Beta-cell reactive T-cell clones from type I diabetes patients are not beta cell specific and recognize multiple antigens

被引:7
作者
Kallan, AA
Roep, BO
Arden, SD
Hutton, JC
deVries, RRP
机构
[1] UNIV LEIDEN HOSP,DEPT IMMUNOHEMATOL,2300 RC LEIDEN,NETHERLANDS
[2] UNIV LEIDEN HOSP,BLOOD BANK,2300 RC LEIDEN,NETHERLANDS
[3] UNIV CAMBRIDGE,ADDENBROOKES HOSP,DEPT CLIN BIOCHEM,CAMBRIDGE,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/S0896-8411(95)80024-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Type I diabetes is the result of an autoimmune destruction of pancreatic beta cells. T cells appear to play a key role in this process. Thus far little information is available on the beta cell antigen or antigens recognized by auto-reactive T cells. Previously, we identified a 38 kD T cell antigen that appears to be localized in the membrane ofinsulin secretory granules and that is recognized by T cells from newly diagnosed type I diabetes patients. Other groups have reported T cell reactivity against glutamic acid decarboxylase (GAD). To obtain an indication of whether or not beta-cell reactive T cells from type I diabetes patients recognize a Limited number of beta-cell antigens, we cloned T-cell lines reactive with rat insulinoma (RIN) membranes from two patients and analysed their antigen specificity. We also studied the antigen specificity of one RIN membrane reactive T-cell clone (1C5), previously isolated from a third patient. From the first patient two identical RIN membrane reactive T-cell clones (7A13) were isolated. The second patient yielded two identical (23A19) RIN membrane reactive T-cell clones, and one that was different (234A33). All clones were CD4(+) and saw antigen in the context of different HLA class II alleles. The reactivity of the clones was, however, not restricted to beta cells: all clones showed cross-reactivity with one or more rat tissues, with some preference for those of neuroendocrine origin, but the cross-reactivity patterns were all different. All four clones recognized different fractions electro-eluted from RIN membranes: 29-36 kDa (7A13), 120-170 (23A19), 29-41 (23A33) and 56-72kDa (1C5). The 23A33 clone reacted with the same 38 kDa fraction electro-eluted from insulinoma membranes as a beta-cell reactive clone (1C6) published previously, but none of the other known beta cell antigen preparations tested were recognized by the T-cell clones. Finally, the subcellular localization of the antigens recognized showed at least two different patterns. These data indicate that beta-cell reactive T cells from the peripheral blood of type I diabetes patients are not necessarily beta-cell specific and may be heterogeneous in regard to their antigen specificity and HLA class II restriction. (C) 1995 Academic Press Limited
引用
收藏
页码:887 / 899
页数:13
相关论文
共 44 条
[1]   RESPONSE OF PERIPHERAL-BLOOD MONONUCLEAR-CELLS TO GLUTAMATE-DECARBOXYLASE IN INSULIN-DEPENDENT DIABETES [J].
ATKINSON, MA ;
KAUFMAN, DL ;
CAMPBELL, L ;
GIBBS, KA ;
SHAH, SC ;
BU, DF ;
ERLANDER, MG ;
TOBIN, AJ ;
MACLAREN, NK .
LANCET, 1992, 339 (8791) :458-459
[2]   AUTOANTIBODIES IN NEWLY DIAGNOSED DIABETIC CHILDREN IMMUNOPRECIPITATE HUMAN PANCREATIC-ISLET CELL-PROTEINS [J].
BAEKKESKOV, S ;
NIELSEN, JH ;
MARNER, B ;
BILDE, T ;
LUDVIGSSON, J ;
LERNMARK, A .
NATURE, 1982, 298 (5870) :167-169
[3]   IDENTIFICATION OF THE 64K AUTOANTIGEN IN INSULIN-DEPENDENT DIABETES AS THE GABA-SYNTHESIZING ENZYME GLUTAMIC-ACID DECARBOXYLASE [J].
BAEKKESKOV, S ;
AANSTOOT, HJ ;
CHRISTGAU, S ;
REETZ, A ;
SOLIMENA, M ;
CASCALHO, M ;
FOLLI, F ;
RICHTEROLESEN, H ;
CAMILLI, PD .
NATURE, 1990, 347 (6289) :151-156
[4]   ISLET-SPECIFIC T-CELL CLONES FROM THE NOD MOUSE RESPOND TO BETA-GRANULE ANTIGEN [J].
BERGMAN, B ;
HASKINS, K .
DIABETES, 1994, 43 (02) :197-203
[5]  
BIEG S, 1993, DIABETOLOGIA, V36, P285
[6]   EFFECT OF CYCLOSPORINE ON PANCREATIC EVENTS AND DEVELOPMENT OF DIABETES IN BB/EDINBURGH RATS [J].
BONE, AJ ;
WALKER, R ;
VAREY, AM ;
COOKE, A ;
BAIRD, JD .
DIABETES, 1990, 39 (04) :508-514
[7]   INSITU CHARACTERIZATION OF AUTOIMMUNE PHENOMENA AND EXPRESSION OF HLA MOLECULES IN THE PANCREAS IN DIABETIC INSULITIS [J].
BOTTAZZO, GF ;
DEAN, BM ;
MCNALLY, JM ;
MACKAY, EH ;
SWIFT, PGF ;
GAMBLE, DR .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 313 (06) :353-360
[8]   ISLET-CELL ANTIBODIES IN DIABETES-MELLITUS WITH AUTOIMMUNE POLY-ENDOCRINE DEFICIENCIES [J].
BOTTAZZO, GF ;
FLORINCH.A ;
DONIACH, D .
LANCET, 1974, 2 (7892) :1279-1283
[9]   ANTI-ADRENAL MEDULLARY ANTIBODIES IN IDDM SUBJECTS AND SUBJECTS AT HIGH-RISK OF DEVELOPING IDDM [J].
BROWN, FM ;
KAMALESH, M ;
ADRI, MNS ;
RABINOWE, SL .
DIABETES CARE, 1988, 11 (01) :30-33
[10]   IDENTIFICATION AND CLONING OF A GRANULE AUTOANTIGEN (CARBOXYPEPTIDASE-H) ASSOCIATED WITH TYPE-I DIABETES [J].
CASTANO, L ;
RUSSO, E ;
ZHOU, L ;
LIPES, MA ;
EISENBARTH, GS .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1991, 73 (06) :1197-1201