Antibodies to the tyrosine phosphatase-like protein IA-2 are highly associated with IDDM, but not with autoimmune endocrine diseases or stiff man syndrome

التفاصيل البيبلوغرافية
العنوان: Antibodies to the tyrosine phosphatase-like protein IA-2 are highly associated with IDDM, but not with autoimmune endocrine diseases or stiff man syndrome
المؤلفون: Michael R. Christie, Werner A. Scherbaum, N. G. Morgenthaler, Daniela Glawe, Hans-Michael Meinck, Mark A. Payton, Jochen Seissler, Peter Achenbach
المصدر: Autoimmunity. 25(4)
سنة النشر: 1997
مصطلحات موضوعية: Adult, Male, endocrine system, Cytoplasm, endocrine system diseases, Adolescent, Immunology, Glutamate decarboxylase, Stiff-Person Syndrome, Autoantigens, Sensitivity and Specificity, Autoimmune Diseases, Islets of Langerhans, Antigen, immune system diseases, Antibody Specificity, Diabetes mellitus, Immunopathology, medicine, Immunology and Allergy, Humans, Receptor-Like Protein Tyrosine Phosphatases, Class 8, Child, Polyendocrinopathies, Autoimmune, Aged, Autoantibodies, Autoimmune disease, Aged, 80 and over, Protein Tyrosine Phosphatase, Non-Receptor Type 1, biology, Glutamate Decarboxylase, Autoantibody, nutritional and metabolic diseases, Infant, Membrane Proteins, Reproducibility of Results, Middle Aged, medicine.disease, Diabetes Mellitus, Type 1, Organ Specificity, Autoimmune polyendocrine syndrome, Child, Preschool, biology.protein, Female, Antibody, Protein Tyrosine Phosphatases
الوصف: Antibodies to the 40 kD antigen (identified as tyrosine phosphatase IA-2) and glutamate decarboxylase (GAD65) are strongly associated with insulin dependent diabetes mellitus (IDDM). However, antibodies to GAD (GADA) can appear in the absence of IDDM, particularly in stiff man syndrome (SMS) and in some individuals with autoimmune polyendocrine syndrome type II (APS II) and organ specific autoimmune diseases. The aim of this study was to compare the specificity of IA-2 antibodies (IA-2A) and GADA for IDDM by determining their frequency in different patient groups. IA-2A were present in 64/114 (56%) IDDM patients and 9/19 (47%) APS II patients with IDDM but in only 4/28 (14%) SMS patients. 1/24 (4%) APS II patients without IDDM and 1/113 (0.9%) patients with organ specific autoimmune disease had low level IA-2A. In contrast GADA were present in 77/114 (68%) IDDM patients and 17/19 (89%) APS II patients with IDDM, but also in 25/28 (89%) SMS patients, 5/24 (21%) APS II patients without IDDM and 22/113 (19%) patients with organ specific autoimmune diseases. Furthermore, within the group of new onset IDDM, IA-2A seemed to be associated with ICA and age: 63% of ICA positive IDDM patients had IA-2A (74% had GADA) increasing to 77% in the group below 20 years of age (69% for GADA). Our results demonstrate that IA-2A may be more specific for IDDM than GADA, as the latter are also present in patients with SMS, APS II without IDDM and organ specific autoimmune diseases. IA-2A were less frequent in older patients with IDDM than GADA or ICA. A combination of IA-2A and GADA detected 84% of total and 93% of ICA positive IDDM patients.
تدمد: 0891-6934
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcb9d98df3c52a12fc50ba22ad221bbdTest
https://pubmed.ncbi.nlm.nih.gov/9344328Test
رقم الانضمام: edsair.doi.dedup.....fcb9d98df3c52a12fc50ba22ad221bbd
قاعدة البيانات: OpenAIRE