GAD65-Reactive T cells in a Non-diabetic Stiff-man Syndrome Patient

• Published in: Journal of autoimmunity Vol. 12; no. 4; pp. 289 - 296
• Main Authors: Schloot, Nanette C, Batstra, Manou C, Duinkerken, Gaby, De Vries, René R.P, Dyrberg, Thomas, Chaudhuri, Abhijit, Behan, Peter O, Roep, Bart O
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.06.1999
• Subjects: Adult; Autoantibodies - blood; Cytokines - biosynthesis; Epitope Mapping; Epitopes, T-Lymphocyte; Female; Glutamate Decarboxylase - immunology; HLA-DR Antigens - physiology; Humans; insulin-dependent diabetes mellitus, GAD65, autoimmune, T lymphocytes, stiff-man syndrome; Lymphocyte Activation; Male; Middle Aged; Stiff-Person Syndrome - immunology; T-Lymphocytes - immunology; insulin-dependent diabetes mellitus, GAD65, autoimmune, T lymphocytes, stiff-man syndrome
• DOI: 10.1006/jaut.1999.0280
• ISSN: 0896-8411

GAD65 (glutamic acid decarboxylase) is an important autoantigen in both type 1 (insulin-dependent) diabetes mellitus (IDDM) and the neurological autoimmune disease stiff-man syndrome (SMS), and is expressed in pancreatic islets as well as the nervous system. Still, only 30% of SMS patients also have type 1 diabetes. To study regulation of T cell responsiveness to GAD65, we investigated a non-diabetic SMS patient with HLA-DR3/7 (predisposing to type 1 diabetes) and high levels of type 1 diabetes-associated autoantibodies against GAD65 and islet cells, and compared the results with those of her diabetic son and two other SMS patients. T cell responses to GAD65 were repeatedly absent in primary stimulation, whereas IA-2, islet antigen and tetanus toxoid induced significant T cell proliferation. However, after in vitro restimulation, GAD65 reactive T cell lines and clones were obtained that were HLA-DR3 restricted, and cross-reactive with a homogenate of purified human pancreatic islets. These T cells produced the immunoregulatory cytokine IL-10 in combination with IFN-γ and IL-4 (Th0). The dominant T cell epitope was mapped to the central region of GAD65. Although no primary response to whole GAD65 was detectable, the naturally processed GAD65 peptide epitope was recognized vigorously in the primary stimulation assay. The lack of detectable primary T cell responses to GAD65, together with the GAD65-specific cytokine production of restimulated T cells, suggest that GAD65-specific cellular autoimmunity in this patient is suppressed and may be related to the absence of diabetes despite humoral autoreactivity and genetic predisposition.