死区:结果表明,该手术的安全性和成功率均为 100%,细胞治疗患者未观察到长期肿瘤发生。在细胞治疗的患者中,循环内皮祖细胞(EPCs)/Matrigel 治疗后的血管生成能力明显高于粒细胞集落刺激因子治疗前(均为 p):頸動脈內輸注自體 CD34 +細胞是安全的,可改善急性IS患者的長期治療效果。试验注册ISRCTN,ISRCTN15677760。2018年4月23日注册-回顾性注册,https://doi.org/10.1186/ISRCTN15677760。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long term outcomes of intracarotid arterial transfusion of circulatory-derived autologous CD34 + cells for acute ischemic stroke patients-A randomized, open-label, controlled phase II clinical trial.

Background: This phase II randomized controlled trial tested whether the intracarotid arterial administration (ICAA) of autologous CD34 + cells to patients within 14 ± 7 days after acute ischemic stroke (IS) could be safe and further improve short- and long-term outcomes.

Methods: Between January 2018 and March 2022, 28 consecutive patients were equally randomly allocated to the cell-treated group (CD34 + cells/3.0 × 107/patient) or the control group (receiving optimal medical therapy). CD34 + cells were transfused into the ipsilateral brain infarct zone of cell-treated patients via the ICAA in the catheterization room.

Results: The results demonstrated 100% safety and success rates for the procedure, and no long-term tumorigenesis was observed in cell-treated patients. In cell-treated patients, the angiogenesis capacity of circulating endothelial progenitor cells (EPCs)/Matrigel was significantly greater after treatment than before treatment with granulocyte colony-stimulating factor (all p < 0.001). Blood samples from the right internal jugular vein of the cell-treated patients presented significantly greater levels of the stromal cell-derived factor 1α/EPC at 5, 10 and 30 min compared with 0 min (all p < 0.005). The National Institute of Health Stroke Scale scores were similar upon presentation, but a greater response was observed by Days 30 and 90 in the cell-treated group than in the control group. Tc-99 m brain perfusion was significantly greater at 180 days in the cell-treated group than in the control group (p = 0.046). The combined long-term end points (defined as death/recurrent stroke/or severe disability) were notably lower in the control group compared with the cell-treated group (14.3% vs. 50.0%, p = 0.103).

Conclusion: Intracarotid transfusion of autologous CD34 + cells is safe and might improve long-term outcomes in patients with acute IS. Trial registration ISRCTN, ISRCTN15677760. Registered 23 April 2018- Retrospectively registered, https://doi.org/10.1186/ISRCTN15677760.

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来源期刊
Stem Cell Research & Therapy
Stem Cell Research & Therapy CELL BIOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
13.20
自引率
8.00%
发文量
525
审稿时长
1 months
期刊介绍: Stem Cell Research & Therapy serves as a leading platform for translational research in stem cell therapies. This international, peer-reviewed journal publishes high-quality open-access research articles, with a focus on basic, translational, and clinical research in stem cell therapeutics and regenerative therapies. Coverage includes animal models and clinical trials. Additionally, the journal offers reviews, viewpoints, commentaries, and reports.
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