Peters M S, Schroeter A L, Kephart G M, Gleich G J
J Invest Dermatol. 1983 Jul;81(1):39-43. doi: 10.1111/1523-1747.ep12538380.
The role of the eosinophil in the pathogenesis of cutaneous diseases is not known. The eosinophil granule major basic protein (MBP), constituting the core and accounting for greater than 50% of the eosinophil granule, is toxic to helminths and mammalian cells. To determine whether eosinophil degranulation occurs in lesions of chronic urticaria, we performed an indirect immunofluorescence assay on sections of formalin-fixed, paraffin-embedded tissue, utilizing affinity chromatography-purified antibody to MBP. Twelve of 28 biopsies showed evidence of degranulation as judged by the deposition of MBP outside the eosinophil. The positive staining was of 3 types: (1) small blood vessel walls (5 patients), (2) dispersion of granular material (9 patients), and (3) focal or diffuse immunofluorescence of connective tissue fibers (11 patients). These results suggest a possible role for the cytotoxic molecule MBP in the evolution of lesions of chronic urticaria.
嗜酸性粒细胞在皮肤病发病机制中的作用尚不清楚。嗜酸性粒细胞颗粒主要碱性蛋白(MBP)构成颗粒核心,占嗜酸性粒细胞颗粒的50%以上,对蠕虫和哺乳动物细胞有毒性。为了确定慢性荨麻疹皮损中是否发生嗜酸性粒细胞脱颗粒,我们利用亲和层析纯化的抗MBP抗体,对福尔马林固定、石蜡包埋组织切片进行间接免疫荧光检测。28例活检中有12例显示有脱颗粒证据,依据是MBP在嗜酸性粒细胞外沉积来判断。阳性染色有3种类型:(1)小血管壁(5例患者),(2)颗粒物质弥散(9例患者),以及(3)结缔组织纤维的局灶性或弥漫性免疫荧光(11例患者)。这些结果提示细胞毒性分子MBP在慢性荨麻疹皮损演变中可能起作用。