Pareja Eugenia, Gómez-Lechón M José, Tolosa Laia
Unidad de Hepatología Experimental, Instituto de Investigación Sanitaria La Fe, Valencia, Spain.
Unidad Hepatobiliopancreáctica, Hospital Universitario Doctor Peset, Valencia, Spain.
Ann Transl Med. 2020 Apr;8(8):566. doi: 10.21037/atm.2020.02.164.
The only curative treatment for severe end-stage liver disease (ESLD) is liver transplantation (LT) but it is limited by the shortage of organ donors. The increase of the incidence of liver disease has led to develop new therapeutic approaches such as liver cell transplantation. Current challenges that limit a wider application of this therapy include a limited cell source and the poor engraftment in the host liver of cryopreserved hepatocytes after thawing. Induced pluripotent stem cells (iPSCs) that can be differentiated into hepatocyte-like cells (HLCs) are being widely explored as an alternative to human hepatocytes because of their unlimited proliferation capacity and their potential ability to avoid the immune system. Their large-scale production could provide a new tool to produce enough HLCs for treating patients with metabolic diseases, acute liver failure (ALF), those with ESLD or patients not considered for organ transplantation. In this review we discuss current challenges for generating differentiated cells compatible with human application as well as in-depth safety evaluation. This analysis highlights the uncertainties and deficiencies that should be addressed before their clinical use but also points out the potential benefits that will produce a great impact in the field of hepatology.
终末期肝病(ESLD)的唯一治愈性治疗方法是肝移植(LT),但它受到器官供体短缺的限制。肝病发病率的增加促使人们开发新的治疗方法,如肝细胞移植。限制这种疗法更广泛应用的当前挑战包括细胞来源有限以及解冻后冷冻保存的肝细胞在宿主肝脏中的植入效果不佳。由于诱导多能干细胞(iPSC)具有无限增殖能力以及避免免疫系统的潜在能力,能够分化为肝细胞样细胞(HLC),因此作为人类肝细胞的替代物正受到广泛探索。其大规模生产可为治疗代谢性疾病、急性肝衰竭(ALF)、ESLD患者或不适合器官移植的患者生产足够的HLC提供一种新工具。在本综述中我们讨论了生成适用于人类的分化细胞的当前挑战以及深入的安全性评估。该分析突出了在其临床应用前应解决的不确定性和不足,但也指出了将对肝病学领域产生重大影响的潜在益处。