Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3)

Detalhes bibliográficos
Autor(a) principal: Silva, Andréa N. M. Rangel da
Data de Publicação: 2009
Outros Autores: Nascimento, Eduardo J. M., Cordeiro, Marli Tenório, Gil, Laura H. V. G., Abath, Frederico Guilherme Coutinho, Montenegro, Silvia M. L., Marques, Ernesto T. A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da FIOCRUZ (ARCA)
Texto Completo: https://www.arca.fiocruz.br/handle/icict/27190
Resumo: O trabalho contou com o apoio do Ministério da Saúde, do programa FIOCRUZ-PDTIS RVR 09, do Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) e do Instituto Nacional de Saúde dos Estados Unidos (NIH) concedidos no U19 AI05641. A SML Montenegro é beneficiária de bolsas do CNPq. Os financiadores não tiveram nenhum papel no desenho do estudo, coleta e análise de dados, decisão de publicar ou preparação do manuscrito. Uma patente (PI0704650-2) foi solicitada para os epítopos apresentados neste manuscrito.
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spelling Silva, Andréa N. M. Rangel daNascimento, Eduardo J. M.Cordeiro, Marli TenórioGil, Laura H. V. G.Abath, Frederico Guilherme CoutinhoMontenegro, Silvia M. L.Marques, Ernesto T. A.2018-06-29T13:38:41Z2018-06-29T13:38:41Z2009SILVA, A. N. M. R. da et al. Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3). PloS One, v. 4, n. 10, p. 1-9, 13 Oct. 2009.1932-6203https://www.arca.fiocruz.br/handle/icict/2719010.1371/journal.pone.0007425O trabalho contou com o apoio do Ministério da Saúde, do programa FIOCRUZ-PDTIS RVR 09, do Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) e do Instituto Nacional de Saúde dos Estados Unidos (NIH) concedidos no U19 AI05641. A SML Montenegro é beneficiária de bolsas do CNPq. Os financiadores não tiveram nenhum papel no desenho do estudo, coleta e análise de dados, decisão de publicar ou preparação do manuscrito. Uma patente (PI0704650-2) foi solicitada para os epítopos apresentados neste manuscrito.Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Laboratório de Virologia e Terapia Experimental. Recife, PE, Brasil.The Johns Hopkins School of Medicine. Division of Infectious Diseases. Department of Medicine. Baltimore, Maryland, United States of America.Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Laboratório de Virologia e Terapia Experimental. Recife, PE, Brasil / Secretaria de Saúde do Estado de Pernambuco. Central Laboratory of Public Health. Recife, PE, Brasil.Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Departamento de Imunologia. Recife, PE, Brasil.Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Departamento de Imunologia. Recife, PE, Brasil.Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Departamento de Imunologia. Recife, PE, Brasil.Fundação Oswaldo Cruz. Instituto Aggeu Magalhães. Laboratório de Virologia e Terapia Experimental. Recife, PE, Brasil / The Johns Hopkins School of Medicine. Division of Infectious Diseases. Department of Medicine. Baltimore, Maryland, United States of America / The Johns Hopkins School of Medicine. Department of Pharmacology and Molecular Sciences. Baltimore, Maryland, United States of America.Background: Dengue virus infection is a growing global public health concern in tropical and subtropical regions of the world. Dengue vaccine development has been hampered by concerns that cross-reactive immunological memory elicited by a candidate vaccine could increase the risk of development of more severe clinical forms. One possible strategy to reduce risks associated with a dengue vaccine is the development of a vaccine composed of selected critical epitopes of each of the serotypes. Methodology/Principal Findings: Synthetic peptides were used to identify B-cell epitopes in the envelope (E) glycoprotein of dengue virus type 3 (DENV-3). Eleven linear, immunodominant epitopes distributed in five regions at amino acid (aa) positions: 51–65, 71–90, 131–170, 196–210 and 246–260 were identified by employing an enzyme- linked immunosorbent assay (ELISA), using a pool of human sera from dengue type 3 infected individuals. Peptides 11 (aa51–65), 27 and 28 (aa131–150) also reacted with dengue 1 (DENV-1) and dengue 2 (DENV-2) patient sera as analyzed through the ROC curves generated for each peptide by ELISA and might have serotype specific diagnostic potential. Mice immunized against each one of the five immunogenic regions showed epitopes 51–65, 131–170, 196–210 and 246–260 elicited the highest antibody response and epitopes131–170, 196–210 and 246–260, elicited IFN-c production and T CD4+ cell response, as evaluated by ELISA and ELISPOT assays respectively. Conclusions/Significance: Our study identified several useful immunodominant IgG-specific epitopes on the envelope of DENV-3. They are important tools for understanding the mechanisms involved in antibody dependent enhancement and immunity. 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dc.title.pt_BR.fl_str_mv Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3)
title Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3)
spellingShingle Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3)
Silva, Andréa N. M. Rangel da
Dengue
Vacina
Infecção
Animais
Dengue / imunologia
Dengue / virologia
Vacinas contra Dengue
Vírus da Dengue / química
Ensaio de Imunoadsorção Enzimática
Epítopos / química
Epítopos do Linfócito B / Química
Humanos
Imunoglobulina G / química
Memória imunológica
Ratos
Ratos, endogâmicos BALB C
Conformação Molecular
Curva ROC
Proteínas de envelope viral / química
title_short Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3)
title_full Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3)
title_fullStr Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3)
title_full_unstemmed Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3)
title_sort Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3)
author Silva, Andréa N. M. Rangel da
author_facet Silva, Andréa N. M. Rangel da
Nascimento, Eduardo J. M.
Cordeiro, Marli Tenório
Gil, Laura H. V. G.
Abath, Frederico Guilherme Coutinho
Montenegro, Silvia M. L.
Marques, Ernesto T. A.
author_role author
author2 Nascimento, Eduardo J. M.
Cordeiro, Marli Tenório
Gil, Laura H. V. G.
Abath, Frederico Guilherme Coutinho
Montenegro, Silvia M. L.
Marques, Ernesto T. A.
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Silva, Andréa N. M. Rangel da
Nascimento, Eduardo J. M.
Cordeiro, Marli Tenório
Gil, Laura H. V. G.
Abath, Frederico Guilherme Coutinho
Montenegro, Silvia M. L.
Marques, Ernesto T. A.
dc.subject.other.pt_BR.fl_str_mv Dengue
Vacina
Infecção
topic Dengue
Vacina
Infecção
Animais
Dengue / imunologia
Dengue / virologia
Vacinas contra Dengue
Vírus da Dengue / química
Ensaio de Imunoadsorção Enzimática
Epítopos / química
Epítopos do Linfócito B / Química
Humanos
Imunoglobulina G / química
Memória imunológica
Ratos
Ratos, endogâmicos BALB C
Conformação Molecular
Curva ROC
Proteínas de envelope viral / química
dc.subject.decs.pt_BR.fl_str_mv Animais
Dengue / imunologia
Dengue / virologia
Vacinas contra Dengue
Vírus da Dengue / química
Ensaio de Imunoadsorção Enzimática
Epítopos / química
Epítopos do Linfócito B / Química
Humanos
Imunoglobulina G / química
Memória imunológica
Ratos
Ratos, endogâmicos BALB C
Conformação Molecular
Curva ROC
Proteínas de envelope viral / química
description O trabalho contou com o apoio do Ministério da Saúde, do programa FIOCRUZ-PDTIS RVR 09, do Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) e do Instituto Nacional de Saúde dos Estados Unidos (NIH) concedidos no U19 AI05641. A SML Montenegro é beneficiária de bolsas do CNPq. Os financiadores não tiveram nenhum papel no desenho do estudo, coleta e análise de dados, decisão de publicar ou preparação do manuscrito. Uma patente (PI0704650-2) foi solicitada para os epítopos apresentados neste manuscrito.
publishDate 2009
dc.date.issued.fl_str_mv 2009
dc.date.accessioned.fl_str_mv 2018-06-29T13:38:41Z
dc.date.available.fl_str_mv 2018-06-29T13:38:41Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv SILVA, A. N. M. R. da et al. Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3). PloS One, v. 4, n. 10, p. 1-9, 13 Oct. 2009.
dc.identifier.uri.fl_str_mv https://www.arca.fiocruz.br/handle/icict/27190
dc.identifier.issn.pt_BR.fl_str_mv 1932-6203
dc.identifier.doi.none.fl_str_mv 10.1371/journal.pone.0007425
identifier_str_mv SILVA, A. N. M. R. da et al. Identification of continuous human B-cell epitopes in the envelope glycoprotein of dengue virus type 3 (DENV-3). PloS One, v. 4, n. 10, p. 1-9, 13 Oct. 2009.
1932-6203
10.1371/journal.pone.0007425
url https://www.arca.fiocruz.br/handle/icict/27190
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