Expression of co-stimulatory molecules by Kupffer cells in chronic hepatitis of hepatitis C virus etiology

被引:61
作者
Burgio, VL
Ballardini, G
Artini, M
Caratozzolo, M
Bianchi, FB
Levrero, M
机构
[1] Univ La Sapienza, Policlin Umberto I, Ist Clin Med 1, I-00161 Rome, Italy
[2] Univ La Sapienza, Ist Clin Chirurg 4, I-00161 Rome, Italy
[3] Univ La Sapienza, Fdn Andrea Cesalpino, I-00161 Rome, Italy
[4] Univ Cagliari, Dipartimento Sci Med, Cagliari, Italy
[5] Univ Bologna, Policlin S Orsola, Med Clin 2, I-40126 Bologna, Italy
关键词
D O I
10.1002/hep.510270620
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
In this paper we show that in viral hepatitis most Kupffer cells (KCs) are activated and express high levels of CD80, CD40, and class-II MHC molecules, thus acquiring the phenotype of professional antigen presenting cells (APCs). Activated KCs display a close contact with CD4+ T lymphocytes and form KCs-T lymphocyte clusters. Clusters are found within the sinusoids, across the sinusoid wall, and within the liver parenchima as well, as a consequence of transendothelial migration (TEM), The positivity of activated KCs for hepatitis C virus (HCV) antigens, which likely reflects phagocytosis of infected hepatocytes, suggests that KCs-T cell clusters represent the morphological expression of the functional interaction between KCs acting as professional APCs and antigen-experienced CD4+ T lymphocytes within the liver. These phenotypic and morphological changes are distinct features of livers in chronic hepatitis patients compared with controls.
引用
收藏
页码:1600 / 1606
页数:7
相关论文
共 22 条
[2]   HEPATITIS-C VIRUS (HCV) GENOTYPE, TISSUE HCV ANTIGENS, HEPATOCELLULAR EXPRESSION OF HLA-A,B,C, AND INTERCELLULAR ADHESION-1 MOLECULES - CLUES TO PATHOGENESIS OF HEPATOCELLULAR DAMAGE AND RESPONSE TO INTERFERON TREATMENT IN PATIENTS WITH CHRONIC HEPATITIS-C [J].
BALLARDINI, G ;
GROFF, P ;
PONTISSO, P ;
GIOSTRA, F ;
FRANCESCONI, R ;
LENZI, M ;
ZAULI, D ;
ALBERTI, A ;
BIANCHI, FB .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (05) :2067-2075
[3]  
BARNABA V, 1994, J IMMUNOL, V152, P3074
[4]   THE ACUTE-PHASE RESPONSE [J].
BAUMANN, H ;
GAULDIE, J .
IMMUNOLOGY TODAY, 1994, 15 (02) :74-80
[5]  
CHISARI FV, 1995, ANNU REV IMMUNOL, V13, P29, DOI 10.1146/annurev.iy.13.040195.000333
[6]   Subepithelial B cells in the human palatine tonsil .1. Morphologic, cytochemical and phenotypic characterization [J].
Dono, M ;
Burgio, VL ;
Tacchetti, C ;
Favre, A ;
Zupo, S ;
Taborelli, G ;
Chiorazzi, N ;
Grossi, CE ;
Ferrarini, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1996, 26 (09) :2035-2042
[7]   A central role of CD40 ligand in the regulation of CD4(+) T-cell responses [J].
Grewal, IS ;
Flavell, RA .
IMMUNOLOGY TODAY, 1996, 17 (09) :410-414
[8]   AN ANTIGEN-INDEPENDENT CONTACT MECHANISM AS AN EARLY STEP IN T-CELL-PROLIFERATIVE RESPONSES TO DENDRITIC CELLS [J].
INABA, K ;
ROMANI, N ;
STEINMAN, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (02) :527-542
[9]   COSTIMULATION AND THE REGULATION OF ANTIMICROBIAL IMMUNITY [J].
KAYE, PM .
IMMUNOLOGY TODAY, 1995, 16 (09) :423-427
[10]   THE ROLE OF THE CD28 RECEPTOR DURING T-CELL RESPONSES TO ANTIGEN [J].
LINSLEY, PS ;
LEDBETTER, JA .
ANNUAL REVIEW OF IMMUNOLOGY, 1993, 11 :191-212