Dexamethasone Inhibits CD4 T Cell Deletion Mediated by Macrophages from Human Immunodeficiency Virus–Infected Persons
Author(s) -
Thorsten Orlikowsky,
Zongmin Wang,
Anita Dudhane,
Günther Dannecker,
D. Niethammer,
Gary P. Wormser,
Michael K. Hoffmann,
Harold W. Horowitz
Publication year - 2001
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/323997
Subject(s) - peripheral blood mononuclear cell , dexamethasone , apoptosis , immune system , antibody , macrophage , immunology , biology , antigen , t cell , virology , monoclonal antibody , in vitro , endocrinology , biochemistry
Prednisolone slows the loss of CD4 T cells in individuals with human immunodeficiency virus (HIV) disease and inhibits antigen-induced apoptosis of recently HIV-infected CD4 cells in vitro. This study investigated whether dexamethasone inhibits the ability of macrophages to delete CD4 T cells via anti-CD4 antibody or immune-complexed HIV envelope protein gp120. Peripheral blood mononuclear cells from HIV-negative persons were incubated with CD4-reactive ch412 monoclonal antibody or with gp120/IgG immune complexes and resident macrophages, with and without dexamethasone. Dexamethasone inhibited CD4 cell deletion in a dose-dependent manner. The deletion of normal CD4 cells by macrophages from HIV-infected patients also was inhibited by dexamethasone. Furthermore, up-regulation of CD95 expression on T cells exposed to anti-CD4 and gp120/IgG, which predisposes T cells to CD95-mediated apoptosis, is inhibited by dexamethasone in a dose-dependent fashion. Dexamethasone inhibits the macrophage-mediated deletion of CD4 lymphocytes in HIV-infected persons.
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