Genetic modification of pigs for solid organ xenotransplantation

被引:23
作者
Gock, Hilton
Nottle, Mark
Lew, Andrew M.
d'Apice, Anthony J. F.
Cowan, Peter
机构
[1] St Vincents Hosp, Immunol Res Ctr, Melbourne, Vic 3065, Australia
[2] Univ Melbourne, Dept Med, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
DECAY-ACCELERATING FACTOR; ALPHA-1,3-GALACTOSYLTRANSFERASE KNOCKOUT PIGS; COMPLEMENT-REGULATORY PROTEINS; CELL NUCLEAR TRANSFER; ALPHA 1,3-GALACTOSYLTRANSFERASE KNOCKOUT; PRIMATE RENAL XENOTRANSPLANTATION; MEMBRANE COFACTOR PROTEIN; CD46 TRANSGENIC PIG; EX-VIVO MODEL; HYPERACUTE REJECTION;
D O I
10.1016/j.trre.2010.10.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Xenotransplantation of solid organs will only ever become a clinical reality with genetic modification of the pig, which is now widely accepted as the most likely donor species for humans. The understanding of the barriers to xenotransplantation has required advances in genetic technologies to resolve these problems. Hyperacute rejection has been overcome by overexpression of complement regulatory proteins or targeted disruption of the enzyme associated with the major carbohydrate xenoantigen. The subsequent barriers of disordered coagulation, induced antibody, and cell-mediated rejection remain challenging. The mechanisms for these incompatibilities are being deciphered, and multiple genetic manipulations to resolve these issues are currently in progress. Moreover, new technologies offer help to producing sizeable numbers of modified pigs in a timely manner. This article retraces the basis and foreshadows progress of the genetically modified pig for xenotransplantation as it advances toward the clinic. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:9 / 20
页数:12
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