EXPRESSION OF B7 (CD80) AND CD40 ANTIGENS AND THE CD40 LIGAND IN HODGKINS-DISEASE IS INDEPENDENT OF LATENT EPSTEIN-BARR-VIRUS INFECTION

被引:0
作者
MURRAY, PG
OATES, J
REYNOLDS, GM
CROCKER, J
YOUNG, LS
机构
[1] UNIV BIRMINGHAM, INST CANC STUDIES, BIRMINGHAM B15 2TT, W MIDLANDS, ENGLAND
[2] BIRMINGHAM HEARTLANDS HOSP, DEPT HISTOPATHOL, BIRMINGHAM B9 5ST, W MIDLANDS, ENGLAND
[3] UNIV BIRMINGHAM, DEPT PATHOL, BIRMINGHAM, W MIDLANDS, ENGLAND
来源
JOURNAL OF CLINICAL PATHOLOGY-CLINICAL MOLECULAR PATHOLOGY EDITION | 1995年 / 48卷 / 02期
关键词
HODGKINS DISEASE; B7 (CD80) ANTIGEN; CD40; ANTIGEN; LIGAND;
D O I
暂无
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aim-To examine the expression of CD40 and B7 (CD80) antigens and the CD40 ligand in Hodgkin's disease. Methods-Antigen and ligand expression was studied in 17 cases of Hodgkin's disease using immunohistochemistry. The study included 11 cases of Hodgkin's disease in which latent Epstein-Barr virus (EBV) infection could be demonstrated within tumour cells by in situ hybridisation for the EBV encoded early RNAs (EBERs). Results-In all cases, irrespective of EBV status, Reed-Sternberg cells and their variants (HRS cells) showed strong expression of both B7 and CD40 antigens. CD40 ligand expression was not shown in HRS cells but was confined to a subset of small lymphocytes some of which were seen to be in intimate contact with HRS cells. Paraffin wax sections from a further 60 cases of Hodgkin's disease were examined for CD40 and EBER expression alone. The CD40 antigen was identified in HRS cells in all of these cases irrespective of EBER expression. Conclusions-As CD40 and B7 expression are features of professional antigen presenting cells, these results provide further evidence that HRS cells may have antigen presenting properties and that this may contribute to the characteristic recruitment and activation of non-malignant lymphocytes which is a feature of Hodgkin's disease. The ability of HRS cells to activate T-h cells may in turn contribute to their own survival through the induction of the gp39/CD40 pathway.
引用
收藏
页码:M105 / M108
页数:4
相关论文
共 24 条
[1]   ANALYSIS OF ANTIGEN RECEPTOR GENES IN HODGKINS-DISEASE [J].
ANGEL, CA ;
PRINGLE, JH ;
NAYLOR, J ;
WEST, KP ;
LAUDER, I .
JOURNAL OF CLINICAL PATHOLOGY, 1993, 46 (04) :337-340
[2]   MOLECULAR AND BIOLOGICAL CHARACTERIZATION OF A MURINE LIGAND FOR CD40 [J].
ARMITAGE, RJ ;
FANSLOW, WC ;
STROCKBINE, L ;
SATO, TA ;
CLIFFORD, KN ;
MACDUFF, BM ;
ANDERSON, DM ;
GIMPEL, SD ;
DAVISSMITH, T ;
MALISZEWSKI, CR ;
CLARK, EA ;
SMITH, CA ;
GRABSTEIN, KH ;
COSMAN, D ;
SPRIGGS, MK .
NATURE, 1992, 357 (6373) :80-82
[3]   RAPID INSITU HYBRIDIZATION FOR THE DIAGNOSIS OF LATENT EPSTEIN-BARR-VIRUS INFECTION [J].
BARLETTA, JM ;
KINGMA, DW ;
LING, Y ;
CHARACHE, P ;
MANN, RB ;
AMBINDER, RF .
MOLECULAR AND CELLULAR PROBES, 1993, 7 (02) :105-109
[4]  
CURRAN RC, 1977, LANCET, V2, P349
[5]  
DELABIE J, 1993, BLOOD, V82, P2845
[6]  
DELSOL G, 1993, AM J PATHOL, V142, P1729
[7]  
FISHER RI, 1985, J IMMUNOL, V135, P3568
[8]  
FISHER RI, 1983, J IMMUNOL, V130, P2666
[9]   B-CELL SURFACE ANTIGEN-B7 PROVIDES A COSTIMULATORY SIGNAL THAT INDUCES T-CELLS TO PROLIFERATE AND SECRETE INTERLEUKIN-2 [J].
GIMMI, CD ;
FREEMAN, GJ ;
GRIBBEN, JG ;
SUGITA, K ;
FREEDMAN, AS ;
MORIMOTO, C ;
NADLER, LM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (15) :6575-6579
[10]   CLONAL REARRANGEMENTS OF T-CELL RECEPTOR AND IMMUNOGLOBULIN GENES AND IMMUNOPHENOTYPIC ANTIGEN EXPRESSION IN DIFFERENT SUBCLASSES OF HODGKINS-DISEASE [J].
GRIESSER, H ;
FELLER, AC ;
MAK, TW ;
LENNERT, K .
INTERNATIONAL JOURNAL OF CANCER, 1987, 40 (02) :157-160