Participation of Th17 and Treg Cells in Pediatric Bronchial Asthma
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概要
- 論文の詳細を見る
The immune response plays an important role in the development of allergic diseases. It is established that a complex network of various immunocytes such as Th2, non-Th2 (Th17), and regulatory T (Treg) participate in allergic reactions. In this study, we examined the frequencies of Th17 cells (IL-17-positive cells) and Treg cells (FOXP3-positive cells) in the peripheral blood and elucidated their participation in pediatric allergic diseases such as bronchial asthma and food allergies. Our study included 35 subjects, 27 with allergic diseases (19 with asthma and 8 with food allergies) and 8 were controls (without any allergic diseases); their age ranged from 1 to 13 years. The frequency of Th17 cells (IL-17-positive cells) among the CD4+T cells in the peripheral blood was 2.33±1.29% in patients with bronchial asthma, 1.53±1.34% in those with food allergies, and 1.50±0.809% in controls. These results indicated that only the patients with bronchial asthma had a trend towards a higher frequency of Th17 cells (p=0.1558). The ratio of Th17 cells to Treg cells did not show any statistical correlation among the patients with bronchial asthma. However, when we excluded the patients with a severe type of asthma, we could obtain an inverse trend between the ratio of Th17 cells to Treg cells (p=0.1655). This study suggested that Th17 cells and Treg cells participate in pediatric allergic reactions such as bronchial asthma.
著者
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RONCADOR Giovanna
Monoclonal Antibodies Unit, Biotechnology Program, Centro Nacional de Investigaciones Oncologicas
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Banham Alison
Nuffield Department Of Clinical Laboratory Sciences John Radcliffe Hospital
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Nakano Yasuko
Department Of Medicinal Information School Of Pharmaceutical Sciences Showa University
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Itabashi Kazuo
Department Of Pediatrics Showa University School Of Medicine
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Negoro Takaharu
Department Of Biochemistry School Of Medicine Showa University
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Yamamoto Yoshiki
Department Of Materials Engineering School Of Engineering The University Of Tokyo
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SUNAGA Susumu
Department of Allergy and Internal Medicine, Kinki University School of Medicine
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Wakagi Akiko
Department of Pharmacogenomics, School of Pharmacy, Showa University
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Hoshi Akane
Department of Pharmacogenomics, School of Pharmacy, Showa University
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Akiyama Haruyo
Department of Pharmacogenomics, School of Pharmacy, Showa University
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Tobe Takashi
Center of Pharmaceutical Education, School of Pharmacy, Showa University
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Roncador Giovanna
Monoclonal Antibodies Unit Biotechnology Program Centro Nacional De Investigaciones Oncologicas
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Itabashi Kazuo
Department Of Pediatrics Showa University Hospital
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Itabashi Kazuo
Department of Pediatrics, School of Medicine, Showa University
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Sunaga Susumu
Department of Pediatrics, Tokyo Metropolitan Health and Medical Treatment Corporation Ebara Hospital
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Roncador Giovanna
Monoclonal Antibodies Unit, Biotechnology Program, Centro Nacional de Investigaciones Oncolo'gicas (CNIO)
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Yamamoto Yoshiki
Department of Pediatrics, Tokyo Metropolitan Health and Medical Treatment Corporation Ebara Hospital
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Banham Alison
Nuffield Department of Clinical Laboratory Sciences, University of Oxford, Level 4 Academic Block, John Radcliffe Hospital
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Negoro Takaharu
Department of Pharmacogenomics, School of Pharmacy, Showa University
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Nakano Yasuko
Department of Chemistry, Faculty of Science, Hokkaido University
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