T cell repertoire in the liver of patients with autoimmune hepatitis

被引:18
作者
Yoshizawa, K
Ota, M
Katsuyama, Y
Ichijo, T
Inada, H
Umemura, T
Tanaka, E
Kiyosawa, K
机构
[1] Shinshu Univ, Sch Med, Dept Internal Med 2, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Sch Med, Dept Legal Med, Matsumoto, Nagano 3908621, Japan
[3] Shinshu Univ, Sch Med, Dept Pharm, Matsumoto, Nagano 3908621, Japan
关键词
autoimmune hepatitis; T cell receptor; complementarity determining region 3; T cell clones; CDR3 size spectratyping;
D O I
10.1016/S0198-8859(99)00058-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Despite a large number of T cells infiltrating into the liver of patients with autoimmune hepatitis (AIH), little is known about their roles or target antigens. To investigate the roles of these T cells in the pathogenesis of AIH, we have studied the clonality of alpha beta T cell populations in liver tissue by size spectratyping the complementarity-determining region (CDR)3 size lengths of T cell receptor (TCR) V beta-chain transcripts. Analysis of nine AIH patients who had the HLA DR4 haplotype showed clonal expansion in all samples. More than two T cell clones expanded in most patients. Although the expression of the TCR V beta genes was different among the nine patients, clonal expansion of T cells expressing either TCR V beta 2, 3, 4, 16, or 22 was observed in two patients or more. TCR V beta 4 clones expanded in 5 cases. Cloning and sequencing of TCR V beta CDR3 from PCR products revealed no whole CDR3-shared clones among different patients. In conclusion, several T cell clonotypes first recognize target antigens, then expand and accumulate in the liver of AIH patients. These suggest heterogeneity of autoantigens and the complexity of AIH immunopathogenesis in individual patients. (C) American Society for Histocompatibility and Immunogenetics, 1999. Published by Elsevier Science Inc.
引用
收藏
页码:806 / 815
页数:10
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