Advances in mechanisms of allergic disease in 2016.

J Allergy Clin Immunol

Department of Medicine, Vanderbilt University Medical Center, Nashville, Tenn.

Published: December 2017

This review highlights advances in mechanisms of allergic disease, particularly type 2 innate lymphoid cells; T2 lymphocytes; eicosanoid regulation of inflammation; extracellular vesicles in allergic responses; IL-33; microbiome properties, especially as they relate to mucosal barrier function; and a series of findings concerning the allergic inflammatory cells eosinophils, basophils, and mast cells. During the last year, mechanistic advances occurred in understanding type 2 innate lymphoid cells, particularly related to their response to ozone, involvement with experimental food allergy responses, and regulation by IL-33. Novel ways of regulating T2 cells through epigenetic regulation of GATA-3 through sirtuin-1, a class III histone deacetylase, were published. The understanding of eicosanoid regulation of inflammation increased and focused on additional properties of phospholipase A and the role of prostaglandin D and its receptors and inhibitory prostaglandin E pathways. Mechanisms through which extracellular vesicles are released and contribute to allergic responses were reported. There was a deeper appreciation of mucosal barrier function, the epithelial alarmin IL-33, and the microbiome. Finally, there were advances concerning allergic inflammatory cells (mast cells, basophils, and eosinophils) that will undoubtedly have an effect on disease understanding and new therapeutic strategies.

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http://dx.doi.org/10.1016/j.jaci.2017.08.029DOI Listing

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