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Childhood allergic asthma is associated with increased IL-13 and FOXP3 histone acetylation
Epigenetic mechanisms including DNA methylation and histone acetylation play a major role in controlling the polarization of naive T cells toward different effector T cells such as TH1, TH2, and regulatory T (Treg) cells and may thus modify the risk for disease development by modulating the developm...
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Published in: | Journal of allergy and clinical immunology 2015-07, Vol.136 (1), p.200-202 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Epigenetic mechanisms including DNA methylation and histone acetylation play a major role in controlling the polarization of naive T cells toward different effector T cells such as TH1, TH2, and regulatory T (Treg) cells and may thus modify the risk for disease development by modulating the developmental function of these T-cell populations.1 Recently, the link between epigenetic modifications and the risk for asthma development was investigated in several cohort studies, which mainly focused on DNA methylation,2 whereas little is known about the role of histone modifications including histone acetylation during asthma manifestation. Histone acetylation as an epigenetic marker for transcriptional activation was measured in a subgroup of 4- to 15-year-old steroid-naive children with AA and HC children from the Munich Clinical Asthma Research Association (CLARA) study population (n(AA) = 14, n(HCs) = 18).3 Children with AA were characterized by increased eosinophils, IgE, and fractional exhaled nitric oxide compared with HC children and showed a significant bronchodilator response4 according to American Thoracic Society/European Respiratory Society guidelines. |
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ISSN: | 0091-6749 1097-6825 |
DOI: | 10.1016/j.jaci.2015.01.027 |