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Maternally Acquired Zika Antibodies Enhance Dengue Disease Severity in Mice.
Fowler, Angela M; Tang, William W; Young, Matthew P; Mamidi, Anila; Viramontes, Karla M; McCauley, Melanie D; Carlin, Aaron F; Schooley, Robert T; Swanstrom, Jesica; Baric, Ralph S; Govero, Jennifer; Diamond, Michael S; Shresta, Sujan.
Afiliação
  • Fowler AM; Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
  • Tang WW; Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
  • Young MP; Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
  • Mamidi A; Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
  • Viramontes KM; Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
  • McCauley MD; Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.
  • Carlin AF; Department of Medicine, University of California San Diego, La Jolla, CA 92093, USA.
  • Schooley RT; Department of Medicine, University of California San Diego, La Jolla, CA 92093, USA.
  • Swanstrom J; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Baric RS; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Govero J; Departments of Medicine, Molecular Microbiology, Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Diamond MS; Departments of Medicine, Molecular Microbiology, Pathology & Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Shresta S; Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA; Department of Medicine, University of California San Diego, La Jolla, CA 92093, USA. Electronic address: sujan@lji.org.
Cell Host Microbe ; 24(5): 743-750.e5, 2018 11 14.
Article em En | MEDLINE | ID: mdl-30439343
ABSTRACT
Antibody (Ab)-dependent enhancement can exacerbate dengue virus (DENV) infection due to cross-reactive Abs from an initial DENV infection, facilitating replication of a second DENV. Zika virus (ZIKV) emerged in DENV-endemic areas, raising questions about whether existing immunity could affect these related flaviviruses. We show that mice born with circulating maternal Abs against ZIKV develop severe disease upon DENV infection. Compared with pups of naive mothers, those born to ZIKV-immune mice lacking type I interferon receptor in myeloid cells (LysMCre+Ifnar1fl/fl) exhibit heightened disease and viremia upon DENV infection. Passive transfer of IgG isolated from mice born to ZIKV-immune mothers resulted in increased viremia in naive recipient mice. Treatment with Abs blocking inflammatory cytokine tumor necrosis factor linked to DENV disease or Abs blocking DENV entry improved survival of DENV-infected mice born to ZIKV-immune mothers. Thus, the maternal Ab response to ZIKV infection or vaccination might predispose to severe dengue disease in infants.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticorpos Facilitadores / Dengue / Vírus da Dengue / Zika virus / Infecção por Zika virus / Anticorpos Antivirais Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Anticorpos Facilitadores / Dengue / Vírus da Dengue / Zika virus / Infecção por Zika virus / Anticorpos Antivirais Tipo de estudo: Prognostic_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article