Department of Environmental Medicine, Poznan University of Medical Sciences, Poznań, Poland.
Universal Scientific Education and Research Network (USERN).
J Med Virol. 2024 Sep;96(9):e29900. doi: 10.1002/jmv.29900.
Despite remarkable progress in the treatment of hepatitis C virus (HCV) infection, it remains a significant global health burden, necessitating the development of an effective prophylactic vaccine. This review paper presents the current landscape of HCV vaccine candidates and approaches, including more traditional, based on inactivated virus, and more modern, such as subunit protein, vectored, based on nucleic acids (DNA and mRNA) and virus-like particles. The concept of the HCV vaccine is first put in the context of viral genetic diversity and adaptive responses to HCV infection, an understanding of which is crucial in guiding the development of an effective vaccine against such a complex virus. Because ethical dimensions are also significant in vaccine research, development, and potential deployment, we also address them in this paper. The road to a safe and effective vaccine to prevent HCV infection remains bumpy due to the genetic variation of HCV and its ability to evade immune responses. The progress in cell-culture systems allowed for the production of an inactivated HCV vaccine candidate, which can induce cross-neutralizing antibodies in vitro, but whether this could prevent infection in humans is unknown. Subunit protein vaccine candidates that entered clinical trials elicited HCV-specific humoral and cellular responses, though it remains to be shown whether they translate into effective prevention of HCV infection or progression of infection to a chronic state. Such responses were also induced by a clinically tested vector-based vaccine candidate, which decreased the viral HCV load but did not prevent chronic HCV infection. These disappointments were not readily predicted from preclinical animal studies. The vaccine platforms employing virus-like particles, DNA, and mRNA provide opportunities for the HCV vaccine, but their potential in this context has yet to be shown. Ensuring the designed vaccine is based on conserved epitope(s) and elicits broadly neutralizing immune responses is also essential. Given failures in developing a prophylactic HCV vaccine, it is crucial to continue supporting national strategies, including funding for screening and treatment programs. However, these actions are likely insufficient to permanently control the HCV burden, encouraging further mobilization of significant resources for HCV vaccine research as a missing element in the elimination of viral hepatitis as a global public health.
尽管丙型肝炎病毒 (HCV) 感染的治疗取得了显著进展,但它仍是一个重大的全球健康负担,需要开发有效的预防性疫苗。本文综述了 HCV 疫苗候选物和方法,包括更传统的基于灭活病毒的疫苗,以及更现代的基于亚单位蛋白、载体、核酸 (DNA 和 mRNA) 和病毒样颗粒的疫苗。首先,本文将 HCV 疫苗的概念置于 HCV 遗传多样性和对 HCV 感染的适应性反应的背景下,这对于指导针对如此复杂病毒的有效疫苗的开发至关重要。由于疫苗研究、开发和潜在部署中还存在伦理维度,我们也在本文中讨论了这些问题。由于 HCV 的遗传变异性及其逃避免疫反应的能力,预防 HCV 感染的安全有效的疫苗的研发道路仍然崎岖不平。细胞培养系统的进步允许生产灭活的 HCV 疫苗候选物,该候选物可在体外诱导交叉中和抗体,但尚不清楚这是否能预防人体感染。进入临床试验的亚单位蛋白疫苗候选物可诱导 HCV 特异性体液和细胞反应,但仍有待证明它们是否能有效预防 HCV 感染或感染进展为慢性状态。一种经过临床测试的基于载体的疫苗候选物也诱导了这种反应,该候选物降低了 HCV 的病毒载量,但不能预防慢性 HCV 感染。这些失望的结果并没有从临床前动物研究中轻易预测到。使用病毒样颗粒、DNA 和 mRNA 的疫苗平台为 HCV 疫苗提供了机会,但它们在这方面的潜力尚未得到证明。确保设计的疫苗基于保守表位并诱导广泛中和的免疫反应也是至关重要的。鉴于预防性 HCV 疫苗的开发失败,继续支持国家战略,包括为筛查和治疗计划提供资金至关重要。然而,这些行动可能不足以永久控制 HCV 负担,鼓励进一步调动大量资源用于 HCV 疫苗研究,作为消除全球公共卫生中病毒性肝炎的缺失环节。