
pmid: 11886260
This report describes induction of HIV-1 resistance and synthesis of resistance factors in immortal CD4-positive T lymphocytes. SupT1 cells were infected by NL4-3 attenuated by a defect in the vif gene through coculture with infected primary lymphocytes. Cell lines from this infection, termed R1, expressed CD4 and CXCR4, carried low levels of HIV-1 DNA, but expressed no other detectable viral products and were resistant to infection by wild-type HIV-1. Investigation of challenge infection in resistant R1 lines demonstrated entry, reverse transcription, and integration by incoming HIV-1 but no synthesis of viral RNA. By assay of marker gene expression, we found that Tat was unable to activate LTR-driven transcription in R1 lines. HIV-1-resistant R1 lines secreted soluble factors that inhibited productive infection of primary lymphocytes by several strains of HIV-1 and blocked viral RNA synthesis in newly infected cells. Resistance factors also blocked the induction of HIV-1 transcription in ACH-2 cells as assayed by viral antigen expression and Northern blot of viral RNA. Soluble factors produced by HIV-1-resistant, immortal R1 cells may form the basis of new approaches to control HIV-1 infection.
CD4-Positive T-Lymphocytes, Gene Products, vif, Transcription, Genetic, Virus Integration, Virus Replication, Virus Latency, Virology, DNA, Viral, HIV-1, vif Gene Products, Human Immunodeficiency Virus, Humans, Cell Line, Transformed
CD4-Positive T-Lymphocytes, Gene Products, vif, Transcription, Genetic, Virus Integration, Virus Replication, Virus Latency, Virology, DNA, Viral, HIV-1, vif Gene Products, Human Immunodeficiency Virus, Humans, Cell Line, Transformed
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