Hepatocyte transplantation for inborn errors of metabolism

被引:22
作者
Burlina, AB [1 ]
机构
[1] Univ Padua, Childrens Hosp, Dept Pediat, Metab Unit, I-35128 Padua, Italy
关键词
D O I
10.1023/B:BOLI.0000031095.57411.8d
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Liver transplantation for inborn errors of metabolism has proved effective in some (mostly liver-associated) inborn errors of metabolism. Significant morbidity and mortality rates have been extensively reported due to disease recurrence or to complications of the immunosuppressive regimen. On the basis of clinical trials in animals as well as in humans, the use of isolated hepatocytes offers a unique opportunity for treating inborn errors of metabolism. The state of art of the technique applied to this field is reviewed here and related practical problems are examined. No final conclusions can be drawn, but further insight into the use of alternative sources of cells, including stem/progenitor cells associated with cryobiology and immunological research, will offer new opportunities for cell therapy for inborn errors of metabolism in the near future.
引用
收藏
页码:373 / 383
页数:11
相关论文
共 49 条
[31]   Repopulation of rat liver by fetal hepatoblasts and adult hepatocytes transduced ex vivo with lentiviral vectors [J].
Oertel, M ;
Rosencrantz, R ;
Chen, YQ ;
Thota, PN ;
Sandhu, JS ;
Dabeva, MD ;
Pacchia, AL ;
Adelson, ME ;
Dougherty, JP ;
Shafritz, DA .
HEPATOLOGY, 2003, 37 (05) :994-1005
[32]   Hepatocyte transplantation: clinical and experimental application [J].
Ohashi, K ;
Park, F ;
Kay, MA .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2001, 79 (11) :617-630
[33]   Ex vivo hepatic gene therapy of a mouse model of Hereditary Tyrosinemia Type I [J].
Overturf, K ;
Al-Dhalimy, M ;
Manning, K ;
Ou, CN ;
Finegold, M ;
Grompe, M .
HUMAN GENE THERAPY, 1998, 9 (03) :295-304
[34]   Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type I [J].
Overturf, K ;
AlDhalimy, M ;
Tanguay, R ;
Brantly, M ;
Ou, CN ;
Finegold, M ;
Grompe, M .
NATURE GENETICS, 1996, 12 (03) :266-273
[35]  
QIAN JH, 1985, J IMMUNOL, V134, P3656
[36]   Safety and feasibility of liver-directed ex vivo gene therapy for homozygous familial hypercholesterolemia [J].
Raper, SE ;
Grossman, M ;
Rader, DJ ;
Thoene, JG ;
Clark, BJ ;
Kolansky, DM ;
Muller, DWM ;
Wilson, JM .
ANNALS OF SURGERY, 1996, 223 (02) :116-126
[37]   Medical progress: Prometheus's vulture and the stem-cell promise. [J].
Rosenthal, N .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (03) :267-274
[38]   Pediatric liver transplantation in metabolic disease: Clinical decision making [J].
Shneider, BL .
PEDIATRIC TRANSPLANTATION, 2002, 6 (01) :25-29
[39]   Hepatocyte transplantation in a 4-year-old girl with peroxisomal biogenesis disease: Technique, safety, and metabolic follow-up [J].
Sokal, EM ;
Smets, F ;
Bourgois, A ;
Van Maldergem, L ;
Buts, JP ;
Reding, R ;
Otte, JB ;
Evrard, V ;
Latinne, D ;
Vincent, MF ;
Moser, A ;
Soriano, HE .
TRANSPLANTATION, 2003, 76 (04) :735-738
[40]   Hepatocyte transplantation: New possibilities for therapy [J].
Strom, S ;
Fisher, R .
GASTROENTEROLOGY, 2003, 124 (02) :568-571