Durable cellular immune response against inactivated ZIKV and envelope proteins in ZIKV-infected women during pregnancy

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dc.contributor(LMP) Lab. Multipropósitopt_BR
dc.contributor(LV) Lab. Virologiapt_BR
dc.contributor.authorApostolico, Juliana de Souzapt_BR
dc.contributor.authorLunardelli, Victória Alves Santospt_BR
dc.contributor.authorBoscardin, Silvia Beatrizpt_BR
dc.contributor.authorBotosso, Viviane Fongaropt_BR
dc.contributor.authorAstray, Renato Mancinipt_BR
dc.contributor.authorJorge Kalilpt_BR
dc.contributor.authorRoque Pacheco de Almeidapt_BR
dc.contributor.authorEdecio Cunha-Netopt_BR
dc.contributor.authorDaniela Santoro Rosapt_BR
dc.date.accessioned2024-06-21T17:52:31Z-
dc.date.available2024-06-21T17:52:31Z-
dc.date.issued2023pt_BR
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/5387-
dc.description.abstractIntroduction: Zika virus (ZIKV) infection has been associated to Guillain-Barré syndrome in adults and congenital malformations during pregnancy, leading to the manifestation of congenital Zika syndrome (CZS). The ZIKV envelope protein (EZIKV), prominently displayed on the virus surface, is a primary target for the humoral immune response. However, limited information exists regarding its capacity to induce cellular immunity, particularly in pregnant women with a history of ZIKV infection. The EZIKV protein comprises three domains: the central domain (EDI), a dimerization domain (EDII), and a domain responsible for binding to the cell surface receptor (EDIII). To examine the regions of EZIKV targeted by cellular immunity, we examined cellular immune responses in a cohort of mothers infected with ZIKV, whose infants exhibited microcephaly. Methods: To assess the ZIKV-specific response, we used inactivated virus and different recombinant viral envelope proteins (EZIKV, EDI/IIZIKV and EDIIIZIKV). All women in the study contracted the infection during pregnancy, with 72% experiencing symptoms such as fever, rash, joint pain, and retro-orbital pain. Peripheral blood mononuclear cells (PMBC) were collected post- ZIKV diagnosis confirmation, with a median time of 18 months (IQR 13.5-19) after parturition. Using the ELISpot assay, we quantified specific interferon-gamma (IFNγ) producing cells by stimulating PBMC with either inactivated ZIKV particles or equimolar amounts of recombinant EZIKV, EDI/IIZIKV and EDIIIZIKV. Results and discussion: Our findings demonstrate the induction of IFN-γ producing cells in PBMC from ZIKV-convalescent mothers, whose infants manifested microcephaly, upon stimulation with both inactivated ZIKV particles and recombinant proteins. The identification of immunodominant regions within ZIKV can contribute for the development of targeted treatments and vaccine candidates tailored for pregnant women.pt_BR
dc.description.sponsorship(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulopt_BR
dc.description.sponsorship(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológicopt_BR
dc.format.extent1369608pt_BR
dc.language.isoEnglishpt_BR
dc.relation.ispartofFrontiers in Tropical Diseasespt_BR
dc.rightsOpen accesspt_BR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_BR
dc.titleDurable cellular immune response against inactivated ZIKV and envelope proteins in ZIKV-infected women during pregnancypt_BR
dc.typeArticlept_BR
dc.rights.licenseCC BYpt_BR
dc.identifier.doi10.3389/fitd.2024.1369608pt_BR
dc.contributor.external(UNIFESP) Universidade Federal de São Paulopt_BR
dc.contributor.external(USP) Universidade de São Paulopt_BR
dc.contributor.external(III-INCT) Instituto Nacional de Ciências e Tecnologiapt_BR
dc.contributor.external(UFS) Universidade Federal de Sergipept_BR
dc.identifier.citationvolume5pt_BR
dc.subject.keywordZika viruspt_BR
dc.subject.keywordcellular immune responsept_BR
dc.subject.keywordT cellspt_BR
dc.subject.keywordpregnancypt_BR
dc.subject.keywordmicrocephalypt_BR
dc.relation.ispartofabbreviatedFront Trop Dispt_BR
dc.identifier.citationabntv. 5, 1369608, abr. 2024pt_BR
dc.identifier.citationvancouver2024 Apr; 5:1369608pt_BR
dc.contributor.butantanBotosso, Viviane Fongaro|:Pesquisador|:(LV) Lab. Virologiapt_BR
dc.contributor.butantanAstray, Renato Mancini|:Pesquisador|:(LMP) Lab. Multipropósitopt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2017-1741-7pt_BR
dc.sponsorship.butantan(FAPESP) Fundação de Amparo à Pesquisa do Estado de São Paulo¦¦2021/13004-0pt_BR
dc.sponsorship.butantan(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦440400/2016-3pt_BR
dc.sponsorship.butantan(CNPq) Conselho Nacional de Desenvolvimento Científico e Tecnológico¦¦465434/2014pt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
dc.description.dbindexedYespt_BR
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item.openairetypeArticle-
item.languageiso639-1English-
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