嗜酸性粒细胞趋化因子
斑秃
免疫学
单因子
趋化因子
巨噬细胞炎性蛋白
特应性皮炎
外周血单个核细胞
医学
银屑病
过敏性
CCL22型
单核细胞
过敏
炎症
生物
趋化因子受体
生物化学
体外
作者
Yoshihiro Kuwano,Manabu Fujimoto,Rei Watanabe,Nobuko Ishiura,H. Nakashima,Yuki Ohno,Shoichiro Yano,Norihito Yazawa,Hitoshi Okochi,Kunihiko Tamaki
标识
DOI:10.1111/j.1365-2133.2007.07943.x
摘要
Background Although chemokines play an important role in various inflammatory diseases, there have been few studies about the role of chemokines in alopecia areata (AA). Objectives To determine serum levels of chemokines in patients with AA and their clinical correlations. Methods Serum samples from 85 patients with AA, 20 patients with atopic dermatitis, 20 patients with psoriasis vulgaris and 28 normal controls were examined by the cytometric bead array assay assessing monokine induced by interferon (IFN)-γ (MIG), RANTES, interleukin-8 (IL-8), IFN-inducible protein-10, monocyte chemoattractant protein-1, macrophage inflammatory protein (MIP)-1α, MIP-1β and eotaxin levels. Secreted chemokine levels from peripheral blood mononuclear cells (PBMC) of patients with AA were also investigated. Results Serum MIG, RANTES, IL-8 and eotaxin levels were selectively increased in patients with AA compared with normal controls. Levels of MIG, RANTES and IL-8 secreted from PBMC of patients with AA were also increased. Furthermore, elevated serum MIG and RANTES levels significantly correlated with the disease activity. RANTES levels were nonsignificantly associated with a predisposition to atopy. Conclusions These results suggest that MIG and RANTES play an important role in the development of AA and are useful as markers of disease activity and as therapeutic targets.
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