TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock

Detalhes bibliográficos
Autor(a) principal: Brunialti, Milena Karina Coló [UNIFESP]
Data de Publicação: 2006
Outros Autores: Martins, Paulo Sergio [UNIFESP], Carvalho, Heraclito Barbosa DE [UNIFESP], Machado, Flávia Ribeiro [UNIFESP, Barbosa, L. M., Salomão, Reinaldo [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1097/01.shk.0000217815.57727.29
http://repositorio.unifesp.br/handle/11600/28800
Resumo: Bacterial recognition and induced cellular activation are fundamental for the host control of infection, yet the limit between protective and harmful response is still inexact. Forty-one patients were enrolled in this study: 14 with sepsis, 12 with severe sepsis, and 15 with septic shock. Seventeen healthy volunteers (HV) were included as control. the expression of TLR2, TLR4, CD14, CD11b, and CD11c was analyzed on monocytes surface in whole blood. sCD14 was measured in serum, and TNF-alpha, IL-6, and IL-10 cytokine levels were measured in PBMC supernatants after LIPS, IL-1 beta, and TNF-alpha stimuli by ELISA. An increase in sCD14 and a decreased mCD14 were found in patients as compared with HV (P < 0.001). However, no differences in the expression of TLR2, TLR4, and CD11c were found among the groups. A trend toward differential expression of CD11b was observed, with higher values found in patients with sepsis as compared with HV. A negative regulation of the inflammatory cytokine production was observed in patients with severe sepsis and shock septic in relation to sepsis and HV, regardless of the stimulus. No significant difference in IL-10 production was found among the groups. in this study, we show that the inflammatory response is associated with the continuum of clinical manifestations of sepsis, with a strong inflammatory response in the early phase (sepsis) and a refractory picture in the late phases (severe sepsis and septic shock). Correlation between cell surface receptors and cytokine production after IL-1 beta and TNF-alpha stimuli and the observation of a single and same standard response with the different stimulus suggest a pattern of immunology response that is not dependent only on the expression of the evaluated receptors and that is likely to have a regulation in the intracellular signaling pathways.
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spelling TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shockToll-like receptorLPSTNF-alphaIL-6IL-10immunophenotypingBacterial recognition and induced cellular activation are fundamental for the host control of infection, yet the limit between protective and harmful response is still inexact. Forty-one patients were enrolled in this study: 14 with sepsis, 12 with severe sepsis, and 15 with septic shock. Seventeen healthy volunteers (HV) were included as control. the expression of TLR2, TLR4, CD14, CD11b, and CD11c was analyzed on monocytes surface in whole blood. sCD14 was measured in serum, and TNF-alpha, IL-6, and IL-10 cytokine levels were measured in PBMC supernatants after LIPS, IL-1 beta, and TNF-alpha stimuli by ELISA. An increase in sCD14 and a decreased mCD14 were found in patients as compared with HV (P < 0.001). However, no differences in the expression of TLR2, TLR4, and CD11c were found among the groups. A trend toward differential expression of CD11b was observed, with higher values found in patients with sepsis as compared with HV. A negative regulation of the inflammatory cytokine production was observed in patients with severe sepsis and shock septic in relation to sepsis and HV, regardless of the stimulus. No significant difference in IL-10 production was found among the groups. in this study, we show that the inflammatory response is associated with the continuum of clinical manifestations of sepsis, with a strong inflammatory response in the early phase (sepsis) and a refractory picture in the late phases (severe sepsis and septic shock). Correlation between cell surface receptors and cytokine production after IL-1 beta and TNF-alpha stimuli and the observation of a single and same standard response with the different stimulus suggest a pattern of immunology response that is not dependent only on the expression of the evaluated receptors and that is likely to have a regulation in the intracellular signaling pathways.Universidade Federal de São Paulo, Immunol Lab, Div Infect Dis, Escola Paulista Med, BR-04039032 São Paulo, BrazilUniv São Paulo, Fac Med, Dept Epidemiol, São Paulo, BrazilUniversidade Federal de São Paulo, Hosp São Paulo, Intens Care Unit, BR-04039032 São Paulo, BrazilSanta Marcelina Hosp, Div Infect Dis, São Paulo, BrazilUniversidade Federal de São Paulo, Immunol Lab, Div Infect Dis, Escola Paulista Med, BR-04039032 São Paulo, BrazilUniversidade Federal de São Paulo, Hosp São Paulo, Intens Care Unit, BR-04039032 São Paulo, BrazilWeb of ScienceLippincott Williams & WilkinsUniversidade Federal de São Paulo (UNIFESP)Universidade de São Paulo (USP)Santa Marcelina HospBrunialti, Milena Karina Coló [UNIFESP]Martins, Paulo Sergio [UNIFESP]Carvalho, Heraclito Barbosa DE [UNIFESP]Machado, Flávia Ribeiro [UNIFESPBarbosa, L. M.Salomão, Reinaldo [UNIFESP]2016-01-24T12:41:03Z2016-01-24T12:41:03Z2006-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion351-357http://dx.doi.org/10.1097/01.shk.0000217815.57727.29Shock. Philadelphia: Lippincott Williams & Wilkins, v. 25, n. 4, p. 351-357, 2006.10.1097/01.shk.0000217815.57727.291073-2322http://repositorio.unifesp.br/handle/11600/28800WOS:000236652100006engShockinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T10:41:03Zoai:repositorio.unifesp.br/:11600/28800Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-01-24T10:41:03Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock
title TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock
spellingShingle TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock
Brunialti, Milena Karina Coló [UNIFESP]
Toll-like receptor
LPS
TNF-alpha
IL-6
IL-10
immunophenotyping
title_short TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock
title_full TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock
title_fullStr TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock
title_full_unstemmed TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock
title_sort TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock
author Brunialti, Milena Karina Coló [UNIFESP]
author_facet Brunialti, Milena Karina Coló [UNIFESP]
Martins, Paulo Sergio [UNIFESP]
Carvalho, Heraclito Barbosa DE [UNIFESP]
Machado, Flávia Ribeiro [UNIFESP
Barbosa, L. M.
Salomão, Reinaldo [UNIFESP]
author_role author
author2 Martins, Paulo Sergio [UNIFESP]
Carvalho, Heraclito Barbosa DE [UNIFESP]
Machado, Flávia Ribeiro [UNIFESP
Barbosa, L. M.
Salomão, Reinaldo [UNIFESP]
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Santa Marcelina Hosp
dc.contributor.author.fl_str_mv Brunialti, Milena Karina Coló [UNIFESP]
Martins, Paulo Sergio [UNIFESP]
Carvalho, Heraclito Barbosa DE [UNIFESP]
Machado, Flávia Ribeiro [UNIFESP
Barbosa, L. M.
Salomão, Reinaldo [UNIFESP]
dc.subject.por.fl_str_mv Toll-like receptor
LPS
TNF-alpha
IL-6
IL-10
immunophenotyping
topic Toll-like receptor
LPS
TNF-alpha
IL-6
IL-10
immunophenotyping
description Bacterial recognition and induced cellular activation are fundamental for the host control of infection, yet the limit between protective and harmful response is still inexact. Forty-one patients were enrolled in this study: 14 with sepsis, 12 with severe sepsis, and 15 with septic shock. Seventeen healthy volunteers (HV) were included as control. the expression of TLR2, TLR4, CD14, CD11b, and CD11c was analyzed on monocytes surface in whole blood. sCD14 was measured in serum, and TNF-alpha, IL-6, and IL-10 cytokine levels were measured in PBMC supernatants after LIPS, IL-1 beta, and TNF-alpha stimuli by ELISA. An increase in sCD14 and a decreased mCD14 were found in patients as compared with HV (P < 0.001). However, no differences in the expression of TLR2, TLR4, and CD11c were found among the groups. A trend toward differential expression of CD11b was observed, with higher values found in patients with sepsis as compared with HV. A negative regulation of the inflammatory cytokine production was observed in patients with severe sepsis and shock septic in relation to sepsis and HV, regardless of the stimulus. No significant difference in IL-10 production was found among the groups. in this study, we show that the inflammatory response is associated with the continuum of clinical manifestations of sepsis, with a strong inflammatory response in the early phase (sepsis) and a refractory picture in the late phases (severe sepsis and septic shock). Correlation between cell surface receptors and cytokine production after IL-1 beta and TNF-alpha stimuli and the observation of a single and same standard response with the different stimulus suggest a pattern of immunology response that is not dependent only on the expression of the evaluated receptors and that is likely to have a regulation in the intracellular signaling pathways.
publishDate 2006
dc.date.none.fl_str_mv 2006-04-01
2016-01-24T12:41:03Z
2016-01-24T12:41:03Z
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/10.1097/01.shk.0000217815.57727.29
Shock. Philadelphia: Lippincott Williams & Wilkins, v. 25, n. 4, p. 351-357, 2006.
10.1097/01.shk.0000217815.57727.29
1073-2322
http://repositorio.unifesp.br/handle/11600/28800
WOS:000236652100006
url http://dx.doi.org/10.1097/01.shk.0000217815.57727.29
http://repositorio.unifesp.br/handle/11600/28800
identifier_str_mv Shock. Philadelphia: Lippincott Williams & Wilkins, v. 25, n. 4, p. 351-357, 2006.
10.1097/01.shk.0000217815.57727.29
1073-2322
WOS:000236652100006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Shock
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 351-357
dc.publisher.none.fl_str_mv Lippincott Williams & Wilkins
publisher.none.fl_str_mv Lippincott Williams & Wilkins
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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