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Utility of adenovirus-mediated Fas ligand and bcl-2 gene transfer to modulate rat liver allograft survival |
De-Sheng Wang, Yu Li, Ke-Feng Dou, Kai-Zong Li and Zhen-Shun Song |
Xi'an, China
Author Affiliations: Department of Hepatobiliary Surgery, Xijing Hospital (Wang DS, Dou KF, Li KZ and Song ZS), and Research Centre of Cell Engineering (Li Y), Fourth Military Medical University, Xi'an 710032, China
Corresponding Author: De-Sheng Wang, PhD, Department of Hepatobiliary Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China (Tel: 86-29-84775259; Fax: 86-29-84773564; Email: wangdesh@163.com) |
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Abstract BACKGROUND: Expression of Fas ligand (FasL) on the graft by gene transduction is expected to introduce apoptosis to lymphocytes to protect rejection, but the FasL-expressing graft cells may also induce apoptosis as the graft usually expresses Fas antigens. In this study, a strong antiapoptotic gene, bcl-2, was cotransfected with the FasL gene in rat liver graft to protect against Fas-mediated cell death and to prolong recipient survival.
METHODS: Orthotopic liver transplantation was done in a strain combination of DA to LEW rats. After donor vascular isolation, adenovirus-mediated FasL and bcl-2 genes were cotransfected in the liver graft.
RESULTS: Intragraft expression of FasL mRNA was constitutively expressed after adenovirus-mediated transduction, although expression of FasL increased mildly in control grafts. Bcl-2 mRNA was highly expressed at 2 days after reperfusion. In contrast, lower expression of bcl-2 was observed in the control group. The average survival of the gene transferred allografts increased from (9.8+1.3) days to (18.5+8.7) days compared with the control group.
CONCLUSION: Our results indicate that rat liver allografts can be protected against host immune responses by adenovirus-mediated FasL and bcl-2 transfection, and that bcl-2 expression prevents the graft from Fas-mediated apoptosis.
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