Inserm U1259 MAVIVH, Université de Tours and CHRU de Tours, 37000 Tours, France.
Viruses. 2023 May 11;15(5):1151. doi: 10.3390/v15051151.
The introduction of direct-acting antivirals (DAAs) has revolutionized hepatitis C treatment. Short courses of treatment with these drugs are highly beneficial to patients, eliminating hepatitis C virus (HCV) without adverse effects. However, this outstanding success is tempered by the continuing difficulty of eradicating the virus worldwide. Thus, access to an effective vaccine against HCV is strongly needed to reduce the burden of the disease and contribute to the elimination of viral hepatitis. The recent failure of a T-cell vaccine based on the use of viral vectors expressing the HCV non-structural protein sequences to prevent chronic hepatitis C in drug users has pointed out that the induction of neutralizing antibodies (NAbs) will be essential in future vaccine candidates. To induce NAbs, vaccines must contain the main target of this type of antibody, the HCV envelope glycoproteins (E1 and E2). In this review, we summarize the structural regions in E1 and E2 proteins that are targeted by NAbs and how these proteins are presented in the vaccine candidates currently under development.
直接作用抗病毒药物(DAAs)的引入彻底改变了丙型肝炎的治疗方式。这些药物的短期疗程对患者非常有益,可消除丙型肝炎病毒(HCV)而无不良反应。然而,这一卓越的成功因全球范围内持续难以消灭该病毒而受到影响。因此,迫切需要一种有效的 HCV 疫苗来减轻疾病负担,并有助于消除病毒性肝炎。最近,一种基于使用表达 HCV 非结构蛋白序列的病毒载体的 T 细胞疫苗未能预防药物使用者的慢性丙型肝炎,这表明诱导中和抗体(NAbs)将是未来疫苗候选物的关键。为了诱导 NAbs,疫苗必须包含这种抗体的主要靶标,即 HCV 包膜糖蛋白(E1 和 E2)。在这篇综述中,我们总结了 E1 和 E2 蛋白中被 NAbs 靶向的结构区域,以及这些蛋白在目前正在开发的疫苗候选物中的呈现方式。