ST2-Mediated Neutrophilic Airway Inflammation: A Therapeutic Target for Patients With Uncontrolled Asthma.

Asthma IL-33 IL1RL1 protein cytokines inflammation macrophages neutrophils therapeutics

Journal

Allergy, asthma & immunology research
ISSN: 2092-7355
Titre abrégé: Allergy Asthma Immunol Res
Pays: Korea (South)
ID NLM: 101518382

Informations de publication

Date de publication:
Jan 2024
Historique:
received: 13 02 2023
revised: 05 06 2023
accepted: 05 08 2023
medline: 24 1 2024
pubmed: 24 1 2024
entrez: 23 1 2024
Statut: ppublish

Résumé

Suppression of tumorigenicity 2 (ST2) has been proposed as the receptor contributing to neutrophilic inflammation in patients with type 2-low asthma. However, the exact role of ST2 in neutrophil activation remains poorly understood. A total of 105 asthmatic patients (classified into 3 groups according to control status: the controlled asthma [CA], partly-controlled asthma [PA], and uncontrolled asthma [UA] groups), and 104 healthy controls were enrolled to compare serum levels of soluble ST2 (sST2) and interleukin (IL)-33. Moreover, the functions of ST2 in neutrophils and macrophages (Mϕ) were evaluated Serum sST2 levels were significantly higher in the UA group than in the CA or PA groups ( These results suggest that IL-33 induces the activation of neutrophils and Mϕ via ST2 receptors, leading to neutrophilic airway inflammation and poor control status of asthma. ST2 could be a therapeutic target for neutrophilic airway inflammation in patients with UA.

Identifiants

pubmed: 38262389
pii: 16.22
doi: 10.4168/aair.2024.16.1.22
doi:

Types de publication

Journal Article

Langues

eng

Pagination

22-41

Subventions

Organisme : National Research Foundation of Korea
ID : 2020R1I1A1A01073900
Pays : Korea
Organisme : Ministry of Health and Welfare
ID : HR16C0001
Pays : Korea

Informations de copyright

Copyright © 2024 The Korean Academy of Asthma, Allergy and Clinical Immunology • The Korean Academy of Pediatric Allergy and Respiratory Disease.

Déclaration de conflit d'intérêts

There are no financial or other issues that might lead to conflict of interest.

Auteurs

Quang Luu Quoc (QL)

Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Department of Biomedical Sciences, Ajou University School of Medicine, Suwon, Korea.

Thi Bich Tra Cao (TBT)

Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Department of Biomedical Sciences, Ajou University School of Medicine, Suwon, Korea.

Jae-Hyuk Jang (JH)

Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.

Yoo Seob Shin (YS)

Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Department of Biomedical Sciences, Ajou University School of Medicine, Suwon, Korea.

Youngwoo Choi (Y)

Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Department of Biomaterials Science, College of Natural Resources and Life Science, Pusan National University, Miryang, Korea. ychoi@pusan.ac.kr.

Hae-Sim Park (HS)

Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.
Department of Biomedical Sciences, Ajou University School of Medicine, Suwon, Korea. hspark@ajou.ac.kr.

Classifications MeSH