Agarwal M K, Jones R T, Yunginger J W
J Allergy Clin Immunol. 1982 Dec;70(6):432-6. doi: 10.1016/0091-6749(82)90005-7.
To develop a model for mold allergen extract standardization, we studied eight commercial Alternaria extracts from various suppliers by a variety of immunochemical and physicochemical techniques, including measurement of Alt-I, a purified allergenic fraction of Alternaria. Wide variations were noted in the allergenic and antigenic potencies of these extracts. Estimates of Alt-I content measured by Alt-I RAST inhibition and by radioimmunoassay correlated significantly (p less than 0.05), but Alt-I activity by either method could not be correlated with allergenic potency as measured by RAST inhibiton using solid-phase Alternaria. Each test extract produced unique and differing patterns of Coomassie blue-stained bands in isoelectrofocusing gels and in crossed immunoelectrophoresis gels using rabbit antibodies to Alternaria. The optimal method for mold allergen standardization involves a combination of RAST inhibiton, isoelectrofocusing, and crossed immunoelectrophoresis techniques, and, if possible, quantitation of individual allergens.
为建立一种霉菌变应原提取物标准化模型,我们通过多种免疫化学和物理化学技术研究了来自不同供应商的8种商业链格孢提取物,包括对链格孢一种纯化变应原组分Alt-I的测定。这些提取物的变应原和抗原效力存在很大差异。通过Alt-I RAST抑制法和放射免疫分析法测得的Alt-I含量估计值显著相关(p小于0.05),但两种方法测得的Alt-I活性均与使用固相链格孢的RAST抑制法测得的变应原效力无关。在等电聚焦凝胶和使用兔抗链格孢抗体的交叉免疫电泳凝胶中,每种测试提取物都产生了独特且不同的考马斯亮蓝染色条带模式。霉菌变应原标准化的最佳方法包括RAST抑制法、等电聚焦法和交叉免疫电泳技术的结合,以及尽可能对单个变应原进行定量。