TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis

Detalhes bibliográficos
Autor(a) principal: Redondo, Ana Carolina Costa
Data de Publicação: 2014
Outros Autores: Ceccon, Maria Esther Jurfest Rivero, Silveira-Lessa, Ana Lúcia, Quinello, Camila, Palmeira, Patricia, Carvalho, Werther Brunow [UNIFESP], Carneiro-Sampaio, Magda Maria Sales
Tipo de documento: Artigo
Idioma: eng
por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/j.jped.2013.12.012
http://repositorio.unifesp.br/handle/11600/38117
Resumo: Objective: To analyze toll-like receptor (TLR)-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis.Methods: This prospective study included 27 full-term newborns aged 8 to 29 days, with clinical and laboratory diagnosis of late-onset sepsis. Ten newborns (37%) had positive cultures. Cytokines were measured by cytometric bead array in peripheral blood, while TLR-2, TLR-4 expression, and median fluorescence intensity (MFI) were determined by immunophenotyping peripheral whole blood monocytes, and were analyzed with a BD FACSDiva flow cytometer (Becton, Dickinson and Company, USA). A comparison was performed with healthy adults.Results: Microorganisms were identified in 37% of these septic newborns, and all of them had high levels of pro-inflammatory cytokines (IL-8, IL-6, IL-1 beta) and anti-inflammatory cytokine (IL-10) corroborating the inflammatory/septic process. in monocytes, the frequency of TLR-4 expression was higher in infected newborns (p = 0.01).Conclusion: This study investigated the innate immune response in septic newborns. Septic newborns that relied almost exclusively on the innate immune system showed little in vivo response at nnonocyte activation, suggesting impaired immune response and increased susceptibility to infection. (C) 2014 Sociedade Brasileira de Pediatria. Published by Elsevier Editora Ltda. All rights reserved.
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spelling TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsisExpressão do TLR-2 e do TLR-4 em monócitos de recém-nascidos a termo com sepse tardiaSepsis/immunologyInnate immunityToll-like receptor 2Toll-like receptor 4NewbornMonocytesSepse/imunologiaImunidade inataReceptor 2 toll-likeReceptor 4 toll-likeRecém-nascidosMonócitosObjective: To analyze toll-like receptor (TLR)-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis.Methods: This prospective study included 27 full-term newborns aged 8 to 29 days, with clinical and laboratory diagnosis of late-onset sepsis. Ten newborns (37%) had positive cultures. Cytokines were measured by cytometric bead array in peripheral blood, while TLR-2, TLR-4 expression, and median fluorescence intensity (MFI) were determined by immunophenotyping peripheral whole blood monocytes, and were analyzed with a BD FACSDiva flow cytometer (Becton, Dickinson and Company, USA). A comparison was performed with healthy adults.Results: Microorganisms were identified in 37% of these septic newborns, and all of them had high levels of pro-inflammatory cytokines (IL-8, IL-6, IL-1 beta) and anti-inflammatory cytokine (IL-10) corroborating the inflammatory/septic process. in monocytes, the frequency of TLR-4 expression was higher in infected newborns (p = 0.01).Conclusion: This study investigated the innate immune response in septic newborns. Septic newborns that relied almost exclusively on the innate immune system showed little in vivo response at nnonocyte activation, suggesting impaired immune response and increased susceptibility to infection. (C) 2014 Sociedade Brasileira de Pediatria. Published by Elsevier Editora Ltda. All rights reserved.Objetivos: Analisar a expressão dos TLR-2 e TLR-4 em monócitos de recém-nascidos com sepse tardia. Métodos: Trata-se de um estudo prospectivo com 27 recém-nascidos a termo entre 8 e 29 dias de vida com diagnóstico clínico e laboratorial de sepse tardia dos quais dez (37%) apresentaram cultura positiva. As citocinas foram determinadas por teste de CBA em sangue periférico enquanto que a expressão e MFI (mediana de intensidade de fluorescência) dos TLR-2 e TLR-4 foi determinado por imunofenotipagem em monócitos de sangue periférico total através de análise pelo citômetro de fluxo BD FACSDiva. O grupo usado para comparação foi de adultos saudáveis. Resultados: Microrganismos foram identificados em 37% dos pacientes e estes juntamente com os pacientes com sepse clínica tiveram níveis elevados de citocinas pró-inflamatórias (IL-8, IL-6, IL-1) e de citocina anti-inflamatória (IL-10) corroborando o processo inflamatório/infeccioso. No monócito, a frequência de expressão do TLR-4 foi mais elevada (p = 0,01). Conclusões: Este estudo analisou a resposta imune inata no recém-nascido com sepse. Recém--nascidos sépticos que dependem quase exclusivamente do sistema imune inato apresentaram pouca resposta in vivo na ativação de monócitos o que sugere uma resposta imune deficiente e maior susceptibilidade à infecção.Univ São Paulo, Fac Med, Hosp Clin, Neonatal Intens Care Unit,Inst Crianca, São Paulo, BrazilUniv São Paulo, Dept Parasitol, Inst Ciencias Biomed, São Paulo, BrazilUniv São Paulo, Fac Med, Hosp Clin, Lab Med Invest LIM 36,Inst Crianca, São Paulo, BrazilUniv São Paulo, Fac Med, Dept Neonatol, São Paulo, BrazilUniv São Paulo, Fac Med, Dept Pediat, São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Soc Brasil PediatriaUniversidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Redondo, Ana Carolina CostaCeccon, Maria Esther Jurfest RiveroSilveira-Lessa, Ana LúciaQuinello, CamilaPalmeira, PatriciaCarvalho, Werther Brunow [UNIFESP]Carneiro-Sampaio, Magda Maria Sales2016-01-24T14:37:45Z2016-01-24T14:37:45Z2014-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion472-478application/pdfapplication/pdfhttp://dx.doi.org/10.1016/j.jped.2013.12.012Jornal de Pediatria. Rio de Janeiro, Rj: Soc Brasil Pediatria, v. 90, n. 5, p. 472-478, 2014.10.1016/j.jped.2013.12.012S0021-75572014000500472-en.pdfS0021-75572014000500472-pt.pdf0021-7557S0021-75572014000500472http://repositorio.unifesp.br/handle/11600/38117WOS:000342121700007engporJornal de Pediatriainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T16:52:10Zoai:repositorio.unifesp.br/:11600/38117Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T16:52:10Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis
Expressão do TLR-2 e do TLR-4 em monócitos de recém-nascidos a termo com sepse tardia
title TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis
spellingShingle TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis
Redondo, Ana Carolina Costa
Sepsis/immunology
Innate immunity
Toll-like receptor 2
Toll-like receptor 4
Newborn
Monocytes
Sepse/imunologia
Imunidade inata
Receptor 2 toll-like
Receptor 4 toll-like
Recém-nascidos
Monócitos
title_short TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis
title_full TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis
title_fullStr TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis
title_full_unstemmed TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis
title_sort TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis
author Redondo, Ana Carolina Costa
author_facet Redondo, Ana Carolina Costa
Ceccon, Maria Esther Jurfest Rivero
Silveira-Lessa, Ana Lúcia
Quinello, Camila
Palmeira, Patricia
Carvalho, Werther Brunow [UNIFESP]
Carneiro-Sampaio, Magda Maria Sales
author_role author
author2 Ceccon, Maria Esther Jurfest Rivero
Silveira-Lessa, Ana Lúcia
Quinello, Camila
Palmeira, Patricia
Carvalho, Werther Brunow [UNIFESP]
Carneiro-Sampaio, Magda Maria Sales
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Redondo, Ana Carolina Costa
Ceccon, Maria Esther Jurfest Rivero
Silveira-Lessa, Ana Lúcia
Quinello, Camila
Palmeira, Patricia
Carvalho, Werther Brunow [UNIFESP]
Carneiro-Sampaio, Magda Maria Sales
dc.subject.por.fl_str_mv Sepsis/immunology
Innate immunity
Toll-like receptor 2
Toll-like receptor 4
Newborn
Monocytes
Sepse/imunologia
Imunidade inata
Receptor 2 toll-like
Receptor 4 toll-like
Recém-nascidos
Monócitos
topic Sepsis/immunology
Innate immunity
Toll-like receptor 2
Toll-like receptor 4
Newborn
Monocytes
Sepse/imunologia
Imunidade inata
Receptor 2 toll-like
Receptor 4 toll-like
Recém-nascidos
Monócitos
description Objective: To analyze toll-like receptor (TLR)-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis.Methods: This prospective study included 27 full-term newborns aged 8 to 29 days, with clinical and laboratory diagnosis of late-onset sepsis. Ten newborns (37%) had positive cultures. Cytokines were measured by cytometric bead array in peripheral blood, while TLR-2, TLR-4 expression, and median fluorescence intensity (MFI) were determined by immunophenotyping peripheral whole blood monocytes, and were analyzed with a BD FACSDiva flow cytometer (Becton, Dickinson and Company, USA). A comparison was performed with healthy adults.Results: Microorganisms were identified in 37% of these septic newborns, and all of them had high levels of pro-inflammatory cytokines (IL-8, IL-6, IL-1 beta) and anti-inflammatory cytokine (IL-10) corroborating the inflammatory/septic process. in monocytes, the frequency of TLR-4 expression was higher in infected newborns (p = 0.01).Conclusion: This study investigated the innate immune response in septic newborns. Septic newborns that relied almost exclusively on the innate immune system showed little in vivo response at nnonocyte activation, suggesting impaired immune response and increased susceptibility to infection. (C) 2014 Sociedade Brasileira de Pediatria. Published by Elsevier Editora Ltda. All rights reserved.
publishDate 2014
dc.date.none.fl_str_mv 2014-09-01
2016-01-24T14:37:45Z
2016-01-24T14:37:45Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.jped.2013.12.012
Jornal de Pediatria. Rio de Janeiro, Rj: Soc Brasil Pediatria, v. 90, n. 5, p. 472-478, 2014.
10.1016/j.jped.2013.12.012
S0021-75572014000500472-en.pdf
S0021-75572014000500472-pt.pdf
0021-7557
S0021-75572014000500472
http://repositorio.unifesp.br/handle/11600/38117
WOS:000342121700007
url http://dx.doi.org/10.1016/j.jped.2013.12.012
http://repositorio.unifesp.br/handle/11600/38117
identifier_str_mv Jornal de Pediatria. Rio de Janeiro, Rj: Soc Brasil Pediatria, v. 90, n. 5, p. 472-478, 2014.
10.1016/j.jped.2013.12.012
S0021-75572014000500472-en.pdf
S0021-75572014000500472-pt.pdf
0021-7557
S0021-75572014000500472
WOS:000342121700007
dc.language.iso.fl_str_mv eng
por
language eng
por
dc.relation.none.fl_str_mv Jornal de Pediatria
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 472-478
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Soc Brasil Pediatria
publisher.none.fl_str_mv Soc Brasil Pediatria
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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