Decreased expression levels of CD22 and L-selectin on peripheral blood B lymphocytes from patients with bullous pemphigoid

被引:4
作者
Inaoki, Makoto
Echigo, Takeshi
Hayashi, Hiroaki
Nagaoka, Tetsuya
Hasegawa, Minoru
Takehara, Kazuhiko
Fujimoto, Wataru
Tedder, Thomas F.
Sato, Shinichi
机构
[1] Kanazawa Univ, Dept Dermatol, Grad Sch Med Sci, Ishikawa 9208641, Japan
[2] Kawasaki Med Sch, Dept Dermatol, Okayama 7010192, Japan
[3] Duke Univ, Med Ctr, Dept Immunol, Durham, NC 27710 USA
[4] Nagasaki Univ, Grad Sch Biomed Sci, Dept Dermatol, Nagasaki 8528501, Japan
关键词
autoantibody; bullous pemphigoid; CD22; L-selectin; leukocyte activation;
D O I
10.1016/j.jaut.2006.09.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Bullous pemphigoid (BP), an autoimmune subepidermal-blistering disease of the elderly, is caused by antibodies against BP antigens at the epidermal basement membrane zone (BMZ). CD22 is a B lymphocyte specific response regulator, which is down-regulated after B-cell activation. Old CD22-deficient mice produce class-switched autoantibodies. To assess the role of CD22 in the pathogenesis of BP, we examined CD22 expression on B cells from BP patients and correlated its expression with clinical parameters. B cell expression of CD22 was 20% lower in BP patients when compared to healthy control subjects. In addition, B cells from BP patients showed decreased expression of L-selectin, which is an indicator of leukocyte activation, and CD22 expression levels were correlated with L-selectin expression. These results suggest that the decreased CD22 expression may be associated with the activation of B cells in 13P. CD22 expression levels in BP patients did not correlate with the levels of anti-epidermal BMZ antibodies, and old CD22-deficient mice did not develop the anti-epidermal BMZ antibody. These results suggest that a decrease in CD22 expression may not be associated with BP-specific antibody production. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:196 / 202
页数:7
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