Bankwitz Dorothea, Krey Thomas, Pietschmann Thomas
Twincore Zentrum für Experimentelle und Klinische Infektionsforschung, Institut für Experimentelle Virologie, Feodor-Lynen-Str. 7, 30625, Hannover, Deutschland.
Medizinische Hochschule Hannover, RESIST Exzellenzcluster EXC2155, Hannover, Deutschland.
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2022 Feb;65(2):183-191. doi: 10.1007/s00103-021-03477-9. Epub 2022 Jan 11.
The incidence of hepatitis C virus (HCV) infections remains high even more than 10 years after approval of the first direct-acting antivirals for treatment of hepatitis C. In some countries, more people are newly infected with the virus than patients cured by antiviral therapy. The development of a prophylactic vaccine could prevent virus transmission and thereby make a significant contribution to control the global burden of this disease. In this article, we review the unique challenges and current approaches to HCV vaccine development.HCV is a highly diverse and versatile virus that mostly escapes the immune system and establishes chronic infections. However, up to one third of the exposed individuals can spontaneously resolve HCV infections, which indicates that protective immunity can be achieved. Numerous studies on determinants of protective immunity against HCV show an increasingly complete picture of what a vaccine must achieve. It is very likely that both strong neutralizing antibodies and powerful cytotoxic T cells are needed to reliably protect against chronic HCV infection. The key question is which approaches allow maturation of particularly broadly effective antibodies and T cells. This will be necessary to protect against the high number of different HCV variants. The recent successes of mRNA vaccines open new doors for HCV vaccine research and development. Combined with a deeper understanding of the structure and function of the viral envelope proteins, the identification of cross-protective antibody and T‑cell epitopes as well as the use of standardized methods to quantify the effectiveness of vaccine candidates, new perspectives arise for the development of a vaccine.
即使在首批用于治疗丙型肝炎的直接抗病毒药物获批10多年后,丙型肝炎病毒(HCV)感染的发生率仍然很高。在一些国家,新感染该病毒的人数超过了通过抗病毒治疗治愈的患者人数。预防性疫苗的研发可以预防病毒传播,从而为控制这种疾病的全球负担做出重大贡献。在本文中,我们综述了HCV疫苗研发面临的独特挑战和当前方法。HCV是一种高度多样且适应性强的病毒,大多能逃避免疫系统并建立慢性感染。然而,高达三分之一的暴露个体能够自发清除HCV感染,这表明可以实现保护性免疫。关于针对HCV的保护性免疫决定因素的大量研究越来越全面地展现了疫苗必须达到的目标。很可能需要强大的中和抗体和有力的细胞毒性T细胞才能可靠地预防慢性HCV感染。关键问题是哪种方法能使特别广泛有效的抗体和T细胞成熟。这对于预防大量不同的HCV变体是必要的。mRNA疫苗最近的成功为HCV疫苗的研发打开了新的大门。结合对病毒包膜蛋白结构和功能的更深入理解、交叉保护性抗体和T细胞表位的鉴定以及使用标准化方法来量化候选疫苗的有效性,疫苗研发出现了新的前景。