Document 0852 DOCN M9440852 TI Population dynamics of CD4+ T cells lacking Thy-1 in murine retrovirus-induced immunodeficiency syndrome (MAIDS). DT 9404 AU Moutschen MP; Colombi S; Deprez M; Van Wijk F; Hotermans C; Martin MT; Greimers R; Boniver J; Department of Pathology, University of Liege, Belgium. SO Scand J Immunol. 1994 Feb;39(2):216-24. Unique Identifier : AIDSLINE MED/94126672 AB Increased numbers of CD4+ Thy-1- cells have been described in the spleen (SP) of mice with retrovirus-induced immunodeficiency (MAIDS). Since this phenotypic abnormality might have considerable functional importance, the expansion of the CD4+ Thy-1- subset in MAIDS was characterized further. CD4+ Thy-1- and Thy-1+ T-cells from infected mice expressed similar densities of CD3 and TCR alpha/beta. In contrast, the Thy-1- subset was uniformly CD44hi, even early in the disease when part of Thy-1+ cells were still CD44lo. The emergence of CD4+ Thy-1- cells occurred first in SP and lymph nodes and was observed later in thymus. The important fraction of CD4+ cells lacking Thy-1 normally present in Peyer's patches was only weakly modified. Despite the major expansion of the CD4+ Thy-1- phenotype, the proliferating fraction was not higher in this subset than in CD4+ Thy-1+ cells from infected mice. Persistence after hydroxyurea administration was identical in both subsets, indicating similar mean cell lifespans. Taken together, these results show that the major expansion of CD4+ Thy-1- T-cells in MAIDS is not ascribable solely to increased proliferation within this subset. Phenotypic analysis suggests that CD4+ Thy-1- cells result from the differentiation of Thy-1+ cells induced by activation signals related to retroviral infection. DE Animal Antigens, CD3/ANALYSIS Antigens, Surface/ANALYSIS Carrier Proteins/ANALYSIS Leukocyte Count Lymph Nodes/IMMUNOLOGY Male Membrane Glycoproteins/ANALYSIS Mice Mice, Inbred C57BL Murine Acquired Immunodeficiency Syndrome/*IMMUNOLOGY Phenotype Receptors, Antigen, T-Cell, alpha-beta/ANALYSIS Receptors, Cell Surface/ANALYSIS Receptors, Lymphocyte Homing/ANALYSIS Spleen/IMMUNOLOGY Support, Non-U.S. Gov't T-Lymphocyte Subsets/*IMMUNOLOGY T4 Lymphocytes/*IMMUNOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).