Chimeric 2C10R4 anti-CD40 antibody therapy is critical for long-term survival of GTKO.hCD46.hTBM pig-to-primate cardiac xenograft

被引:376
作者
Mohiuddin, Muhammad M. [1 ]
Singh, Avneesh K. [1 ]
Corcoran, Philip C. [1 ]
Thomas, Marvin L., III [2 ]
Clark, Tannia [3 ]
Lewis, Billeta G. [2 ]
Hoyt, Robert F. [4 ]
Eckhaus, Michael [2 ]
Pierson, Richard N., III [5 ]
Belli, Aaron J. [6 ]
Wolf, Eckhard [7 ]
Klymiuk, Nikolai [7 ]
Phelps, Carol [8 ]
Reimann, Keith A. [6 ]
Ayares, David [8 ]
Horvath, Keith A. [1 ]
机构
[1] NHLBI, Cardiothorac Surg Res Program, NIH, Bldg 10, Bethesda, MD 20892 USA
[2] NIH, Div Vet Resources, ORS, Bldg 10, Bethesda, MD 20892 USA
[3] NICHD, NIH, Bethesda, MD 20892 USA
[4] Leidos Biomed Res Inc, Bethesda, MD 20892 USA
[5] Univ Maryland, Med Ctr, Baltimore, MD 20201 USA
[6] Univ Massachusetts, Sch Med, MassBiol, Boston, MA 02126 USA
[7] Univ Munich, D-81377 Munich, Germany
[8] Revivicor Inc, Blacksburg, VA 24060 USA
关键词
GENE-KNOCKOUT PIGS; COSTIMULATION BLOCKADE; HEART-TRANSPLANTATION; HUMAN THROMBOMODULIN; TRANSGENIC PIGS; XENOTRANSPLANTATION; REJECTION; BABOONS; PROGRESS; EXTENDS;
D O I
10.1038/ncomms11138
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Preventing xenograft rejection is one of the greatest challenges of transplantation medicine. Here, we describe a reproducible, long-term survival of cardiac xenografts from alpha 1-3 galactosyltransferase gene knockout pigs, which express human complement regulatory protein CD46 and human thrombomodulin (GTKO.hCD46.hTBM), that were transplanted into baboons. Our immunomodulatory drug regimen includes induction with anti-thymocyte globulin and alpha CD20 antibody, followed by maintenance with mycophenolate mofetil and an intensively dosed alpha CD40 (2C10R4) antibody. Median (298 days) and longest (945 days) graft survival in five consecutive recipients using this regimen is significantly prolonged over our recently established survival benchmarks (180 and 500 days, respectively). Remarkably, the reduction of aCD40 antibody dose on day 100 or after 1 year resulted in recrudescence of anti-pig antibody and graft failure. In conclusion, genetic modifications (GTKO.hCD46.hTBM) combined with the treatment regimen tested here consistently prevent humoral rejection and systemic coagulation pathway dysregulation, sustaining long-term cardiac xenograft survival beyond 900 days.
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页数:10
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