Document 0842 DOCN M95A0842 TI In vitro activation leads to the binding of T-cell markers to the surface of B-lymphocytes. DT 9510 AU Rabinowitz R; Massiah E; Hadar R; Schlesinger M; Hubert H. Humphrey Center for Experimental Medicine, Hebrew; University, Hadassah Medical School, Jerusalem, Israel. SO Clin Immunol Immunopathol. 1995 Aug;76(2):148-54. Unique Identifier : AIDSLINE MED/95339607 AB The aim of the present study was to determine whether activation of human T-cells in vitro results in the expression of markers characteristic for T-cells on the surface of B-lymphocytes and to correlate antigenic changes with the release of soluble T-cell antigens. Peripheral blood lymphocytes (PBL) were exposed in vitro to phytohemagglutinin (PHA) for 3 days. Changes in the phenotype of the cells were determined by flow cytometry and the level of soluble T-cell antigens was assessed by ELISA. PHA-activated PBL released elevated quantities of soluble CD2, CD4, and CD8 compared with control cultures. Following PHA stimulation the proportion of CD4+ CD8+ and HLA-DR+ cells increased. In addition, after 3 days of activation with PHA about 80% of the CD19+ cells (B-cells) reacted with F(ab)2 fragments of CD2 monoclonal antibodies (MoAbs). A high proportion of B-cells in activated cultures also reacted with F(ab)2 fragments of anti-CD8 MoAb and anti-CD4 MoAb. The removal of either CD4+ or CD8+ T-cells from the cultures prior to stimulations with PHA drastically reduced the proportion of B-cells expressing CD4 or CD8, respectively. The attachment of T-cell markers to the surface B-lymphocytes may constitute a new mechanism for B-cell regulation by T-cells. DE Antigens, CD/*BIOSYNTHESIS Antigens, CD2/BIOSYNTHESIS Antigens, CD4/BIOSYNTHESIS Antigens, CD8/BIOSYNTHESIS Antigens, Surface/*PHYSIOLOGY B-Lymphocytes/*METABOLISM Biological Markers/ANALYSIS Cells, Cultured CD4-Positive T-Lymphocytes/IMMUNOLOGY CD8-Positive T-Lymphocytes/IMMUNOLOGY Human Lymphocyte Transformation/IMMUNOLOGY Phytohemagglutinins/PHARMACOLOGY Protein Binding/PHYSIOLOGY Solubility Support, Non-U.S. Gov't T-Lymphocytes/DRUG EFFECTS/*IMMUNOLOGY/*METABOLISM JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).