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Understanding the complexity of IgE-related phenotypes from childhood to young adulthood: A Mechanisms of the Development of Allergy (MeDALL) seminar.

J. Allergy Clin. Immunol. 129, 943-954 (2012)
DOI
Open Access Green as soon as Postprint is submitted to ZB.
Mechanisms of the Development of Allergy (MeDALL), a Seventh Framework Program European Union project, aims to generate novel knowledge on the mechanisms of initiation of allergy. Precise phenotypes of IgE-mediated allergic diseases will be defined in MeDALL. As part of MeDALL, a scientific seminar was held on January 24, 2011, to review current knowledge on the IgE-related phenotypes and to explore how a multidisciplinary effort could result in a new integrative translational approach. This article provides a summary of the meeting. It develops challenges in IgE-related phenotypes and new clinical and epidemiologic approaches to the investigation of allergic phenotypes, including cluster analysis, scale-free models, candidate biomarkers, and IgE microarrays; the particular case of severe asthma was reviewed. Then novel approaches to the IgE-associated phenotypes are reviewed from the individual mechanisms to the systems, including epigenetics, human in vitro immunology, systems biology, and animal models. The last chapter deals with the understanding of the population-based IgE-associated phenotypes in children and adolescents, including age effect in terms of maturation, observed effects of early-life exposures and shift of focus from early life to pregnancy, gene-environment interactions, cohort effects, and time trends in patients with allergic diseases. This review helps to define phenotypes of allergic diseases in MeDALL.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Allergy; Mechanisms of the Development of Allergy; Seventh Framework Program; phenotypes; IgE; asthma; ASTHMA RESEARCH-PROGRAM; OBSTRUCTIVE PULMONARY-DISEASE; WORLD-HEALTH-ORGANIZATION; T-REGULATORY-CELLS; BIRTH-COHORT; CLUSTER-ANALYSIS; RUSSIAN KARELIA; LUNG-FUNCTION; BRONCHIAL HYPERRESPONSIVENESS; DIAGNOSTIC GATEKEEPERS
Reviewing status