Immune checkpoint inhibitor-related T-cell-mediated rejection increases the risk of perioperative graft loss after liver transplantation.

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Tác giả: Tao Ding, Guangxiang Gu, Kun He, Kenglong Huang, Haoming Lin, Yutian Lin, Chao Liu, Xinjun Lu, Kwan Man, Li Pang, Wenrui Wu, Leibo Xu, Yanfang Ye, Fapeng Zhang

Ngôn ngữ: eng

Ký hiệu phân loại: 393.2 Cremation

Thông tin xuất bản: China : Chinese medical journal , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 749977

 BACKGROUND: Pre-transplant exposure to immune checkpoint inhibitors (ICIs) significantly increases the risk of allograft rejection after liver transplantation (LT)
  however, whether ICI-related rejection leads to increased graft loss remains controversial. Therefore, this study aimed to investigate the association between ICI-related allograft rejection and perioperative graft loss. METHODS: This was a retrospective analysis of adult liver transplant recipients with early biopsy-proven T-cell-mediated rejection (TCMR) at Liver Transplantation Center of Sun Yat-sen Memorial Hospital from June 2019 to September 2024. The pathological features, clinical characteristics, and perioperative graft survival were analyzed. RESULTS: Twenty-eight patients who underwent early TCMR between June 2019 and September 2024 were included. Based on pre-LT ICI exposure, recipients were categorized into ICI-related TCMR (irTCMR, n = 12) and conventional TCMR (cTCMR, n = 16) groups. Recipients with irTCMR had a higher median Banff rejection activity index (RAI) (6 vs. 5, P = 0.012) and more aggressive tissue damage and inflammation. Recipients with irTCMR showed higher proportion of treatment resistance, achieving a complete resolution rate of only 8/12 compared to 16/16 for cTCMR. Graft loss occurred in 5/12 of irTCMR recipients within 90 days after LT, with no graft loss in cTCMRs recipients. Cox analysis demonstrated that irTCMR with an ICI washout period of <
 30 days was an independent risk factor for perioperative graft loss (hazard ratio [HR], 6.540
  95% confidence interval [CI], 1.067-40.067, P = 0.042). CONCLUSION: IrTCMR is associated with severe pathological features, increased resistance to treatment, and higher graft loss in adult liver transplant recipients.
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