Katayama K, Kasahara A, Sasaki Y, Kashiwagi T, Naito M, Masuzawa M, Katoh M, Yoshihara H, Kamada T, Mukuda T, Hijioka T, Hori M, Hayashi N
Department of Internal Medicine, Osaka Kouseinenkin Hospital, 2-2, Yamadaoka, Suita-city, Osaka, Japan.
J Viral Hepat. 2001 May;8(3):180-5. doi: 10.1046/j.1365-2893.2001.00274.x.
The aim of this study was to clarify the immunological and virological responses to pre-administration of interferon-gamma prior to initiation of interferon-alpha treatment in patients with refractory chronic hepatitis C. Twenty-two nonresponders to 6-months of IFN-alpha treatment were enrolled. The hepatitis C virus (HCV) genotype was Ib in all. Natural IFN-gamma (1 MIU/day) was administered daily for 14 days followed by natural IFN-alpha (5 MIU/day) daily for 14 days and then three times weekly for 22 weeks. Serum immunological parameters (IL-10, neopterin, BMG, sCD8, sCD4, IL-6, IL-12) were measured as were the levels of several cytokines (IFN-gamma, TNF-alpha, IL-2, IL-4, IL-5, IL-6, IL-10). Three patients dropped out; two because of the occurrence of other diseases and one because of an adverse effect. At the end of the period of IFN-alpha treatment, HCV-RNA had become negative in six of 19 patients (end-of treatment response; ETR). Six months after the completion of IFN administration, a virological sustained response (SR) was seen in two of 19 patients. The mean serum levels of IL-10 were significantly decreased 6 weeks after the start of treatment. Other immunological parameter levels increased significantly during the period of IFN-gamma administration, and tended to return to the pretreatment level after the start of IFN-alpha administration. Univariate logistic regression analysis showed that the initial change in the levels of these parameters or the change in the ratios of Th1/Th2 parameter levels are useful factors indicative of the end of the treatment response. These findings suggest that priming with IFN-gamma prior to the initiation of IFN-alpha treatment in patients with refractory chronic hepatitis C can modulate the host immune response and this might contribute to viral clearance.
本研究的目的是阐明难治性慢性丙型肝炎患者在开始使用α干扰素治疗前预先给予γ干扰素后的免疫和病毒学反应。招募了22名对6个月α干扰素治疗无反应者。所有患者的丙型肝炎病毒(HCV)基因型均为Ib型。每天给予天然γ干扰素(1MIU/天),持续14天,随后每天给予天然α干扰素(5MIU/天),持续14天,然后每周3次,持续22周。检测血清免疫参数(IL-10、新蝶呤、β2微球蛋白、可溶性CD8、可溶性CD4、IL-6、IL-12)以及几种细胞因子(γ干扰素、肿瘤坏死因子-α、IL-2、IL-4、IL-5、IL-6、IL-10)的水平。3名患者退出研究;2名是因为出现其他疾病,1名是因为出现不良反应。在α干扰素治疗期结束时,19名患者中有6名患者的HCV-RNA转为阴性(治疗结束反应;ETR)。在完成干扰素给药6个月后,19名患者中有2名出现病毒学持续应答(SR)。治疗开始6周后,IL-10的平均血清水平显著下降。在给予γ干扰素期间,其他免疫参数水平显著升高,在开始给予α干扰素后趋于恢复到治疗前水平。单因素逻辑回归分析表明,这些参数水平的初始变化或Th1/Th2参数水平比值的变化是提示治疗结束反应的有用因素。这些发现表明,在难治性慢性丙型肝炎患者开始α干扰素治疗前用γ干扰素进行预激可以调节宿主免疫反应,这可能有助于病毒清除。