Methylisothiazolinone: Dermal and respiratory immune responses in mice

被引:22
作者
Devos, Fien C. [1 ]
Pollaris, Lore [1 ]
Van Den Broucke, Sofie [1 ]
Seys, Sven [2 ]
Goossens, An [3 ]
Nemery, Benoit [1 ]
Hoet, Peter H. M. [1 ]
Vanoirbeek, Jeroen A. J. [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Environm & Hlth, Dept Publ Hlth & Primary Care, B-3000 Leuven, Belgium
[2] Katholieke Univ Leuven, Clin Immunol Lab, Dept Microbiol & Immunol, B-3000 Leuven, Belgium
[3] Katholieke Univ Leuven, Lab Dermatoimmunol, Dept Microbiol & Immunol, B-3000 Leuven, Belgium
关键词
Methylisothiazolinone; Sensitizer; Mice; Chemical-induced asthma; Skin/lung; LYMPH-NODE ASSAY; CONTACT ALLERGY; TOLUENE DIISOCYANATE; PRESERVATIVE SENSITIVITY; SENSITIZATION; DERMATITIS; AIRBORNE; PAINT; REACTIVITY; EXPOSURE;
D O I
10.1016/j.toxlet.2015.04.009
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Methylisothiazolinone (MI), a widely used chemical preservative in industrial and household products, and cosmetics, has been associated with allergic contact dermatitis. However, the asthmogenic capacity of MI is currently unknown. In this study, we investigated the capacity of MI to elicit asthma-like responses in a validated mouse model. On days 1 and 8, mice (C57Bl/6 and BALB/c) were dermally treated with MI or vehicle on each ear. On day 15, mice received a single intranasal challenge with MI or vehicle. Immediately after the challenge, the early ventilatory response was measured using a double chamber plethysmograph. One day later, airway hyperreactivity, pulmonary inflammation and immune-related parameters were assessed. Dermal treatment with MI in both C57Bl/6 and BALB/c mice induced increased T-and B-cell proliferation in the auricular lymph nodes, along with IFN-gamma production and limited increases in total serum IgE, confirming dermal sensitization. An airway challenge with MI led to an early ventilatory response (decreased breathing frequency), indicative for acute sensory irritation. However, 24 h later no allergic respiratory response (no airway hyperreactivity (AHR) nor pulmonary inflammation) was found in either mouse strains. Our study indicates that MI can be classified as a strong dermal sensitizer and irritant, but not an asthmogen after initial dermal sensitization, followed by an airway challenge. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:179 / 188
页数:10
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