Gallagher P, Jones K
Arthritis Rheum. 1982 Jan;25(1):75-9. doi: 10.1002/art.1780250112.
The cause of cranial arteritis is unknown, but the demonstration of immunoglobulin and complement in temporal artery biopsies by immunofluorescence suggest that it may be a disease of disordered immunity. Because of the inevitable problems of histologic interpretation associated with the fluorescent technique, 15 temporal artery biopsies from patients with active arteritis were examined by an immunoperoxidase method. Varying amounts of IgA, IgG, and IgM were identified in plasma cells and macrophages. Extracellular IgG was identified in 1 case, but there was no staining for complement. These findings provide no support for the concept of cranial arteritis as a form of immune complex vasculitis.
颅动脉炎的病因尚不清楚,但通过免疫荧光在颞动脉活检中显示免疫球蛋白和补体提示它可能是一种免疫紊乱性疾病。由于与荧光技术相关的组织学解释存在不可避免的问题,对15例活动性动脉炎患者的颞动脉活检采用免疫过氧化物酶法进行检查。在浆细胞和巨噬细胞中发现了不同量的IgA、IgG和IgM。1例发现细胞外IgG,但补体无染色。这些发现不支持颅动脉炎是免疫复合物性血管炎的一种形式这一概念。