Mpingabo Patrick I, Ylade Michelle, Aogo Rosemary A, Crisostomo Maria Vinna, Thiono Devina J, Daag Jedas Veronica, Agrupis Kristal-An, Escoto Ana Coello, Raimundi-Rodriguez Guillermo L, Odio Camila D, Fernandez Maria Abad, White Laura, de Silva Aravinda M, Deen Jacqueline, Katzelnick Leah C
Viral Epidemiology and Immunity Unit, Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892-3203, USA.
Institute of Child Health and Human Development, National Institutes of Health, University of the Philippines-Manila, Ermita, 1000 Manila, Philippines.
Sci Transl Med. 2025 Jul 23;17(808):eadq0571. doi: 10.1126/scitranslmed.adq0571.
Cross-reactive antibodies to epitopes that span envelope proteins on the virion surface are hypothesized to protect against dengue virus (DENV) infection and disease. Here, we measured antibodies targeting a quaternary epitope called the envelope dimer epitope (EDE) as well as neutralizing and binding antibodies and evaluated their association with DENV infection, vaccine response, and disease outcome in dengue-vaccinated ( = 164) and dengue-unvaccinated children ( = 88) within a longitudinal cohort in Cebu, Philippines ( = 2996). Antibodies targeting EDE were prevalent and associated with broad neutralization of mature DENV1 to DENV4 virions in those with evidence of at least two prior DENV infections but were mostly absent in those with only one prior infection. Subsequent infection and vaccination boosted titers of EDE-like antibodies, neutralizing antibodies, and DENV-binding antibodies. EDE-like antibodies were associated with reduced risk of symptomatic dengue and more severe dengue and statistically explained the protective effect of binding and neutralizing antibodies on dengue. Thus, antibodies targeting quaternary epitopes help explain the broad cross-protection observed in those with multiple prior DENV exposures, making them useful for evaluation and development of future vaccines and therapeutics.
据推测,针对病毒粒子表面包膜蛋白上的表位的交叉反应性抗体可预防登革热病毒(DENV)感染和疾病。在此,我们检测了靶向一种称为包膜二聚体表位(EDE)的四级表位的抗体以及中和抗体和结合抗体,并在菲律宾宿务的一个纵向队列(n = 2996)中评估了它们与登革热疫苗接种儿童(n = 164)和未接种登革热疫苗儿童(n = 88)的DENV感染、疫苗反应及疾病结局之间的关联。靶向EDE的抗体普遍存在,在那些有至少两次既往DENV感染证据的个体中,与成熟DENV1至DENV4病毒粒子的广泛中和相关,但在仅有一次既往感染的个体中大多不存在。后续感染和疫苗接种提高了EDE样抗体、中和抗体和DENV结合抗体的滴度。EDE样抗体与有症状登革热和更严重登革热的风险降低相关,并且在统计学上解释了结合抗体和中和抗体对登革热的保护作用。因此,靶向四级表位的抗体有助于解释在有多次既往DENV暴露的个体中观察到的广泛交叉保护现象,使其对未来疫苗和治疗方法的评估与开发具有重要意义。