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Selective Suppression of Antibody Production with the Aid of Radiolabelled Birch Pollen Allergen
Authors:G. Filipp,,G. Biró  ,,W. D. Hartung, G. Lehmann
Affiliation:Klinik-Rotes-Kreuz, Dept. of Allergology and Clinical Immunology, and Dept. of Oto-Rhino-Laryngology, Saarbrücken, II. Medical Clinic, Medical Faculty, University of Saarland, Homburg/Saar, and Institute for Analytical and Biological Chemistry, University of Saarland, Saabriicken, Fed. Rep. of Germany
Abstract:In accordance with the clonal selection theory we intended to prevent the development of artificially induced birch pollen allergy in rabbits with the aid of the radiolabelled' pollen allergen (75–1000 μCi125 I-pollen/animal) intravenously administered prior to pollen sensitization. The birch pollen allergen, in accordance with Burnet's working hypothesis, reacts only with a genetically determining B cell subpopulation. The fixation of the radiolabelled birch pollen allergen to the receptors of the competent B cell clone causes the lesion of the latter. Compared with the control group, this group of rabbits showed an extensive suppression of anaphylactic reagin-like PCA-antibodies, and haemagglutinating antibodies in the blood as well as in nasal secretion. In addition, we tried to influence the already ongoing synthesis of the antibodies with the aid of a subsequent intravenously administered radiolabelled birch pollen allergen (750–1000 μCi125 I-pollen/animal). An intensive suppression of the synthesis of antibodies could also be proved in this case. The simultaneous immunization of the control rabbits with birch pollen and egg albumin resulted in the production of antibodies against both antigens, as expected. The hot-labelled birch pollen antigen intravenously injected before or after immunization with egg albumin and birch pollen led selectively to suppression of anti-birch-pollen PCA antibodies. The synthesis of anti-egg albumin PCA antibodies was unaffected.
Keywords:hot labelled allergen    125I-labelled birch pollen allergen    radioactive damage of B-cell clone    selective immunosuppression
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