INSERM, Unité 785, Villejuif, France.
Hepatology. 2013 Feb;57(2):689-99. doi: 10.1002/hep.26024. Epub 2013 Jan 8.
The development of potentially severe non-graft-versus-host disease (GVHD) hepatitis resembling autoimmune hepatitis (AIH) has been reported after bone marrow transplantation (BMT). The aim of this study was to better characterize this form of hepatitis, particularly through the identification of autoantigens recognized by patient sera. Five patients who received an allogeneic BMT for the treatment of hematological diseases developed liver dysfunction with histological features suggestive of AIH. Before and during the onset of hepatic dysfunction, sera were tested on immunoblottings performed with cytosolic, microsomal, mitochondrial, and nuclear proteins from rat liver homogenate and resolved by two-dimensional electrophoresis. Antigenic targets were identified by mass spectrometry. During the year that followed BMT, all patients presented with GVHD. Acute hepatitis then occurred after the withdrawal, or during the tapering, of immunosuppressive therapy. At that time, no patients had a history of liver toxic drug absorption, patent viral infection, or any histopathological findings consistent with GVHD. Immunoreactive spots stained by sera collected at the time of hepatic dysfunction were more numerous and more intensely expressed than those stained by sera collected before. Considerable patient-dependent pattern heterogeneity was observed. Among the 259 spots stained exclusively by sera collected at the time of hepatitis, a total of 240 spots were identified, corresponding to 103 different proteins. Twelve of them were recognized by sera from 3 patients.
This is the first immunological description of potentially severe non-GVHD hepatitis occurring after BMT, determined using a proteomic approach and enabling a discussion of the mechanisms that transform an alloimmune reaction into an autoimmune response. Any decision to withdraw immunosuppression after allogeneic BMT should be made with caution.
骨髓移植(BMT)后可发生类似于自身免疫性肝炎(AIH)的潜在严重非移植物抗宿主病(GVHD)肝炎。本研究旨在更好地描述这种肝炎,特别是通过鉴定患者血清识别的自身抗原。5 例因血液系统疾病接受同种异体 BMT 的患者发生肝功能障碍,组织学特征提示 AIH。在肝功能障碍发生之前和期间,用大鼠肝匀浆的胞质、微粒体、线粒体和核蛋白进行免疫印迹检测血清,并通过二维电泳分离。通过质谱鉴定抗原靶标。在 BMT 后 1 年内,所有患者均出现 GVHD。随后在免疫抑制治疗停药或减量期间发生急性肝炎。此时,没有患者有肝毒性药物吸收、显性病毒感染或任何与 GVHD 一致的组织病理学发现。在肝功能障碍时收集的血清染色的免疫反应性斑点比在肝前收集的血清染色的斑点更多且表达更强烈。观察到相当大的患者依赖性模式异质性。在仅由肝炎时收集的血清染色的 259 个斑点中,共鉴定出 240 个斑点,对应于 103 种不同的蛋白质。其中 12 种被 3 例患者的血清识别。
这是使用蛋白质组学方法首次对 BMT 后发生的潜在严重非 GVHD 肝炎进行的免疫学描述,可讨论将同种免疫反应转化为自身免疫反应的机制。在同种异体 BMT 后决定撤回免疫抑制应谨慎做出。