Virus-Induced Asthma Exacerbations: SIRT1 Targeted Approach.

SIRT1 asthma cellular senescence exacerbations virus infection

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
13 Aug 2020
Historique:
received: 01 07 2020
revised: 06 08 2020
accepted: 10 08 2020
entrez: 23 8 2020
pubmed: 23 8 2020
medline: 23 8 2020
Statut: epublish

Résumé

The prevalence of asthma has increased worldwide. Asthma exacerbations triggered by upper respiratory tract viral infections remain a major clinical problem and account for hospital admissions and time lost from work. Virus-induced asthma exacerbations cause airway inflammation, resulting in worsening asthma and deterioration in the patients' quality of life, which may require systemic corticosteroid therapy. Despite recent advances in understanding the cellular and molecular mechanisms underlying asthma exacerbations, current therapeutic modalities are inadequate for complete prevention and treatment of these episodes. The pathological role of cellular senescence, especially that involving the silent information regulator 2 homolog sirtuin (SIRT) protein family, has recently been demonstrated in stable and exacerbated chronic respiratory disease states. This review discusses the role of SIRT1 in the pathogenesis of bronchial asthma. It also discusses the role of SIRT1 in inflammatory cells that play an important role in virus-induced asthma exacerbations. Recent studies have hypothesized that SIRT1 is one of major contributors to cellular senescence. SIRT1 levels decrease in Th2 and non-Th2-related airway inflammation, indicating the role of SIRT1 in several endotypes and phenotypes of asthma. Moreover, several models have demonstrated relationships between viral infection and SIRT1. Therefore, targeting SIRT1 is a novel strategy that may be effective for treating virus-induced asthma exacerbations in the future.

Identifiants

pubmed: 32823491
pii: jcm9082623
doi: 10.3390/jcm9082623
pmc: PMC7464235
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Yosuke Fukuda (Y)

Department of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Shinagawa-ku, Tokyo 142-8555, Japan.

Kaho Akimoto (K)

Department of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Shinagawa-ku, Tokyo 142-8555, Japan.

Tetsuya Homma (T)

Department of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Shinagawa-ku, Tokyo 142-8555, Japan.

Jonathan R Baker (JR)

Airway Disease, National Heart and Lung Institute, Imperial College, London SW3 6LY, UK.

Kazuhiro Ito (K)

Airway Disease, National Heart and Lung Institute, Imperial College, London SW3 6LY, UK.

Peter J Barnes (PJ)

Airway Disease, National Heart and Lung Institute, Imperial College, London SW3 6LY, UK.

Hironori Sagara (H)

Department of Medicine, Division of Respiratory Medicine and Allergology, Showa University School of Medicine, 1-5-8 Shinagawa-ku, Tokyo 142-8555, Japan.

Classifications MeSH