Department of Medicine and Stem Cell Institute, University of Minnesota, Minneapolis, MN 55455, USA.
Transl Res. 2010 Sep;156(3):147-54. doi: 10.1016/j.trsl.2010.07.008. Epub 2010 Aug 1.
Human embryonic stem cells (hESCs) and induced pluripotent stem cells (iPSCs) provide an accessible, genetically tractable, and homogenous starting cell population to efficiently study human blood cell development. These cell populations provide platforms to develop new cell-based therapies to treat both malignant and nonmalignant hematological diseases. Our group previously demonstrated the ability of hESC-derived hematopoietic precursors to produce functional natural killer (NK) cells as well as an explanation of the underlying mechanism responsible for the inefficient development of T and B cells from hESCs. hESCs and iPSCs, which can be engineered reliably in vitro, provide an important new model system to study human lymphocyte development and produce enhanced cell-based therapies with the potential to serve as a "universal" source of antitumor lymphocytes. This review will focus on the application of hESC-derived NK cells with currently used and novel therapeutics for clinical trials, barriers to translation, and future applications through genetic engineering approaches.
人类胚胎干细胞 (hESCs) 和诱导多能干细胞 (iPSCs) 为高效研究人类血细胞发育提供了一种易于获取、遗传上易于操作且同质的起始细胞群体。这些细胞群体为开发新的基于细胞的疗法提供了平台,以治疗恶性和非恶性血液疾病。我们的小组之前证明了 hESC 衍生的造血前体细胞产生功能性自然杀伤 (NK) 细胞的能力,以及解释了 hESC 中 T 和 B 细胞发育效率低下的潜在机制。hESCs 和 iPSCs 可以在体外可靠地进行工程改造,为研究人类淋巴细胞发育提供了一个重要的新模型系统,并产生了增强的基于细胞的疗法,有可能成为抗肿瘤淋巴细胞的“通用”来源。本综述将重点介绍 hESC 衍生的 NK 细胞在临床试验中目前使用的和新型治疗方法的应用、转化的障碍,以及通过遗传工程方法的未来应用。