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There is established concept that dendritic cells (DCs) play essential roles in the development of allergic immune responses. However, the influence of H 1  receptor antagonists on DC functions is not well defined. The aim of the present study was to examine the effect of epinastine hydrochloride (EP), the most notable histamine H 1  receptor antagonists in Japan, on  Dermatophagoides farinae (Der f) -pulsed mouse bone marrow-derived DCs in vitro and in vivo. EP at more than 25 ng/mL could significantly inhibit the production of IL-6, TNF- α  and IL-10 from  Der f -pulsed DCs, which was increased by  Der f  challenge in vitro. On the other hand, EP increased the ability of  Der f -pulsed DCs to produce IL-12. Intranasal instillation of  Der f -pulsed DCs resulted in nasal eosinophilia associated with a significant increase in IL-5 levels in nasal lavage fluids.  Der f -pulsed and EP-treated DCs significantly inhibited nasal eosinophila and reduced IL-5. These results indicate that EP inhibits the development of Th2 immune responses through the modulation of DC functions and results in favorable modification of clinical status of allergic diseases.

mediators of inflammation

Influence of Epinastine Hydrochloride, an -Receptor Antagonist, on the Function of Mite Allergen-Pulsed Murine Bone Marrow-Derived Dendritic Cells In Vitro and In Vivo