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Human antibody responses after dengue virus infection are highly cross-reactive to Zika virus

  • Lalita Priyamvada
  • , Kendra M. Quicke
  • , William H. Hudson
  • , Nattawat Onlamoon
  • , Jaturong Sewatanon
  • , Srilatha Edupuganti
  • , Kovit Pattanapanyasat
  • , Kulkanya Chokephaibulkit
  • , Mark J. Mulligan
  • , Patrick C. Wilson
  • , Rafi Ahmed
  • , Mehul S. Suthar
  • , Jens Wrammert
  • Emory University School of Medicine
  • Siriraj Hospital
  • MC 1035

Research output: Contribution to journalArticlepeer-review

493 Citations (Scopus)

Abstract

Zika virus (ZIKV) is an emerging mosquito-borne flavivirus of significant public health concern. ZIKV shares a high degree of sequence and structural homology compared with other flaviviruses, including dengue virus (DENV), resulting in immunological cross-reactivity. Improving our current understanding of the extent and characteristics of this immunological cross-reactivity is important, as ZIKV is presently circulating in areas that are highly endemic for dengue. To assess the magnitude and functional quality of cross-reactive immune responses between these closely related viruses, we tested acute and convalescent sera from nine Thai patients with PCR-confirmed DENV infection against ZIKV. All of the sera tested were cross-reactive with ZIKV, both in binding and in neutralization. To deconstruct the observed serum cross-reactivity in depth, we also characterized a panel of DENV-specific plasmablast-derived monoclonal antibodies (mAbs) for activity against ZIKV. Nearly half of the 47 DENV-reactive mAbs studied bound to both whole ZIKV virion and ZIKV lysate, of which a subset also neutralized ZIKV. In addition, both sera and mAbs from the dengue-infected patients enhanced ZIKV infection of Fc gamma receptor (FcγR)-bearing cells in vitro. Taken together, these findings suggest that preexisting immunity to DENV may impact protective immune responses against ZIKV. In addition, the extensive cross-reactivity may have implications for ZIKV virulence and disease severity in DENV-experienced populations.

Original languageEnglish
Pages (from-to)7852-7857
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume113
Issue number28
DOIs
Publication statusPublished - 12 Jul 2016

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Antibodies
  • B-cell responses
  • Cross-reactivity
  • Zika virus

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