Medicine

Raphael P. H. Meier

2026.1.1XENOTRANSPLANTATION

DOI: 10.1111/xen.70107

tlooto Summary

This case highlights both the promise of xenogeneic hepatic support and the physiologic limits that currently preclude durable therapy, including thrombocytopenia, complement–coagulation incompatibility, portal‐flow competition, and challenges in assessing dual‐graft function.

Abstract

Genetically engineered porcine organs are redefining the boundaries of clinical xenotransplantation. Zhang et al. now report the first functional pig-to-human liver xenotransplantation in a living patient, demonstrating that a 10-gene-edited auxiliary porcine liver can engraft, produce bile, and synthesize metabolic and coagulation factors in vivo. The xenograft supported a high-risk hepatectomy with borderline remnant volume and contributed to early postoperative stability, although xenotransplant-associated thrombotic microangiopathy ultimately required graft removal. The case highlights both the promise of xenogeneic hepatic support and the physiologic limits that currently preclude durable therapy, including thrombocytopenia, complement-coagulation incompatibility, portal-flow competition, and challenges in assessing dual-graft function. These results establish proof-of-concept for temporary porcine liver support in humans and outline key priorities for next-generation designs: optimized thromboregulation, mitigation of xTMA, improved immunomodulation, and strategies for controlled transition to native-liver autonomy.

Citation format

MEIER, Raphael P. H. Functional xenogeneic liver support in a living human: Promise, lessons, and next steps. XENOTRANSPLANTATION, 2026, 33(1): e70107.