Schalén C, Christensen P, Grubb A, Samuelsson G, Svensson M L
Acta Pathol Microbiol Scand C. 1980 Apr;88(2):77-82. doi: 10.1111/j.1699-0463.1980.tb00076.x.
The alkaline extract of group A streptococci type 4 was separated by electrophoresis and diffused against 27 normal human sera. One of the precipitates appeared with 85% of the sear. Addition of purified IgA myeloma protein or sera containing IgA M-components to the extract changed the electrophoretic mobility of the precipitate anodically. Purified IgG Fc-fragments or sera containing IgG M-component did not affect the mobility of the precipitate. It was concluded that this precipitate contained the streptococcal receptor for human IgA. A non-precipitating IgG Fc-receptor, with agglutinating capacity for cells coated with human IgG1 but not IgG3, was localized by preparative electrophoresis to the same electrophoretic region as the IgA receptor. The mobility of the IgG receptor remained unaltered on addition of IgA myeloma protein permitting a separation of the two receptors by preparative electrophoresis. The receptors were distinct from the group specific carbohydrate, peptidoglycan and lipoteicholic acid. No M antigen or opacity factor were demonstrated in the extract.
对4型A组链球菌的碱性提取物进行电泳分离,并与27份正常人血清进行扩散试验。其中一种沉淀物出现在85%的血清中。向提取物中添加纯化的IgA骨髓瘤蛋白或含有IgA M成分的血清,会使沉淀物的电泳迁移率向阳极方向改变。纯化的IgG Fc片段或含有IgG M成分的血清不会影响沉淀物的迁移率。得出的结论是,这种沉淀物含有人类IgA的链球菌受体。一种对包被有人类IgG1而非IgG3的细胞具有凝集能力的非沉淀性IgG Fc受体,通过制备电泳定位于与IgA受体相同的电泳区域。添加IgA骨髓瘤蛋白后,IgG受体的迁移率保持不变,从而可以通过制备电泳将两种受体分离。这些受体与群特异性碳水化合物、肽聚糖和脂磷壁酸不同。提取物中未检测到M抗原或不透明因子。