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Nanomedicines in the treatment of patients with hepatitis C co-infected with HIV – focus on pegylated interferon-alpha

机译:纳米药物在艾滋病合并感染的丙型肝炎患者中的治疗-重点关注聚乙二醇化干扰素-α

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摘要

In immuno-competent individuals, the natural course of chronic hepatitis C virus (HCV) infection is highly variable and 5%–30% of patients develop cirrhosis over 20 years. Co-infection with HCV and human immunodeficiency virus (HIV) is an important prognostic factor and associated with more frequent and accelerated progression to cirrhosis. Until recently HIV/AIDS-related complications were life limiting in patients co-infected with HCV; the introduction of highly active antiretroviral treatment (HAART) and the better prognosis of HIV infection has made HCV-related complications an emerging health problem in HCV/HIV co-infected individuals. Treatment of chronic HCV infection has also evolved since the introduction of interferon-alpha. Recently, introduction of pegylated interferon-alpha (peginterferon-alpha) has resulted in an increase in sustained virus clearance rates of up to 80% in selected genotypes and patient populations. The safety and efficacy of modern anti HCV treatment regimens – based on peginterferon-alpha in combination with ribavirin – was evaluated in 4 controlled trials. Sustained clearance of hepatitis C virus can be achieved in up to 35% of patients with HIV/HCV co-infection, and novel HCV treatment regimens based on peginterferon-alpha have no negative effect on the control of HIV disease. In conclusion, if HIV infection is well controlled and CD4+ cell counts >100/mm3, treatment of chronic hepatitis C with peginterferon in combination with ribavirin is safe and should be given for 48 weeks regardless of the HCV genotype. Introduction of peginterferon-alpha has significantly improved adherence to treatment and treatment efficacy; in particular sustained virologic response in patients with HCV genotype 1 or 4 infection improved, but sustained viral clearance in only 7%–38% of patients infected with genotype 1 and 4 cannot be the final step in development of effective treatments in patients with HCV/HIV co-infection.
机译:在具有免疫能力的个体中,慢性丙型肝炎病毒(HCV)感染的自然过程是高度可变的,并且5%–30%的患者在20年内会发展为肝硬化。 HCV和人类免疫缺陷病毒(HIV)合并感染是重要的预后因素,与肝硬化的更频繁和加速发展有关。直到最近,与HCV并发感染的患者中与HIV / AIDS相关的并发症仍然限制了生命。高效抗逆转录病毒治疗(HAART)的引入以及HIV感染的更佳预后使HCV相关并发症成为HCV / HIV合并感染个体中正在出现的健康问题。自从引入干扰素-α以来,慢性HCV感染的治疗也得到了发展。最近,聚乙二醇化干扰素-α(peginterferon-alpha)的引入导致选定基因型和患者群体的持续病毒清除率提高了80%。在4项对照试验中评估了现代抗HCV治疗方案(基于聚乙二醇干扰素-α联合利巴韦林)的安全性和有效性。可以在多达35%的HIV / HCV合并感染患者中实现丙型肝炎病毒的持续清除,并且基于聚乙二醇干扰素α的新型HCV治疗方案对控制HIV疾病没有负面影响。总之,如果HIV感染得到良好控制并且CD4 + 细胞计数> 100 / mm 3 ,则聚乙二醇干扰素联合利巴韦林治疗慢性丙型肝炎是安全的,应该无论HCV基因型如何,均给予48周。引入聚乙二醇干扰素-α可以显着改善对治疗的依从性和治疗效果。特别是HCV基因型1或4感染患者的持续病毒学应答有所改善,但是只有7%–38%的基因型1和4感染患者的持续病毒清除率并不是开发有效治疗HCV / HIV合并感染。

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