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
BACKGROUND: Despite the remarkable success of highly active antiretroviral therapy (HAART) in loweri...
While current antiretroviral therapy has significantly improved, challenges still remain in life-lon...
International audienceDespite being at the origin of one of the world's most devastating public heal...
AbstractWe have recently developed an HIV-1 packaging cell line, Ψ422, as an improved tool for anti-...
AbstractPackaging cell lines derived from human immunodeficiency virus-1 (HIV-1) are promising tools...
AbstractWe compared the efficiency of human immunodeficiency virus (HIV-1) vectors that express a ma...
AbstractLentiviral vectors based on human immunodeficiency virus type 1 (HIV-1) possess the ability ...
Today, lentiviral vectors are favorable vectors for RNA interference delivery in anti-HIV therapeuti...
Genetic modification of T lymphocytes holds great potential for treatments of cancer, T cell disorde...
Background: Murine leukemia virus (MLV) vector particles can be pseudotyped with a truncated variant...
AbstractWe have constructed a series of retroviral vectors in which the expression of antisense RNA ...
AbstractHIV-regulated expression of the diphtheria toxin A fragment gene (HIV-DT-A) is a potential g...
HIV currently infects 35 million people worldwide and antiretroviral treatments are expensive, lifel...
AbstractUsing retroviral supernatants derived from the amphotropic murine packaging cell line PA317 ...
A Hut-78 cell clone (F12) harboring a nonproducer human immunodeficiency virus (HIV-1) variant shows...
BACKGROUND: Despite the remarkable success of highly active antiretroviral therapy (HAART) in loweri...
While current antiretroviral therapy has significantly improved, challenges still remain in life-lon...
International audienceDespite being at the origin of one of the world's most devastating public heal...
AbstractWe have recently developed an HIV-1 packaging cell line, Ψ422, as an improved tool for anti-...
AbstractPackaging cell lines derived from human immunodeficiency virus-1 (HIV-1) are promising tools...
AbstractWe compared the efficiency of human immunodeficiency virus (HIV-1) vectors that express a ma...
AbstractLentiviral vectors based on human immunodeficiency virus type 1 (HIV-1) possess the ability ...
Today, lentiviral vectors are favorable vectors for RNA interference delivery in anti-HIV therapeuti...
Genetic modification of T lymphocytes holds great potential for treatments of cancer, T cell disorde...
Background: Murine leukemia virus (MLV) vector particles can be pseudotyped with a truncated variant...
AbstractWe have constructed a series of retroviral vectors in which the expression of antisense RNA ...
AbstractHIV-regulated expression of the diphtheria toxin A fragment gene (HIV-DT-A) is a potential g...
HIV currently infects 35 million people worldwide and antiretroviral treatments are expensive, lifel...
AbstractUsing retroviral supernatants derived from the amphotropic murine packaging cell line PA317 ...
A Hut-78 cell clone (F12) harboring a nonproducer human immunodeficiency virus (HIV-1) variant shows...
BACKGROUND: Despite the remarkable success of highly active antiretroviral therapy (HAART) in loweri...
While current antiretroviral therapy has significantly improved, challenges still remain in life-lon...
International audienceDespite being at the origin of one of the world's most devastating public heal...