Katzelnick Leah C, Montoya Magelda, Gresh Lionel, Balmaseda Angel, Harris Eva
Division of Infectious Diseases and Vaccinology, School of Public Health, University of California, Berkeley, CA 94720-3370; Centre for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, United Kingdom;
Centre for Pathogen Evolution, Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, United Kingdom;
Proc Natl Acad Sci U S A. 2016 Jan 19;113(3):728-33. doi: 10.1073/pnas.1522136113. Epub 2016 Jan 4.
The four dengue virus serotypes (DENV1-4) are mosquito-borne flaviviruses that infect ∼ 390 million people annually; up to 100 million infections are symptomatic, and 500,000 cases progress to severe disease. Exposure to a heterologous DENV serotype, the specific infecting DENV strains, and the interval of time between infections, as well as age, ethnicity, genetic polymorphisms, and comorbidities of the host, are all risk factors for severe dengue. In contrast, neutralizing antibodies (NAbs) are thought to provide long-lived protection against symptomatic infection and severe dengue. The objective of dengue vaccines is to provide balanced protection against all DENV serotypes simultaneously. However, the association between homotypic and heterotypic NAb titers and protection against symptomatic infection remains poorly understood. Here, we demonstrate that the titer of preinfection cross-reactive NAbs correlates with reduced likelihood of symptomatic secondary infection in a longitudinal pediatric dengue cohort in Nicaragua. The protective effect of NAb titers on infection outcome remained significant when controlled for age, number of years between infections, and epidemic force, as well as with relaxed or more stringent criteria for defining inapparent DENV infections. Further, individuals with higher NAb titers immediately after primary infection had delayed symptomatic infections compared with those with lower titers. However, overall NAb titers increased modestly in magnitude and remained serotype cross-reactive in the years between infections, possibly due to reexposure. These findings establish that anti-DENV NAb titers correlate with reduced probability of symptomatic DENV infection and provide insights into longitudinal characteristics of antibody-mediated immunity to DENV in an endemic setting.
四种登革病毒血清型(DENV1 - 4)是通过蚊子传播的黄病毒,每年感染约3.9亿人;其中多达1亿例感染出现症状,50万例发展为重症疾病。接触异源DENV血清型、特定感染的DENV毒株、感染之间的时间间隔,以及宿主的年龄、种族、基因多态性和合并症,都是重症登革热的危险因素。相比之下,中和抗体(NAbs)被认为可提供长期保护,防止出现症状性感染和重症登革热。登革热疫苗的目标是同时针对所有DENV血清型提供均衡保护。然而,同型和异型NAb滴度与预防症状性感染之间的关联仍知之甚少。在此,我们证明,在尼加拉瓜一个纵向儿科登革热队列中,感染前交叉反应性NAb的滴度与症状性二次感染可能性降低相关。在控制年龄、感染间隔年数、流行强度以及放宽或更严格定义隐性DENV感染的标准后,NAb滴度对感染结果的保护作用仍然显著。此外,与滴度较低的个体相比,初次感染后立即具有较高NAb滴度的个体出现症状性感染的时间延迟。然而,总体NAb滴度在感染间隔年数中适度升高,并且在这些年中仍保持血清型交叉反应性,这可能是由于再次接触所致。这些发现表明,抗DENV NAb滴度与症状性DENV感染概率降低相关,并为流行地区DENV抗体介导免疫的纵向特征提供了见解。