Restricted usage of T-cell receptor Vγ-Vδ genes and expression of costimulatory molecules in Takayasu's arteritis

被引:32
作者
Seko, Y [1 ]
Takahashi, N
Tada, Y
Yagita, H
Okumura, K
Nagai, R
机构
[1] Univ Tokyo, Grad Sch Med, Dept Cardiovasc Med, Tokyo 1138655, Japan
[2] Juntendo Univ, Sch Med, Dept Immunol, Tokyo 1138421, Japan
[3] Asahi Life Fdn, Inst Adult Dis, Tokyo 1600023, Japan
[4] Yamanashi Med Coll, Dept Surg 2, Yamanashi 4093898, Japan
关键词
Takayasu's arteritis; T-cell receptor (TCR); gamma delta T-cell; costimulatory molecule; cell-mediated autoimmunity;
D O I
10.1016/S0167-5273(00)00194-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To further investigate the immunological mechanisms involved in Takayasu's arteritis, we analyzed the T-cell receptor (TCR) V gamma and V delta gene usage by infiltrating gamma delta T-cells and the expression of costimulatory molecules B7-1, B7-2, CD40, CD27 ligand (CD27L), CD30L, OX40L in the arterial tissue of a patient with Takayasu's arteritis. We found that the repertoires of TCR V gamma as well as V delta gene transcripts of the infiltrating cells were restricted as compared with those of peripheral blood lymphocytes from a patient with Takayasu's arteritis. This strongly suggests that gamma delta T-cells as well as alpha beta T-cells, as we previously reported, were specifically involved in the pathogenesis of Takayasu's arteritis. We also found that B7-1, B7-2, CD40, CD27L, CD30L, and OX40L were expressed in the arterial tissue, suggesting the roles for these costimulatory molecules in T-cell-mediated vascular injury in Takayasu's arteritis. Our findings strongly support the involvement of T-cell-mediated immunological mechanisms in the pathogenesis of Takayasu's arteritis. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:S77 / S83
页数:7
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