TY - JOUR
T1 - Staphylococcus aureus enterotoxin sensitization involvement and its association with the CysLTR1 variant in different asthma phenotypes
AU - Matsumoto, Hisako
AU - Kanemitsu, Yoshihiro
AU - Nagasaki, Tadao
AU - Tohda, Yuji
AU - Horiguchi, Takahiko
AU - Kita, Hideo
AU - Kuwabara, Kazunobu
AU - Tomii, Keisuke
AU - Otsuka, Kojiro
AU - Fujimura, Masaki
AU - Ohkura, Noriyuki
AU - Tomita, Katsuyuki
AU - Yokoyama, Akihito
AU - Ohnishi, Hiroshi
AU - Nakano, Yasutaka
AU - Oguma, Tetsuya
AU - Hozawa, Soichiro
AU - Izuhara, Yumi
AU - Ito, Isao
AU - Oguma, Tsuyoshi
AU - Inoue, Hideki
AU - Tajiri, Tomoko
AU - Iwata, Toshiyuki
AU - Ono, Junya
AU - Ohta, Shoichiro
AU - Hirota, Tomomitsu
AU - Kawaguchi, Takahisa
AU - Tamari, Mayumi
AU - Yokoyama, Tetsuji
AU - Tabara, Yasuharu
AU - Matsuda, Fumihiko
AU - Izuhara, Kenji
AU - Niimi, Akio
AU - Mishima, Michiaki
N1 - Publisher Copyright:
© 2016 American College of Allergy, Asthma & Immunology
PY - 2017/2/1
Y1 - 2017/2/1
N2 - 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 TH2 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.
AB - 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 TH2 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.
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U2 - 10.1016/j.anai.2016.11.013
DO - 10.1016/j.anai.2016.11.013
M3 - Article
C2 - 28034578
AN - SCOPUS:85009178457
SN - 1081-1206
VL - 118
SP - 197
EP - 203
JO - Annals of Allergy, Asthma and Immunology
JF - Annals of Allergy, Asthma and Immunology
IS - 2
ER -