Promiscuous T cells selected by Escherichia coli:: OGDC-E2 in primary biliary cirrhosis

被引:18
作者
Tanimoto, H
Shimoda, S
Nakamura, M
Ishibashi, H
Kawano, A
Kamihira, T
Matsushita, S
Gershwin, ME
Harada, M
机构
[1] Kyushu Univ, Grad Sch Med Sci, Higashi Ku, Fukuoka 8128582, Japan
[2] Natl Nagasaki Med Ctr, Omura, Japan
[3] Saitama Med Sch, Dept Allergy & Immunol, Moroyama, Saitama 35004, Japan
[4] Univ Calif Davis, Div Rheumatol Allergy & Clin Immunol, Sch Med, Davis, CA 95616 USA
关键词
autoimmunity; bacterial antigens; cross-reactivity; 2-oxo-dehydrogenase;
D O I
10.1016/S0896-8411(03)00024-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The etiology of primary biliary cirrhosis (PBC) remains enigmatic. One theory that has attracted attention proposes that PBC is induced via molecular mimicry with Escherichia coli. If molecular mimicry is responsible for the immunogenic response in PBC, then T cell clones specific for E coli antigens should stimulate and be cross-reactive with peptides specific for the human immunodominant autoepitopes. To address this issue, we developed T cell clones specific for E. coli OGDC-E2 peptide. Importantly. we demonstrate the presence of T cell clones specific for E. coli OGDC-E2 that react promiscuously with the human mitochondrial equivalents. Indeed, there was a significant increase in the liver derived T cell precursor frequency of such reactivity and such liver clones were only found in patients with PBC. In conclusion, these data suggest that PBC is a multi-hit disease involving, a genetic predisposition, a mucosal response, and activation of promiscuous T cells; such activation may occur either directly from bacterial antigens, or indirectly through chemically-modified bacterial antigens. Dissection of the mechanisms involved will lead not only to understanding the immunogenetic basis of PBC, but likely its pathogenic etiology. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:255 / 263
页数:9
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