MHC class II-expressing hepatocytes function as antigen-presenting cells and activate specific CD4 T lymphocytes

被引:127
作者
Herkel, J
Jagemann, B
Wiegard, C
Lazaro, JFG
Lueth, S
Kanzler, S
Blessing, M
Schmitt, E
Lohse, AW
机构
[1] Univ Mainz, Dept Med 1, D-55101 Mainz, Germany
[2] Univ Mainz, Dept Immunol, D-55101 Mainz, Germany
关键词
D O I
10.1053/jhep.2003.50191
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The ability to activate CD4 T cells is restricted to antigen-presenting cells that express major histocompatibility complex (MHC) class II molecules. Parenchymal cells normally do not express MHC class II molecules; however, in clinical hepatitis, viral or autoimmune, hepatocytes often exhibit aberrant MHC class II expression. It is not known whether MHC class II-expressing hepatocytes can function as antigen-presenting cells, but it has been suggested that aberrant MHC class II expression by parenchymal cells may cause autoimmune disease. Therefore, we generated transgenic mice that specifically overexpress class II transactivator molecules in hepatocytes. Hepatocytes from these mice exhibited stable MHC class II expression and were used to stimulate CD4 T cells from T-cell receptor transgenic mice and CD4 T-cell lines. MHC II-expressing hepatocytes featured costimulatory CD80 molecules and could serve as antigen-presenting cells that were able to process protein antigen and to activate specific CD4 T cells. Nevertheless, the transgenic mice with aberrant hepatocellular MHC class II expression did not exhibit any symptoms of autoimmune disease. In conclusion, MHC II-expressing hepatocytes, as found in clinical hepatitis, can present antigen and activate CD4 T cells. The ability of hepatocytes to present antigen on MHC II molecules does not seem to be a sufficient cause for inflammatory autoimmunity and hepatitis. However, we still need to explore whether such antigen presentation is occurring in vivo. The transgenic mice described in this study may serve as a model to study the immune interaction of hepatocytes and CD4 T cells in both in vitro and in vivo.
引用
收藏
页码:1079 / 1085
页数:7
相关论文
共 44 条
[1]   Death by neglect as a deletional mechanism of peripheral tolerance [J].
Bertolino, P ;
Trescol-Biémont, MC ;
Thomas, J ;
Fazekas de St Groth, B ;
Pihlgren, M ;
Marvel, J ;
Rabourdin-Combe, C .
INTERNATIONAL IMMUNOLOGY, 1999, 11 (08) :1225-1237
[2]  
BOTRAZZO GF, 1983, LANCET, V2, P1115
[3]   INDUCTION OF IMMUNOLOGICAL TOLERANCE BY PORCINE LIVER ALLOGRAFTS [J].
CALNE, RY ;
SELLS, RA ;
PENA, JR ;
DAVIS, DR ;
MILLARD, PR ;
HERBERTSON, BM ;
BINNS, RM ;
DAVIES, DAL .
NATURE, 1969, 223 (5205) :472-+
[4]   HEPATIC SUPPRESSION OF SENSITIZATION TO ANTIGEN ABSORBED INTO PORTAL SYSTEM [J].
CANTOR, HM ;
DUMONT, AE .
NATURE, 1967, 215 (5102) :744-&
[5]   Pathogenesis of chronic hepatitis C: Immunological features of hepatic injury and viral persistence [J].
Cerny, A ;
Chisari, FV .
HEPATOLOGY, 1999, 30 (03) :595-601
[6]   HEPATITIS-B VIRUS IMMUNOPATHOGENESIS [J].
CHISARI, FV ;
FERRARI, C .
ANNUAL REVIEW OF IMMUNOLOGY, 1995, 13 :29-60
[7]  
CHOMCZYNSKI P, 1993, BIOTECHNIQUES, V15, P532
[8]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[9]   Impairment of CD4+ T cell responses during chronic virus infection prevents neutralizing antibody responses against virus escape mutants [J].
Ciurea, A ;
Hunziker, L ;
Klenerman, P ;
Hengartner, H ;
Zinkernagel, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 193 (03) :297-305
[10]   B220 - A B-CELL-SPECIFIC MEMBER OF THE T200 GLYCOPROTEIN FAMILY [J].
COFFMAN, RL ;
WEISSMAN, IL .
NATURE, 1981, 289 (5799) :681-683