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Liver Regenerative Medicine: From Hepatocyte Transplantation toBioartificial Livers and Bioengineered Grafts

机译:肝再生医学:从肝细胞移植到生物人工肝和生物工程移植物

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摘要

Donor organ shortage is the main limitation to liver transplantation as a treatment for end-stage liver disease (ESLD) and acute liver failure (ALF). Liver regenerative medicine may in the future offer an alternative form of therapy for these diseases, be it through cell transplantation, bioartificial liver (BAL) devices, or bioengineered whole organ liver transplantation. All three strategies have shown promising results in the past decade. However, before they are incorporated into widespread clinical practice, the ideal cell type for each treatment modality must be found, and an adequate amount of metabolically active, functional cells must be able to be produced. Research is ongoing in hepatocyte expansion techniques, use of xenogeneic cells, and differentiation of stem cell-derived hepatocyte-like cells (HLCs). HLCs are a few steps away from clinical application, but may be very useful in individualized drug development and toxicity testing, as well as disease modeling. Finally, safety concerns including tumorigenicity and xenozoonosis must also be addressed before cell transplantation, BAL devices, and bioengineered livers occupy their clinical niche. This review aims to highlight the most recent advances and provide an updated view of the current state ofaffairs in the field of liver regenerative medicine.
机译:供体器官短缺是肝移植作为终末期肝病(ESLD)和急性肝衰竭(ALF)的治疗方法的主要局限性。肝脏再生医学将来可能会通过细胞移植,生物人工肝(BAL)装置或生物工程化的全器官肝移植为这些疾病提供另一种治疗方式。在过去的十年中,这三种策略均显示出可喜的成果。但是,在将它们纳入广泛的临床实践之前,必须找到每种治疗方式的理想细胞类型,并且必须能够产生足够数量的代谢活性功能细胞。肝细胞扩增技术,异种细胞的使用以及干细胞衍生的肝细胞样细胞(HLC)的分化研究正在进行中。 HLC距临床应用仅几步之遥,但在个性化药物开发和毒性测试以及疾病建模中可能非常有用。最后,在细胞移植,BAL装置和生物工程肝脏占据其临床地位之前,还必须解决包括致瘤性和xenozoonosis等安全问题。这篇综述旨在突出最新进展,并提供有关当前状态的更新视图。肝脏再生医学领域的事务。

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