Similar T-cell oligoclonality in antimitochondrial antibody-positive and -negative primary biliary cirrhosis

被引:11
作者
Mayo, MJ
Lipsky, PE
Miller, SN
Stastny, P
Combes, B
机构
[1] Univ Texas, SW Med Ctr, Dept Internal Med, Div Hepatol, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Internal Med, Div Rheumat Dis, Dallas, TX 75390 USA
[3] Univ Texas, SW Med Ctr, Dept Internal Med, Div Transplant Immunol, Dallas, TX 75390 USA
关键词
autoimmunity; cholangitis; cholangiopathy; liver;
D O I
10.1023/A:1005609100900
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Approximately 5% of patients with clinical and histological features suggestive of primary biliary cirrhosis do not have anti-mitochondrial antibodies that can be detected by current methodologies. Although the role of these autoantibodies in the pathogenesis of liver disease is uncertain, T lymphocytes within the portal tracts are felt to be important mediators of bile duct destruction. In order to investigate the hypothesis that a similar T-cell process may be involved in both antimitochondrial antibody-positive and -negative primary biliary cirrhosis, we characterized the oligoclonally expanded T cells in both types of patients by analysis of complementarity determining region 3 length in peripheral blood mononuclear cells. The distribution of oligoclonally expanded T cells was similar in both groups. This finding does not support a distinct T-cell-mediated pathogenesis for anti-mitochondrial antibody-positive and -negative primary biliary cirrhosis but rather suggests that similar processes may be involved in the immunopathogenesis of both.
引用
收藏
页码:345 / 351
页数:7
相关论文
共 31 条
[1]   AUTOIMMUNE CHOLANGIOPATHY - PART OF THE SPECTRUM OF AUTOIMMUNE CHRONIC ACTIVE HEPATITIS [J].
BENARI, Z ;
DHILLON, AP ;
SHERLOCK, S .
HEPATOLOGY, 1993, 18 (01) :10-15
[2]   LIMITED T-CELL RECEPTOR DIVERSITY IN LIVER-INFILTRATING LYMPHOCYTES FROM PATIENTS WITH PRIMARY BILIARY-CIRRHOSIS [J].
DIU, A ;
MOEBIUS, U ;
FERRADINI, L ;
GENEVEE, C ;
ROMANROMAN, S ;
CLAUDON, M ;
DELORME, D ;
MEUER, S ;
HERCEND, T ;
PRAZ, F .
JOURNAL OF AUTOIMMUNITY, 1993, 6 (05) :611-619
[3]   AN EXPERIMENTALLY VALIDATED PANEL OF SUBFAMILY-SPECIFIC OLIGONUCLEOTIDE PRIMERS (V-ALPHA-1-W29/V-BETA-1-W24) FOR THE STUDY OF HUMAN T-CELL RECEPTOR VARIABLE V-GENE SEGMENT USAGE BY POLYMERASE CHAIN-REACTION [J].
GENEVEE, C ;
DIU, A ;
NIERAT, J ;
CAIGNARD, A ;
DIETRICH, PY ;
FERRADINI, L ;
ROMANROMAN, S ;
TRIEBEL, F ;
HERCEND, T .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (05) :1261-1269
[4]   AUTOIMMUNE CHOLANGITIS - A VARIANT OF PRIMARY BILIARY-CIRRHOSIS - CLINICOPATHOLOGICAL AND SEROLOGIC CORRELATIONS IN 200 CASES [J].
GOODMAN, ZD ;
MCNALLY, PR ;
DAVIS, DR ;
ISHAK, KG .
DIGESTIVE DISEASES AND SCIENCES, 1995, 40 (06) :1232-1242
[5]   PRIMARY BILIARY-CIRRHOSIS - ASSOCIATIONS WITH CLASS-II MAJOR HISTOCOMPATIBILITY COMPLEX ANTIGENS [J].
GORES, GJ ;
MOORE, SB ;
FISHER, LD ;
POWELL, FC ;
DICKSON, ER .
HEPATOLOGY, 1987, 7 (05) :889-892
[6]   Analysis of T-cell receptor beta of the T-cell clones reactive to the human PDC-E2 163-176 peptide in the context of HLA-DR53 in patients with primary biliary cirrhosis [J].
Ichiki, Y ;
Shimoda, S ;
Hara, H ;
Shigematsu, H ;
Nakamura, M ;
Hayashida, K ;
Ishibashi, H ;
Niho, Y .
HEPATOLOGY, 1997, 26 (03) :728-733
[7]   Comparison of the clinical features and clinical course of antimitochondrial antibody-positive and -negative primary biliary cirrhosis [J].
Invernizzi, P ;
Crosignani, A ;
Battezzati, PM ;
Covini, G ;
DeValle, G ;
Larghi, A ;
Zuin, M ;
Podda, M .
HEPATOLOGY, 1997, 25 (05) :1090-1095
[8]   T-CELL RESPONSES TO THE COMPONENTS OF PYRUVATE-DEHYDROGENASE COMPLEX IN PRIMARY BILIARY-CIRRHOSIS [J].
JONES, DEJ ;
PALMER, JM ;
JAMES, OFW ;
YEAMAN, SJ ;
BASSENDINE, MF ;
DIAMOND, AG .
HEPATOLOGY, 1995, 21 (04) :995-1002
[9]   T-cell autoimmunity in primary biliary cirrhosis [J].
Jones, DEJ .
CLINICAL SCIENCE, 1996, 91 (05) :551-558
[10]  
Kim WR, 1997, HEPATOLOGY, V26, P22