Aspirin-exacerbated respiratory disease (AERD): Current understanding of AERD.


Journal

Allergology international : official journal of the Japanese Society of Allergology
ISSN: 1440-1592
Titre abrégé: Allergol Int
Pays: England
ID NLM: 9616296

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 26 04 2019
accepted: 06 05 2019
pubmed: 27 6 2019
medline: 21 12 2019
entrez: 26 6 2019
Statut: ppublish

Résumé

The characteristics in AERD are severe adult-onset asthma, eosinophilic rhinosinusitis with nasal polyposis, and CysLT overproduction. The cause of AERD have remained unclear, however the decrease in the production of PGE2 caused by the reduction in COX-2 activity is considered to main pathological mechanism of AERD. The mast cell activation and the interaction between platelets and granulocytes are lead to the CysLT overproduction and severe eosinophilic inflammation. The ongoing activation of mast cells is important key pathogenesis in not only stable AERD but exacerbated AERD by aspirin and NSAIDs. In recent years, type 2 inflammation caused by ILC2 activation in patients with AERD have been attracting attention. Omalizumab is effective option for AERD via suppression of mast cell activation and CysLT overproduction. Dupilumab improves sinus symptoms especially in patients with AERD. In near future, anti-platelet drug, CRTH2 antagonist, and anti-TSLP antibody may be useful candidates of therapeutic options in patients with AERD.

Identifiants

pubmed: 31235242
pii: S1323-8930(19)30058-9
doi: 10.1016/j.alit.2019.05.001
pii:
doi:

Substances chimiques

Anti-Asthmatic Agents 0
Anti-Inflammatory Agents, Non-Steroidal 0
Aspirin R16CO5Y76E

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

289-295

Informations de copyright

Copyright © 2019 Japanese Society of Allergology. Production and hosting by Elsevier B.V. All rights reserved.

Auteurs

Masami Taniguchi (M)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan. Electronic address: taniguchi.masami.ne@mail.hosp.go.jp.

Chihiro Mitsui (C)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

Hiroaki Hayashi (H)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

Emiko Ono (E)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

Keiichi Kajiwara (K)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

Haruhisa Mita (H)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

Kentaro Watai (K)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

Yosuke Kamide (Y)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

Yuma Fukutomi (Y)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

Kiyoshi Sekiya (K)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

Noritaka Higashi (N)

National Hospital Organization Sagamihara National Hospital, Clinical Research Center, Kanagawa, Japan.

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Classifications MeSH