Goumans Marie-José, Maring Janita A, Smits Anke M
Department of Molecular Cell Biology and Center for Biomedical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Heart. 2014 Aug;100(15):1153-7. doi: 10.1136/heartjnl-2014-305646.
It has been over a decade since the concept of cell-based therapy was coined as a method to treat patients who suffered the consequences of myocardial infarction (MI). Shortly after promising preclinical results emerged, a rapid translation to the clinic was made using stem cells isolated from a variety of sources, including bone marrow mononuclear cells (BM-MNC), mesenchymal stem cells (MSC) and cardiac progenitor cells (CPC). The hypothesis was that transplanted stem cells would provide cues that enhance the wound healing process, and locally differentiate into new contractile cardiac tissue. However, although the clinical trials have been shown to be safe, only a relatively small effect on cardiac function has been observed. It has become clear that each cell type applied in cell-based therapy has its own ability for cardiac repair. Basic knowledge of each cell population's behaviour and its ability to interfere in different stages of post-MI wound healing may enable us to design an optimised cell-based therapy.
自基于细胞的疗法被提出作为治疗心肌梗死(MI)患者的一种方法以来,已经过去了十多年。在出现有前景的临床前结果后不久,就迅速将从多种来源分离的干细胞应用于临床,这些来源包括骨髓单个核细胞(BM-MNC)、间充质干细胞(MSC)和心脏祖细胞(CPC)。其假设是,移植的干细胞将提供促进伤口愈合过程的线索,并在局部分化为新的可收缩心脏组织。然而,尽管临床试验已证明是安全的,但对心脏功能的影响相对较小。很明显,基于细胞的疗法中应用的每种细胞类型都有其自身的心脏修复能力。了解每个细胞群体的行为及其干扰心肌梗死后伤口愈合不同阶段的能力,可能使我们能够设计出优化的基于细胞的疗法。