Potent Lentiviral Restriction by a Synthetic Feline TRIM5 Cyclophilin A Fusion

被引:15
作者
Dietrich, Isabelle [1 ]
Macintyre, Angela [1 ]
McMonagle, Elizabeth [1 ]
Price, Amanda J. [2 ]
James, Leo C. [2 ]
McEwan, William A. [2 ]
Hosie, Margaret J. [1 ]
Willett, Brian J. [1 ]
机构
[1] Univ Glasgow, Retrovirus Res Lab, Inst Comparat Med, Fac Vet Med, Glasgow G61 1QH, Lanark, Scotland
[2] MRC Lab Mol Biol, Div Prot & Nucle Acid Chem, Cambridge CB1 0QH, England
基金
英国惠康基金;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; TRIM5-ALPHA RESTRICTION; HIV-1; INFECTION; REVERSE TRANSCRIPTION; RHESUS TRIM5-ALPHA; HUMAN-CELLS; T-CELLS; REPLICATION; CAPSIDS; RECOGNITION;
D O I
10.1128/JVI.00858-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:8980 / 8985
页数:6
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