Begovac Josip, Romih Vanja
Department of HIV/AIDS, Dr Fran Mihaljević University Hospital for Infectious Diseases, Zagreb, Croatia.
Acta Med Croatica. 2009 Dec;63(5):423-9.
Hepatitis C virus (HCV) and human immunodeficiency virus (HIV) co-infected individuals have a higher risk of advanced liver fibrosis compared to those that are HCV mono-infected. Treatment of HCV offers the possibility of virus eradication, thus every person with detectable HCV viral load is a candidate for treatment. Treatment is recommended for all HCV/HIV co-infected patients with: 1) repeatedly elevated aminotransferase levels; 2) F2 stage of liver fibrosis or higher regardless of alanine aminotransferase level; and 3) more than 200 CD4+ T-lymphocytes per microL of blood. Treatment is not recommended for patients that are active injection drug users, consume large amounts of alcohol, or have or had a severe psychiatric disorder. Liver biopsy is generally recommended, however, because of faster progression to liver fibrosis in HIV and HCV co-infected patients, if the patient declines liver biopsy it should not exclude him from treatment. Treatment with a combination of pegylated interferon and weight-based ribavirin (1000 mg/day if <75 kg and 1200 mg/day if >75 kg) is recommended. Pegylated interferon is used as 180 microg for alfa-2a form and 1.5 mg/kg for alfa-2b form once weekly subcutaneously. HCV RNA should be measured after 4 weeks of treatment, and later as needed, in weeks 12, 24, 48 or 72. For evaluation of a sustained viral response, HCV RNA should be measured 24 weeks after the end of treatment. In patients with rapid viral response (undetectable levels of HCV RNA after 4 weeks of treatment), treatment duration is 24 weeks (genotypes 2 and 3) or 48 weeks (genotypes 1 and 4). In patients without rapid viral response but with an adequate response after 12 and 24 weeks, we generally recommend treatment for 48 weeks, however, 72 weeks of treatment can be considered for genotypes 1 and 4. Treatment discontinuation is recommended in patients with <2 log viral load decline after 12 weeks or with a detectable viral load after 24 weeks of treatment. If concurrent treatment of HCV and HIV is necessary, treatment with zidovudine and didanosine should be avoided and caution is needed with the administration of potentially hepatotoxic antiretroviral drugs such as nevirapine and ritonavir.
与丙型肝炎病毒(HCV)单一感染的个体相比,丙型肝炎病毒(HCV)和人类免疫缺陷病毒(HIV)合并感染的个体发生晚期肝纤维化的风险更高。丙型肝炎病毒治疗提供了根除病毒的可能性,因此每个可检测到丙型肝炎病毒载量的人都是治疗的候选对象。对于所有合并感染HCV/HIV的患者,在出现以下情况时建议进行治疗:1)转氨酶水平反复升高;2)无论丙氨酸转氨酶水平如何,肝纤维化达到F2期或更高;3)每微升血液中CD4+T淋巴细胞超过200个。对于活跃的注射吸毒者、大量饮酒者或患有严重精神疾病或曾患有严重精神疾病的患者,不建议进行治疗。然而,一般建议进行肝活检,由于HIV和HCV合并感染患者肝纤维化进展更快,如果患者拒绝肝活检,这不应该排除其接受治疗。建议采用聚乙二醇化干扰素和基于体重的利巴韦林联合治疗(体重<75 kg者为1000 mg/天,体重>75 kg者为1200 mg/天)。聚乙二醇化干扰素,α-2a型为180 μg,α-2b型为1.5 mg/kg,每周一次皮下注射。治疗4周后应检测HCV RNA,之后根据需要在第12、24、48或72周检测。为评估持续病毒学应答,应在治疗结束后24周检测HCV RNA。对于病毒快速应答(治疗4周后HCV RNA水平不可检测)的患者,治疗疗程为24周(基因2型和3型)或48周(基因1型和4型)。对于无病毒快速应答但在12周和24周后有充分应答的患者,我们一般建议治疗48周,然而,对于基因1型和4型患者可考虑治疗72周。对于治疗12周后病毒载量下降<2 log或治疗24周后病毒载量可检测到的患者,建议停药。如果有必要同时治疗HCV和HIV,应避免使用齐多夫定和去羟肌苷,并且在使用潜在肝毒性抗逆转录病毒药物如奈韦拉平和利托那韦时需要谨慎。