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Current perspective on eicosanoids in asthma and allergic diseases - EAACI Task Force consensus report, part I

Sokolowska, M; Rovati, G E; Diamant, Z; Untersmayr, E; Schwarze, J; Lukasik, Z; Sava, F; Angelina, A; Palomares, O; Akdis, C A; O‘Mahony, L; Sanak, M; Dahlen, S-E; Woszczek, G (2021). Current perspective on eicosanoids in asthma and allergic diseases - EAACI Task Force consensus report, part I. Allergy, 76(1):114-130.

Abstract

Eicosanoids are biologically active lipid mediators, comprising prostaglandins, leukotrienes, thromboxanes, and lipoxins, involved in several pathophysiological processes relevant to asthma, allergies, and allied diseases. Prostaglandins and leukotrienes are the most studied eicosanoids and established inducers of airway pathophysiology including bronchoconstriction and airway inflammation. Drugs inhibiting the synthesis of lipid mediators or their effects, such as leukotriene synthesis inhibitors, leukotriene receptors antagonists, and more recently prostaglandin D2 receptor antagonists, have been shown to modulate features of asthma and allergic diseases. This review, produced by an European Academy of Allergy and Clinical Immunology (EAACI) task force, highlights our current understanding of eicosanoid biology and its role in mediating human pathology, with a focus on new findings relevant for clinical practice, development of novel therapeutics, and future research opportunities.

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Swiss Institute of Allergy and Asthma Research
Dewey Decimal Classification:610 Medicine & health
Scopus Subject Areas:Health Sciences > Immunology and Allergy
Life Sciences > Immunology
Uncontrolled Keywords:Immunology, Immunology and Allergy
Language:English
Date:1 January 2021
Deposited On:11 Jan 2021 09:33
Last Modified:24 Dec 2024 02:40
Publisher:Wiley-Blackwell Publishing, Inc.
ISSN:0105-4538
OA Status:Closed
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:https://doi.org/10.1111/all.14295
PubMed ID:32279330
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