Document 0007 DOCN M9470007 TI Allergen-induced expression of cell surface markers on lymphocytes of Chi t I-sensitized patients. DT 9409 AU Liebers V; Raulf M; Baur X; Berufsgenossenschaftliches Forschungsinstitut fur Arbeitsmedizin; (BGFA), Ruhr-Universitat Bochum, Germany. SO Allergy. 1994 Mar;49(3):163-9. Unique Identifier : AIDSLINE MED/94256625 AB Lymphocyte cultures of persons sensitized to the hemoglobin allergen Chi t I show a highly significant response to the allergen measured in the lymphocyte stimulation assay by (3H)-thymidine uptake. In this study, we investigated by flow cytometry the expression of different cell surface markers on lymphocytes after in vitro stimulation for 7 d with or without the allergen Chi t I. We determined the expression of the low-affinity receptor for IgE (CD23) on lymphocytes of Chi t I-sensitized patients and Chi t I-exposed as well as nonexposed controls. CD23 expression was significantly higher in patients than in nonexposed controls. Exposed but healthy subjects showed intermediate values. We also determined the expression of activation markers CD25 (IL-2 receptor) and HLA-DR on the lymphocytes of patients and nonexposed controls. HLA-DR expression on non-T cells (CD3-) was significantly higher in patients than in controls. HLA-DR on T cells (CD3+), and CD25 as well as CD23 expression, could be significantly enhanced after antigen-specific stimulation in patients but not in controls, whereas alpha/beta-T-cell-receptor expression was significantly reduced in patients. Differences between patients and controls were not observed in response to tetanus toxoid (TT) and phytohemagglutinin (PHA). Our results demonstrate antigen-specific influences on the expression of cell surface molecules. These findings may be valuable diagnostic information. DE Allergens/*IMMUNOLOGY Animal Antigens, Surface/*BIOSYNTHESIS/IMMUNOLOGY B-Lymphocytes/*IMMUNOLOGY/METABOLISM Cells, Cultured Chironomidae/*IMMUNOLOGY Comparative Study CD4-CD8 Ratio Flow Cytometry Hemoglobins/*IMMUNOLOGY Human HLA-DR Antigens/BIOSYNTHESIS IgE/BIOSYNTHESIS Lymphocyte Transformation Phytohemagglutinins/IMMUNOLOGY Receptors, Interleukin-2/*BIOSYNTHESIS Support, Non-U.S. Gov't T-Lymphocytes/*IMMUNOLOGY/METABOLISM Tetanus Toxoid/IMMUNOLOGY Time Factors JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).