Wells' syndrome: A pathogenic role for circulating CD4(+)CD7(-) T cells expressing interleukin-5 mRNA

被引:19
|
作者
Yagi, H [1 ]
Tokura, Y [1 ]
Matsushita, K [1 ]
Hanaoka, K [1 ]
Furukawa, F [1 ]
Takigawa, M [1 ]
机构
[1] HAMAMATSU UNIV SCH MED, DEPT DERMATOL, HAMAMATSU, SHIZUOKA 43131, JAPAN
关键词
IDIOPATHIC HYPEREOSINOPHILIC SYNDROME; MONOCLONAL-ANTIBODIES; BLOOD; CD7; EOSINOPHILS; LYMPHOCYTE; SUBSET;
D O I
10.1111/j.1365-2133.1997.tb03934.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Wells' syndrome, or eosinophilic cellulitis, is a rare dermatosis characterized histologically by a dermal infiltrate of eosinophils, lymphocytes and histiocytes between collagen bundles and amorphous or granular eosinophilic deposits on collagen, constituting name figures, We report a 54-year-old woman with eosinophilic cellulitis whose peripheral blood showed a marked eosinophilia and a high proportion of CD4(+)CD7(-) cells before treatment. Reverse transcriptase-polymerase chain reaction revealed that CD4(+)CD7(-) cells, but neither CD4(+)CD7(+) nor CD4(-)CD8(+) cells, in the circulating mononuclear cells expressed mRNA for interleukin (IL)-5, the major cytokine involved in eosinophilia. The proportion of CD4(+)CD7(-) cells decreased, and expression of mRNA for IL-5 disappeared in the peripheral blood, when the disease was treated by the administration of intravenous recombinant interferon-gamma. These findings suggest that circulating CD4(+)CD7(-) T cells play a pivotal role in the pathogenesis of eosinophilic cellulitis by producing IL-5.
引用
收藏
页码:918 / 923
页数:6
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