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J Virol ; 84(17): 8980-5, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20554781

ABSTRACT

A synthetic feline TRIM5-cyclophilin A fusion protein (feTRIMCyp) was generated and transduced into feline cells. feTRIMCyp was highly efficient at preventing infection with human (HIV) and feline (FIV) immunodeficiency virus pseudotypes, and feTRIMCyp-expressing cells resisted productive infection with either FIV-Fca or FIV-Pco. The restriction of FIV infection by feTRIMCyp was reversed by the cyclosporine (Cs) derivatives NIM811 and Debio-025 but less so by Cs itself. FeTRIMCyp and FIV infections of the cat offer a unique opportunity to evaluate TRIMCyp-based approaches to genetic therapy for HIV infection and the treatment of AIDS.


Subject(s)
Carrier Proteins/metabolism , Cyclophilin A/metabolism , Feline Acquired Immunodeficiency Syndrome/virology , HIV Infections/virology , HIV-1/physiology , Immunodeficiency Virus, Feline/physiology , Virus Internalization , Animals , Antiviral Restriction Factors , Carrier Proteins/chemical synthesis , Carrier Proteins/genetics , Cats , Cell Line , Cyclophilin A/chemical synthesis , Cyclophilin A/genetics , Disease Models, Animal , Feline Acquired Immunodeficiency Syndrome/prevention & control , HIV Infections/prevention & control , Humans , Recombinant Fusion Proteins/chemical synthesis , Recombinant Fusion Proteins/genetics , Recombinant Fusion Proteins/metabolism , Tripartite Motif Proteins , Ubiquitin-Protein Ligases
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