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Serum-soluble TRAIL levels in patients with severe persistent allergic asthma: Its relation to omalizumab treatment

BACKGROUND: In this study we compare the Omalizumab treatment modality in the dynamics of cell apoptosis regulating molecules in both severe persistent asthma patients who had no other any allergic disease, newly diagnosed patients with allergic asthma, and healthy volunteers. MATERIAL/METHODS: Seve...

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Autores principales: Yalcin, Arzu Didem, Bisgin, Atil, Kargi, Aysegul, Gorczynski, Reginald M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560751/
https://www.ncbi.nlm.nih.gov/pubmed/22367138
http://dx.doi.org/10.12659/MSM.882504
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author Yalcin, Arzu Didem
Bisgin, Atil
Kargi, Aysegul
Gorczynski, Reginald M.
author_facet Yalcin, Arzu Didem
Bisgin, Atil
Kargi, Aysegul
Gorczynski, Reginald M.
author_sort Yalcin, Arzu Didem
collection PubMed
description BACKGROUND: In this study we compare the Omalizumab treatment modality in the dynamics of cell apoptosis regulating molecules in both severe persistent asthma patients who had no other any allergic disease, newly diagnosed patients with allergic asthma, and healthy volunteers. MATERIAL/METHODS: Severe persistent allergic asthma patients were subjected to measurement of serum soluble TRAIL (TNF-related apoptosis-inducing ligand) levels during the active disease phase and the stable phase which occurred 4 months after Omalizumab treatment. Serum sTRAIL concentrations were measured by a solid phase sandwich enzyme-linked immunosorbent assay. Concentration levels were compared with those of age- and sex-matched newly diagnosed patients with allergic asthma, and healthy controls. All assays were carried out in duplicate. Total serum IgE levels, antinuclear antibody (ANA), rheumatoid factor (RF), hepatitis markers, C3, C4 and eosinophil levels were evaluated in all patients. RESULTS: ANA, RF, hepatitis markers were negative in all patients. Complement 3 and 4 levels were normal in all patients. Prick tests in all patients were detected in mite and grass allergy. These results correlated with specific IgE. There were no differences between the healthy controls, newly diagnosed allergic asthma patients, and non-treated severe persistent allergic asthma patients during the active phase. Interestingly, the levels in variances of the patients who had the effective omalizumab treatment were significantly lower than the healthy controls, while the mean values were not statistically significant. CONCLUSIONS: Our study gives a different perspective on severe persistent allergic asthma and omalizumab treatment efficacy at the cell apoptosis-linked step by the serum sTRAIL levels.
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spelling pubmed-35607512013-04-24 Serum-soluble TRAIL levels in patients with severe persistent allergic asthma: Its relation to omalizumab treatment Yalcin, Arzu Didem Bisgin, Atil Kargi, Aysegul Gorczynski, Reginald M. Med Sci Monit Public Investigation BACKGROUND: In this study we compare the Omalizumab treatment modality in the dynamics of cell apoptosis regulating molecules in both severe persistent asthma patients who had no other any allergic disease, newly diagnosed patients with allergic asthma, and healthy volunteers. MATERIAL/METHODS: Severe persistent allergic asthma patients were subjected to measurement of serum soluble TRAIL (TNF-related apoptosis-inducing ligand) levels during the active disease phase and the stable phase which occurred 4 months after Omalizumab treatment. Serum sTRAIL concentrations were measured by a solid phase sandwich enzyme-linked immunosorbent assay. Concentration levels were compared with those of age- and sex-matched newly diagnosed patients with allergic asthma, and healthy controls. All assays were carried out in duplicate. Total serum IgE levels, antinuclear antibody (ANA), rheumatoid factor (RF), hepatitis markers, C3, C4 and eosinophil levels were evaluated in all patients. RESULTS: ANA, RF, hepatitis markers were negative in all patients. Complement 3 and 4 levels were normal in all patients. Prick tests in all patients were detected in mite and grass allergy. These results correlated with specific IgE. There were no differences between the healthy controls, newly diagnosed allergic asthma patients, and non-treated severe persistent allergic asthma patients during the active phase. Interestingly, the levels in variances of the patients who had the effective omalizumab treatment were significantly lower than the healthy controls, while the mean values were not statistically significant. CONCLUSIONS: Our study gives a different perspective on severe persistent allergic asthma and omalizumab treatment efficacy at the cell apoptosis-linked step by the serum sTRAIL levels. International Scientific Literature, Inc. 2012-03-01 /pmc/articles/PMC3560751/ /pubmed/22367138 http://dx.doi.org/10.12659/MSM.882504 Text en © Med Sci Monit, 2012 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
spellingShingle Public Investigation
Yalcin, Arzu Didem
Bisgin, Atil
Kargi, Aysegul
Gorczynski, Reginald M.
Serum-soluble TRAIL levels in patients with severe persistent allergic asthma: Its relation to omalizumab treatment
title Serum-soluble TRAIL levels in patients with severe persistent allergic asthma: Its relation to omalizumab treatment
title_full Serum-soluble TRAIL levels in patients with severe persistent allergic asthma: Its relation to omalizumab treatment
title_fullStr Serum-soluble TRAIL levels in patients with severe persistent allergic asthma: Its relation to omalizumab treatment
title_full_unstemmed Serum-soluble TRAIL levels in patients with severe persistent allergic asthma: Its relation to omalizumab treatment
title_short Serum-soluble TRAIL levels in patients with severe persistent allergic asthma: Its relation to omalizumab treatment
title_sort serum-soluble trail levels in patients with severe persistent allergic asthma: its relation to omalizumab treatment
topic Public Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560751/
https://www.ncbi.nlm.nih.gov/pubmed/22367138
http://dx.doi.org/10.12659/MSM.882504
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