• 1 January 1981
    • journal article
    • research article
    • Vol. 46 (1), 44-53
Abstract
A simple 2-step method for the detection of specific antigen within immune complexes is described. The immune complexes are precipitated from serum by polyethylene glycol, dissociated by incubation in acid pH buffer and adsorbed onto the surface of polystyrene tubes. The antigen is detected by the binding of a radiolabeled affinity-purified specific antibody. The assay can detect the antigen within both antigen- and antibody-excess immune complexes of any Ig class, and can allow semiquantitative comparison of different samples. Immune complexes containing food protein antigens after eating were found in the serum of both normal subjects and atopic patients; the latter group showed higher mean levels of antigen-specific immune complexes. The method can be adopted for large-scale screening of clinical samples for suspected antigens if suitable antisera are available.