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Human antibody responses after dengue virus infection are highly cross-reactive to Zika virus.
Priyamvada, Lalita; Quicke, Kendra M; Hudson, William H; Onlamoon, Nattawat; Sewatanon, Jaturong; Edupuganti, Srilatha; Pattanapanyasat, Kovit; Chokephaibulkit, Kulkanya; Mulligan, Mark J; Wilson, Patrick C; Ahmed, Rafi; Suthar, Mehul S; Wrammert, Jens.
Afiliação
  • Priyamvada L; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322; Division of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322;
  • Quicke KM; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322; Division of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322;
  • Hudson WH; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322; Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322;
  • Onlamoon N; Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand;
  • Sewatanon J; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322; Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322; Department of Microbiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand;
  • Edupuganti S; The Hope Clinic of the Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322; Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, GA 30322;
  • Pattanapanyasat K; Department of Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand;
  • Chokephaibulkit K; Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand;
  • Mulligan MJ; The Hope Clinic of the Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322; Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, GA 30322;
  • Wilson PC; Section of Rheumatology, The Knapp Center for Lupus and Immunology Research, Department of Medicine, University of Chicago, Chicago, IL 60637.
  • Ahmed R; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322; Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322; jwramme@emory.edu rahmed@emory.edu.
  • Suthar MS; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322; Division of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322;
  • Wrammert J; Emory Vaccine Center, Emory University School of Medicine, Atlanta, GA 30322; Division of Infectious Disease, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322; jwramme@emory.edu rahmed@emory.edu.
Proc Natl Acad Sci U S A ; 113(28): 7852-7, 2016 07 12.
Article em En | MEDLINE | ID: mdl-27354515
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dengue / Vírus da Dengue / Zika virus / Formação de Anticorpos Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dengue / Vírus da Dengue / Zika virus / Formação de Anticorpos Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article