In this study, we investigate the mechanisms by which ischemia-free liver transplantation (IFLT) mitigates ischemia-reperfusion injury (IRI) and identify key therapeutic targets. Clinical data from 200 patients were collected to evaluate perioperative recovery and overall outcomes. Liver tissues were obtained from donors at the preprocurement, end-of-preservation, and postperfusion stages. Gene expression profiles were examined using single-cell transcriptomic analysis. Phenotypic and functional characteristics were evaluated using flow cytometry, and protein expression was assessed using immunofluorescence, immunohistochemistry, and enzyme-linked immunosorbent assay. Animal models of IRI were employed to examine the effects of HIF-2α inhibition in vivo. PT-2385 was administered to inhibit HIF-2α, and 100 µg of anti-mouse CD8α monoclonal antibody was injected to deplete CD8+ T cells. Patients in the IFLT group exhibited a lower incidence of early allograft dysfunction and a higher 1-yr survival rate. Differential gene expression analysis of IRI-related genes in 14 paired liver samples from conventional liver transplantation revealed significant upregulation of HIF-2α in postreperfusion tissues, predominantly expressed in CD69+CD103-CD8+ T cells. The up-regulated genes were enriched in TNF-related signaling pathways. Inhibition of HIF-2α reduced the number of CD69+CD103-CD8+ T cells and alleviated liver injury in vivo. In IFLT, genes in this pathway were not significantly upregulated. Under HIF-2α stimulation, CD69+CD103-CD8+ T cells exacerbate organ and tissue injury through TNF-related signaling. In IFLT, the absence of significant pathway upregulation suggests effective prevention of IRI.
Chen et al. (Wed,) studied this question.