Ex Parte VERMA et al - Page 2


                 Appeal No.  2000-1930                                                       Page 2                   
                 Application No.  08/232,452                                                                          

                        29.    Transduced primary fibroblasts contained in a collagen matrix                          
                               suitable for implantation into the loose connective tissue of the                      
                               dermis of a subject, wherein said transduced fibroblasts are                           
                               infected with a recombinant retroviral vector that contains                            
                               exogenous genetic material encoding a gene product, wherein said                       
                               transduced fibroblasts express said gene product, and wherein                          
                               expression of said gene product is under the control of a                              
                               constitutive promoter.                                                                 
                        30. A method for immunizing a subject against immunogenic,                                    
                               exogenous material, said method comprising:                                            
                                      implanting in the loose connective tissue of the dermis of a                    
                               subject, an extracellular collagen matrix containing transduced                        
                               subject-derived primary fibroblasts, wherein said transduced                           
                               fibroblasts are infected with a recombinant retroviral vector                          
                               containing exogenous genetic material encoding an immunogenic                          
                               gene product, and wherein said transduced fibroblasts express                          
                               said gene product.                                                                     

                        The examiner relies upon the following references:                                            
                 Bell et al. (Bell), ”The reconstitution of living skin,” The Journal of Investigative                
                 Dermatology, Vol. 81, No. 1, pp. 2s-10s (1983)                                                       
                 Miller et al. (Miller), ”Transfer of genes into human somatic cells using retrovirus                 
                 vectors,” Cold Spring Harbor Symposia on Quantitative Biology, Vol. LI,                              
                 pp.1013-1019 (1986)                                                                                  
                 Garver Jr., et al. (Garver I), ”Production of glycosylated physiologically ‘normal’                  
                 human α1-antitrypsin by mouse fibroblasts modified by insertion of a human                           
                 α1-antitrypsin cDNA using a retroviral vector,” Proc. Natl. Acad. Sci. USA, Vol.                     
                 84, pp.1050-1054 (1987)                                                                              
                 Palmer et al. (Palmer), ”Efficient retrovirus-mediated transfer and expression of a                  
                 human adenosine deaminase gene in diploid skin fibroblasts from an adenosine                         
                 deaminase-deficient human,” Proc. Natl. Acad. Sci. USA, Vol. 84, pp. 1055-1059                       
                 (1987)                                                                                               
                 Selden et al. (Selden), ”Implantation of genetically engineered fibroblasts into                     
                 mice:  Implications for gene therapy,” Science, Vol. 236, pp. 714-718 (1987)                         








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