Cargando…
Improved Immune Responses Against Zika Virus After Sequential Dengue and Zika Virus Infection in Humans
The high levels of dengue-virus (DENV) seroprevalence in areas where the Zika virus (ZIKV) is circulating and the cross-reactivity between these two viruses have raised concerns on the risk of increased ZIKV disease severity for patients with a history of previous DENV infections. To determine the r...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164826/ https://www.ncbi.nlm.nih.gov/pubmed/30205518 http://dx.doi.org/10.3390/v10090480 |
_version_ | 1783359692639043584 |
---|---|
author | Delgado, Félix G. Torres, Karina I. Castellanos, Jaime E. Romero-Sánchez, Consuelo Simon-Lorière, Etienne Sakuntabhai, Anavaj Roth, Claude |
author_facet | Delgado, Félix G. Torres, Karina I. Castellanos, Jaime E. Romero-Sánchez, Consuelo Simon-Lorière, Etienne Sakuntabhai, Anavaj Roth, Claude |
author_sort | Delgado, Félix G. |
collection | PubMed |
description | The high levels of dengue-virus (DENV) seroprevalence in areas where the Zika virus (ZIKV) is circulating and the cross-reactivity between these two viruses have raised concerns on the risk of increased ZIKV disease severity for patients with a history of previous DENV infections. To determine the role of DENV preimmunity in ZIKV infection, we analyzed the T- and B-cell responses against ZIKV in donors with or without previous DENV infection. Using peripheral blood mononuclear cells (PBMCs) from donors living in an endemic area in Colombia, we have identified, by interferon (IFN)-γ enzyme-linked immunospot (ELISPOT) assay, most of the immunodominant ZIKV T-cell epitopes in the nonstructural (NS) proteins NS1, NS3, and NS5. Analyses of the T- and B-cell responses in the same donors revealed a stronger T-cell response against peptides conserved between DENV and ZIKV, with a higher level of ZIKV-neutralizing antibodies in DENV-immune donors in comparison with DENV-naïve donors. Strikingly, the potential for antibody-mediated enhancement of ZIKV infection was reduced in donors with sequential DENV and ZIKV infection in comparison with donors with DENV infection only. Altogether, these data suggest that individuals with DENV immunity present improved immune responses against ZIKV. |
format | Online Article Text |
id | pubmed-6164826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61648262018-10-11 Improved Immune Responses Against Zika Virus After Sequential Dengue and Zika Virus Infection in Humans Delgado, Félix G. Torres, Karina I. Castellanos, Jaime E. Romero-Sánchez, Consuelo Simon-Lorière, Etienne Sakuntabhai, Anavaj Roth, Claude Viruses Article The high levels of dengue-virus (DENV) seroprevalence in areas where the Zika virus (ZIKV) is circulating and the cross-reactivity between these two viruses have raised concerns on the risk of increased ZIKV disease severity for patients with a history of previous DENV infections. To determine the role of DENV preimmunity in ZIKV infection, we analyzed the T- and B-cell responses against ZIKV in donors with or without previous DENV infection. Using peripheral blood mononuclear cells (PBMCs) from donors living in an endemic area in Colombia, we have identified, by interferon (IFN)-γ enzyme-linked immunospot (ELISPOT) assay, most of the immunodominant ZIKV T-cell epitopes in the nonstructural (NS) proteins NS1, NS3, and NS5. Analyses of the T- and B-cell responses in the same donors revealed a stronger T-cell response against peptides conserved between DENV and ZIKV, with a higher level of ZIKV-neutralizing antibodies in DENV-immune donors in comparison with DENV-naïve donors. Strikingly, the potential for antibody-mediated enhancement of ZIKV infection was reduced in donors with sequential DENV and ZIKV infection in comparison with donors with DENV infection only. Altogether, these data suggest that individuals with DENV immunity present improved immune responses against ZIKV. MDPI 2018-09-07 /pmc/articles/PMC6164826/ /pubmed/30205518 http://dx.doi.org/10.3390/v10090480 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Delgado, Félix G. Torres, Karina I. Castellanos, Jaime E. Romero-Sánchez, Consuelo Simon-Lorière, Etienne Sakuntabhai, Anavaj Roth, Claude Improved Immune Responses Against Zika Virus After Sequential Dengue and Zika Virus Infection in Humans |
title | Improved Immune Responses Against Zika Virus After Sequential Dengue and Zika Virus Infection in Humans |
title_full | Improved Immune Responses Against Zika Virus After Sequential Dengue and Zika Virus Infection in Humans |
title_fullStr | Improved Immune Responses Against Zika Virus After Sequential Dengue and Zika Virus Infection in Humans |
title_full_unstemmed | Improved Immune Responses Against Zika Virus After Sequential Dengue and Zika Virus Infection in Humans |
title_short | Improved Immune Responses Against Zika Virus After Sequential Dengue and Zika Virus Infection in Humans |
title_sort | improved immune responses against zika virus after sequential dengue and zika virus infection in humans |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6164826/ https://www.ncbi.nlm.nih.gov/pubmed/30205518 http://dx.doi.org/10.3390/v10090480 |
work_keys_str_mv | AT delgadofelixg improvedimmuneresponsesagainstzikavirusaftersequentialdengueandzikavirusinfectioninhumans AT torreskarinai improvedimmuneresponsesagainstzikavirusaftersequentialdengueandzikavirusinfectioninhumans AT castellanosjaimee improvedimmuneresponsesagainstzikavirusaftersequentialdengueandzikavirusinfectioninhumans AT romerosanchezconsuelo improvedimmuneresponsesagainstzikavirusaftersequentialdengueandzikavirusinfectioninhumans AT simonloriereetienne improvedimmuneresponsesagainstzikavirusaftersequentialdengueandzikavirusinfectioninhumans AT sakuntabhaianavaj improvedimmuneresponsesagainstzikavirusaftersequentialdengueandzikavirusinfectioninhumans AT rothclaude improvedimmuneresponsesagainstzikavirusaftersequentialdengueandzikavirusinfectioninhumans |