International Journal of Molecular Sciences (Jun 2017)

Fexofenadine Suppresses Delayed-Type Hypersensitivity in the Murine Model of Palladium Allergy

  • Ryota Matsubara,
  • Kenichi Kumagai,
  • Hiroaki Shigematsu,
  • Kazutaka Kitaura,
  • Yasunari Nakasone,
  • Satsuki Suzuki,
  • Yoshiki Hamada,
  • Ryuji Suzuki

DOI
https://doi.org/10.3390/ijms18071357
Journal volume & issue
Vol. 18, no. 7
p. 1357

Abstract

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Palladium is frequently used in dental materials, and sometimes causes metal allergy. It has been suggested that the immune response by palladium-specific T cells may be responsible for the pathogenesis of delayed-type hypersensitivity in study of palladium allergic model mice. In the clinical setting, glucocorticoids and antihistamine drugs are commonly used for treatment of contact dermatitis. However, the precise mechanism of immune suppression in palladium allergy remains unknown. We investigated inhibition of the immune response in palladium allergic mice by administration of prednisolone as a glucocorticoid and fexofenadine hydrochloride as an antihistamine. Compared with glucocorticoids, fexofenadine hydrochloride significantly suppressed the number of T cells by interfering with the development of antigen-presenting cells from the sensitization phase. Our results suggest that antihistamine has a beneficial effect on the treatment of palladium allergy compared to glucocorticoids.

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