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Virology ; 406(2): 302-11, 2010 Oct 25.
Article in English | MEDLINE | ID: mdl-20708209

ABSTRACT

HIV-1 infection studies of primary CD8(+) T-cells are hampered by difficulty in obtaining a significant number of targets for infection and low levels of productive infection. Further, there exists a paucity of CD8-expressing T-cell lines to address questions pertaining to the study of CD8(+) T-cells in the context of HIV-1 infection. In this study, a set of CD8(+) T-cell clones were originated through HTLV-I transformation in vitro, and the properties of these cells were examined. The clones were susceptible to T-cell tropic strains of the virus and exhibited HIV-1 production 20-fold greater than primary CD4(+) T-cells. Productive infection resulted in a decrease in expression of CD8 and CXCR4 molecules on the surface of the CD8(+) T-cell clones and antibodies to these molecules abrogated viral binding and replication. These transformed cells provide an important tool in the study of CD8(+) T-cells and may provide important insights into the mechanism(s) behind HIV-1 induced CD8(+) T-cell dysfunction.


Subject(s)
CD8-Positive T-Lymphocytes/virology , Cell Transformation, Viral , HIV Infections/immunology , HIV-1/immunology , Human T-lymphotropic virus 1/physiology , CD8 Antigens/genetics , CD8 Antigens/metabolism , CD8-Positive T-Lymphocytes/immunology , Cells, Cultured , HIV Infections/genetics , HIV Infections/virology , Humans , Receptors, CXCR4/genetics , Receptors, CXCR4/immunology
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