Ren Fen-Yu, Jin Hai, Piao Xi-Xu, Piao Feng-Shun
Department of Gastroenterology and Hepatology, Yanbian University Hospital, Yanji 133000, Jilin Province, China.
World J Gastroenterol. 2007 Nov 7;13(41):5440-5. doi: 10.3748/wjg.v13.i41.5440.
To investigate the anti-viral mechanism of combination therapy of interferon (IFN)-alpha and ribavirin in patients with chronic hepatitis B.
Twenty patients were assigned to receive either IFN-alpha plus ribavirin (group A, n = 14) or no treatment as a control (group B, n = 6). Patients were analyzed for T-cell proliferative responses specific for hepatitis B virus (HBV)-antigen and cytokine production by peripheral blood mononuclear cells (PBMCs).
Combination therapy induced HBV-antigen specific CD4+ T-cell proliferative responses in four patients (28.6%). Production of high levels of HBV-specific IFN-gamma, tumor necrosis factor (TNF)-alpha, interleukin (IL)-12 by PBMCs was found in five patients (35.7%), who showed significantly lower HBV DNA levels in serum at 12 mo after treatment ended (P = 0.038) and at 24 mo of follow-up (P = 0.004) than those without high levels of cytokine production.
HBV-antigen specific CD4+ T cells may directly control HBV replication and secretion of anti-viral T helper 1 (Th1) cytokines by PBMCs during combination therapy of chronic hepatitis B with ribavirin and IFN-alpha.
研究干扰素(IFN)-α与利巴韦林联合治疗慢性乙型肝炎患者的抗病毒机制。
将20例患者分为两组,分别接受IFN-α联合利巴韦林治疗(A组,n = 14)或不接受任何治疗作为对照(B组,n = 6)。分析患者外周血单个核细胞(PBMC)对乙型肝炎病毒(HBV)抗原的T细胞增殖反应及细胞因子产生情况。
联合治疗使4例患者(28.6%)产生了HBV抗原特异性CD4+ T细胞增殖反应。5例患者(35.7%)的PBMC产生了高水平的HBV特异性干扰素-γ、肿瘤坏死因子(TNF)-α、白细胞介素(IL)-12,这些患者在治疗结束后12个月(P = 0.038)和随访24个月时(P = 0.004)血清HBV DNA水平显著低于未产生高水平细胞因子的患者。
在慢性乙型肝炎患者接受利巴韦林和IFN-α联合治疗期间,HBV抗原特异性CD4+ T细胞可能直接控制HBV复制以及PBMC分泌抗病毒辅助性T细胞1(Th1)细胞因子。