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

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. Between January 2018 and March 2022, 28...

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Veröffentlicht in:Stem cell research & therapy 2024-11, Vol.15 (1), p.443-18, Article 443
Hauptverfasser: Lin, Hung-Sheng, Sung, Pei-Hsun, Huang, Shu-Hua, Lin, Wei-Che, Chiang, John Y, Ma, Ming-Chun, Chen, Yi-Ling, Chen, Kuan-Hung, Lee, Fan-Yen, Ko, Sheung-Fat, Yip, Hon-Kan
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Sprache:eng
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Zusammenfassung: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. Between January 2018 and March 2022, 28 consecutive patients were equally randomly allocated to the cell-treated group (CD34 + cells/3.0 × 10 /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. 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 
ISSN:1757-6512
1757-6512
DOI:10.1186/s13287-024-04021-7