Donor-specific Immune Senescence as a Candidate Biomarker of Operational Tolerance Following Liver Transplantation in Adults: Results of a Prospective, Multicenter Cohort Study

医学 前瞻性队列研究 生物标志物 衰老 移植 队列 队列研究 肝移植 免疫学 免疫系统 内科学 肿瘤科 生物化学 化学
作者
Naoki Tanimine,James F. Markmann,Michelle A. Wood,Anthony J. Demetris,Kristen Mason,Juliete A.F. Silva,Josh Levitsky,Sandy Feng,Abhinav Humar,Jean C. Emond,Abraham Shaked,Göran B. Klintmalm,Alberto Sánchez‐Fueyo,Drew Lesniak,Cynthia Breeden,Gerald T. Nepom,Nancy D. Bridges,Julia Goldstein,Christian P. Larsen,Michele Desmarais
出处
期刊:American Journal of Transplantation [Wiley]
被引量:3
标识
DOI:10.1016/j.ajt.2024.10.022
摘要

Immunosuppression can be withdrawn from selected liver transplant recipients, although robust clinical predictors of tolerance remain elusive. The Immune Tolerance Network ITN056ST study (OPTIMAL) assessed clinical outcomes and mechanistic correlates of phased immunosuppression withdrawal (ISW) in non-autoimmune, non-viral adult liver transplant recipients. Enrolled subjects were ≥3 years post-transplant with minimal/absent inflammation or fibrosis on a screening liver biopsy. The primary endpoint was operational tolerance at 52 weeks following complete ISW. Of 61 subjects who initiated ISW, 34 failed during ISW and 10 restarted immunosuppression due to clinically manifest acute rejection. Of the 17 subjects remaining off immunosuppression at 1 year, 10 were ultimately deemed tolerant by biopsy. There were no cases of chronic rejection or graft loss. The majority of subjects (78.6%), including those who experienced rejection, ended the study on same or less calcineurin inhibitor than at baseline. 28.3% developed de novo DSA during ISW, which persisted in 11.3%. A minority (16.4%) of histologically and clinically stable long-term adult liver transplant recipients can successfully discontinue and remain off immunosuppression. Increased frequency of donor-specific T cell senescence, C4d deposition and higher density of immune synapses on the screening liver biopsy emerged as potential candidate biomarkers for operational tolerance. NCT02533180.
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