AbstractWe describe a recombinant vesicular stomatitis virus lacking its glycoprotein gene and expressing instead the HIV-1 receptor CD4 and a coreceptor, CXCR4. This virus was unable to infect normal cells but did infect, propagate on, and kill cells that were first infected with HIV-1 and therefore had the HIV membrane fusion protein on their surface. Killing of HIV-1-infected cells controlled HIV infection in a T cell line and reduced titers of infectious HIV-1 in the culture by as much as 104-fold. Such a targeted virus could have therapeutic value in reducing HIV viral load. Our results also demonstrate a general strategy of targeting one virus to the envelope protein of another virus to control infection
The bacterial defense system CRISPR (clustered regularly interspaced short palindromic repeats) has ...
Human T-cell leukemia virus type 1 (HTLV-1) causes serious and intractable diseases in some carriers...
AbstractWe have recently developed an HIV-1 packaging cell line, Ψ422, as an improved tool for anti-...
HIV entry into target cells requires the interaction of the HIV envelope glycoprotein (Env) with a p...
<p><b>A.</b> HIV-1 Csy4 targeting vectors. HIV-1: HIV-1 gene structure; HIV-RGH: the HIV-1 reporter ...
AbstractWe have constructed VSV recombinants lacking the viral glycoprotein gene and instead express...
Abstract Background Efficient targeted gene transfer and cell type specific transgene expression are...
CXC-chemokine receptor (CXCR4) is one principle coreceptor for the entry of T cell line (T)tropic HI...
Traditional vaccine methods have long been employed to control widespread infectious diseases, but s...
For HIV to enter cells, the viral surface protein Envelope (Env) must sequentially bind the host pro...
The vif gene of human immunodeficiency virus type 1 (HIV-1) encodes a basic Mr 23,000 protein that i...
Traditional vaccine methods have long been employed to control widespread infectious diseases, but s...
AbstractHuman immunodeficiency virus (HIV) drugs designed to interfere with obligatory utilization o...
Recombinant viral vectors are useful tools for AIDS vaccine development. However, expression of HIV-...
Human immunodeficiency virus type 1 (HIV-1)-based viral vector is widely used as a biomaterial to tr...
The bacterial defense system CRISPR (clustered regularly interspaced short palindromic repeats) has ...
Human T-cell leukemia virus type 1 (HTLV-1) causes serious and intractable diseases in some carriers...
AbstractWe have recently developed an HIV-1 packaging cell line, Ψ422, as an improved tool for anti-...
HIV entry into target cells requires the interaction of the HIV envelope glycoprotein (Env) with a p...
<p><b>A.</b> HIV-1 Csy4 targeting vectors. HIV-1: HIV-1 gene structure; HIV-RGH: the HIV-1 reporter ...
AbstractWe have constructed VSV recombinants lacking the viral glycoprotein gene and instead express...
Abstract Background Efficient targeted gene transfer and cell type specific transgene expression are...
CXC-chemokine receptor (CXCR4) is one principle coreceptor for the entry of T cell line (T)tropic HI...
Traditional vaccine methods have long been employed to control widespread infectious diseases, but s...
For HIV to enter cells, the viral surface protein Envelope (Env) must sequentially bind the host pro...
The vif gene of human immunodeficiency virus type 1 (HIV-1) encodes a basic Mr 23,000 protein that i...
Traditional vaccine methods have long been employed to control widespread infectious diseases, but s...
AbstractHuman immunodeficiency virus (HIV) drugs designed to interfere with obligatory utilization o...
Recombinant viral vectors are useful tools for AIDS vaccine development. However, expression of HIV-...
Human immunodeficiency virus type 1 (HIV-1)-based viral vector is widely used as a biomaterial to tr...
The bacterial defense system CRISPR (clustered regularly interspaced short palindromic repeats) has ...
Human T-cell leukemia virus type 1 (HTLV-1) causes serious and intractable diseases in some carriers...
AbstractWe have recently developed an HIV-1 packaging cell line, Ψ422, as an improved tool for anti-...