Center for Tropical Medicine and Infectious Disease, Kaohsiung Medical University, Kaohsiung 80708, Taiwan; Division of Infectious Disease, Department of Internal Medicine, Kaohsiung Medical, University Hospital, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Center for Tropical Medicine and Infectious Disease, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Biomed Pharmacother. 2021 Dec;144:112304. doi: 10.1016/j.biopha.2021.112304. Epub 2021 Oct 8.
Dengue virus (DENV) is a global health threat causing about half of the worldwide population to be at risk of infection, especially the people living in tropical and subtropical area. Although the dengue disease caused by dengue virus (DENV) is asymptomatic and self-limiting in most people with first infection, increased severe dengue symptoms may be observed in people with heterotypic secondary DENV infection. Since there is a lack of specific antiviral medication, the development of dengue vaccines is critical in the prevention and control this disease. Several targets and strategies in the development of dengue vaccine have been demonstrated. Currently, Dengvaxia, a live-attenuated chimeric yellow-fever/tetravalent dengue vaccine (CYD-TDV) developed by Sanofi Pasteur, has been licensed and approved for clinical use in some countries. However, this vaccine has demonstrated low efficacy in children and dengue-naïve individuals and also increases the risk of severe dengue in young vaccinated recipients. Accordingly, many novel strategies for the dengue vaccine are under investigation and development. Here, we conducted a systemic literature review according to PRISMA guidelines to give a concise overview of various aspects of the vaccine development process against DENVs, mainly targeting five potential strategies including live attenuated vaccine, inactivated virus vaccine, recombinant subunit vaccine, viral-vector vaccine, and DNA vaccine. This study offers the comprehensive view of updated information and current progression of immunogen selection as well as strategies of vaccine development against DENVs.
登革病毒(DENV)是一种全球健康威胁,使全球约一半的人口面临感染风险,特别是生活在热带和亚热带地区的人群。尽管由登革病毒(DENV)引起的登革热疾病在大多数初次感染的人身上是无症状和自限性的,但在具有异型二次 DENV 感染的人中可能会观察到更严重的登革热症状。由于缺乏特异性抗病毒药物,因此开发登革热疫苗对于预防和控制这种疾病至关重要。已经证明了登革热疫苗开发中的几个目标和策略。目前,赛诺菲巴斯德公司开发的减毒嵌合黄热病/四价登革热疫苗(CYD-TDV)Dengvaxia 已在一些国家获得许可和批准用于临床使用。然而,该疫苗在儿童和无登革热病史的人群中的疗效较低,并且会增加年轻接种者患重症登革热的风险。因此,许多新的登革热疫苗策略正在研究和开发中。在这里,我们根据 PRISMA 指南进行了系统的文献回顾,简要概述了针对 DENVs 的疫苗开发过程的各个方面,主要针对五种潜在策略,包括减毒活疫苗、灭活病毒疫苗、重组亚单位疫苗、病毒载体疫苗和 DNA 疫苗。本研究提供了针对 DENVs 的免疫原选择和疫苗开发策略的最新信息和当前进展的综合观点。