Progress towards clinical xenotransplantation

被引:29
作者
Schuurman, Henk-Jan [1 ,2 ]
Pierson, Richard N., III [3 ]
机构
[1] Spring Point Project, Minneapolis, MN 55402 USA
[2] Univ Minnesota, Dept Surg, Diabet Inst Immunol & Transplantat, Minneapolis, MN 55455 USA
[3] Univ Maryland, Div Cardiac Surg, VA Maryland Hlth Care Syst, Surg Clin Care Ctr, Baltimore, MD 21201 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2008年 / 13卷
关键词
antibody-mediated rejection; anticoagulants; anti-gal antibody; anti-pig antibody; baboon; cell/tissue transplantation; cellular rejection; chimerism; chronic rejection; cloning; coagulation; complement; complement inhibitors; complement regulatory protein; costimulatory blockade; cross-species pathogen transmission; cynomolgus monkey; cytomegalovirus; dissiminated intravascular coagulopathy; encapsulation; endothelial cells; endothelial cell activation; ethics; extracorporeal perfusion; extracorporeal liver perfusion; ex vivo perfusion; ex vivo lung perfusion; galactose-alpha(1-3)galactose; galactosyl transferase; GalT knock-out; gene targeting; genetic modification; heart transplantation; hepatocyte transplantation; hyperacute rejection; innate immunity; immunosuppression; immune tolerance; islet transplantation; islet cell encapsulation; kidney transplantation; liver assist device; liver transplantation; lung transplantation; lymphotropic gamma-herpesvirus; macrophage; miniature swine; naturally existing antibody; nonhuman primates; pig; porcine; porcine endogenous retrovirus; pulmonary intravascular macrophages; regulatory guidance; rhesus monkey; sertoli cells; solid organ transplantation; species disparity; swine; thrombosis; transgenesis; xenosis; xeno-transplantation; xeno-tolerance; zoonosis;
D O I
10.2741/2671
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Xenotransplantation has progressed from early heroic experiments on the path to meet the ever increasing demands of tissue and organ transplantation in patients with end-stage organ failure. The pig species is regarded as the most promising donor species. However, due to the evolutionary distance, innovative approaches are to be developed to permit life-supporting function in humans. Transplantation of organs from non-human primates has increased our knowledge on rejection mechanisms and provided opportunitities for testing modified immunosuppression of the host and genetic modification of the donor. The development of transgenic animals expressing human complement-regulatory factors, and of animals lacking the target for naturally occurring anti-pig antibodies, has essentially eradicated hyperacute rejection of solid organs. However, there is still a need for tolerable immunosuppression or immune-tolerance regimens to provide broadly available procedures in the clinical setting. Safety concerns especially cross-species transmission of infectious pathogens, in particular of porcine endogenous retrovirus. Many studies have indicated that this is highly unlikely. At present, cell and tissue transplantation of islets of Langerhans to diabetic patients is close to being tested in well-designed clinical trials. Further research is required before other porcine xenografts can offer a broadly available therapeutic option in clinical medicine.
引用
收藏
页码:204 / 220
页数:17
相关论文
共 158 条
[1]  
ABOUNA GM, 1997, XENOTRANSPLANTATION, P785
[2]  
Allan Jonathan S, 1996, Sci Eng Ethics, V2, P486, DOI 10.1007/BF02583936
[3]  
Allan JS, 2003, CURR TOP MICROBIOL, V278, P101
[4]   Hyperacute lung rejection in the pig-to-human model. 2. Synergy between soluble and membrane complement inhibition [J].
Azimzadeh, A ;
Zorn, GL ;
Blair, KSA ;
Zhang, JP ;
Pfeiffer, S ;
Harrison, RA ;
Cozzi, E ;
White, DJG ;
Pierson, RN .
XENOTRANSPLANTATION, 2003, 10 (02) :120-131
[5]   BABOON-TO-HUMAN CARDIAC XENOTRANSPLANTATION IN A NEONATE [J].
BAILEY, LL ;
NEHLSENCANNARELLA, SL ;
CONCEPCION, W ;
JOLLEY, WB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1985, 254 (23) :3321-3329
[6]  
BARNARD CN, 1977, S AFR MED J, V52, P1035
[7]   Xenogeneic thymokidney and thymic tissue transplantation in a pig-to-baboon model: I. Evidence for pig-specific T-cell unresponsiveness [J].
Barth, RN ;
Yamamoto, S ;
LaMattina, JC ;
Kumagai, N ;
Kitamura, H ;
Vagefi, PA ;
Awwad, M ;
Colvin, RB ;
Cooper, DKC ;
Sykes, M ;
Sachs, DH ;
Yamada, K .
TRANSPLANTATION, 2003, 75 (10) :1615-1624
[8]   Xenotransplantation: regulatory challenges [J].
Bloom, ET .
CURRENT OPINION IN BIOTECHNOLOGY, 2001, 12 (03) :312-316
[9]   Pig endogenous retroviruses and xenotransplantation [J].
Blusch, JH ;
Patience, C ;
Martin, U .
XENOTRANSPLANTATION, 2002, 9 (04) :242-251
[10]  
Bühler L, 2000, TRANSPLANTATION, V70, P1323