AbstractWe have recently developed an HIV-1 packaging cell line, Ψ422, as an improved tool for anti-HIV gene therapy. After stable transfection with an HIV-1 or HIV-2 vector, Ψ422 has been shown to synthesize virions able to transduce CD4+T cells and macrophages. We now report that HIV vectors per se, in the absence of antiviral genes, inhibit HIV infection of transduced cells. This antiviral effect was shown to be due, at least in part, to a TAR and RRE decoy effect. These data highlight further advantages of HIV-derived gene delivery systems for HIV therapy, in addition to CD4 cell targeting and the ability to transduce nondividing cells
Gene therapy can be an option to overcome the side effects of chemotherapy and prevent the developme...
Retroviral vectors were engineered to express either sense (MoTiN-TRΨe+) or sense and antisense (MoT...
AbstractTargeting the HIV entry and assembly pathways holds promise for development of novel anti-HI...
AbstractWe have recently developed an HIV-1 packaging cell line, Ψ422, as an improved tool for anti-...
International audienceDespite being at the origin of one of the world's most devastating public heal...
Stem cell gene therapy approaches for Human Immunodeficiency Virus (HIV) infection have been explore...
A primary advantage of lentiviral vectors is their ability to pass through the nuclear envelope into...
Abstract Background Efficient targeted gene transfer and cell type specific transgene expression are...
AbstractPackaging cell lines derived from human immunodeficiency virus-1 (HIV-1) are promising tools...
A Hut-78 cell clone (F12) harboring a nonproducer human immunodeficiency virus (HIV-1) variant shows...
While current antiretroviral therapy has significantly improved, challenges still remain in life-lon...
International audienceTargeting viral entry is the most likely gene therapy strategy to succeed in p...
Highly active antiretroviral therapy (HAART) has vastly improved outcomes for patients infected with...
BACKGROUND: RNA-based approaches are promising for long-term gene therapy against HIV-1. They can ta...
BACKGROUND: Despite the remarkable success of highly active antiretroviral therapy (HAART) in loweri...
Gene therapy can be an option to overcome the side effects of chemotherapy and prevent the developme...
Retroviral vectors were engineered to express either sense (MoTiN-TRΨe+) or sense and antisense (MoT...
AbstractTargeting the HIV entry and assembly pathways holds promise for development of novel anti-HI...
AbstractWe have recently developed an HIV-1 packaging cell line, Ψ422, as an improved tool for anti-...
International audienceDespite being at the origin of one of the world's most devastating public heal...
Stem cell gene therapy approaches for Human Immunodeficiency Virus (HIV) infection have been explore...
A primary advantage of lentiviral vectors is their ability to pass through the nuclear envelope into...
Abstract Background Efficient targeted gene transfer and cell type specific transgene expression are...
AbstractPackaging cell lines derived from human immunodeficiency virus-1 (HIV-1) are promising tools...
A Hut-78 cell clone (F12) harboring a nonproducer human immunodeficiency virus (HIV-1) variant shows...
While current antiretroviral therapy has significantly improved, challenges still remain in life-lon...
International audienceTargeting viral entry is the most likely gene therapy strategy to succeed in p...
Highly active antiretroviral therapy (HAART) has vastly improved outcomes for patients infected with...
BACKGROUND: RNA-based approaches are promising for long-term gene therapy against HIV-1. They can ta...
BACKGROUND: Despite the remarkable success of highly active antiretroviral therapy (HAART) in loweri...
Gene therapy can be an option to overcome the side effects of chemotherapy and prevent the developme...
Retroviral vectors were engineered to express either sense (MoTiN-TRΨe+) or sense and antisense (MoT...
AbstractTargeting the HIV entry and assembly pathways holds promise for development of novel anti-HI...