Overcoming the barriers to xenotransplantation: prospects for the future

被引:74
作者
Ekser, Burcin [1 ,2 ]
Cooper, David K. C. [1 ]
机构
[1] Univ Pittsburgh, Med Ctr, Thomas E Starzl Transplantat Inst, Pittsburgh, PA 15261 USA
[2] Univ Padua, Dept Surg & Organ Transplantat, Padua, Italy
关键词
antibodies; antipig; coagulation; consumptive coagulopathy; genetically engineered; nonhuman primate; pig; xenotransplantation; PORCINE ENDOTHELIAL-CELLS; DECAY-ACCELERATING FACTOR; PRIMATE RENAL XENOTRANSPLANTATION; N-GLYCOLYLNEURAMINIC ACID; GENE-KNOCKOUT PIGS; DISSEMINATED INTRAVASCULAR COAGULATION; XENOGRAFT HYPERACUTE REJECTION; TO-HUMAN XENOTRANSPLANTATION; ACUTE VASCULAR REJECTION; LIFE-SUPPORTING FUNCTION;
D O I
10.1586/ECI.09.81
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cross-species transplantation (xenotransplantation) has immense potential to solve the critical need for organs, tissues and cells for clinical transplantation. The increasing availability of genetically engineered pigs is enabling progress to be made in pig-to-nonhuman primate experimental models. Potent pharmacologic immunosuppressive regimens have largely prevented T-cell rejection and a T-cell-dependent elicited antibody response. However, coagulation dysfunction between the pig and primate is proving to be a major problem, and this can result in life-threatening consumptive coagulopathy. This complication is unlikely to be overcome until pigs expressing a human 'antithrombotic' or 'anticoagulant' gene, such as thrombomodulin, tissue factor pathway inhibitor or CD39, become available. Progress in islet xenotransplantation has been more encouraging, and diabetes has been controlled in nonhuman primates for periods in excess of 6 months, although this has usually been achieved using immunosuppressive protocols that might not be clinically applicable. Further advances are required to overcome the remaining barriers.
引用
收藏
页码:219 / 230
页数:12
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