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Staphylococcus aureus enterotoxin sensitization involvement and its association with the CysLTR1 variant in different asthma phenotypes

Authors :
Mayumi Tamari
Isao Ito
Tetsuya Oguma
Michiaki Mishima
Hideo Kita
Tetsuji Yokoyama
Toshiyuki Iwata
Yasutaka Nakano
Shoichiro Ohta
Yuji Tohda
Keisuke Tomii
Takahiko Horiguchi
Tomomitsu Hirota
Junya Ono
Kenji Izuhara
Hideki Inoue
Kazunobu Kuwabara
Tomoko Tajiri
Yasuharu Tabara
Hisako Matsumoto
Katsuyuki Tomita
Noriyuki Ohkura
Soichiro Hozawa
Takahisa Kawaguchi
Kojiro Otsuka
Akihito Yokoyama
Fumihiko Matsuda
Akio Niimi
Tadao Nagasaki
Masaki Fujimura
Yoshihiro Kanemitsu
Tsuyoshi Oguma
Yumi Izuhara
Hiroshi Ohnishi
Source :
Epub 2016 Dec 27
Publication Year :
2017
Publisher :
McLean, VA : American College of Allergy, Asthma, and Immunology, 2017.

Abstract

Background Sensitization to Staphylococcus aureus enterotoxin (SE) is a known risk factor for asthma susceptibility and severity. However, how SE sensitization is involved in asthma, particularly nonatopic asthma and/or late-onset asthma, remains uncertain. Objective To clarify the involvement of SE sensitization in nonatopic and/or late-onset asthma and its association with a polymorphism of the cysteinyl leukotriene receptor 1 gene ( CysLTR1 ), which was examined because CysLT signaling is closely associated with late-onset eosinophilic asthma. Methods We assessed associations between sensitization to SE (A and/or B) and clinical indexes in 224 patients with asthma (mean age, 62.3 years; 171 women) from a cohort of the Kinki Hokuriku Airway Disease Conference, particularly those with nonatopic asthma (not sensitized to common aeroallergens) and/or late-onset asthma. Associations between SE sensitization and CysLTR1 polymorphism (rs2806489), a potential regulatory variant for atopic predisposition in women, were also assessed in a sex-stratified manner. Results A total of 105 patients (47%) with asthma were sensitized to SE. Among patients with nonatopic asthma (n = 67) or with late-onset asthma (n = 124), those sensitized to SE had significantly higher serum total IgE and periostin levels than those not sensitized. In nonatopic patients, a rapid decrease in forced expiratory volume in 1 second was associated with SE sensitization. In women with asthma, rs2806489 was associated with sensitization to SEB and age at asthma onset. Conclusion SE sensitization contributes to T H 2 inflammation in nonatopic and/or late-onset asthma. In women with asthma, the CysLTR1 variant might be associated with sensitization to SEB and age at asthma onset.

Details

Language :
English
ISSN :
10811206
Volume :
118
Issue :
2
Database :
OpenAIRE
Journal :
Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
Accession number :
edsair.doi.dedup.....6e1b2cfb4b4bdc5fa7c4925bbe2a0ded