TY - JOUR
T1 - Pig-to-non-human primate heart transplantation
T2 - The final step toward clinical xenotransplantation?
AU - Reichart, Bruno
AU - Längin, Matthias
AU - Radan, Julia
AU - Mokelke, Maren
AU - Buttgereit, Ines
AU - Ying, Jiawei
AU - Fresch, Ann Kathrin
AU - Mayr, Tanja
AU - Issl, Lara
AU - Buchholz, Stefan
AU - Michel, Sebastian
AU - Ellgass, Reinhard
AU - Mihalj, Maks
AU - Egerer, Stefanie
AU - Baehr, Andrea
AU - Kessler, Barbara
AU - Kemter, Elisabeth
AU - Kurome, Mayuko
AU - Zakhartchenko, Valeri
AU - Steen, Stig
AU - Sjöberg, Trygve
AU - Paskevicius, Audrius
AU - Krüger, Luise
AU - Fiebig, Uwe
AU - Denner, Joachim
AU - Godehardt, Antonia W.
AU - Tönjes, Ralf R.
AU - Milusev, Anastasia
AU - Rieben, Robert
AU - Sfriso, Riccardo
AU - Walz, Christoph
AU - Kirchner, Thomas
AU - Ayares, David
AU - Lampe, Karen
AU - Schönmann, Uwe
AU - Hagl, Christian
AU - Wolf, Eckhard
AU - Klymiuk, Nikolai
AU - Abicht, Jan Michael
AU - Brenner, Paolo
N1 - Publisher Copyright:
© 2020
PY - 2020/8
Y1 - 2020/8
N2 - Background: The demand for donated human hearts far exceeds the number available. Xenotransplantation of genetically modified porcine organs provides an alternative. In 2000, an Advisory Board of the International Society for Heart and Lung Transplantation set the benchmark for commencing clinical cardiac xenotransplantation as consistent 60% survival of non-human primates after life-supporting porcine heart transplantations. Recently, we reported the stepwise optimization of pig-to-baboon orthotopic cardiac xenotransplantation finally resulting in consistent success, with 4 recipients surviving 90 (n = 2), 182, and 195 days. Here, we report on 4 additional recipients, supporting the efficacy of our procedure. Results: The first 2 additional recipients succumbed to porcine cytomegalovirus (PCMV) infections on Days 15 and 27, respectively. In 2 further experiments, PCMV infections were successfully avoided, and 3-months survival was achieved. Throughout all the long-term experiments, heart, liver, and renal functions remained within normal ranges. Post-mortem cardiac diameters were slightly increased when compared with that at the time of transplantation but with no detrimental effect. There were no signs of thrombotic microangiopathy. The current regimen enabled the prolonged survival and function of orthotopic cardiac xenografts in altogether 6 of 8 baboons, of which 4 were now added. These results exceed the threshold set by the Advisory Board of the International Society for Heart and Lung Transplantation. Conclusions: The results of our current and previous experimental cardiac xenotransplantations together fulfill for the first time the pre-clinical efficacy suggestions. PCMV-positive donor animals must be avoided.
AB - Background: The demand for donated human hearts far exceeds the number available. Xenotransplantation of genetically modified porcine organs provides an alternative. In 2000, an Advisory Board of the International Society for Heart and Lung Transplantation set the benchmark for commencing clinical cardiac xenotransplantation as consistent 60% survival of non-human primates after life-supporting porcine heart transplantations. Recently, we reported the stepwise optimization of pig-to-baboon orthotopic cardiac xenotransplantation finally resulting in consistent success, with 4 recipients surviving 90 (n = 2), 182, and 195 days. Here, we report on 4 additional recipients, supporting the efficacy of our procedure. Results: The first 2 additional recipients succumbed to porcine cytomegalovirus (PCMV) infections on Days 15 and 27, respectively. In 2 further experiments, PCMV infections were successfully avoided, and 3-months survival was achieved. Throughout all the long-term experiments, heart, liver, and renal functions remained within normal ranges. Post-mortem cardiac diameters were slightly increased when compared with that at the time of transplantation but with no detrimental effect. There were no signs of thrombotic microangiopathy. The current regimen enabled the prolonged survival and function of orthotopic cardiac xenografts in altogether 6 of 8 baboons, of which 4 were now added. These results exceed the threshold set by the Advisory Board of the International Society for Heart and Lung Transplantation. Conclusions: The results of our current and previous experimental cardiac xenotransplantations together fulfill for the first time the pre-clinical efficacy suggestions. PCMV-positive donor animals must be avoided.
KW - costimulation blockade
KW - graft growth
KW - heart preservation
KW - orthotopic heart transplantation
KW - xenotransplantation
UR - http://www.scopus.com/inward/record.url?scp=85086102864&partnerID=8YFLogxK
U2 - 10.1016/j.healun.2020.05.004
DO - 10.1016/j.healun.2020.05.004
M3 - Article
C2 - 32527674
AN - SCOPUS:85086102864
SN - 1053-2498
VL - 39
SP - 751
EP - 757
JO - Journal of Heart and Lung Transplantation
JF - Journal of Heart and Lung Transplantation
IS - 8
ER -