Pre-transplant antibody screening and anti-CD154 costimulation blockade promote long-term xenograft survival in a pig-to-primate kidney transplant model

被引:197
作者
Higginbotham, Laura [1 ]
Mathews, Dave [1 ]
Breeden, Cynthia A. [1 ]
Song, Mingqing [1 ]
Farris, Alton Brad, III [2 ]
Larsen, Christian P. [1 ]
Ford, Mandy L. [1 ]
Lutz, Andrew J. [3 ]
Tector, Matthew [4 ]
Newell, Kenneth A. [1 ]
Tector, A. Joseph [3 ]
Adams, Andrew B. [1 ]
机构
[1] Emory Univ, Sch Med, Emory Transplant Ctr, Dept Surg, Atlanta, GA 30322 USA
[2] Emory Univ, Sch Med, Anat Pathol, Atlanta, GA 30322 USA
[3] Indiana Univ Sch Med, Indiana Univ, Hlth Transplant Inst, Dept Surg, Indianapolis, IN 46202 USA
[4] Indiana Univ, Hlth Transplant Dept, Indianapolis, IN 46204 USA
关键词
alpha-1,3-galactosyltransferase; costimulation blockade; human decay-accelerating factor; non-human primate; renal transplantation; transgenic pigs; xenoantigen; xenotransplantation; NONHUMAN-PRIMATES; CARDIAC XENOTRANSPLANTATION; ALLOGRAFT SURVIVAL; CYNOMOLGUS MONKEYS; ENDOTHELIAL-CELLS; RENAL-ALLOGRAFT; GRAFT-SURVIVAL; KNOCKOUT PIGS; BABOONS; BELATACEPT;
D O I
10.1111/xen.12166
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Xenotransplantation has the potential to alleviate the organ shortage that prevents many patients with end-stage renal disease from enjoying the benefits of kidney transplantation. Despite significant advances in other models, pig-to-primate kidney xenotransplantation has met limited success. Preformed anti-pig antibodies are an important component of the xenogeneic immune response. To address this, we screened a cohort of 34 rhesus macaques for anti-pig antibody levels. We then selected animals with both low and high titers of anti-pig antibodies to proceed with kidney transplant from galactose-1,3-galactose knockout/CD55 transgenic pig donors. All animals received T-cell depletion followed by maintenance therapy with costimulation blockade (either anti-CD154 mAb or belatacept), mycophenolate mofetil, and steroid. The animal with the high titer of anti-pig antibody rejected the kidney xenograft within the first week. Low-titer animals treated with anti-CD154 antibody, but not belatacept exhibited prolonged kidney xenograft survival (>133 and >126 vs. 14 and 21days, respectively). Long-term surviving animals treated with the anti-CD154-based regimen continue to have normal kidney function and preserved renal architecture without evidence of rejection on biopsies sampled at day 100. This description of the longest reported survival of pig-to-non-human primate kidney xenotransplantation, now >125days, provides promise for further study and potential clinical translation.
引用
收藏
页码:221 / 230
页数:10
相关论文
共 41 条
[1]   Development of a chimeric anti-CD40 monoclonal antibody that synergizes with LEA29Y to prolong islet allograft survival [J].
Adams, AB ;
Shirasugi, N ;
Jones, TR ;
Durham, MM ;
Strobert, EA ;
Cowan, S ;
Rees, P ;
Hendrix, R ;
Price, K ;
Kenyon, NS ;
Hagerty, D ;
Townsend, R ;
Hollenbaugh, D ;
Pearson, TC ;
Larsen, CP .
JOURNAL OF IMMUNOLOGY, 2005, 174 (01) :542-550
[2]   Calcineurin inhibitor-free CD28 blockade-based protocol protects allogeneic islets in nonhuman primates [J].
Adams, AB ;
Shirasugi, N ;
Durham, MM ;
Strobert, E ;
Anderson, D ;
Rees, P ;
Cowan, S ;
Xu, HY ;
Blinder, Y ;
Cheung, M ;
Hollenbaugh, D ;
Kenyon, NS ;
Pearson, TC ;
Larsen, CP .
DIABETES, 2002, 51 (02) :265-270
[3]   Reactivity of human natural antibodies to endothelial cells from Galα(1,3) gal-deficient pigs [J].
Baumann, Bettina C. ;
Stussi, Georg ;
Huggel, Aatja ;
Rieben, Robert ;
Seebach, Joerg D. .
TRANSPLANTATION, 2007, 83 (02) :193-201
[4]  
Bühler L, 2000, TRANSPLANTATION, V70, P1323
[5]   Reduced Binding of Human Antibodies to Cells From GGTA1/CMAH KO Pigs [J].
Burlak, C. ;
Paris, L. L. ;
Lutz, A. J. ;
Sidner, R. A. ;
Estrada, J. ;
Li, P. ;
Tector, M. ;
Tector, A. J. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2014, 14 (08) :1895-1900
[6]   Identification of human preformed antibody targets in GTKO pigs [J].
Burlak, Christopher ;
Wang, Zheng-Yu ;
Chihara, Ray K. ;
Lutz, Andrew J. ;
Wang, Yueren ;
Estrada, Jose L. ;
Tector, A. Joseph .
XENOTRANSPLANTATION, 2012, 19 (02) :92-101
[7]   Proteomic identification of non-Gal antibody targets after pig-to-primate cardiac xenotransplantation [J].
Byrne, Guerard W. ;
Stalboerger, Paul G. ;
Davila, Eduardo ;
Heppelmann, Carrie J. ;
Gazi, Mozammel H. ;
McGregor, Hugh C. J. ;
LaBreche, Peter T. ;
Davies, William R. ;
Rao, Vinay P. ;
Oi, Keiji ;
Tazelaar, Henry D. ;
Logan, John S. ;
McGregor, Christopher G. A. .
XENOTRANSPLANTATION, 2008, 15 (04) :268-276
[8]   Cloning and expression of porcine β1,4 N-acetylgalactosaminyl transferase encoding a new xenoreactive antigen [J].
Byrne, Guerard W. ;
Du, Zeji ;
Stalboerger, Paul ;
Kogelberg, Heide ;
McGregor, Christopher G. A. .
XENOTRANSPLANTATION, 2014, 21 (06) :543-554
[9]   Identification of New Carbohydrate and Membrane Protein Antigens in Cardiac Xenotransplantation [J].
Byrne, Guerard W. ;
Stalboerger, Paul G. ;
Du, Zeji ;
Davis, Tessa R. ;
McGregor, Christopher G. A. .
TRANSPLANTATION, 2011, 91 (03) :287-292
[10]   Long-term survival of neonatal porcine islets in nonhuman primates by targeting costimulation pathways [J].
Cardona, K ;
Korbutt, GS ;
Milas, Z ;
Lyon, J ;
Cano, J ;
Jiang, W ;
Bello-Laborn, H ;
Hacquoil, B ;
Strobert, E ;
Gangappa, S ;
Weber, CJ ;
Pearson, TC ;
Rajotte, RV ;
Larsen, CP .
NATURE MEDICINE, 2006, 12 (03) :304-306