Liver irradiation: A potential preparative regimen for hepatocyte transplantation

被引:27
作者
Guha, C
Parashar, B
Deb, NJ
Sharma, A
Gorla, GR
Alfieri, A
Roy-Chowdhury, N
Roy-Chowdhury, J
Vikram, B
机构
[1] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Radiat Oncol, Bronx, NY 10467 USA
[2] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
[3] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10467 USA
[4] Montefiore Med Ctr, Albert Einstein Coll Med, Marion Bessin Liver Res Ctr, Bronx, NY 10467 USA
[5] Beth Israel Deaconess Med Ctr, Dept Radiat Oncol, New York, NY 10003 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2001年 / 49卷 / 02期
关键词
hepatocyte transplantation; radiation therapy; radiation-induced liver damage; liver malignancies;
D O I
10.1016/S0360-3016(00)01495-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Advances in the understanding of hepatocyte engraftment and repopulation of the host liver have already led to the use of hepatocyte transplantation (HT) with some success in the treatment of inherited and acquired liver diseases. Wider application of HT is severely limited by the unavailability of large number of transplantable hepatocytes and difficulties associated with transplanting an adequate number of cells for achieving therapeutically satisfactory levels of metabolic correction. Therefore, there is a need for preparative regimens that provide a growth advantage to the transplanted (healthy) hepatocytes over the host's own (diseased) hepatocytes so that the former ran repopulate the host liver. We have recently shown that when the liver of recipient rats was subjected to radiotherapy and partial hepatectomy before HT, the transplanted hepatocytes engrafted in and massively repopulated the liver, and also ameliorated the adverse clinical and histopathological changes associated with hepatic irradiation. This protocol was then used as a preparative regimen for transplanting normal hepatocytes into jaundice mutant rats (Gunn strain), which lack hepatic bilirubin-uridinediphosphoglucuronate glucuronosyltransferase and is a model of Crigler-Najjar syndrome Type I. The results showed long-term correction of the metabolic abnormality, suggesting that the transplanted hepatocytes repopulated an irradiated liver and were metabolically functional. This strategy could be useful in the treatment of various genetic, metabolic, or malignant diseases of the liver. (C) 2001 Elsevier Science Inc.
引用
收藏
页码:451 / 457
页数:7
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