Diepolder H M, Zachoval R, Hoffmann R M, Wierenga E A, Santantonio T, Jung M C, Eichenlaub D, Pape G R
Institute for Immunology, Klinikum Grosshadern, University of Munich, Germany.
Lancet. 1995 Oct 14;346(8981):1006-7. doi: 10.1016/s0140-6736(95)91691-1.
In acute hepatitis C virus (HCV) infection only 20-50% of patients spontaneously clear the virus. To characterise the immune reaction during that phase we studied the response of peripheral blood mononuclear cells (PBMC) to the recombinant HCV proteins core, non-structural protein 3 (NS3), NS4, and NS5 in 14 patients with acute hepatitis C. All eight patients with self-limited disease compared with two of six with evolving chronic infection showed an NS3- specific PBMC response (p = 0.015). Of 65 patients with established chronic hepatitis C, five showed a PBMC response to NS3. NS3-specific CD4 T-cell clones from patients with self-limited infection predominantly produced interferon-gamma and may thus support cytotoxic effector mechanisms important for viral clearance.
在急性丙型肝炎病毒(HCV)感染中,只有20%-50%的患者能自发清除病毒。为了明确该阶段的免疫反应,我们研究了14例急性丙型肝炎患者外周血单个核细胞(PBMC)对重组HCV蛋白核心、非结构蛋白3(NS3)、NS4和NS5的反应。与6例病情进展为慢性感染患者中的2例相比,所有8例自限性疾病患者均表现出NS3特异性PBMC反应(p = 0.015)。在65例确诊为慢性丙型肝炎的患者中,5例表现出PBMC对NS3的反应。自限性感染患者的NS3特异性CD4 T细胞克隆主要产生γ干扰素,因此可能支持对病毒清除很重要的细胞毒性效应机制。