Serum chemokine profiles in patients with alopecia areata

被引:44
作者
Kuwano, Y.
Fujimoto, M.
Watanabe, R.
Ishiura, N.
Nakashima, H.
Ohno, Y.
Yano, S.
Yazawa, N.
Okochi, H.
Tamaki, K.
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Dept Dermatol, Kanazawa, Ishikawa 9208641, Japan
[2] Univ Tokyo, Fac Med, Dept Dermatol, Tokyo 113, Japan
[3] Int Med Ctr Japan, Res Inst, Dept Regenerat Med, Tokyo, Japan
关键词
alopecia areata; atopy; chemokine; monokine induced by interferon-gamma; RANTES;
D O I
10.1111/j.1365-2133.2007.07943.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
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)- c ( MIG), RANTES, interleukin- 8 ( IL- 8), IFN- inducible protein- 10, monocyte chemoattractant protein- 1, macrophage inflammatory protein ( MIP)- 1a, MIP- 1b 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.
引用
收藏
页码:466 / 473
页数:8
相关论文
共 18 条
[1]
Abramovits W, 2005, J AM ACAD DERMATOL, V53, pS86, DOI 10.1016/j.jaad.2005.04.034
[2]
ALAM R, 1993, J IMMUNOL, V150, P3442
[3]
[Anonymous], ACTA DERM VENERE S92, DOI [10.2340/00015555924447, DOI 10.2340/00015555924447]
[4]
Arca E, 2004, EUR J DERMATOL, V14, P33
[5]
Selective expression of chemokine monokine induced by interferon-7 in alopecia areata [J].
Benoit, S ;
Toksoy, A ;
Goebeler, M ;
Gillitzer, R .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (04) :933-935
[6]
ALOPECIA AREATA, THYROID DISEASE AND AUTOIMMUNITY [J].
CUNLIFFE, WJ ;
HALL, R ;
STEVENSO.CJ ;
WEIGHTMA.D .
BRITISH JOURNAL OF DERMATOLOGY, 1969, 81 (12) :877-&
[7]
CYTOKINE MESSENGER-RNA LEVELS IN ALOPECIA-AREATA BEFORE AND AFTER TREATMENT WITH THE CONTACT ALLERGEN DIPHENYLCYCLOPROPENONE [J].
HOFFMANN, R ;
WENZEL, E ;
HUTH, A ;
VANDERSTEEN, P ;
SCHAUFELE, M ;
HENNINGER, HP ;
HAPPLE, R .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1994, 103 (04) :530-533
[8]
A NEW CLASSIFICATION OF ALOPECIA AREATA [J].
IKEDA, T .
DERMATOLOGICA, 1965, 131 (06) :421-&
[9]
Enhanced production of CC-chemokines (RANTES, MCP-1, MIP-1α, MIP-1β, and eotaxin) in patients with atopic dermatitis [J].
Kaburagi, Y ;
Shimada, Y ;
Nagaoka, T ;
Hasegawa, M ;
Takehara, K ;
Sato, S .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 2001, 293 (07) :350-355
[10]
DETECTION OF PLASMA INTERLEUKIN-8 IN ATOPIC-DERMATITIS [J].
KIMATA, H ;
LINDLEY, I .
ARCHIVES OF DISEASE IN CHILDHOOD, 1994, 70 (02) :119-122