Autoantigen-specific memory CD4+ T cells are prevalent early in progression to Type 1 diabetes

被引:33
作者
Oling, Viveka [1 ]
Reijonen, Helena [2 ]
Simell, Olli [3 ]
Knip, Mikael [4 ,5 ,6 ]
Ilonen, Jorma [1 ,7 ]
机构
[1] Univ Turku, Immunogenet Lab, FI-20520 Turku, Finland
[2] Virginia Mason, Benaroya Res Inst, Seattle, WA 98101 USA
[3] Univ Turku, Dept Pediat, FI-20521 Turku, Finland
[4] Univ Helsinki, Hosp Children & Adolescents, FI-00029 Helsinki, Finland
[5] Univ Helsinki, Folkhalsan Res Ctr, FI-00029 Helsinki, Finland
[6] Tampere Univ Hosp, Dept Pediat, FI-33521 Tampere, Finland
[7] Univ Eastern Finland, Dept Clin Microbiol, FI-70211 Kuopio, Finland
关键词
T1D; T cells; GAD65; Insulin; GLUTAMIC-ACID DECARBOXYLASE; CLASS-II TETRAMERS; AT-RISK SUBJECTS; PERIPHERAL-BLOOD; GENERAL-POPULATION; EPITOPES; INSULIN; AUTOANTIBODIES; PREDICTION; CHILDREN;
D O I
10.1016/j.cellimm.2011.12.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autoreactive CD4(+) T cells contribute to the destruction of insulin producing beta cells in Type 1 diabetes (T1D). Using MHC class II tetramers, we have analyzed the frequency of GAD65-(274-286; 555-567) and insulin-(A1-15; A6-21) specific CD4(+)T cells in 31 children with T1D, 65 multiple autoantibody-positive children and 93 HLA- and age-matched controls. In a smaller group of children T-cell responses of memory origin to the same autoantigens were investigated. We observed a higher response to GAD65 555-567 in the autoantibody-positive children than in the controls (P = 0.017). Memory T-cell responses to GAD65 555-567 were more frequent among T1D patients (P = 0.025) and autoantibody-positive (P = 0.054), while all controls were negative (n = 28). In summary, the presence of antigen experienced GAD65-specific T cells in the subjects with diabetes-associated autoimmunity is encouraging for further directions in the prediction of T1D. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:133 / 139
页数:7
相关论文
共 37 条
[1]   Natural history of type 1 diabetes [J].
Achenbach, P ;
Bonifacio, E ;
Koczwara, K ;
Ziegler, AG .
DIABETES, 2005, 54 :S25-S31
[2]   Autoreactive T cell responses show proinflammatory polarization in diabetes but a regulatory phenotype in health [J].
Arif, S ;
Tree, TI ;
Astill, TP ;
Tremble, JM ;
Bishop, AJ ;
Dayan, CM ;
Roep, BO ;
Peakman, M .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 113 (03) :451-463
[3]   COMBINED ANALYSIS OF AUTOANTIBODIES IMPROVES PREDICTION OF IDDM IN ISLET-CELL ANTIBODY-POSITIVE RELATIVES [J].
BINGLEY, PJ ;
CHRISTIE, MR ;
BONIFACIO, E ;
BONFANTI, R ;
SHATTOCK, M ;
FONTE, MT ;
BOTTAZZO, GF ;
GALE, EAM .
DIABETES, 1994, 43 (11) :1304-1310
[4]   Comparative study of GAD65-specific CD4+ T cells in healthy and type 1 diabetic subjects [J].
Danke, NA ;
Yang, JB ;
Greenbaum, C ;
Kwok, WW .
JOURNAL OF AUTOIMMUNITY, 2005, 25 (04) :303-311
[5]   Autoreactive T cells in healthy individuals [J].
Danke, NA ;
Koelle, DM ;
Yee, C ;
Beheray, S ;
Kwok, WW .
JOURNAL OF IMMUNOLOGY, 2004, 172 (10) :5967-5972
[6]   Translational mini-review series on type 1 diabetes: Systematic analysis of T cell epitopes in autoimmune diabetes [J].
Di Lorenzo, T. P. ;
Peakman, M. ;
Roep, B. O. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2007, 148 (01) :1-16
[7]   Predominantly recognized proinsulin T helper cell epitopes in individuals with and without islet cell autoimmunity [J].
Durinovic-Belló, I ;
Boehm, BO ;
Ziegler, AG .
JOURNAL OF AUTOIMMUNITY, 2002, 18 (01) :55-66
[8]  
EISENBARTH GS, 1986, NEW ENGL J MED, V314, P1360
[9]  
Endl J, 2006, DIABETES, V55, P50, DOI 10.2337/diabetes.55.01.06.db05-0387
[10]   Identification of naturally processed T cell epitopes from glutamic acid decarboxylase presented in the context of HLA-DR alleles by T lymphocytes of recent onset IDDM patients [J].
Endl, J ;
Otto, H ;
Jung, G ;
Dreisbusch, B ;
Donie, F ;
Stahl, P ;
Elbracht, R ;
Schmitz, G ;
Meinl, E ;
Hummel, M ;
Ziegler, AG ;
Wank, R ;
Schendel, DJ .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (10) :2405-2415