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Pig-to-human heart xenotransplantation in two recently deceased human recipients.

Nader MoazamiJeffrey M SternKaren KhalilJacqueline I KimNavneet NarulaMassimo MangiolaElaina P WeldonLarisa KagermazovaLes JamesNikki LawsonGreta L PiperPhilip M SommerAlex ReyentovichDaniel BamiraTajinderpal SaraonBernard S KadoshMichael DivitaRandal I GoldbergSyed T HussainJustin ChanJennie NgaiThomas JanNicole M AliVasishta S TatapudiDorry L SegevShivani BisenIan S JaffeBenjamin PiegariHaley KowalskiMaria KokkinakiJeffrey MonahanLori SorrellsLars BurdorfJef D BoekeHarvey PassChandra GoparajuBrendan KeatingDavid AyaresMarc LorberAdam D GriesemerSapna A MehtaDeane E SmithRobert A Montgomery
Published in: Nature medicine (2023)
Genetically modified xenografts are one of the most promising solutions to the discrepancy between the numbers of available human organs for transplantation and potential recipients. To date, a porcine heart has been implanted into only one human recipient. Here, using 10-gene-edited pigs, we transplanted porcine hearts into two brain-dead human recipients and monitored xenograft function, hemodynamics and systemic responses over the course of 66 hours. Although both xenografts demonstrated excellent cardiac function immediately after transplantation and continued to function for the duration of the study, cardiac function declined postoperatively in one case, attributed to a size mismatch between the donor pig and the recipient. For both hearts, we confirmed transgene expression and found no evidence of cellular or antibody-mediated rejection, as assessed using histology, flow cytometry and a cytotoxic crossmatch assay. Moreover, we found no evidence of zoonotic transmission from the donor pigs to the human recipients. While substantial additional work will be needed to advance this technology to human trials, these results indicate that pig-to-human heart xenotransplantation can be performed successfully without hyperacute rejection or zoonosis.
Keyphrases
  • endothelial cells
  • pluripotent stem cells
  • heart failure
  • stem cells
  • atrial fibrillation
  • flow cytometry
  • poor prognosis
  • dna methylation
  • risk assessment
  • high throughput
  • copy number
  • binding protein
  • resting state