Fenwick F, Bassendine M F, Agarwal K, Bevitt D, Pumeechockchai W, Burt A D, Toms G L
The Schools of Clinical Medical Sciences, The Medical School, Newcastle upon Tyne NE2 4HH, UK.
J Clin Pathol. 2006 Feb;59(2):174-8. doi: 10.1136/jcp.2005.028126.
Patients with common variable immunodeficiency may exhibit rapidly progressive hepatitis when infected with hepatitis C virus (HCV), leading to cirrhosis and liver failure. Liver transplantation in these patients may result in a cholestatic form of HCV reinfection with exceptionally high virus loads.
To report an immunohistochemical investigation of the pretransplant and post-transplant liver of one such patient.
METHODS/RESULTS: On immunohistochemical staining of frozen sections with anti-HCV core monoclonal antibody or fluorescein labelled human polyclonal anti-HCV IgG, no HCV antigens were demonstrated in the native cirrhotic liver removed at transplant, despite a viral load of 10(6.4) genomes/g. The transplanted liver, collected six weeks post-transplant, exhibited cholestatic recurrent hepatitis, had an HCV virus load of 10(10) genomes/g of liver, and revealed HCV antigen in the cytoplasm of most hepatocytes, with a pronounced periportal distribution. No virus antigen was demonstrable in other cell types. The core antigen was also detected in paraffin wax embedded, formaldehyde fixed tissue of this liver after high temperature antigen retrieval, but not in the native cirrhotic liver or a selection of HCV positive livers collected pretransplant from immunocompetent patients. Attempts to delineate the distribution of E1, NS3, and NS4 antigens were unsuccessful because monoclonal antibodies to these antigens produced "false positive" staining of foci of hepatocytes in the post-transplant livers of HCV seronegative patients with cholestasis.
This case provided an opportunity to study the natural development of HCV during acute infection in the absence of an immune response, and may help to elucidate the pathogenesis of HCV recurrence in liver allografts.
普通可变免疫缺陷患者感染丙型肝炎病毒(HCV)时可能出现快速进展性肝炎,导致肝硬化和肝衰竭。这些患者进行肝移植可能会导致胆汁淤积型HCV再感染,病毒载量异常高。
报告对一名此类患者移植前和移植后肝脏进行的免疫组织化学研究。
方法/结果:用抗HCV核心单克隆抗体或荧光素标记的人多克隆抗HCV IgG对冰冻切片进行免疫组织化学染色,尽管病毒载量为10(6.4)基因组/克,但在移植时切除的天然肝硬化肝脏中未检测到HCV抗原。移植后六周收集的移植肝脏表现为胆汁淤积性复发性肝炎,HCV病毒载量为10(10)基因组/克肝脏,并且在大多数肝细胞的细胞质中发现了HCV抗原,呈现明显的汇管区周围分布。在其他细胞类型中未检测到病毒抗原。在高温抗原修复后,该肝脏的石蜡包埋、甲醛固定组织中也检测到了核心抗原,但在天然肝硬化肝脏或移植前从免疫功能正常的患者中收集的一组HCV阳性肝脏中未检测到。由于针对这些抗原的单克隆抗体在胆汁淤积的HCV血清阴性患者的移植后肝脏中对肝细胞灶产生“假阳性”染色,因此未能成功描绘E1、NS3和NS4抗原的分布。
该病例为研究急性感染期间无免疫反应时HCV的自然发展提供了机会,并可能有助于阐明肝移植中HCV复发的发病机制。