寨卡病毒
登革热
登革热病毒
病毒学
血清型
黄病毒
抗体依赖性增强
疾病
免疫学
生物
医学
病毒
内科学
作者
Leah C. Katzelnick,César Narvaez,Sonia Arguello,Brenda Lopez Mercado,Damaris Collado,Oscarlett Ampie,Douglas Elizondo,Tatiana Miranda,Fausto Andres Bustos Carrillo,Juan Carlos Mercado,Krista Latta,Amy Schiller,Bruno Segovia-Chumbez,Sergio Ojeda,Nery Sánchez,Miguel Plazaola,Joséfina Coloma,M. Elizabeth Halloran,Lakshmanane Premkumar,Aubree Gordon
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2020-08-28
卷期号:369 (6507): 1123-1128
被引量:213
标识
DOI:10.1126/science.abb6143
摘要
The Zika pandemic sparked intense interest in whether immune interactions among dengue virus serotypes 1 to 4 (DENV1 to -4) extend to the closely related Zika virus (ZIKV). We investigated prospective pediatric cohorts in Nicaragua that experienced sequential DENV1 to -3 (2004 to 2015), Zika (2016 to 2017), and DENV2 (2018 to 2020) epidemics. Risk of symptomatic DENV2 infection and severe disease was elevated by one prior ZIKV infection, one prior DENV infection, or one prior DENV infection followed by one ZIKV infection, compared with being flavivirus-naïve. By contrast, multiple prior DENV infections reduced dengue risk. Further, although high preexisting anti-DENV antibody titers protected against DENV1, DENV3, and ZIKV disease, intermediate titers induced by previous ZIKV or DENV infection enhanced future risk of DENV2 disease and severity, as well as DENV3 severity. The observation that prior ZIKV infection can modulate dengue disease severity like a DENV serotype poses challenges to development of dengue and Zika vaccines.
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