Rajasalu Tarvo, Teesalu Kaupo, Janmey Paul A, Uibo Raivo
Department of Immunology, Institute of General and Molecular Pathology, University of Tartu, 19 Ravila Street, Tartu 51014, Estonia.
Immunol Lett. 2004 Jun 15;94(1-2):153-60. doi: 10.1016/j.imlet.2004.05.002.
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 alpha-internexin (alpha-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 alpha-INX AAbs were higher in patients with hypopituitarism as compared to healthy controls (P = 0.032, Mann-Whitney U-test). These findings suggest that alpha-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 alpha-INX AAbs as one of the predominant neuronal IF AAbs in human sera.
血清中针对细胞溶质抗原的抗垂体抗体(APAs)已被发现与自身免疫性垂体炎、特发性垂体功能减退症以及其他自身免疫性内分泌疾病有关。在此,采用免疫印迹法,在6例特发性垂体功能减退症患者、60例1型糖尿病患者、9例1型自身免疫性多腺体综合征(APS)患者以及74名健康对照者中,寻找血清自身抗体(AAb)对垂体抗原(包括核蛋白和细胞骨架蛋白)的反应性。观察到患者血清中频繁出现针对一种60 kDa人垂体抗原的IgG反应性,通过蛋白质组学方法将来自大鼠脑的交叉反应性62 kDa蛋白鉴定为α-中间丝蛋白(α-INX)。在内分泌自身免疫患者以及健康受试者的大多数血清中均发现了针对这种神经元特异性IV型中间丝(IF)蛋白的IgG和IgM AAbs,两组之间在频率上无显著差异,但垂体功能减退症患者中IgMα-INX AAbs水平高于健康对照者(P = 0.032,曼-惠特尼U检验)。这些发现表明,α-INX AAbs与自身免疫性内分泌疾病无特异性关联,很可能是天然AAb库的一部分。这是首次证明α-INX AAbs是人类血清中主要的神经元IF AAbs之一。