Clinical Pig Kidney Xenotransplantation: How Close Are We?

被引:48
作者
Cooper, David K. C. [1 ]
Hara, Hidetaka [1 ]
Iwase, Hayato [1 ]
Yamamoto, Takayuki [1 ]
Jagdale, Abhijit [1 ]
Kumar, Vineeta [2 ]
Mannon, Roslyn Bernstein [2 ]
Hanaway, Michael J. [1 ]
Anderson, Douglas J. [1 ]
Eckhoff, Devin E. [1 ]
机构
[1] Univ Alabama Birmingham, Div Transplantat, Dept Surg, ZRB 701,1720 2nd Ave South, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Med, Div Nephrol, Birmingham, AL 35294 USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2020年 / 31卷 / 01期
基金
美国国家卫生研究院;
关键词
DECAY-ACCELERATING FACTOR; TRANSGENIC PIGS; XENOGRAFT SURVIVAL; HEART-TRANSPLANTATION; NULL PIGS; CLASS-II; EXPRESSION; CELLS; BABOONS; ANTIBODIES;
D O I
10.1681/ASN.2019070651
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Patients with ESKD who would benefit from a kidney transplant face a critical and continuing shortage of kidneys from deceased human donors. As a result, such patients wait a median of 3.9 years to receive a donor kidney, by which time approximately 35% of transplant candidates have died while waiting or have been removed from the waiting list. Those of blood group B or 0 may experience a significantly longer waiting period. This problem could be resolved if kidneys from genetically engineered pigs offered an alternative with an acceptable clinical outcome. Attempts to accomplish this have followed two major paths: deletion of pig xenoantigens, as well as insertion of "protective" human transgenes to counter the human immune response. Pigs with up to nine genetic manipulations are now available. In nonhuman primates, administering novel agents that block the CD40/CD154 costimulation pathway, such as an anti-CD40 mAb, suppresses the adaptive immune response, leading to pig kidney graft survival of many months without features of rejection (experiments were terminated for infectious complications). In the absence of innate and adaptive immune responses, the transplanted pig kidneys have generally displayed excellent function. A clinical trial is anticipated within 2 years. We suggest that it would be ethical to offer a pig kidney transplant to selected patients who have a life expectancy shorter than the time it would take for them to obtain a kidney from a deceased human donor. In the future, the pigs will also be genetically engineered to control the adaptive immune response, thus enabling exogenous immunosuppressive therapy to be significantly reduced or eliminated.
引用
收藏
页码:12 / 21
页数:10
相关论文
共 74 条
[1]   Xenoantigen Deletion and Chemical Immunosuppression Can Prolong Renal Xenograft Survival [J].
Adams, Andrew B. ;
Kim, Steven C. ;
Martens, Gregory R. ;
Ladowski, Joseph M. ;
Estrada, Jose L. ;
Reyes, Luz M. ;
Breeden, Cindy ;
Stephenson, Allison ;
Eckhoff, Devin E. ;
Tector, Matt ;
Tector, Alfred Joseph .
ANNALS OF SURGERY, 2018, 268 (04) :564-573
[2]  
[Anonymous], 2017, ANN DAT REP
[3]  
[Anonymous], 2017, Annual data report
[4]   Early graft failure of GalTKO pig organs in baboons is reduced by expression of a human complement pathway-regulatory protein [J].
Azimzadeh, Agnes M. ;
Kelishadi, Sean S. ;
Ezzelarab, Mohamed B. ;
Singh, Avneesh K. ;
Stoddard, Tiffany ;
Iwase, Hayato ;
Zhang, Tianshu ;
Burdorf, Lars ;
Sievert, Evelyn ;
Avon, Chris ;
Cheng, Xiangfei ;
Ayares, David ;
Horvath, Keith A. ;
Corcoran, Philip C. ;
Mohiuddin, Muhammad M. ;
Barth, Rolf N. ;
Cooper, David K. C. ;
Pierson, Richard N., III .
XENOTRANSPLANTATION, 2015, 22 (04) :310-316
[5]   Who can tolerate a marginal kidney? Predicting survival after deceased donor kidney transplant by donor-recipient combination [J].
Bae, Sunjae ;
Massie, Allan B. ;
Thomas, Alvin G. ;
Bahn, Gahyun ;
Luo, Xun ;
Jackson, Kyle R. ;
Ottmann, Shane E. ;
Brennan, Daniel C. ;
Desai, Niraj M. ;
Coresh, Josef ;
Segev, Dorry L. ;
Wang, Jacqueline M. Garonzik .
AMERICAN JOURNAL OF TRANSPLANTATION, 2019, 19 (02) :425-433
[6]   Ureteral stenosis in HDAF pig-to-primate renal xenotransplantation: A phenomenon related to immunological events? [J].
Baldan, N ;
Rigotti, P ;
Calabrese, F ;
Cadrobbi, R ;
Dedja, A ;
Lacopetti, I ;
Boldrin, M ;
Seveso, M ;
Dall'Olmo, L ;
Frison, L ;
De Benedictis, G ;
Bernardini, D ;
Thiene, G ;
Cozzi, E ;
Anconalb, E .
AMERICAN JOURNAL OF TRANSPLANTATION, 2004, 4 (04) :475-481
[7]   Simultaneous expression by porcine aorta endothelial cells of glycosphingolipids bearing the major epitope for human xenoreactive antibodies (Gal alpha 1-3Gal), blood group H determinant and N-glycolylneuraminic acid [J].
Bouhours, D ;
Pourcel, C ;
Bouhours, JF .
GLYCOCONJUGATE JOURNAL, 1996, 13 (06) :947-953
[8]   Pigs expressing the human inhibitory ligand PD-L1 (CD 274) provide a new source of xenogeneic cells and tissues with low immunogenic properties [J].
Buermann, Anna ;
Petkov, Stoyan ;
Petersen, Bjoern ;
Hein, Rabea ;
Lucas-Hahn, Andrea ;
Baars, Wiebke ;
Brinkmann, Antje ;
Niemann, Heiner ;
Schwinzer, Reinhard .
XENOTRANSPLANTATION, 2018, 25 (05)
[9]  
Bühler L, 2000, TRANSPLANTATION, V69, P2296
[10]   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