Demonstration of natural autoantibodies against the neurofilament protein α-internexin in sera of patients with endocrine autoimmunity and healthy individuals

Serum anti-pituitary antibodies (APAs) to cytosolic antigens have been found in association with autoimmune hypophysitis, idiopathic hypopituitarism, and other autoimmune endocrinopathies. Here, an immunoblot method was used to search for serum autoantibody (AAb) reactivities against pituitary antig...

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Bibliographic Details
Published in:Immunology letters Vol. 94; no. 1; pp. 153 - 160
Main Authors: Rajasalu, Tarvo, Teesalu, Kaupo, Janmey, Paul A, Uibo, Raivo
Format: Journal Article
Language:English
Published: Netherlands Elsevier B.V 15-06-2004
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Summary:Serum anti-pituitary antibodies (APAs) to cytosolic antigens have been found in association with autoimmune hypophysitis, idiopathic hypopituitarism, and other autoimmune endocrinopathies. Here, an immunoblot method was used to search for serum autoantibody (AAb) reactivities against pituitary antigens, including nuclear and cytoskeletal proteins, in six patients with idiopathic hypopituitarism, 60 patients with type 1 diabetes, nine patients with autoimmune polyglandular syndrome (APS) type 1, and in 74 healthy controls. Frequent patient serum IgG reactivity was observed against a 60 kDa human pituitary antigen, and the cross-reactive 62 kDa protein from rat brain was identified as α-internexin (α-INX) by proteomic methods. IgG and IgM AAbs to this neuron-specific type IV intermediate filament (IF) protein were found in most sera of patients with endocrine autoimmunity as well as healthy subjects with no significant differences in frequencies between the groups, but the levels of IgM α-INX AAbs were higher in patients with hypopituitarism as compared to healthy controls ( P = 0.032, Mann–Whitney U-test). These findings suggest that α-INX AAbs are not specifically related to autoimmune endocrine diseases and most probably are a part of the natural AAb repertoire. This is the first demonstration of α-INX AAbs as one of the predominant neuronal IF AAbs in human sera.
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ISSN:0165-2478
1879-0542
DOI:10.1016/j.imlet.2004.05.002