Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected Patients

Detalhes bibliográficos
Autor(a) principal: Bernardes Terzian, Ana Carolina [UNESP]
Data de Publicação: 2017
Outros Autores: Schanoski, Alessandra Soares [UNESP], Oliveira Mota, Minh' Tasso de [UNESP], Silva, Rafael Alves da [UNESP], Estofolete, Cassia Fernanda [UNESP], Colombo, Tatiana Elias [UNESP], Rahal, Paula [UNESP], Hanley, Kathryn A., Vasilakis, Nikos, Kalil, Jorge, Nogueiral, Mauricio Lacerda [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1093/cid/cix558
http://hdl.handle.net/11449/163340
Resumo: Background. The pathogenesis of severe dengue disease involves immune components as biomarkers. The mechanism by which some dengue virus (DENV)-infected individuals progress to severe disease is poorly understood. Most studies on the pathogenesis of severe dengue disease focus on the process of antibody-dependent enhancement (ADE) as a primary risk factor. With the circulation of Zika virus (ZIKV) in DENV-endemic areas, many people infected by ZIKV were likely exposed to DENV. The influence of such exposure on Zika disease outcomes remains unknown. Methods. We investigated whether patients previously exposed to DENV exhibited higher viremia when exposed to a subsequent, heterologous dengue or Zika infection than those patients not previously exposed to dengue. We measured viral loads and cytokine profile during patients' acute infections. Results. Neither dengue nor Zika viremia was higher in patients with prior DENV infection, although the power to detect such a difference was only adequate in the ZIKV analysis. Of the 10 cytokines measured, only 1 significant difference was detected: Levels of interleukin 1 beta (IL-1 beta) were lower in dengue-infected patients who had experienced a previous dengue infection than patients infected with dengue for the first time. However, power to detect differences between groups was low. In Zika-infected patients, levels of IL-1 beta showed a significant, positive correlation with viral load. Conclusions. No signs of ADE were observed in vivo in patients with acute ZIKV infection who had prior exposure to DENV.
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spelling Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected PatientsZIKVDENVADEcytokinesBackground. The pathogenesis of severe dengue disease involves immune components as biomarkers. The mechanism by which some dengue virus (DENV)-infected individuals progress to severe disease is poorly understood. Most studies on the pathogenesis of severe dengue disease focus on the process of antibody-dependent enhancement (ADE) as a primary risk factor. With the circulation of Zika virus (ZIKV) in DENV-endemic areas, many people infected by ZIKV were likely exposed to DENV. The influence of such exposure on Zika disease outcomes remains unknown. Methods. We investigated whether patients previously exposed to DENV exhibited higher viremia when exposed to a subsequent, heterologous dengue or Zika infection than those patients not previously exposed to dengue. We measured viral loads and cytokine profile during patients' acute infections. Results. Neither dengue nor Zika viremia was higher in patients with prior DENV infection, although the power to detect such a difference was only adequate in the ZIKV analysis. Of the 10 cytokines measured, only 1 significant difference was detected: Levels of interleukin 1 beta (IL-1 beta) were lower in dengue-infected patients who had experienced a previous dengue infection than patients infected with dengue for the first time. However, power to detect differences between groups was low. In Zika-infected patients, levels of IL-1 beta showed a significant, positive correlation with viral load. Conclusions. No signs of ADE were observed in vivo in patients with acute ZIKV infection who had prior exposure to DENV.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Butantan InstituteBrazilian National Institutes for Science and Technology for Dengue Studies (INCT em Dengue)National Institutes of HealthSao Paulo State Univ, Sao Jose do Rio Preto Sch Med, Sao Jose Do Rio Preto, BrazilSao Paulo State Univ, Butantan Inst, Sao Jose Do Rio Preto, BrazilSao Paulo State Univ, Dept Biol, Inst Biosci Letters & Exact Sci, Sao Jose Do Rio Preto, BrazilNew Mexico State Univ, Las Cruces, NM 88003 USAUniv Texas Med Branch, Galveston, TX 77555 USAUniv Sao Paulo, Sch Med, Sao Paulo, BrazilSao Paulo State Univ, Sao Jose do Rio Preto Sch Med, Sao Jose Do Rio Preto, BrazilSao Paulo State Univ, Butantan Inst, Sao Jose Do Rio Preto, BrazilSao Paulo State Univ, Dept Biol, Inst Biosci Letters & Exact Sci, Sao Jose Do Rio Preto, BrazilFAPESP: 2013/21719-3FAPESP: 2015/12295-0National Institutes of Health: 1U01AI115577-01Oxford Univ Press IncUniversidade Estadual Paulista (Unesp)New Mexico State UnivUniv Texas Med BranchUniversidade de São Paulo (USP)Bernardes Terzian, Ana Carolina [UNESP]Schanoski, Alessandra Soares [UNESP]Oliveira Mota, Minh' Tasso de [UNESP]Silva, Rafael Alves da [UNESP]Estofolete, Cassia Fernanda [UNESP]Colombo, Tatiana Elias [UNESP]Rahal, Paula [UNESP]Hanley, Kathryn A.Vasilakis, NikosKalil, JorgeNogueiral, Mauricio Lacerda [UNESP]2018-11-26T17:41:03Z2018-11-26T17:41:03Z2017-10-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1260-1265application/pdfhttp://dx.doi.org/10.1093/cid/cix558Clinical Infectious Diseases. Cary: Oxford Univ Press Inc, v. 65, n. 8, p. 1260-1265, 2017.1058-4838http://hdl.handle.net/11449/16334010.1093/cid/cix558WOS:000412022500002WOS000412022500002.pdf79910823626712120000-0001-5693-6148Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengClinical Infectious Diseases5,051info:eu-repo/semantics/openAccess2024-01-19T06:33:08Zoai:repositorio.unesp.br:11449/163340Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-01-19T06:33:08Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected Patients
title Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected Patients
spellingShingle Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected Patients
Bernardes Terzian, Ana Carolina [UNESP]
ZIKV
DENV
ADE
cytokines
title_short Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected Patients
title_full Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected Patients
title_fullStr Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected Patients
title_full_unstemmed Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected Patients
title_sort Viral Load and Cytokine Response Profile Does Not Support Antibody-Dependent Enhancement in Dengue-Primed Zika Virus-Infected Patients
author Bernardes Terzian, Ana Carolina [UNESP]
author_facet Bernardes Terzian, Ana Carolina [UNESP]
Schanoski, Alessandra Soares [UNESP]
Oliveira Mota, Minh' Tasso de [UNESP]
Silva, Rafael Alves da [UNESP]
Estofolete, Cassia Fernanda [UNESP]
Colombo, Tatiana Elias [UNESP]
Rahal, Paula [UNESP]
Hanley, Kathryn A.
Vasilakis, Nikos
Kalil, Jorge
Nogueiral, Mauricio Lacerda [UNESP]
author_role author
author2 Schanoski, Alessandra Soares [UNESP]
Oliveira Mota, Minh' Tasso de [UNESP]
Silva, Rafael Alves da [UNESP]
Estofolete, Cassia Fernanda [UNESP]
Colombo, Tatiana Elias [UNESP]
Rahal, Paula [UNESP]
Hanley, Kathryn A.
Vasilakis, Nikos
Kalil, Jorge
Nogueiral, Mauricio Lacerda [UNESP]
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
New Mexico State Univ
Univ Texas Med Branch
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv Bernardes Terzian, Ana Carolina [UNESP]
Schanoski, Alessandra Soares [UNESP]
Oliveira Mota, Minh' Tasso de [UNESP]
Silva, Rafael Alves da [UNESP]
Estofolete, Cassia Fernanda [UNESP]
Colombo, Tatiana Elias [UNESP]
Rahal, Paula [UNESP]
Hanley, Kathryn A.
Vasilakis, Nikos
Kalil, Jorge
Nogueiral, Mauricio Lacerda [UNESP]
dc.subject.por.fl_str_mv ZIKV
DENV
ADE
cytokines
topic ZIKV
DENV
ADE
cytokines
description Background. The pathogenesis of severe dengue disease involves immune components as biomarkers. The mechanism by which some dengue virus (DENV)-infected individuals progress to severe disease is poorly understood. Most studies on the pathogenesis of severe dengue disease focus on the process of antibody-dependent enhancement (ADE) as a primary risk factor. With the circulation of Zika virus (ZIKV) in DENV-endemic areas, many people infected by ZIKV were likely exposed to DENV. The influence of such exposure on Zika disease outcomes remains unknown. Methods. We investigated whether patients previously exposed to DENV exhibited higher viremia when exposed to a subsequent, heterologous dengue or Zika infection than those patients not previously exposed to dengue. We measured viral loads and cytokine profile during patients' acute infections. Results. Neither dengue nor Zika viremia was higher in patients with prior DENV infection, although the power to detect such a difference was only adequate in the ZIKV analysis. Of the 10 cytokines measured, only 1 significant difference was detected: Levels of interleukin 1 beta (IL-1 beta) were lower in dengue-infected patients who had experienced a previous dengue infection than patients infected with dengue for the first time. However, power to detect differences between groups was low. In Zika-infected patients, levels of IL-1 beta showed a significant, positive correlation with viral load. Conclusions. No signs of ADE were observed in vivo in patients with acute ZIKV infection who had prior exposure to DENV.
publishDate 2017
dc.date.none.fl_str_mv 2017-10-15
2018-11-26T17:41:03Z
2018-11-26T17:41:03Z
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.uri.fl_str_mv http://dx.doi.org/10.1093/cid/cix558
Clinical Infectious Diseases. Cary: Oxford Univ Press Inc, v. 65, n. 8, p. 1260-1265, 2017.
1058-4838
http://hdl.handle.net/11449/163340
10.1093/cid/cix558
WOS:000412022500002
WOS000412022500002.pdf
7991082362671212
0000-0001-5693-6148
url http://dx.doi.org/10.1093/cid/cix558
http://hdl.handle.net/11449/163340
identifier_str_mv Clinical Infectious Diseases. Cary: Oxford Univ Press Inc, v. 65, n. 8, p. 1260-1265, 2017.
1058-4838
10.1093/cid/cix558
WOS:000412022500002
WOS000412022500002.pdf
7991082362671212
0000-0001-5693-6148
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Clinical Infectious Diseases
5,051
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1260-1265
application/pdf
dc.publisher.none.fl_str_mv Oxford Univ Press Inc
publisher.none.fl_str_mv Oxford Univ Press Inc
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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