Autoimmunity to islet proteins in children diagnosed with new-onset diabetes

被引:56
作者
Brooks-Worrell, BM
Greenbaum, CJ
Palmer, JP
Pihoker, C
机构
[1] DVA Puget Sound Hlth Care Syst, Dept Med, Seattle, WA 98108 USA
[2] Univ Washington, Dept Med, Seattle, WA 98195 USA
[3] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[4] Childrens Hosp & Med Ctr, Seattle, WA 98105 USA
[5] Virginia Mason, Benaroya Res Inst, Seattle, WA 98105 USA
关键词
D O I
10.1210/jc.2003-031360
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Autoantibody and T cells reacting with islet proteins have been demonstrated in patients with type 1 diabetes. In recent years an increasing number of children have been clinically classified with type 2 (not ketosis prone, evidence of insulin resistance, presence of acanthosis nigricans, and obesity) or indeterminant diabetes (admixture of clinical features of types 1 and 2). In this study, we compared the islet cell autoantibody and T-cell responses to islet proteins in type 2 (n = 19) and indeterminant (n = 16) children (< 18 yr of age) to classic type 1 (n = 37) diabetic patients. We observed that 37 of 37 type 1 diabetic children demonstrated autoantibody and/or T-cell reactivity to islet proteins. Fourteen of the 19 type 2 patients were positive for islet cell autoantibodies, and six of 14 were positive for T-cell responses to islet proteins. For the indeterminant patients, 11 of 16 of the patients were positive for autoantibodies, and six of 16 patients were positive for T-cell responses to islet proteins. These results demonstrate that autoimmunity to islet proteins is present in a high percentage of children classified as indeterminant or type 2 diabetes. Moreover, the presence of obesity or acanthosis nigracans does not reliably distinguish children with or without islet cell autoimmunity.
引用
收藏
页码:2222 / 2227
页数:6
相关论文
共 28 条
[1]
A SIMPLE NEW METHOD FOR USING ANTIGENS SEPARATED BY POLYACRYLAMIDE-GEL ELECTROPHORESIS TO STIMULATE LYMPHOCYTES INVITRO AFTER CONVERTING BANDS CUT FROM WESTERN BLOTS INTO ANTIGEN-BEARING PARTICLES [J].
ABOUZEID, C ;
FILLEY, E ;
STEELE, J ;
ROOK, GAW .
JOURNAL OF IMMUNOLOGICAL METHODS, 1987, 98 (01) :5-10
[2]
Diabetes antibody standardization program: First assay proficiency evaluation [J].
Bingley, PJ ;
Bonifacio, E ;
Mueller, PW .
DIABETES, 2003, 52 (05) :1128-1136
[3]
Intermolecular antigen spreading occurs during the preclinical period of human type 1 diabetes [J].
Brooks-Worrell, B ;
Gersuk, VH ;
Greenbaum, C ;
Palmer, JP .
JOURNAL OF IMMUNOLOGY, 2001, 166 (08) :5265-5270
[4]
Cellular immune responses to human islet proteins in antibody-positive type 2 diabetic patients [J].
Brooks-Worrell, BM ;
Juneja, R ;
Minokadeh, A ;
Greenbaum, CJ ;
Palmer, JP .
DIABETES, 1999, 48 (05) :983-988
[5]
DETERMINATION OF BOVINE LYMPHOCYTE-RESPONSES TO EXTRACTED PROTEINS OF BRUCELLA-ABORTUS BY USING PROTEIN IMMUNOBLOTTING [J].
BROOKSALDER, B ;
SPLITTER, GA .
INFECTION AND IMMUNITY, 1988, 56 (10) :2581-2586
[6]
BrooksWorrell BM, 1996, J IMMUNOL, V157, P5668
[7]
ANTIGENS OF BRUCELLA-ABORTUS S19 IMMUNODOMINANT FOR BOVINE LYMPHOCYTES AS IDENTIFIED BY ONE-DIMENSIONAL AND 2-DIMENSIONAL CELLULAR IMMUNOBLOTTING [J].
BROOKSWORRELL, BM ;
SPLITTER, GA .
INFECTION AND IMMUNITY, 1992, 60 (06) :2459-2464
[8]
Type 2 diabetes mellitus in UK children - an emerging problem [J].
Ehtisham, S ;
Barrett, TG ;
Shaw, NJ .
DIABETIC MEDICINE, 2000, 17 (12) :867-871
[9]
Type 2 diabetes among North American children and adolescents: An epidemiologic review and a public health perspective [J].
Fagot-Campagna, A ;
Pettitt, DJ ;
Engelgau, MM ;
Burrows, NR ;
Geiss, LS ;
Valdez, R ;
Beckles, GLA ;
Saaddine, J ;
Gregg, EW ;
Williamson, DF ;
Narayan, KMV .
JOURNAL OF PEDIATRICS, 2000, 136 (05) :664-672
[10]
RADIOIMMUNOASSAYS FOR GLUTAMIC-ACID DECARBOXYLASE (GAD65) AND GAD65 AUTOANTIBODIES USING S-35 OR H-3 RECOMBINANT HUMAN LIGANDS [J].
FALORNI, A ;
ORTQVIST, E ;
PERSSON, B ;
LERNMARK, A .
JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 186 (01) :89-99