Klintmalm Göran B, Trotter James F, Demetris Anthony
Annette C. and Harold C. Simmons Transplant Institute, Baylor University Medical Center, Dallas, TX.
Division of Transplantation, Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA.
Transplant Direct. 2022 Jun 24;8(7):e1076. doi: 10.1097/TXD.0000000000001076. eCollection 2022 Jul.
T cell-mediated rejection that appears and persists late after transplantation is often associated with development of de novo donor-specific antibodies. Treatment of this condition often presents a conundrum because of the uncertainty regarding the trade-off between immunosuppression-related toxicities/complications and restoration of allograft function and structure.
Herein, we report an illustrative case of a young 20-y-old otherwise healthy woman who underwent liver replacement for Alagille's syndrome from an ABO-compatible, 6 antigen-mismatched crossmatch-negative 24-y-old man. Although triple baseline immunosuppression was used (tacrolimus, mycophenolate mofetil, and prednisone), she developed rejection 3 d after liver replacement. Despite verified continual immunosuppression compliance, 1.5 y after liver replacement she experienced 6 more rejection episodes over the following 18 mo and development of de novo donor-specific antibody.
Treatment with belatacept began 3.5 y after transplantation, normalizing her liver tests with no further rejections. A biopsy obtained 6 y after transplantation (postoperative day 2221) was normal, appearing without inflammation or residual fibrosis.
Belatacept may be a useful treatment approach in this setting.
移植后出现且持续较晚的T细胞介导的排斥反应通常与新发供者特异性抗体的产生有关。由于免疫抑制相关毒性/并发症与恢复同种异体移植物功能和结构之间的权衡存在不确定性,这种情况的治疗常常是一个难题。
在此,我们报告一例说明性病例,一名20岁的年轻健康女性因阿拉吉耶综合征接受了来自一名24岁男性的肝脏移植,该男性与受者ABO血型相容,6个抗原错配且交叉配型阴性。尽管使用了三联基线免疫抑制治疗(他克莫司、霉酚酸酯和泼尼松),但她在肝移植后3天发生了排斥反应。尽管证实其持续遵守免疫抑制治疗方案,但在肝移植1.5年后,她在接下来的18个月内又经历了6次排斥反应,并产生了新发供者特异性抗体。
移植3.5年后开始使用贝拉西普治疗,她的肝功能检查恢复正常,未再发生排斥反应。移植6年后(术后第2221天)获得的活检结果正常,未见炎症或残留纤维化。
在这种情况下,贝拉西普可能是一种有用的治疗方法。