AUTOANTIGEN RECOGNITION BY THYROID-INFILTRATING T-CELLS IN GRAVES-DISEASE

被引:145
作者
DAYAN, CM
LONDEI, M
CORCORAN, AE
GRUBECKLOEBENSTEIN, B
JAMES, RFL
RAPOPORT, B
FELDMANN, M
机构
[1] CHARING CROSS SUNLEY MED RES CTR, 1 LURGAN AVE, LONDON W6 8LW, ENGLAND
[2] UNIV CALIF SAN FRANCISCO, THYROID MOLEC BIOL LAB, SAN FRANCISCO, CA 94121 USA
[3] UNIV VIENNA, DEPT EXPTL PATHOL, A-1010 VIENNA, AUSTRIA
[4] LEICESTER ROYAL INFIRM, DEPT SURG, LEICESTER LE2 7LX, ENGLAND
关键词
T-CELL CLONE; THYROID PEROXIDASE; AUTOIMMUNE THYROIDITIS;
D O I
10.1073/pnas.88.16.7415
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Graves disease is a common form of human autoimmune thyroiditis. It shares many pathological features and HLA associations with other, less easily studied, organ-specific autoimmune conditions such as insulin-dependent diabetes mellitus, and hence it is also a useful model for understanding these other diseases. We have previously shown that thyroid-infiltrating T cells in Graves disease that have been recently activated in vivo specifically recognize autologous thyroid epithelial cells. However, the autoantigens involved were not defined. In this study, we have made use of antigen-independent T-cell cloning techniques to show that at least three different thyroid antigens, three different epitopes on a single antigen, and two HLA class II elements are involved in this recognition process in a single individual. This demonstrates that T cells that are present and activated at the site of a human autoimmune disease may show considerable heterogeneity in their recognition of autoantigen on the target tissue. This contrasts with the limited heterogeneity recently reported in some animal models and has potentially important implications for both our understanding of the autoimmune process in humans and the design of immunotherapies to reverse it.
引用
收藏
页码:7415 / 7419
页数:5
相关论文
共 28 条
  • [1] MAPPING OF AUTOANTIGENIC EPITOPES ON RECOMBINANT THYROID PEROXIDASE FRAGMENTS USING THE POLYMERASE CHAIN-REACTION
    BANGA, JP
    BARNETT, PS
    EWINS, DL
    PAGE, MJ
    MCGREGOR, AM
    [J]. AUTOIMMUNITY, 1990, 6 (04) : 257 - 268
  • [2] AUTOANTIGENIC DETERMINANTS ON HUMAN THYROGLOBULIN .2. DETERMINANTS RECOGNIZED BY AUTOANTIBODIES FROM PATIENTS WITH CHRONIC AUTOIMMUNE-THYROIDITIS COMPARED TO AUTOANTIBODIES FROM HEALTHY-SUBJECTS
    BRESLER, HS
    BUREK, CL
    HOFFMAN, WH
    ROSE, NR
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1990, 54 (01): : 76 - 86
  • [3] COOKE A, 1991, CLIN EXP IMMUNOL, V83, P345
  • [4] T-CELL ANTIGENIC SITES TEND TO BE AMPHIPATHIC STRUCTURES
    DELISI, C
    BERZOFSKY, JA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (20) : 7048 - 7052
  • [5] DELPRETE GF, 1987, ACTA ENDOCRINOL-COP, V115, P111
  • [6] DONIACH D, 1982, CLIN ASPECTS IMMUNOL, V2, P903
  • [7] THE PATHOGENESIS OF GRAVES-DISEASE
    GOSSAGE, AAR
    MUNRO, DS
    [J]. CLINICS IN ENDOCRINOLOGY AND METABOLISM, 1985, 14 (02): : 299 - 330
  • [8] PATHOGENETIC RELEVANCE OF HLA CLASS-II EXPRESSING THYROID FOLLICULAR CELLS IN NONTOXIC GOITER AND IN GRAVES-DISEASE
    GRUBECKLOEBENSTEIN, B
    LONDEI, M
    GREENALL, C
    PIRICH, K
    KASSAL, H
    WALDHAUSL, W
    FELDMANN, M
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (05) : 1608 - 1614
  • [9] CD4+ T-CELL CLONES FROM AUTOIMMUNE THYROID-TISSUE CANNOT BE CLASSIFIED ACCORDING TO THEIR LYMPHOKINE PRODUCTION
    GRUBECKLOEBENSTEIN, B
    TURNER, M
    PIRICH, K
    KASSAL, H
    LONDEI, M
    WALDHAUSL, W
    FELDMANN, M
    [J]. SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 1990, 32 (05) : 433 - 440
  • [10] GRUBECKLOEBENSTEIN B, 1989, CLIN EXP IMMUNOL, V77, P324