Schmeding Maximilian, Kienlein Stefan, Röcken Christoph, Neuhaus Ruth, Neuhaus Peter, Heidenhain Christoph, Neumann Ulf P
Department of General, Visceral and Transplantation Surgery, Charité Campus Virchow Klinikum, Berlin, Germany.
Transpl Immunol. 2010 Aug;23(4):156-60. doi: 10.1016/j.trim.2010.06.002. Epub 2010 Jun 14.
Hepatitis-C is the most common indication for liver transplantation. Recurrence of HCV is universal leading to graft failure in up to 40% of all patients. The differentiation between acute rejection and recurrent hepatitis-C is crucial as rejection treatments are likely to aggravate HCV-recurrence. Histological examination of liver biopsy remains the gold standard for diagnosis of acute rejection but has failed in the past to distinguish between acute rejection and recurrent hepatitis-C. In a retrospective study we have recently reported that C4d as a marker of the activated complement cascade is detectable in a hepatic specimen in acute rejection after liver transplantation and may serve as a valuable tool in differential diagnosis between ACR and HCV-recurrence. We performed a prospective analysis by ELISA measurement of C4d concentration in cryo-preserved liver biopsies of LTX patients who had either experienced acute rejection, hepatitis-C recurrence or displayed no pathological alterations (controls). Opposed to our immunohistologically based findings in paraffinized tissue we were unable to detect significant differences of C4d concentration in ELISA of cryo-preserved liver tissue. Consequently the role and potential value of C4d as a diagnostic marker may not be determined using ELISA-based tissue evaluation.
丙型肝炎是肝移植最常见的指征。丙型肝炎病毒(HCV)复发普遍存在,导致高达40%的患者出现移植肝衰竭。急性排斥反应与复发性丙型肝炎的鉴别至关重要,因为排斥反应的治疗可能会加重HCV复发。肝活检的组织学检查仍然是诊断急性排斥反应的金标准,但过去未能区分急性排斥反应和复发性丙型肝炎。在一项回顾性研究中,我们最近报告称,作为活化补体级联反应标志物的C4d在肝移植后急性排斥反应的肝脏标本中可检测到,可能是鉴别急性细胞性排斥反应(ACR)和HCV复发的有价值工具。我们通过酶联免疫吸附测定(ELISA)对经历过急性排斥反应、HCV复发或无病理改变(对照)的肝移植(LTX)患者的冷冻保存肝活检组织中的C4d浓度进行了前瞻性分析。与我们在石蜡包埋组织中基于免疫组织化学的发现相反,我们无法在冷冻保存肝组织的ELISA中检测到C4d浓度的显著差异。因此,使用基于ELISA的组织评估可能无法确定C4d作为诊断标志物的作用和潜在价值。