Gilles J G, Mareschal J C, Saint-Remy J M
Experimental Medicine Unit, Université Catholique de Louvain, Brussels, Belgium.
J Allergy Clin Immunol. 1988 Jul;82(1):35-9. doi: 10.1016/0091-6749(88)90048-6.
We describe a two-step latex (Lx) agglutination assay for the titration of specific anti-Dermatophagoides pteronyssinus IgE. The samples are first incubated with allergen-coated Lx of 2.3 microns diameter. Bound IgE is digested by pepsin and then titrated by its agglutinating activity on 0.8 micron Lx particles coated with antihuman Fc epsilon rabbit F(ab')2. This latex allergosorbent test detects 100 pg of specific IgE per milliliter and does not depend on the concentration of total IgE. Owing to a tenfold increase in the allergosorbent surface, no competition with the binding of specific anti-D. pteronyssinus IgG is observed. Pepsin digestion eliminates potential interferences caused by autoantibodies against IgE. A good correlation (r = 0.92) is found with Phadebas RAST on a series of 91 samples. The latex allergosorbent test does not make use of radioisotopes and can be performed in less than 6 hours.
我们描述了一种用于滴定特异性抗屋尘螨IgE的两步乳胶(Lx)凝集试验。首先将样品与直径为2.3微米的过敏原包被的Lx一起孵育。结合的IgE用胃蛋白酶消化,然后通过其对包被有抗人Fcε兔F(ab')2的0.8微米Lx颗粒的凝集活性进行滴定。这种乳胶变应原吸附试验可检测到每毫升100 pg的特异性IgE,且不依赖于总IgE的浓度。由于变应原吸附表面增加了10倍,未观察到与特异性抗屋尘螨IgG结合的竞争。胃蛋白酶消化消除了由抗IgE自身抗体引起的潜在干扰。在一系列91个样品上,与Phadebas RAST有良好的相关性(r = 0.92)。乳胶变应原吸附试验不使用放射性同位素,且可在不到6小时内完成。