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肝移植中的抗体介导排斥反应:免疫病理学特征和长期随访。

Antibody-Mediated Rejection in Liver Transplantation: Immuno-Pathological Characteristics and Long-Term Follow-Up.

机构信息

Division of Transplant Surgery, Department of Surgery, University of Texas Medical Branch, UTMB, Galveston, TX, United States.

John Sealy School of Medicine, University of Texas Medical Branch, UTMB, Galveston, TX, United States.

出版信息

Transpl Int. 2024 Aug 29;37:13232. doi: 10.3389/ti.2024.13232. eCollection 2024.

Abstract

The diagnosis of liver antibody-mediated rejection (AMR) is challenging and likely under-recognized. The association of AMR with donor-specific antibodies (DSA), and its clinical course in relation to pathologic findings and treatment are ill defined. We identified cases of liver AMR by following the criteria outlined by the 2016 Banff Working Group. Patient demographics, native liver disease, histopathologic findings, treatment type, clinical outcome, and transaminase levels during AMR diagnosis, treatment, and resolution were determined. Patients (n = 8) with AMR average age was 55.2 years (range: 19-68). Seven of eight cases met the Banff criteria for AMR. Personalized treatment regimens consisted of optimization of immunosuppression, intravenous pulse steroids, plasmapheresis, IVIG, rituximab, and bortezomib. Five patients experienced complete resolution of AMR, return of transaminases to baseline, and decreased DSA at long-term follow-up. One patient developed chronic AMR and two patients required re-transplantation. Follow-up after AMR diagnosis ranged from one to 11 years. Because AMR can present at any time, crossmatch, early biopsy, and routine monitoring of DSA levels should be implemented following transaminase elevation to recognize AMR. Furthermore, treatment should be immediately implemented to reverse AMR and prevent graft failure, chronic damage, re-transplantation, and possibly mortality.

摘要

肝抗体介导的排斥反应(AMR)的诊断具有挑战性,且可能被低估。AMR 与供体特异性抗体(DSA)的关联及其与病理发现和治疗的临床过程尚不清楚。我们通过遵循 2016 年 Banff 工作组概述的标准来确定肝 AMR 病例。确定了患者的人口统计学数据、原发性肝病、组织病理学发现、治疗类型、临床结局以及 AMR 诊断、治疗和缓解期间的转氨酶水平。患有 AMR 的患者(n=8)的平均年龄为 55.2 岁(范围:19-68 岁)。8 例中有 7 例符合 AMR 的 Banff 标准。个体化治疗方案包括优化免疫抑制、静脉注射脉冲类固醇、血浆置换、IVIG、利妥昔单抗和硼替佐米。5 例患者的 AMR 完全缓解,转氨酶恢复基线水平,长期随访时 DSA 减少。1 例患者发生慢性 AMR,2 例患者需要再次移植。AMR 诊断后的随访时间从 1 年到 11 年不等。因为 AMR 随时可能发生,所以在转氨酶升高后应进行交叉配型、早期活检和 DSA 水平的常规监测,以识别 AMR。此外,应立即实施治疗以逆转 AMR,防止移植物衰竭、慢性损伤、再次移植和可能的死亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44d1/11391112/7f2cc1ce7f99/ti-37-13232-g001.jpg

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