Ferraro D, Bonura C, Giglio M, Di Stefano R, Almasio P L, Di Marco V, Craxì A, Cacciola I, Squadrito G, Raimondo G
Department of Hygiene and Microbiology, University of Palermo, Palermo, Italy.
J Biol Regul Homeost Agents. 2003 Apr-Jun;17(2):172-5.
Occult HBV infection in subjects with chronic hepatitis C is related to more severe disease outcome. It has been suggested that it might reduce sensitivity to antiviral treatment.
To assess in HBsAg negative subjects with chronic hepatitis C any effect of the presence of HBV genomes in the liver on the early kinetics of HCV-RNA under PEG-IFN plus ribavirin.
Twenty-two anti-HCV and HCV-RNA positive subjects, with biopsy-proven chronic hepatitis C (M/F 15/7; 50 +/- 8.6 years, 16 genotype 1b) were given PEG-IFN alpha 2b 1.0 microg qw plus ribavirin (800 to 1,200 mg daily according to body weight) for an intended 52 week period. Early virological response was assessed over the first 4 weeks of therapy by quantifying HCV-RNA. Occult HBV infection was assessed by testing for HBV-DNA in the liver before therapy.
HBV genomes were found in the liver of 7 of 22 (31.4%) patients, unrelated to anti-HBc status. Kinetics of HCV-RNA during the first 4 weeks of antiviral treatment was unaffected by occult HBV infection, both in terms of absolute reduction of viral load and of number of cases with a reduction of > or = 2 log10 on treatment.
Occult HBV infection does not affect the early phase of response to combination therapy. Further follow-up of patients into the maintenance phase of antiviral treatment and after stopping it will clarify if and when occult HBV has a role in reducing sustained virological response.
慢性丙型肝炎患者中的隐匿性HBV感染与更严重的疾病转归相关。有人提出,它可能会降低对抗病毒治疗的敏感性。
评估在HBsAg阴性的慢性丙型肝炎患者中,肝脏中HBV基因组的存在对聚乙二醇干扰素联合利巴韦林治疗下HCV-RNA早期动力学的影响。
22例抗-HCV和HCV-RNA阳性、经活检证实为慢性丙型肝炎的患者(男/女15/7;年龄50±8.6岁,16例为1b基因型)接受聚乙二醇干扰素α-2b 1.0μg每周一次联合利巴韦林(根据体重每日800至1200mg)治疗,疗程预定为52周。在治疗的前4周通过定量HCV-RNA评估早期病毒学应答。在治疗前通过检测肝脏中的HBV-DNA评估隐匿性HBV感染。
22例患者中有7例(31.4%)肝脏中发现HBV基因组,与抗-HBc状态无关。在抗病毒治疗的前4周,隐匿性HBV感染对HCV-RNA的动力学没有影响,无论是从病毒载量的绝对降低还是从治疗中病毒载量降低≥2 log10的病例数来看。
隐匿性HBV感染不影响联合治疗的早期应答阶段。对患者在抗病毒治疗维持期及停药后的进一步随访将明确隐匿性HBV是否以及何时在降低持续病毒学应答方面起作用。