TLR-2 and TLR-4 expression in monocytes of newborns with late-onset sepsis
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , |
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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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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1814268271718825984 |