Association between specific IgE to staphylococcal enterotoxin B and the eosinophilic phenotype of asthma.


Journal

The Korean journal of internal medicine
ISSN: 2005-6648
Titre abrégé: Korean J Intern Med
Pays: Korea (South)
ID NLM: 8712418

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 05 01 2024
accepted: 02 04 2024
medline: 11 7 2024
pubmed: 11 7 2024
entrez: 10 7 2024
Statut: ppublish

Résumé

Sensitization to staphylococcal superantigens (SAgs) could contribute to asthma severity. However, its relevance with eosinophilic phenotype has not yet been clarified. This study aimed to investigate associations between serum specific IgE levels to SAg and eosinophilic airway inflammation in adult asthmatics. The serum specific IgE levels to 3 SAgs, including staphylococcal enterotoxin A (SEA) and B (SEB), and toxic shock syndrome toxin-1 (TSST-1) were measured by ImmunoCAP in 230 adult asthmatic patients and 50 healthy controls (HCs). Clinical characteristics and laboratory parameters, including serum total/free IgE, and 2 eosinophil-activation markers, eosinophil cationic protein (ECP), and eosinophil-derived neurotoxin (EDN), were analyzed according to blood eosinophil counts (BEC; 150 cells/μL) and serum specific IgE levels to 3 SAgs (0.35 kU/L). Asthmatic patients showed higher serum specific IgE levels to 3 SAgs than HCs (p < 0.05 for all). The serum total/clinfree IgE levels were significantly higher in asthmatics with positive IgE responses to 3 SAgs than those without (p < 0.05 for all). There were no significant differences in clinical parameters including age, asthma severity, comorbidities, or smoking according to IgE responses to 3 SAgs. Patients with positive IgE responses to SEB (not to SEA/TSST-1) had higher serum specific IgE levels to house dust mites and ECP/EDN as well as higher BEC with positive correlations between serum SEB-specific IgE levels and BEC/ECP/EDN (p < 0.05 for all). These findings suggest that serum SEB-specific IgE levels could contribute to eosinophil activation as well as IgE production in adult asthma.

Sections du résumé

BACKGROUND/AIMS OBJECTIVE
Sensitization to staphylococcal superantigens (SAgs) could contribute to asthma severity. However, its relevance with eosinophilic phenotype has not yet been clarified. This study aimed to investigate associations between serum specific IgE levels to SAg and eosinophilic airway inflammation in adult asthmatics.
METHODS METHODS
The serum specific IgE levels to 3 SAgs, including staphylococcal enterotoxin A (SEA) and B (SEB), and toxic shock syndrome toxin-1 (TSST-1) were measured by ImmunoCAP in 230 adult asthmatic patients and 50 healthy controls (HCs). Clinical characteristics and laboratory parameters, including serum total/free IgE, and 2 eosinophil-activation markers, eosinophil cationic protein (ECP), and eosinophil-derived neurotoxin (EDN), were analyzed according to blood eosinophil counts (BEC; 150 cells/μL) and serum specific IgE levels to 3 SAgs (0.35 kU/L).
RESULTS RESULTS
Asthmatic patients showed higher serum specific IgE levels to 3 SAgs than HCs (p < 0.05 for all). The serum total/clinfree IgE levels were significantly higher in asthmatics with positive IgE responses to 3 SAgs than those without (p < 0.05 for all). There were no significant differences in clinical parameters including age, asthma severity, comorbidities, or smoking according to IgE responses to 3 SAgs. Patients with positive IgE responses to SEB (not to SEA/TSST-1) had higher serum specific IgE levels to house dust mites and ECP/EDN as well as higher BEC with positive correlations between serum SEB-specific IgE levels and BEC/ECP/EDN (p < 0.05 for all).
CONCLUSION CONCLUSIONS
These findings suggest that serum SEB-specific IgE levels could contribute to eosinophil activation as well as IgE production in adult asthma.

Identifiants

pubmed: 38986495
pii: kjim.2024.003
doi: 10.3904/kjim.2024.003
doi:

Substances chimiques

Enterotoxins 0
Immunoglobulin E 37341-29-0
enterotoxin B, staphylococcal 39424-53-8
Superantigens 0
Biomarkers 0
Eosinophil Cationic Protein EC 3.1.27.-
RNASE3 protein, human EC 3.1.27.-
Bacterial Toxins 0
enterotoxin F, Staphylococcal 0
Eosinophil-Derived Neurotoxin EC 3.1.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

659-667

Subventions

Organisme : Korea Health Industry Development Institute
Organisme : Ministry of Health and Welfare
ID : HR16C0001

Commentaires et corrections

Type : CommentIn

Auteurs

Soyoon Sim (S)

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

Youngwoo Choi (Y)

Department of Biomaterials Science (BK21 FOUR Program), College of Natural Resources and Life Science, Pusan National University, Miryang, Korea.

Eun-Mi Yang (EM)

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

Hae-Sim Park (HS)

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

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Classifications MeSH