Excessive CD4 + T cells co‐expressing interleukin‐17 and interferon‐γ in patients with Behçet's disease
Author(s) -
Shimizu J.,
Takai K.,
Fujiwara N.,
Arimitsu N.,
Ueda Y.,
Wakisaka S.,
Yoshikawa H.,
Kaneko F.,
Suzuki T.,
Suzuki N.
Publication year - 2012
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.2011.04543.x
Subject(s) - rar related orphan receptor gamma , interleukin 17 , immunology , biology , interleukin 21 , cytokine , t cell , interleukin , interferon , il 2 receptor , interleukin 12 , interleukin 4 , microbiology and biotechnology , cytotoxic t cell , immune system , in vitro , foxp3 , biochemistry
Summary Excessive T helper type 1 (Th1) cell activity has been reported in Behçet's disease (BD). Recently, association of Th17 cells with certain autoimmune diseases was reported, and we thus investigated circulating Th17 cells in BD. CD4 + CD45RO – (naive) T cells were cultured with Th0‐, Th1‐, Th2‐ and Th17‐related cytokines and antibodies, and their mRNA was studied by real‐time polymerase chain reaction (PCR). When naive CD4 + T cells were cultured with Th1‐ and Th17‐related cytokines, interferon (IFN)‐γ mRNA and interleukin (IL)‐17 mRNA were up‐regulated, respectively, in BD patients. Naive CD4 + T cells cultured in a Th17 cell‐inducing condition expressed IL‐23 receptor (IL‐23R) mRNA excessively. IL‐17 mRNA expression was induced only when naive CD4 + T cells were cultured in the presence of IL‐23. CD4 + T cells cultured with Th17 cytokines expressed excessive RAR‐related orphan receptor C (RORC) mRNA. Using intracellular cytokine staining, we found that CD45RO + (memory) CD4 + T cells producing IL‐17 and IFN‐γ simultaneously were increased significantly. Memory CD4 + T cells producing IFN‐γ but not IL‐17 decreased profoundly in BD patients. CD4 + T cells producing IL‐17 and IFN‐γ simultaneously were found in BD skin lesions. Collectively, we found excessive CD4 + T cells producing IL‐17 and IFN‐γ (Th1/Th17) cells in patients with BD, and possible involvement of IL‐23/IL‐23R pathway for the appearance of excessive Th1/Th17 cells.
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