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T Cell Recognition of Autoantigens in Human Type 1 Diabetes: Clinical Perspectives
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Brezar, Vedran
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Hop St Vincent de Paul, INSERM, U986, F-75014 Paris, France
Univ Paris 05, F-75005 Paris, France Hop St Vincent de Paul, INSERM, U986, F-75014 Paris, France

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[1] Hop St Vincent de Paul, INSERM, U986, F-75014 Paris, France
[2] Univ Paris 05, F-75005 Paris, France
[3] Hop Cochin Hotel Dieu, Assistance Publ Hop Paris, F-75679 Paris, France
来源:
CLINICAL & DEVELOPMENTAL IMMUNOLOGY
|
2011年
关键词:
GLUTAMIC-ACID DECARBOXYLASE;
RANDOMIZED CONTROLLED-TRIAL;
TYROSINE PHOSPHATASE IA-2;
CLASS-II TETRAMERS;
AT-RISK SUBJECTS;
NOD MICE;
TRANSGENIC MICE;
BETA-CELLS;
PROINSULIN EPITOPES;
IMMUNE-RESPONSE;
D O I:
10.1155/2011/513210
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 1 diabetes (T1D) is an autoimmune disease driven by the activation of lymphocytes against pancreatic beta-cells. Among beta-cell autoantigens, preproinsulin has been ascribed a key role in the T1D process. The successive steps that control the activation of autoreactive lymphocytes have been extensively studied in animal models of T1D, but remains ill defined in man. In man, T lymphocytes, especially CD8(+) T cells, are predominant within insulitis. Developing T-cell assays in diabetes autoimmunity is, thus, a major challenge. It is expected to help defining autoantigens and epitopes that drive the disease process, to pinpoint key functional features of epitope-specific T lymphocytes along the natural history of diabetes and to pave the way towards therapeutic strategies to induce immune tolerance to beta-cells. New T-cell technologies will allow defining autoreactive T-cell differentiation programs and characterizing autoimmune responses in comparison with physiologically appropriate immune responses. This may prove instrumental in the discovery of immune correlates of efficacy in clinical trials.
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