Tsai Wen-Yang, Lin Hong-En, Wang Wei-Kung
Department of Tropical Medicine, Medical Microbiology and Pharmacology, John A. Burns School of Medicine, University of Hawaii at ManoaHonolulu, HI, United States.
Front Microbiol. 2017 Jul 20;8:1372. doi: 10.3389/fmicb.2017.01372. eCollection 2017.
The four serotypes of dengue virus (DENV) are the leading cause of arboviral diseases in humans. Decades of efforts have made remarkable progress in dengue vaccine development. Despite the first dengue vaccine (dengvaxia from Sanofi Pasteur), a live-attenuated tetravalent chimeric yellow fever-dengue vaccine, has been licensed by several countries since 2016, its overall moderate efficacy (56.5-60.8%) in the presence of neutralizing antibodies during the Phase 2b and 3 trials, lower efficacy among dengue naïve compared with dengue experienced individuals, and increased risk of hospitalization among young children during the follow-up highlight the need for a better understanding of humoral responses after natural DENV infection. Recent studies of more than 300 human monoclonal antibodies (mAbs) against DENV have led to the discovery of several novel epitopes on the envelope protein recognized by potent neutralizing mAbs. This information together with in-depth studies on polyclonal sera and B-cells following natural DENV infection has tremendous implications for better immunogen design for a safe and effective dengue vaccine. This review outlines the progress in our understanding of mouse mAbs, human mAbs, and polyclonal sera against DENV envelope and precursor membrane proteins, two surface proteins involved in vaccine development, following natural infection; analyses of these discoveries have provided valuable insight into new strategies involving molecular technology to induce more potent neutralizing antibodies and less enhancing antibodies for next-generation dengue vaccine development.
登革病毒(DENV)的四种血清型是人类虫媒病毒疾病的主要病因。数十年来的努力在登革疫苗研发方面取得了显著进展。尽管自2016年以来,首款登革疫苗(赛诺菲巴斯德公司的登革四价活疫苗)已在多个国家获得许可,该疫苗是一种减毒活四价嵌合黄热病-登革疫苗,但其在2b期和3期试验中,在存在中和抗体的情况下总体疗效中等(56.5%-60.8%),与有登革热感染史的个体相比,初次感染登革热的个体中疗效较低,且在随访期间幼儿住院风险增加,这凸显了更好地了解自然感染DENV后的体液免疫反应的必要性。最近对300多种抗DENV人类单克隆抗体(mAb)的研究发现了包膜蛋白上几个新的表位,这些表位可被强效中和mAb识别。这些信息以及对自然感染DENV后的多克隆血清和B细胞的深入研究,对于设计安全有效的登革疫苗的更好免疫原具有重大意义。本综述概述了我们在了解自然感染后针对DENV包膜和前体膜蛋白(疫苗研发中涉及的两种表面蛋白)的小鼠mAb、人类mAb和多克隆血清方面取得的进展;对这些发现的分析为涉及分子技术的新策略提供了有价值的见解,这些策略可诱导产生更强效的中和抗体并减少增强性抗体,以用于下一代登革疫苗的研发。