Alginate microencapsulated human hepatocytes for the treatment of acute liver failure in children

被引:84
作者
Dhawan, Anil [1 ,3 ]
Chaijitraruch, Nataruks [1 ,2 ]
Fitzpatrick, Emer [1 ]
Bansal, Sanjay [1 ]
Filippi, Celine [3 ]
Lehec, Sharon C. [3 ]
Heaton, Nigel D. [4 ]
Kane, Pauline [5 ]
Verma, Anita [6 ]
Hughes, Robin D. [3 ]
Mitry, Ragai R. [3 ]
机构
[1] Kings Coll Hosp London, Paediat Liver GI & Nutr Ctr, London SE5 9RS, England
[2] Chulalongkorn Univ, Dept Paediat, Paediat Gastroenterol & Hepatol, Fac Med, Bangkok, Thailand
[3] Kings Coll London, Dhawan Lab, Mowat Labs, Inst Liver Studies,Kings Coll Hosp, London, England
[4] Kings Coll Hosp London, Inst Liver Studies, Liver Transplant Surg, London, England
[5] Kings Coll Hosp London, Dept Radiol, London, England
[6] Kings Coll Hosp London, Dept Infect Sci & Microbiol, London, England
关键词
Alginate; Hepatocyte microbeads; Microencapsulated human hepatocytes; Acute liver failure; Cell transplantation; Intraperitoneal transplantation; Cryopreservation; IMPROVED SURVIVAL; TRANSPLANTATION; CRYOPRESERVATION; ENCAPSULATION; OUTCOMES; DISEASE;
D O I
10.1016/j.jhep.2019.12.002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background & Aims: Liver transplantation (LT) is the most effective treatment for patients with acute liver failure (ALF), but is limited by surgical risks and the need for life-long immunosuppression. Transplantation of microencapsulated human hepatocytes in alginate is an attractive option over whole liver replacement. The safety and efficacy of hepatocyte microbead transplantation have been shown in animal models. We report our experience of this therapy in children with ALF treated on a named-patient basis. Methods: Clinical grade human hepatocyte microbeads (HMBs) and empty microbeads were tested in immunocompetent healthy rats. Subsequently, 8 children with ALF, who were awaiting a suitable allograft for LT, received intraperitoneal transplantation of HMBs. We monitored complications of the procedure, assessing the host immune response and residual function of the retrieved HMBs, either after spontaneous native liver regeneration or at the time of LT. Results: Intraperitoneal transplantation of HMBs in healthy rats was safe and preserved synthetic and detoxification functions, without the need for immunosuppression. Subsequently, 8 children with ALF received HMBs (4 neonatal haemochromatosis, 2 viral infections and 2 children with unknown cause at time of infusion) at a median age of 14.5 days, range 1 day to 6 years. The procedure was well tolerated without complications. Of the 8 children, 4 avoided LT while 3 were successfully bridged to LT following the intervention. HMBs retrieved after infusions (at the time of LT) were structurally intact, free of host cell adherence and contained viable hepatocytes with preserved functions. Conclusion: The results demonstrate the feasibility and safety of an HMB infusion in children with ALF. Lay summary: Acute liver failure in children is a rare but devastating condition. Liver transplantation is the most effective treatment, but it has several important limitations. Liver cell (hepatocyte) transplantation is an attractive option, as many patients only require short-term liver support while their own liver recovers. Human hepatocytes encapsulated in alginate beads can perform the functions of the liver while alginate coating protects the cells from immune attack. Herein, we demonstrated that transplantation of these beads was safe and feasible in children with acute liver failure. (c) 2019 Published by Elsevier B.V. on behalf of European Association for the Study of the Liver.
引用
收藏
页码:877 / 884
页数:8
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