Uebayashi Elena Yukie, Okajima Hideaki, Yamamoto Miki, Ogawa Eri, Okamoto Tatsuya, Haga Hironori, Hatano Etsurou
Department of Pediatric Surgery, Kyoto University Hospital, Kyoto 606-8507, Japan.
Department of Surgery, Kyoto University Graduate School of Medicine, Kyoto 606-8507, Japan.
J Clin Med. 2022 Aug 18;11(16):4834. doi: 10.3390/jcm11164834.
Antibody-mediated rejection (AMR) of liver allograft transplantation was considered as anecdotal for many decades. However recently, AMR has gained clinical awareness as a potential cause of chronic liver injury, leading to liver allograft fibrosis and eventual graft failure. (1) Methods: Literature on chronic AMR (cAMR) in pediatric post-liver transplant patients was reviewed for epidemiologic data, physiopathology, diagnosis, and treatment approaches. (2) Results: Accurate incidence of cAMR in pediatric liver transplantation remains unknown. Diagnostic criteria of cAMR were suggested by the Banff Working Group in 2016 and are based on standardized histopathological findings, C4d staining pattern, associated with the presence of donor-specific antibodies (DSA). Physio-pathological mechanisms are not clear for the technically difficult-to-obtain animal models reproducing cAMR. Treatment protocols are not established, being limited to case reports and case series, based on experience in ABO incompatible transplantation and kidney transplantation. Immunosuppression compliance with adequate dose adjustment may prevent cAMR. Conversion of Cyclosporine to Tacrolimus may improve pathological findings if treated in early phase. The association of steroids, Mycophenolate Mofetil (MMF) and mTOR inhibitors have shown some synergistic effects. Second-line treatments such as intravenous immunoglobulin (IVIG) and plasma exchange may decrease antibody titers based on ABO incompatible transplant protocols. The use of anti-CD20 (Rituximab) and proteasome inhibitors (Bortezomib) is controversial due to the lack of qualified studies. Therefore, multicenter randomized trials are needed to establish the best therapeutic strategy. In refractory cases, re-transplantation is the only treatment for allograft failure. (3) Conclusions: This literature review collects recent clinical, histopathological, and therapeutical advances of cAMR in liver allograft transplantation of pediatric patients. There are many physio-pathological aspects of cAMR to be clarified. Further efforts with multicenter prospective protocols to manage patients with cAMR are needed to improve its outcome.
数十年来,肝移植中的抗体介导性排斥反应(AMR)一直被视为罕见病例。然而,近年来,AMR作为慢性肝损伤的潜在原因已引起临床关注,可导致肝移植纤维化并最终导致移植失败。(1)方法:回顾了有关小儿肝移植术后慢性AMR(cAMR)的文献,以获取流行病学数据、生理病理学、诊断和治疗方法。(2)结果:小儿肝移植中cAMR的准确发病率尚不清楚。2016年,班夫工作组提出了cAMR的诊断标准,该标准基于标准化的组织病理学发现、C4d染色模式以及与供体特异性抗体(DSA)的存在相关。对于难以通过技术手段获得的重现cAMR的动物模型,其生理病理机制尚不清楚。治疗方案尚未确立,仅限于基于ABO血型不相容移植和肾移植经验的病例报告和病例系列。免疫抑制的充分剂量调整依从性可能预防cAMR。如果在早期进行治疗,将环孢素转换为他克莫司可能会改善病理结果。类固醇、霉酚酸酯(MMF)和mTOR抑制剂联合使用已显示出一些协同作用。基于ABO血型不相容移植方案,静脉注射免疫球蛋白(IVIG)和血浆置换等二线治疗可能会降低抗体滴度。由于缺乏合格的研究,抗CD20(利妥昔单抗)和蛋白酶体抑制剂(硼替佐米)的使用存在争议。因此,需要进行多中心随机试验以确立最佳治疗策略。在难治性病例中,再次移植是移植失败的唯一治疗方法。(3)结论:本文献综述收集了小儿患者肝移植中cAMR的最新临床、组织病理学和治疗进展。cAMR的许多生理病理方面尚待阐明。需要通过多中心前瞻性方案进一步努力管理cAMR患者,以改善其治疗结果。