LYMPHOCYTES IN THYMOMAS ARE TOLERANT TO SELF-MHC

被引:6
作者
FUJII, Y
OKUMURA, M
INADA, K
NAKAHARA, K
机构
[1] Immunology Laboratory, First Department of Surgery, Osaka University Medical School, Osaka, 553
关键词
D O I
10.1016/0008-8749(91)90092-P
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neoplastic epithelial cells of thymoma apparently retain the function of the cortical epithelial cells of normal thymus because a large number of nonneoplastic T cells in thymomas are often CD4 + 8+. However, the lack of medullary structure suggests that thymomas may lack some of the function of the normal thymus, especially the function of the medullary interdigitating cells to induce tolerance to self-antigens on T cells. Thymoma is often associated with autoimmune diseases, most frequently, myasthenia gravis. This suggests that the microenvironment of a thymoma may not be able to induce T cell tolerance to self-antigens. We addressed this question by testing the lymphocytes in thymomas for proliferative responses to mitogens and allogeneic or autologous stimulator cells. The lymphocytes in thymomas proliferated consistently in response to PHA and to allogeneic cells even when the response to OKT3 was undetectable. However, neither the thymoma lymphocytes nor the peripheral blood lymphocytes in these patients proliferated in response to autologous cells. © 1991.
引用
收藏
页码:438 / 447
页数:10
相关论文
共 38 条
[1]   THYMOMA-SPECIFIC ANTIBODIES IN SERA FROM PATIENTS WITH MYASTHENIA-GRAVIS DEMONSTRATED BY INDIRECT HEMAGGLUTINATION [J].
AARLI, JA ;
LEFVERT, AK ;
TONDER, O .
JOURNAL OF NEUROIMMUNOLOGY, 1981, 1 (04) :421-427
[2]   NONTOLERANCE AND AUTOANTIBODIES TO A TRANSGENIC SELF ANTIGEN EXPRESSED IN PANCREATIC BETA-CELLS [J].
ADAMS, TE ;
ALPERT, S ;
HANAHAN, D .
NATURE, 1987, 325 (6101) :223-228
[3]   TOLERANCE IN TRANSGENIC MICE EXPRESSING MAJOR HISTOCOMPATIBILITY MOLECULES EXTRATHYMICALLY ON PANCREATIC-CELLS [J].
BURKLY, LC ;
LO, D ;
FLAVELL, RA .
SCIENCE, 1990, 248 (4961) :1364-1368
[4]   T-CELL TOLERANCE BY CLONAL ANERGY IN TRANSGENIC MICE WITH NONLYMPHOID EXPRESSION OF MHC CLASS-II I-E [J].
BURKLY, LC ;
LO, D ;
KANAGAWA, O ;
BRINSTER, RL ;
FLAVELL, RA .
NATURE, 1989, 342 (6249) :564-566
[5]   EVIDENCE FOR PERIPHERAL MECHANISMS INDUCING TISSUE TOLERANCE DURING ONTOGENY [J].
CORBEL, C ;
MARTIN, C ;
OHKI, H ;
COLTEY, M ;
HLOZANEK, I ;
LEDOUARIN, NM .
INTERNATIONAL IMMUNOLOGY, 1990, 2 (01) :33-40
[6]   SEQUENTIAL-ANALYSES OF THE DEVELOPMENT OF LYMPHOPROLIFERATIVE DISORDERS IN RATS RECEIVING CYCLOSPORINE [J].
DEMETRIS, AJ ;
NALESNIK, MA ;
KUNZ, HW ;
GILL, TJ ;
SHINOZUKA, H .
TRANSPLANTATION, 1984, 38 (03) :239-246
[7]   IMMUNE-RESPONSES OF THYMUS LYMPHOCYTE EMBRYONIC CHIMERAS - STUDIES ON TOLERANCE AND MAJOR HISTOCOMPATIBILITY COMPLEX RESTRICTION IN XENOPUS [J].
FLAJNIK, MF ;
DUPASQUIER, L ;
COHEN, N .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1985, 15 (06) :540-547
[8]   LYMPHOCYTES IN THYMOMA - ASSOCIATION WITH MYASTHENIA-GRAVIS IS CORRELATED WITH INCREASED NUMBER OF SINGLE-POSITIVE CELLS [J].
FUJII, Y ;
HAYAKAWA, M ;
INADA, K ;
NAKAHARA, K .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1990, 20 (10) :2355-2358
[9]   ABNORMAL DIFFERENTIATION OF THYMOCYTES IN MICE TREATED WITH CYCLOSPORIN-A [J].
GAO, EK ;
LO, D ;
CHENEY, R ;
KANAGAWA, O ;
SPRENT, J .
NATURE, 1988, 336 (6195) :176-179
[10]  
HATTORI A, 1987, AM J PATHOL, V128, P111