US2006177934A1PendingUtilityA1

Lentiviral LTR-deleted vector

Assignee: OXFORD BIOMEDICA LTDPriority: Oct 29, 1996Filed: Mar 3, 2006Published: Aug 10, 2006
Est. expiryOct 29, 2016(expired)· nominal 20-yr term from priority
C12N 15/62C07K 2319/00C12N 2799/027C12N 9/88C12N 2830/00C12N 2830/50C12N 9/0071C12N 2830/15C12N 2830/48C12N 15/86C12N 2740/16043A61K 48/00C12N 2740/15043C12N 2830/60
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Claims

Abstract

A vector capable of transducing non-dividing and/or slowly dividing cells is provided, wherein the vector is a lentiviral LTR-deleted vector. Also provided is a method for producing a protein of interest in a non-dividing or slowly dividing cell by transducing the cell with a lentiviral LTR-deleted vector and expressing the protein of interest in the cell. In addition, target cells containing the lentiviral LIR-deleted vector are provided.

Claims

exact text as granted — not AI-modified
1 . A lentiviral vector capable of transducing a non-dividing or slowly-dividing cell, said vector comprising a lentiviral LTR-deleted vector.  
     
     
         2 . The vector according to  claim 1 , further comprising a nucleotide sequence encoding a protein of interest.  
     
     
         3 . A method for producing a protein of interest in a non-dividing or slowly-dividing cell, comprising the steps of: 
 a) transducing the cell with the vector according to  claim 2;  and    b) expressing the protein of interest in the cell.    
     
     
         4 . The method according to  claim 3 , wherein the non-dividing cell is a neuron.  
     
     
         5 . A target cell in vitro comprising the vector of  claim 1 .  
     
     
         6 . A target cell in vitro comprising the vector of  claim 2 .  
     
     
         7 . A method of performing gene delivery on a target cell comprising the steps of: 
 a) transducing the target cell with the vector according to  claim 2;  and    b) delivering the nucleotide sequence to the target cell.

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