The transition from specific to nonspecific desensitization in human basophils.
Open Access
- 1 December 1981
- journal article
- research article
- Published by Oxford University Press (OUP) in The Journal of Immunology
- Vol. 127 (6) , 2410-2414
- https://doi.org/10.4049/jimmunol.127.6.2410
Abstract
Human basophils can be desensitized to IgE-mediated stimuli either specifically (to the desensitizing antigen only) or nonspecifically (to all antigens). It has been suggested that the specificity of desensitization depends on the number of membrane-bound, antigen-specific IgE antibody molecules per basophil. We have varied the number of IgE antibody molecules/basophil by passive sensitization of mixed leukocyte preparations with increasing concentrations of purified IgE anti-penicillin (BPO) antibody. The cells were then desensitized with penicillin-human serum albumin (BPO-HSA). Desensitization was specific (lack of response to BPO-HSA only) with 1000 specific antibody molecules/basophil, and increasingly nonspecific (greater than 70% desensitization to rechallenge with anti-IgE and ragweed antigen E as well as lack of response to BPO-HSA) as the number of antibody molecules was increased to 14,000. This formally established that the number of specific IgE antibody molecules/basophil determines the mode of desensitization.This publication has 4 references indexed in Scilit:
- Role of beta-adrenergic receptors in catecholamine-induced desensitization of adenylate cyclase in human astrocytoma cells.Journal of Biological Chemistry, 1978
- The mechanism of action of soluble lymphocyte mediatorsCellular Immunology, 1977
- Measurement of IgE on Human Basophils: Relation to Serum IgE and Anti-IgE-Induced Histamine ReleaseThe Journal of Immunology, 1977
- REGULATION OF ADENYLATE CYCLASE-COUPLED BETA-ADRENERGIC-RECEPTOR BINDING-SITES BY BETA-ADRENERGIC CATECHOLAMINES INVITRO1976