Dust mite allergen, glutathione S-transferase, induces T cell immunoglobulin mucin domain-4 in dendritic cells to facilitate initiation of airway allergy

作者：Mo, L. -H.; Yang, L. -T.; Zeng, L.; Xu, L. -Z.; Zhang, H. -P.; Li, L. -J.; Liu, J. -Q.; Xiao, X. -J.; Zheng, P. -Y.; Liu, Z. -G.^*; Yang, P. -C.^*

来源：Clinical and Experimental Allergy, 2017, 47(2): 264-270.

DOI：10.1111/cea.12800

• allergen
• allergy
• animal model
• asthma
• specific immunotherapy

Background Allergens from dust mites play a critical role in the pathogenesis of airway allergy. The mechanism by which dust mite allergens induce allergic diseases is not fully understood yet. Objective This study tests a hypothesis that the eighth subtypes of Dermatophagoides farina allergen (Derf8) play an important role in the induction of airway allergy. Methods The protein of Derf8 was synthesized via molecular cloning approach. Dendritic cells (DC) were stimulated with Derf8 in the culture, and then, the expression of T cell immunoglobulin mucin domain 4 (TIM4) in dendritic cells (DC) was analysed. The role of Derf8 in the induction of airway allergy was evaluated with a mouse model. Results Exposure to Derf8 markedly induced the TIM4 expression in DCs by modulating the chromatin at the TIM4 promoter locus. Derf8 played a critical role in the expansion of the T helper 2 response in the mouse airway via inducing DCs to produce TIM4. Administration with Derf8- depleted dust mite extracts (DME) inhibited the allergic inflammation and induced regulatory T cells in mice with airway allergy. Conclusion Derf8 plays an important role in the initiation of dust mite allergy. Vaccination with Derf8- deficient DME is more efficient to inhibit the dust mite allergic inflammation than using wild DME.

• 出版日期2017-2
• 单位深圳大学; 郑州大学