Evaluation of cytokines (MIG, IFN-gamma, TNF-alpha, IL-4, IL-5, and IL-10) during the different evolutive phases of chagasic esophagopathy

The production of cytokines (MIG, IFN-gamma, TNF-alpha, IL-4, IL-5, and IL-10) was studied in 39 individuals, including 28 with chagasic esophagopathy and 11 nonchagasic patients with gastroesophageal reflux disease. A sandwich enzyme immunoassay employing monoclonal antibody pairs specific for each...

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Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 119(2006), 2 vom: 30. Mai, Seite 213-8
1. Verfasser: Crema, Eduardo (VerfasserIn)
Weitere Verfasser: Monteiro, Isabela de Oliveira, Gomes, Marília Gabriela Zanier, Silva, Alex Augusto, Rodrigues Júnior, Virmondes
Format: Aufsatz
Sprache:English
Veröffentlicht: 2006
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Comparative Study Journal Article Research Support, Non-U.S. Gov't CXCL9 protein, human Chemokine CXCL9 Chemokines, CXC Cytokines Interleukin-5 Tumor Necrosis Factor-alpha Interleukin-10 mehr... 130068-27-8 Interleukin-4 207137-56-2 Interferon-gamma 82115-62-6
Beschreibung
Zusammenfassung:The production of cytokines (MIG, IFN-gamma, TNF-alpha, IL-4, IL-5, and IL-10) was studied in 39 individuals, including 28 with chagasic esophagopathy and 11 nonchagasic patients with gastroesophageal reflux disease. A sandwich enzyme immunoassay employing monoclonal antibody pairs specific for each cytokine was used. IFN-gamma and MIG production was significantly higher in patients with megaesophagus compared to control. Furthermore, in the absence of stimulation TNF-alpha levels were lower in the chagasic group than in the control group. In addition, significantly lower TNF-alpha levels were observed for the advanced form of the disease compared to the nonadvanced form. These results support the hypothesis that, although patients with advanced phase of megaesophagus present low number of CD4+ T lymphocytes, PBMC from this patients are able to respond up specific antigen stimulation
Beschreibung:Date Completed 31.05.2006
Date Revised 21.11.2008
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035