心肌损伤细胞治疗的临床试验

Q4 Medicine
A. Popandopulo, M. Solopov, V. V. Turchyn, V. Bushe
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引用次数: 0

摘要

心脏病的高死亡率要求开发新的治疗方法。传统的治疗方法可以提供一种代偿作用,提高患者的生活质量,但不能消除心肌损失。临床前研究表明,干细胞和祖细胞移植可刺激心脏组织再生。这篇综述描述了使用区域干细胞、祖细胞和从ESC/iPSCs分化的细胞治疗心肌损伤的临床试验。临床研究结果证实了细胞治疗心肌损伤的安全性和有效性。然而,由于对移植细胞对心肌的作用机制的认识不足,以及临床前试验的成功引发的临床试验的快速部署,可能最多只能观察到适度的治疗效果。在使用区域干细胞的研究中,不可能可靠地证实它们分化为心肌细胞并融入心肌的能力,并且观察到的心功能改善与旁分泌信号有关。心脏ESC/iPSC衍生物更适合修复丢失的心肌,但由于这些类型细胞的临床试验数量仍然很少,需要进一步的研究来证实其安全性和有效性。在制定未来细胞治疗临床试验设计时,需要严格考虑细胞的作用机制、疾病的病理生理,选择最优的一组终点。所进行的研究的经验使人们认识到需要发展个性化的细胞疗法,根据这种疗法,细胞来源和给药途径的选择应基于患者的个体特征。越来越多的临床试验和对移植细胞对受损心肌作用机制的积极研究表明,这种类型的细胞治疗在不久的将来有机会进入临床实践。2021年10月4日收到。2021年12月13日修订。2021年12月20日接受。经费来源:本研究未获得赞助。利益冲突:作者声明无利益冲突。作者的贡献:作者对本文的贡献相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical trials of myocardium injury cell therapy
The high mortality rate from heart disease requires the development of new therapeutic approaches. Traditional treatments can provide a compensatory effect, improve the patient's quality of life, but not eliminate myocardial loss. Preclinical studies indicate that the regeneration of cardiac tissue can be stimulated through transplantation of stem and progenitor cells.The review describes clinical trials of myocardial injury therapy using regional stem cells, progenitor cells, and cells differentiated from ESC/iPSCs. The results of clinical studies have confirmed the safety and availability of cell therapy for myocardial injury. However, insufficient knowledge of the mechanisms of action of transplanted cells on the myocardium and the rapid deployment of clinical trials initiated by the success of preclinical trials made it possible to observe, at best, only a moderate therapeutic effect. In studies using regional stem cells, it was not possible to reliably confirm their ability to differentiate into cardiomyocytes and integrate into the myocardium, and the observed improvements in heart function are associated with paracrine signaling. Cardiac ESC/iPSC derivatives are more suitable for the restoration of the lost myocardium, but since the number of clinical trials with these types of cells is still small, additional studies are required to confirm their safety and efficacy.When developing the design of future clinical trials of cell therapy, it is necessary to strictly take into account the mechanism of cell action, the pathophysiology of the disease, and select the optimal set of endpoints. The experience of the conducted research leads to an understanding of the need to develop personalized cell therapy, according to which the choice of the source of cells and the route of administration should be based on the individual characteristics of the patient.The growing number of clinical trials and the active study of the mechanisms of action of transplanted cells on damaged myocardium suggest that this type of cell therapy has a chance to enter clinical practice in the near future.Received 4 October 2021. Revised 13 December 2021. Accepted 20 December 2021.Funding: The study did not have sponsorship.Conflict of interest: Authors declare no conflict of interest.Contribution of the authors: The authors contributed equally to this article.
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来源期刊
Patologiya krovoobrashcheniya i kardiokhirurgiya
Patologiya krovoobrashcheniya i kardiokhirurgiya Medicine-Cardiology and Cardiovascular Medicine
CiteScore
1.00
自引率
0.00%
发文量
42
审稿时长
12 weeks
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