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Archives of Toxicology

Publication date: 2016-01-01
Volume: 90 Pages: 1709 - 1717
Publisher: Springer-Verlag

Author:

Pollaris, Lore
Devos, Fien ; De Vooght, Vanessa ; Seys, Sven ; Nemery, Benoit ; Hoet, Peter ; Vanoirbeek, Jeroen

Keywords:

Science & Technology, Life Sciences & Biomedicine, Toxicology, 4,4 '-Methylene diphenyl diisocyanate, 2,4-Toluene diisocyanate, Cross-reactivity, Occupational asthma, C57Bl/6 mice, SKIN EXPOSURE, IMMUNOLOGICAL DETERMINANTS, RESPIRATORY SYMPTOMS, DERMAL SENSITIZATION, OCCUPATIONAL ASTHMA, ISOCYANATE ASTHMA, IMMUNE-RESPONSES, MDI, TDI, SPECIFICITY, 4,4′-Methylene diphenyl diisocyanate, Air Pollutants, Occupational, Animals, Asthma, Cross Reactions, Disease Models, Animal, Immunoglobulin E, Isocyanates, Male, Mice, Inbred C57BL, Th1-Th2 Balance, Toluene 2,4-Diisocyanate, 1115 Pharmacology and Pharmaceutical Sciences, 3101 Biochemistry and cell biology, 3214 Pharmacology and pharmaceutical sciences

Abstract:

Both 2,4-toluene diisocyanate (TDI) and 4,4-methylene diphenyl diisocyanate (MDI) can cause occupational asthma. In this study, we optimized our mouse model of chemical-induced asthma in the C57Bl/6 mice strain using the model agent TDI. Furthermore, we validated MDI in this mouse model and investigated whether cross-reactivity between TDI and MDI is present. On days 1 and 8, C57Bl/6 mice were dermally treated (20 µl/ear) with 3 % MDI, 2 % TDI or the vehicle acetone olive oil (AOO) (3:2). On day 15, they received a single oropharyngeal challenge with 0.04 % MDI, 0.01 % TDI or the vehicle AOO (4:1). One day later, airway hyperreactivity (AHR) and pulmonary inflammation in the bronchoalveolar lavage (BAL) were assessed. Furthermore, total serum IgE levels, lymphocyte subpopulations in auricular lymph nodes and cytokine levels in supernatants of lymphocytes were measured. Both dermal sensitization with TDI or MDI resulted in increased total serum IgE levels along with T and B cell proliferation in the auricular lymph nodes. The auricular lymphocytes showed an increased release of both Th2 and Th1 cytokines. Mice sensitized and challenged with either TDI or MDI showed AHR, along with a predominant neutrophil lung inflammation. Mice sensitized with MDI and challenged with TDI or the other way around showed no AHR, nor BAL inflammation. Both TDI and MDI are able to induce an asthma-like response in this mouse model. However, cross-reactivity between both diisocyanates remained absent.