Afucosylation of anti-dengue IgG is associated with enhanced susceptibility to dengue virus infection postvaccination

登革热病毒 登革热 接种疫苗 免疫学 病毒学 抗体 免疫球蛋白G 病毒 抗体依赖性增强 登革热疫苗 岩藻糖基化 医学 生物 糖蛋白 分子生物学 聚糖
作者
Usama Ashraf,Saborni Chakraborty,Courtney Scallan,Nathan C. Lo,Maria Theresa Alera,Aaron Farmer,Mary Noreen Cabalfin-Chua,Nelson L. Michael,Alan L. Rothman,Taia T. Wang
出处
期刊:Science Translational Medicine [American Association for the Advancement of Science]
卷期号:17 (817): eadx7231-eadx7231
标识
DOI:10.1126/scitranslmed.adx7231
摘要

Dengue viruses (DENVs) cause 390 million infections annually, although only ~25% of these infections are symptomatic. Whereas antibody features linked to severe DENV disease are well studied, factors influencing infection susceptibility remain less clear. Here, we examined immunoglobulin G (IgG) characteristics before and after DENV vaccination (Dengvaxia) in individuals with a history of prior DENV exposure, comparing those who developed postvaccination infections to those who remained infection free. Elevated anti-DENV afucosylation, present before or after vaccination, was associated with increased likelihood of infection after vaccination. These data were further supported by mechanistic studies, which revealed that nonneutralizing, afucosylated, post-Dengvaxia IgG enhanced DENV replication in mice. This enhancement was dependent on CD16, the receptor for the afucosylated IgG Fc domain. Together, these findings support a model in which the presence of afucosylated IgG promotes virus replication, increasing the likelihood of productive infection upon DENV exposure. Moreover, these results highlight that IgG1 fucosylation is a predictor of risk for breakthrough DENV infection despite vaccination and support the importance of investigating strategies to regulate Fc fucosylation during vaccination.
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