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 Stem Cell Research & Therapy Pub Date : 2024-11-20 DOI:10.1186/s13287-024-04021-7
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。
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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.
期刊最新文献
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