CYTOKINE PROFILE IN LONG-TERM USE OF INHALED CORTICOSTEROID IN ASTHMATIC CHILDREN RECEIVING SPECIFIC IMMUNOTHERAPY

INTRODUCTION: Inhaled corticosteroids are widely used for the management of persistent asthma, including by those who receive specific immunotherapy. OBJECTIVE: Our goal was to elucidate the cytokine profile in long-term use of corticosteroid inhalation in asthmatic children who were receiving speci...

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Veröffentlicht in:Pediatrics (Evanston) 2008-01, Vol.121 (Supplement_2), p.S91-S91
1. Verfasser: Harsono, Ariyanto
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description INTRODUCTION: Inhaled corticosteroids are widely used for the management of persistent asthma, including by those who receive specific immunotherapy. OBJECTIVE: Our goal was to elucidate the cytokine profile in long-term use of corticosteroid inhalation in asthmatic children who were receiving specific immunotherapy. METHODS: We performed a randomized, paralleled, comparative study of asthmatic children allocated into 3 groups: those in group A received inhaled budesonide, those in group B received specific immunotherapy, and those in group C received both specific immunotherapy and inhaled budesonide. The primary outcomes were interleukin 4 (IL-4), IL-5, interferon γ (IFN-γ), and IL-2 levels and forced expiratory volume in 1 second (FEV1) reversibility. RESULTS: Significant differences were observed before and after treatment in all groups (P < .05). Patients who received inhaled budesonide showed attenuation of IL-4, IL-5, IFN-γ, and IL-2 and 29% failure of FEV1 reversibility. Patients who received immunotherapy showed attenuation of IL-4 and IL-5, elevation of IFN-γ and IL-2, and 24% failure of improvement of FEV1 reversibility. Patients who received inhaled corticosteroids and immunotherapy showed attenuation of IL-4 and IL-5, elevation of IFN-γ and IL-2, and 100% improvement of FEV1 reversibility. Analysis of the discriminator yielded IL-2 as the primary discriminator, which correlated with the decrease of IL-5. CONCLUSIONS: Long-term use of inhaled corticosteroids by children with asthma who received immunotherapy resulted in elevation of IFN-γ and IL-2 and a decrease of IL-4 and IL-5. Addition of inhaled corticosteroids to immunotherapy resulted in marked attenuation of IL-5 and correlated with greater elevation of IL-2.
doi_str_mv 10.1542/peds.2007-2022H
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OBJECTIVE: Our goal was to elucidate the cytokine profile in long-term use of corticosteroid inhalation in asthmatic children who were receiving specific immunotherapy. METHODS: We performed a randomized, paralleled, comparative study of asthmatic children allocated into 3 groups: those in group A received inhaled budesonide, those in group B received specific immunotherapy, and those in group C received both specific immunotherapy and inhaled budesonide. The primary outcomes were interleukin 4 (IL-4), IL-5, interferon γ (IFN-γ), and IL-2 levels and forced expiratory volume in 1 second (FEV1) reversibility. RESULTS: Significant differences were observed before and after treatment in all groups (P &lt; .05). Patients who received inhaled budesonide showed attenuation of IL-4, IL-5, IFN-γ, and IL-2 and 29% failure of FEV1 reversibility. Patients who received immunotherapy showed attenuation of IL-4 and IL-5, elevation of IFN-γ and IL-2, and 24% failure of improvement of FEV1 reversibility. Patients who received inhaled corticosteroids and immunotherapy showed attenuation of IL-4 and IL-5, elevation of IFN-γ and IL-2, and 100% improvement of FEV1 reversibility. Analysis of the discriminator yielded IL-2 as the primary discriminator, which correlated with the decrease of IL-5. CONCLUSIONS: Long-term use of inhaled corticosteroids by children with asthma who received immunotherapy resulted in elevation of IFN-γ and IL-2 and a decrease of IL-4 and IL-5. Addition of inhaled corticosteroids to immunotherapy resulted in marked attenuation of IL-5 and correlated with greater elevation of IL-2.</description><identifier>ISSN: 0031-4005</identifier><identifier>EISSN: 1098-4275</identifier><identifier>DOI: 10.1542/peds.2007-2022H</identifier><identifier>CODEN: PEDIAU</identifier><language>eng</language><publisher>Evanston: American Academy of Pediatrics</publisher><subject>Asthma ; Children &amp; youth ; Cytokines ; Immunotherapy ; Medical treatment ; Pediatrics ; Steroids ; Studies</subject><ispartof>Pediatrics (Evanston), 2008-01, Vol.121 (Supplement_2), p.S91-S91</ispartof><rights>Copyright American Academy of Pediatrics Jan 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Harsono, Ariyanto</creatorcontrib><title>CYTOKINE PROFILE IN LONG-TERM USE OF INHALED CORTICOSTEROID IN ASTHMATIC CHILDREN RECEIVING SPECIFIC IMMUNOTHERAPY</title><title>Pediatrics (Evanston)</title><description>INTRODUCTION: Inhaled corticosteroids are widely used for the management of persistent asthma, including by those who receive specific immunotherapy. OBJECTIVE: Our goal was to elucidate the cytokine profile in long-term use of corticosteroid inhalation in asthmatic children who were receiving specific immunotherapy. METHODS: We performed a randomized, paralleled, comparative study of asthmatic children allocated into 3 groups: those in group A received inhaled budesonide, those in group B received specific immunotherapy, and those in group C received both specific immunotherapy and inhaled budesonide. The primary outcomes were interleukin 4 (IL-4), IL-5, interferon γ (IFN-γ), and IL-2 levels and forced expiratory volume in 1 second (FEV1) reversibility. RESULTS: Significant differences were observed before and after treatment in all groups (P &lt; .05). Patients who received inhaled budesonide showed attenuation of IL-4, IL-5, IFN-γ, and IL-2 and 29% failure of FEV1 reversibility. Patients who received immunotherapy showed attenuation of IL-4 and IL-5, elevation of IFN-γ and IL-2, and 24% failure of improvement of FEV1 reversibility. Patients who received inhaled corticosteroids and immunotherapy showed attenuation of IL-4 and IL-5, elevation of IFN-γ and IL-2, and 100% improvement of FEV1 reversibility. Analysis of the discriminator yielded IL-2 as the primary discriminator, which correlated with the decrease of IL-5. CONCLUSIONS: Long-term use of inhaled corticosteroids by children with asthma who received immunotherapy resulted in elevation of IFN-γ and IL-2 and a decrease of IL-4 and IL-5. 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OBJECTIVE: Our goal was to elucidate the cytokine profile in long-term use of corticosteroid inhalation in asthmatic children who were receiving specific immunotherapy. METHODS: We performed a randomized, paralleled, comparative study of asthmatic children allocated into 3 groups: those in group A received inhaled budesonide, those in group B received specific immunotherapy, and those in group C received both specific immunotherapy and inhaled budesonide. The primary outcomes were interleukin 4 (IL-4), IL-5, interferon γ (IFN-γ), and IL-2 levels and forced expiratory volume in 1 second (FEV1) reversibility. RESULTS: Significant differences were observed before and after treatment in all groups (P &lt; .05). Patients who received inhaled budesonide showed attenuation of IL-4, IL-5, IFN-γ, and IL-2 and 29% failure of FEV1 reversibility. Patients who received immunotherapy showed attenuation of IL-4 and IL-5, elevation of IFN-γ and IL-2, and 24% failure of improvement of FEV1 reversibility. Patients who received inhaled corticosteroids and immunotherapy showed attenuation of IL-4 and IL-5, elevation of IFN-γ and IL-2, and 100% improvement of FEV1 reversibility. Analysis of the discriminator yielded IL-2 as the primary discriminator, which correlated with the decrease of IL-5. CONCLUSIONS: Long-term use of inhaled corticosteroids by children with asthma who received immunotherapy resulted in elevation of IFN-γ and IL-2 and a decrease of IL-4 and IL-5. Addition of inhaled corticosteroids to immunotherapy resulted in marked attenuation of IL-5 and correlated with greater elevation of IL-2.</abstract><cop>Evanston</cop><pub>American Academy of Pediatrics</pub><doi>10.1542/peds.2007-2022H</doi></addata></record>
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subjects Asthma
Children & youth
Cytokines
Immunotherapy
Medical treatment
Pediatrics
Steroids
Studies
title CYTOKINE PROFILE IN LONG-TERM USE OF INHALED CORTICOSTEROID IN ASTHMATIC CHILDREN RECEIVING SPECIFIC IMMUNOTHERAPY
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