Publication

Impact of pre-existing dengue immunity on human antibody and memory B cell responses to Zika

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Last modified
  • 05/21/2025
Type of Material
Authors
    Paulina Andrade, University of California BerkeleyCiara Gimblet-Ochieng, University of North CarolinaFaraz Modirian, University of California BerkeleyMatthew Collins, Emory UniversityMaritza Cardenas, University of California BerkeleyLeah C. Katzelnick, University of California BerkeleyMagelda Montoya, University of California BerkeleyDaniela Michlmayr, University of California BerkeleyGuillermina Kuan, Ministry of HealthAngel Balmaseda, Sustainable Sciences InstituteJosefina Coloma, University of California BerkeleyAravinda M. de Silva, University of North CarolinaEva Harris, University of California Berkeley
Language
  • English
Date
  • 2019-02-26
Publisher
  • Nature Research (part of Springer Nature): Fully open access journals
Publication Version
Copyright Statement
  • © 2019, The Author(s).
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 2041-1723
Volume
  • 10
Issue
  • 1
Start Page
  • 938
End Page
  • 938
Grant/Funding Information
  • The Pediatric Dengue Cohort Study was also supported by the Pediatric Dengue Vaccine Initiative grant VE-1 (E.H.) from the Bill and Melinda Gates Foundation and by the FIRST grant (E.H. and J.C.) from the Bill and Melinda Gates Foundation and the Instituto Carlos Slim de la Salud.
  • This work was supported by grants P01AI106695 (EH), U19AI118610 (EH), and R01AI099631 (AB) from the National Institute of Allergy and Infectious Diseases (NIH).
Supplemental Material (URL)
Abstract
  • Little is known about enduring memory B cell (MBC) responses to Zika virus (ZIKV) and their relationship with circulating antibodies. Here we comprehensively assess MBC frequency and specificity alongside serum binding and neutralizing antibody responses to ZIKV ~2 weeks and ~8 months postinfection in 31 pediatric subjects with 0, 1 or >1 prior infections with the related dengue virus (DENV). ZIKV infection elicits a robust type-specific MBC response, and the majority of late convalescent anti-ZIKV serum neutralizing activity is attributable to ZIKV-specific antibodies. The number of prior DENV infections does not influence type-specific or cross-reactive MBC responses, although ZIKV has the highest cross-reactivity with DENV3. DENV cross-reactive MBCs expanded by ZIKV infection decline in number and proportion by late convalescence. Finally, ZIKV induces greater cross-reactivity in the MBC pool than in serum antibodies. Our data suggest immunity to DENV only modestly shapes breadth and magnitude of enduring ZIKV antibody responses.
Author Notes
Keywords
Research Categories
  • Biology, Microbiology
  • Biology, Virology
  • Health Sciences, Immunology

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