Rapid culture and quantitation of human immunodeficiency virus type 1 from patient cells without the use of mitogen-stimulated donor cells.

We cultured HIV-infected CD4 ⴙ T cells alone or with FDCs and measured subsequent virus expression using HIV-p24 production and reverse transcription- PCR analyses.. When cultured

This study shows that a therapeutic immunization strategy employing intradermal administration of MVA.HIVA to chronically HIV-1-infected individuals under HAART sup- pression is able

To determine if caffeine has any effect on HIV-1 transduc- tion of nondividing cells, we infected exponentially dividing and nocodazole-arrested 293T cells with an HIV-1-based vec-

Some murine monoclonal antibodies (MAbs) to Tat protein block exogenous Tat-medi- ated transactivation (31) or attenuate primary HIV-1 infection and replication in chronically

Changes in plasma viral load, CD4 ⫹ cell count, ARV drug resistance, and HIV-1 V3 loop population-based genotypes of four chronically HIV-1-infected patients with therapeutic

In the in vitro rapid-turnover assay system, infection of Jurkat cells (activated CD4 ⫹ T cells) by Rap5 virus and the subsequent death of the infected cells either by

The amount of virus binding to fixed Raji cells was similar to the amount of binding to untreated Raji cells (data not shown), and the levels of HIV replication during coculture

Because OM10 cells remain CD4 positive despite being chronically infected with HIV-1 (5), we next determined if the genistein-induced increase in HIV-1 replication was due