Jansen Of Lorkeers S J, Hart E, Tang X L, Chamuleau M E D, Doevendans P A, Bolli R, Chamuleau S A J
Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.
J Cardiovasc Transl Res. 2014 Jul;7(5):475-82. doi: 10.1007/s12265-014-9570-8. Epub 2014 May 16.
Stem cell therapy is a promising strategy in promoting cardiac repair in the setting of ischemic heart disease. Clinical and preclinical studies have shown that cell therapy improves cardiac function. Whether autologous or allogeneic cells should be used, and the need for immunosuppression in non-autologous settings, is a matter of debate. Cyclosporin A (CsA) is frequently used in preclinical trials to reduce cell rejection after non-autologous cell therapy. The direct effect of CsA on the function and survival of stem cells is unclear. Furthermore, the appropriate daily dosage of CsA in animal models has not been established. In this review, we discuss the pros and cons of the use of CsA on an array of stem cells both in vitro and in vivo. Furthermore, we present a small collection of data put forth by our group supporting the efficacy and safety of a specific daily CsA dosage in a pig model.
干细胞疗法是促进缺血性心脏病心脏修复的一种有前景的策略。临床和临床前研究表明,细胞疗法可改善心脏功能。使用自体细胞还是异体细胞,以及在非自体情况下是否需要免疫抑制,是一个有争议的问题。环孢素A(CsA)在临床前试验中经常被用于减少非自体细胞治疗后的细胞排斥反应。CsA对干细胞功能和存活的直接影响尚不清楚。此外,动物模型中CsA的合适每日剂量尚未确定。在这篇综述中,我们讨论了在体外和体内使用CsA对一系列干细胞的利弊。此外,我们展示了我们小组提出的一小部分数据,支持在猪模型中特定每日CsA剂量的有效性和安全性。