TLR2, TLR4, CD14, CD11b, and CD11c expressions on monocytes surface and cytokine production in patients with sepsis, severe sepsis, and septic shock
Autor(a) principal: | |
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Data de Publicação: | 2006 |
Outros Autores: | , , , , |
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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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 |
_version_ |
1814268377820037120 |