肝胆相照论坛

标题: 肝细胞移植的临床应用:现状,适用性,局限性和未来展望 [打印本页]

作者: StephenW    时间: 2020-2-28 12:45     标题: 肝细胞移植的临床应用:现状,适用性,局限性和未来展望

Clinical application of hepatocyte transplantation: current status, applicability, limitations and future outlook.
Minh Phuong Nguyen, Vandana Jain, Valeria Iansante, Ragai R. Mitry, Celine Filippi & Anil Dhawan
Received 20 Dec 2019, Accepted 20 Feb 2020, Accepted author version posted online: 26 Feb 2020

    Download citation https://doi.org/10.1080/17474124.2020.1733975 CrossMark Logo CrossMark

Accepted author version
Introduction

Hepatocyte transplantation (HT) is a promising alternative to liver transplantation for treatment of liver-based metabolic diseases and acute liver failure (ALF). However, shortage of good-quality liver tissues, early cell loss post-infusion, reduced cell engraftment and function restricts clinical application.Areas covered: A comprehensive literature search was performed to cover pre-clinical and clinical HT studies. The review discusses the latest developments to address HT limitations: cell sources from marginal/suboptimal donors to neonatal livers, differentiating pluripotent stem cells into hepatocyte-like cells, in vitro expansion, prevention of immune response to transplanted cells by encapsulation or using innate immunity-inhibiting agents, and enhancing engraftment through partial hepatectomy or irradiation.Expert Opinion: To date, published data are highly encouraging specially the alginate-encapsulated hepatocyte treatment of children with ALF. Hepatocyte functions can be further improved through co-culturing with mesenchymal stromal cells. Moreover, ex-vivo genetic correction will enable the use of autologous cells in future personalized medicine.
Keywords: Hepatocyte transplantation, mature hepatocytes, neonatal hepatocytes, mesenchymal stromal cells, encapsulation, engraftment, cryopreservation, alpha-1 antitrypsin, in vitro expansion, partial hepatectomy, irradiation
Disclaimer
As a service to authors and researchers we are providing this version of an accepted manuscript (AM). Copyediting, typesetting, and review of the resulting proofs will be undertaken on this manuscript before final publication of the Version of Record (VoR). During production and pre-press, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal relate to these versions also.

Additional information
Funding
This paper has not been funded.
Article Highlights

    Hepatocyte transplantation is a highly promising alternative to whole liver transplantation with excellent therapeutic benefit for patients suffering from numerous liver diseases

    One of the major limitations of hepatocyte transplantation is up to 70% massive early cell loss after infusion but a recent study suggests that alpha-1 antitrypsin can significantly reduce immune response responsible for that by inhibiting the coagulation and complement pathways

    Neonatal-derived hepatocytes have been shown to be superior to adult mature hepatocytes with higher cell viability and yield on isolation and overall better recovery post-thawing with greater maintained hepatic functions

    Engraftment of transplanted hepatocytes can be improved through selective and highly proliferative stimulus following partial hepatectomy

    Current strategies to advance transplantation of hepatocytes include large-scale production of cells through in vitro expansion, differentiation of pluripotent stem cells into hepatic lineages and cell encapsulation

    Primary hepatocytes can be alginate-embedded and have proved great efficacy in providing treatment to patients with lived-based metabolic disorders, ‘bridge’ to liver transplantation and temporary therapy while native liver can regenerate thus discarding the need for whole organ replacement

    Human hepatocyte microbeads have demonstrated high safety and efficacy in children with acute liver failure

    The source of cells for transplantation is starting to come from patients themselves where successful correction and infusion of autologous cells won’t trigger any immune rejection
作者: StephenW    时间: 2020-2-28 12:45

肝细胞移植的临床应用:现状,适用性,局限性和未来展望。
Minh Phuong Nguyen,Vandana Jain,Valeria Iansante,Ragai R.Mitry,Celine Filippi和Anil Dhawan
2019年12月20日收到,2020年2月20日接受,在线作者版本被接受:2020年2月26日

下载引文https://doi.org/10.1080/17474124.2020.1733975 CrossMark徽标CrossMark

接受的作者版本
介绍

肝细胞移植(HT)是用于治疗基于肝的代谢疾病和急性肝衰竭(ALF)的有希望的替代肝移植方法。但是,缺乏优质的肝组织,输注后早期细胞丢失,细胞植入减少和功能受到限制,临床应用受到限制。研究范围:进行了全面的文献检索以涵盖临床前和临床HT研究。该评论讨论了解决HT局限性的最新进展:从边缘/次优供体到新生儿肝脏的细胞来源,将多能干细胞分化为肝细胞样细胞,体外扩增,通过封装或使用先天性免疫来防止对移植细胞的免疫反应-专家意见:迄今为止,已发表的数据特别鼓励使用藻酸盐包裹的肝细胞治疗ALF儿童。通过与间质基质细胞共培养,可以进一步改善肝细胞功能。此外,离体基因校正将使自体细胞可用于未来的个性化医学中。
关键词:肝细胞移植,成熟肝细胞,新生儿肝细胞,间充质基质细胞,包囊,植入,冷冻保存,α-1抗胰蛋白酶,体外扩增,部分肝切除术,照射
免责声明
为了向作者和研究人员提供服务,我们提供了此版本的接受手稿(AM)。在最终出版记录版本(VoR)之前,将对本手稿进行复制编辑,排版和审阅。在制作和印前过程中,可能会发现可能影响内容的错误,并且适用于该期刊的所有法律免责声明也与这些版本有关。

附加信息
资金
该论文尚未获得资助。
文章重点

肝细胞移植是全肝移植的极有希望的替代方法,对患有多种肝病的患者具有极好的治疗效果

肝细胞移植的主要局限之一是输注后高达70%的大量早期细胞丢失,但最近的一项研究表明,α-1抗胰蛋白酶可以通过抑制凝血和补体途径来显着降低引起该反应的免疫反应

已显示新生儿来源的肝细胞优于成人成熟的肝细胞,具有更高的细胞活力和分离产率,并且融化后总体上具有更好的恢复功能,并具有更好的肝功能

肝部分切除术后可以通过选择性和高度增殖的刺激来改善移植肝细胞的植入

当前促进肝细胞移植的策略包括通过体外扩增大规模生产细胞,将多能干细胞分化为肝谱系和细胞封装

原代肝细胞可以被藻酸盐包埋,并已被证明在为患有基于生命的代谢性疾病,“搭桥”肝移植和临时治疗的患者提供治疗方面具有巨大功效,而天然肝可以再生,从而无需全器官置换

人肝细胞微珠对急性肝功能衰竭儿童具有很高的安全性和有效性

移植细胞的来源开始来自患者本身,成功地校正和输注自体细胞不会触发任何免疫排斥




欢迎光临 肝胆相照论坛 (http://hbvhbv.info/forum/) Powered by Discuz! X1.5