Autoantibodies in diabetes

被引:202
作者
Pihoker, C [1 ]
Gilliam, LK
Hampe, CS
Lernmark, Å
机构
[1] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[2] Univ Washington, Dept Med, Seattle, WA 98195 USA
关键词
D O I
10.2337/diabetes.54.suppl_2.S52
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Islet cell autoantibodies are strongly associated with the development of type 1 diabetes. The appearance of autoantibodies to one or several of the autoantigens-GAD65, IA-2, or insulin-signals an autoimmune pathogenesis of beta-cell killing. A beta-cell attack may be best reflected by the emergence of autoantibodies dependent on the genotype risk factors, isotype, and subtype of the autoantibodies as well as their epitope specificity. It is speculated that progression to P-cell loss and clinical onset of type 1 diabetes is reflected in a developing pattern of epitope-specific autoantibodies. Although the appearance of autoantibodies does not follow a distinct pattern, the presence of multiple autoantibodies has the highest positive predictive value for type I diabetes. In the absence of reliable T-cell tests, dissection of autoantibody responses in subjects of genetic risk should prove useful in identifying triggers of islet autoimmunity by examining seroconversion and maturation of the autoantibody response that may mark time to onset of type 1 diabetes. The complexity of the disease process is exemplified by multiple clinical phenotypes, including autoimmune diabetes masquerading as type 2 diabetes in youth and adults. Autoantibodies may also provide prognostic information in clinically heterogeneous patient populations when examined longitudinally.
引用
收藏
页码:S52 / S61
页数:10
相关论文
共 111 条
[1]   Stratification of type 1 diabetes risk on the basis of islet autoantibody characteristics [J].
Achenbach, P ;
Warncke, K ;
Reiter, J ;
Naserke, HE ;
Williams, AJK ;
Bingley, PJ ;
Bonifacio, E ;
Ziegler, AG .
DIABETES, 2004, 53 (02) :384-392
[2]  
Amer Diabet Assoc, 2005, DIABETES CARE, V28, pS37
[3]  
[Anonymous], INT HDB SUICIDE ATTE
[4]   Prediction of autoantibody positivity and progression to type 1 diabetes: Diabetes Autoimmunity Study in the Young (DAISY) [J].
Barker, JM ;
Barriga, KJ ;
Yu, LP ;
Miao, DM ;
Erlich, HA ;
Norris, JM ;
Eisenbarth, GS ;
Rewers, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (08) :3896-3902
[5]   Two distinctly HLA-associated contiguous linear epitopes uniquely expressed within the islet antigen 2 molecule are major autoantibody epitopes of the diabetes-specific tyrosine phosphatase-like protein autoantigens [J].
Bearzatto, M ;
Naserke, H ;
Piquer, S ;
Koczwara, K ;
Lampasona, V ;
Williams, A ;
Christie, MR ;
Bingley, PJ ;
Ziegler, AG ;
Bonifacio, E .
JOURNAL OF IMMUNOLOGY, 2002, 168 (08) :4202-4208
[6]  
Berzina L, 2002, ANN NY ACAD SCI, V958, P312
[7]   Epitope analysis of GAD65Ab using fusion proteins and rFab [J].
Binder, KA ;
Banga, JP ;
Madec, AM ;
Ortqvist, E ;
Luo, D ;
Hampe, CS .
JOURNAL OF IMMUNOLOGICAL METHODS, 2004, 295 (1-2) :101-109
[8]   Diabetes antibody standardization program: First assay proficiency evaluation [J].
Bingley, PJ ;
Bonifacio, E ;
Mueller, PW .
DIABETES, 2003, 52 (05) :1128-1136
[9]   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
[10]   Prediction of IDDM in the general population - Strategies based on combinations of autoantibody markers [J].
Bingley, PJ ;
Bonifacio, E ;
Williams, AJK ;
Genovese, S ;
Bottazzo, GF ;
Gale, EAM .
DIABETES, 1997, 46 (11) :1701-1710