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The pruritogenic mediator endothelin‐1 shifts the dendritic cell–T‐cell response toward Th17/Th1 polarization
Author(s) -
Nakahara T.,
KidoNakahara M.,
Ohno F.,
Ulzii D.,
Chiba T.,
Tsuji G.,
Furue M.
Publication year - 2018
Publication title -
allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.363
H-Index - 173
eISSN - 1398-9995
pISSN - 0105-4538
DOI - 10.1111/all.13322
Subject(s) - psoriasis , immunology , immune system , dendritic cell , mediator , interleukin 17 , t cell , medicine , endocrinology
Endothelin‐1 ( ET ‐1) is associated with skin diseases such as atopic dermatitis ( AD ) and psoriasis. ET ‐1 is enhanced in the skin of patients AD and psoriasis. In addition, plasma levels of ET ‐1 are elevated in AD and psoriasis. Although both AD and psoriasis are T‐cell–mediated skin diseases, the association between ET ‐1 and the T‐cell immune response has not been clarified. To evaluate the role of ET ‐1 in inflammatory skin disease, we sought to investigate the effects of ET ‐1 on the functions of dendritic cells ( DC s) and subsequent immune responses. For this purpose, we immunohistochemically confirmed the upregulation of ET ‐1 in the epidermis of patients with AD or psoriasis. ET ‐1 directly induced phenotypic maturation of bone marrow‐derived DC s ( BMDC s). In addition, ET ‐1 augmented the production of several cytokines and allogeneic stimulatory capacity of BMDC s. Interestingly, ET ‐1–activated BMDC s primed T cells to produce Th1 and Th17 cytokines, but not Th2 cytokines. These findings indicate that ET ‐1 polarizes the DC –T‐cell response toward Th17/1 differentiation and may augment the persistent course of inflammatory skin diseases.