Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsis

Detalhes bibliográficos
Autor(a) principal: Martins, Paulo S. [UNIFESP]
Data de Publicação: 2008
Outros Autores: Brunialti, Milena K. C. [UNIFESP], Martos, Leandro S. W. [UNIFESP], Machado, Flavia R. [UNIFESP], Assuncao, Murillo S. [UNIFESP], Blecher, Sergio, Salomão, Reinaldo [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1186/cc6801
http://repositorio.unifesp.br/handle/11600/30243
Resumo: Background Infection control depends on adequate microbe recognition and cell activation, yet inflammatory response may lead to organ dysfunction in sepsis. the aims of this study were to evaluate cell activation in the context of sepsis and its correlation with organ dysfunction.Methods A total of 41 patients were prospectively enrolled: 14 with sepsis, 12 with severe sepsis and 15 with septic shock. A total of 17 healthy volunteers were included as a control group. Patients were admitted to the Intensive Care Units and Emergency Rooms of Hospital São Paulo ( Federal University of São Paulo) and Hospital Santa Marcelina, São Paulo, Brazil. Toll- like receptor ( TLR) 2, TLR4, CD11b, CD11c and CD66b expression on neutrophil surfaces and oxidative metabolism measured by non- fluorescent dichlorofluorescein ( DCFH) oxidation in neutrophils and monocytes, using whole blood, were evaluated using flow cytometry. Organ dysfunction was measured using the sepsis- associated organ failure assessment ( SOFA) score.Results TLR2 expression on neutrophils was found to be downregulated in septic shock patients compared to healthy volunteers ( p = 0.05). No differences were found in CD11b and CD11c expression. CD66b expression was increased in the patient group compared to the control group ( p = 0.01). Neutrophil and monocyte oxidative burst was increased in septic patients compared to the control group at baseline and after stimulation with phorbol myristate acetate ( PMA), formylmethionylleucyl- phenylalanine ( fMLP), lipopolysaccharide ( LPS) and Staphylococcus aureus ( p < 0.001 and p < 0.01, respectively, for neutrophils and monocytes in all tested conditions). A strong correlation was observed between neutrophil and monocyte oxidative metabolism. A SOFA score of 7 discriminated patients between survivors and non- survivors ( area under the curve for reactive oxygen species ( ROS) was 0.78; p = 0.02). ROS generation in patients with sepsis and septic shock with SOFA scores > 7 was higher than in patients with SOFA scores < 7, both in neutrophils and monocytes. However, oxidative burst in patients with sepsis was as high as in septic shock.Conclusion Surface receptors expression on neutrophils may be modulated across the continuum of sepsis, and enhanced or decreased expression may be found depending on the receptor considered. ROS generation is upregulated both in neutrophils and monocytes in septic patients, and it is differently modulated depending on the stage of the disease and the stimuli used.
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spelling Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsisBackground Infection control depends on adequate microbe recognition and cell activation, yet inflammatory response may lead to organ dysfunction in sepsis. the aims of this study were to evaluate cell activation in the context of sepsis and its correlation with organ dysfunction.Methods A total of 41 patients were prospectively enrolled: 14 with sepsis, 12 with severe sepsis and 15 with septic shock. A total of 17 healthy volunteers were included as a control group. Patients were admitted to the Intensive Care Units and Emergency Rooms of Hospital São Paulo ( Federal University of São Paulo) and Hospital Santa Marcelina, São Paulo, Brazil. Toll- like receptor ( TLR) 2, TLR4, CD11b, CD11c and CD66b expression on neutrophil surfaces and oxidative metabolism measured by non- fluorescent dichlorofluorescein ( DCFH) oxidation in neutrophils and monocytes, using whole blood, were evaluated using flow cytometry. Organ dysfunction was measured using the sepsis- associated organ failure assessment ( SOFA) score.Results TLR2 expression on neutrophils was found to be downregulated in septic shock patients compared to healthy volunteers ( p = 0.05). No differences were found in CD11b and CD11c expression. CD66b expression was increased in the patient group compared to the control group ( p = 0.01). Neutrophil and monocyte oxidative burst was increased in septic patients compared to the control group at baseline and after stimulation with phorbol myristate acetate ( PMA), formylmethionylleucyl- phenylalanine ( fMLP), lipopolysaccharide ( LPS) and Staphylococcus aureus ( p < 0.001 and p < 0.01, respectively, for neutrophils and monocytes in all tested conditions). A strong correlation was observed between neutrophil and monocyte oxidative metabolism. A SOFA score of 7 discriminated patients between survivors and non- survivors ( area under the curve for reactive oxygen species ( ROS) was 0.78; p = 0.02). ROS generation in patients with sepsis and septic shock with SOFA scores > 7 was higher than in patients with SOFA scores < 7, both in neutrophils and monocytes. However, oxidative burst in patients with sepsis was as high as in septic shock.Conclusion Surface receptors expression on neutrophils may be modulated across the continuum of sepsis, and enhanced or decreased expression may be found depending on the receptor considered. ROS generation is upregulated both in neutrophils and monocytes in septic patients, and it is differently modulated depending on the stage of the disease and the stimuli used.Universidade Federal de São Paulo, Escola Paulista Med, Div Infect Dis, São Paulo, BrazilUniversidade Federal de São Paulo, Intens Care Unit, São Paulo, BrazilHosp St Marcelina, Intens Care Unit, São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Div Infect Dis, São Paulo, BrazilUniversidade Federal de São Paulo, Intens Care Unit, São Paulo, BrazilWeb of ScienceBiomed Central LtdUniversidade Federal de São Paulo (UNIFESP)Hosp St MarcelinaMartins, Paulo S. [UNIFESP]Brunialti, Milena K. C. [UNIFESP]Martos, Leandro S. W. [UNIFESP]Machado, Flavia R. [UNIFESP]Assuncao, Murillo S. [UNIFESP]Blecher, SergioSalomão, Reinaldo [UNIFESP]2016-01-24T13:49:19Z2016-01-24T13:49:19Z2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion10application/pdfhttp://dx.doi.org/10.1186/cc6801Critical Care. London: Biomed Central Ltd, v. 12, n. 1, 10 p., 2008.10.1186/cc6801WOS000254812500065.pdf1466-609Xhttp://repositorio.unifesp.br/handle/11600/30243WOS:000254812500065engCritical Careinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-07T20:01:35Zoai:repositorio.unifesp.br/:11600/30243Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-07T20:01:35Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsis
title Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsis
spellingShingle Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsis
Martins, Paulo S. [UNIFESP]
title_short Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsis
title_full Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsis
title_fullStr Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsis
title_full_unstemmed Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsis
title_sort Expression of cell surface receptors and oxidative metabolism modulation in the clinical continuum of sepsis
author Martins, Paulo S. [UNIFESP]
author_facet Martins, Paulo S. [UNIFESP]
Brunialti, Milena K. C. [UNIFESP]
Martos, Leandro S. W. [UNIFESP]
Machado, Flavia R. [UNIFESP]
Assuncao, Murillo S. [UNIFESP]
Blecher, Sergio
Salomão, Reinaldo [UNIFESP]
author_role author
author2 Brunialti, Milena K. C. [UNIFESP]
Martos, Leandro S. W. [UNIFESP]
Machado, Flavia R. [UNIFESP]
Assuncao, Murillo S. [UNIFESP]
Blecher, Sergio
Salomão, Reinaldo [UNIFESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Hosp St Marcelina
dc.contributor.author.fl_str_mv Martins, Paulo S. [UNIFESP]
Brunialti, Milena K. C. [UNIFESP]
Martos, Leandro S. W. [UNIFESP]
Machado, Flavia R. [UNIFESP]
Assuncao, Murillo S. [UNIFESP]
Blecher, Sergio
Salomão, Reinaldo [UNIFESP]
description Background Infection control depends on adequate microbe recognition and cell activation, yet inflammatory response may lead to organ dysfunction in sepsis. the aims of this study were to evaluate cell activation in the context of sepsis and its correlation with organ dysfunction.Methods A total of 41 patients were prospectively enrolled: 14 with sepsis, 12 with severe sepsis and 15 with septic shock. A total of 17 healthy volunteers were included as a control group. Patients were admitted to the Intensive Care Units and Emergency Rooms of Hospital São Paulo ( Federal University of São Paulo) and Hospital Santa Marcelina, São Paulo, Brazil. Toll- like receptor ( TLR) 2, TLR4, CD11b, CD11c and CD66b expression on neutrophil surfaces and oxidative metabolism measured by non- fluorescent dichlorofluorescein ( DCFH) oxidation in neutrophils and monocytes, using whole blood, were evaluated using flow cytometry. Organ dysfunction was measured using the sepsis- associated organ failure assessment ( SOFA) score.Results TLR2 expression on neutrophils was found to be downregulated in septic shock patients compared to healthy volunteers ( p = 0.05). No differences were found in CD11b and CD11c expression. CD66b expression was increased in the patient group compared to the control group ( p = 0.01). Neutrophil and monocyte oxidative burst was increased in septic patients compared to the control group at baseline and after stimulation with phorbol myristate acetate ( PMA), formylmethionylleucyl- phenylalanine ( fMLP), lipopolysaccharide ( LPS) and Staphylococcus aureus ( p < 0.001 and p < 0.01, respectively, for neutrophils and monocytes in all tested conditions). A strong correlation was observed between neutrophil and monocyte oxidative metabolism. A SOFA score of 7 discriminated patients between survivors and non- survivors ( area under the curve for reactive oxygen species ( ROS) was 0.78; p = 0.02). ROS generation in patients with sepsis and septic shock with SOFA scores > 7 was higher than in patients with SOFA scores < 7, both in neutrophils and monocytes. However, oxidative burst in patients with sepsis was as high as in septic shock.Conclusion Surface receptors expression on neutrophils may be modulated across the continuum of sepsis, and enhanced or decreased expression may be found depending on the receptor considered. ROS generation is upregulated both in neutrophils and monocytes in septic patients, and it is differently modulated depending on the stage of the disease and the stimuli used.
publishDate 2008
dc.date.none.fl_str_mv 2008-01-01
2016-01-24T13:49:19Z
2016-01-24T13:49:19Z
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/10.1186/cc6801
Critical Care. London: Biomed Central Ltd, v. 12, n. 1, 10 p., 2008.
10.1186/cc6801
WOS000254812500065.pdf
1466-609X
http://repositorio.unifesp.br/handle/11600/30243
WOS:000254812500065
url http://dx.doi.org/10.1186/cc6801
http://repositorio.unifesp.br/handle/11600/30243
identifier_str_mv Critical Care. London: Biomed Central Ltd, v. 12, n. 1, 10 p., 2008.
10.1186/cc6801
WOS000254812500065.pdf
1466-609X
WOS:000254812500065
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Critical Care
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 10
application/pdf
dc.publisher.none.fl_str_mv Biomed Central Ltd
publisher.none.fl_str_mv Biomed Central Ltd
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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