Xenotransplantation: immunological hurdles and progress toward tolerance

被引:123
作者
Griesemer, Adam [1 ]
Yamada, Kazuhiko [2 ]
Sykes, Megan [1 ]
机构
[1] Columbia Univ Coll Phys & Surg, Columbia Ctr Translat Immunol, New York, NY 10032 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Transplantat Biol Res Ctr, Boston, MA USA
关键词
xenotransplantation; tolerance; thymus transplant; mixed chimerism; genetically modified swine; NK cells; NATURAL-KILLER-CELLS; PORCINE ENDOGENOUS RETROVIRUS; THYMIC LOBE TRANSPLANTATION; ISLET XENOGRAFT REJECTION; N-GLYCOLYLNEURAMINIC ACID; GENE-KNOCKOUT PIGS; HUMAN T-CELLS; MHC CLASS-I; BONE-MARROW-TRANSPLANTATION; NON-MYELOABLATIVE REGIMEN;
D O I
10.1111/imr.12152
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The discrepancy between organ need and organ availability represents one of the major limitations in the field of transplantation. One possible solution to this problem is xenotransplantation. Research in this field has identified several obstacles that have so far prevented the successful development of clinical xenotransplantation protocols. The main immunologic barriers include strong T-cell and B-cell responses to solid organ and cellular xenografts. In addition, components of the innate immune system can mediate xenograft rejection. Here, we review these immunologic and physiologic barriers and describe some of the strategies that we and others have developed to overcome them. We also describe the development of two strategies to induce tolerance across the xenogeneic barrier, namely thymus transplantation and mixed chimerism, from their inception in rodent models through their current progress in preclinical large animal models. We believe that the addition of further beneficial transgenes to Gal knockout swine, combined with new therapies such as Treg administration, will allow for successful clinical application of xenotransplantation.
引用
收藏
页码:241 / 258
页数:18
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