Is There Still Hope for the Prophylactic Hepatitis C Vaccine? a Review of Different Approaches Publisher Pubmed



Rzymski P^{1, 2} ; Jibril AT^{2, 3} ; Rahmah L^{2, 4, 5} ; Abarikwu SO^{2, 6} ; Hashem F^{2, 7} ; Lawati AA^{2, 8} ; Morrison FMM^{2, 9} ; Marquez LP^{2, 10} ; Mohamed K^{2, 7} ; Khan A^{2, 11, 12, 13} ; Mushtaq S^{2, 11, 12} ; Minakova K^{2, 14} ; Poniedzialek B¹ ; Zarebskamichaluk D¹⁵ Show All Authors Show Affiliations
Source: Journal of Medical Virology Published:2024

Abstract

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. © 2024 Wiley Periodicals LLC.