Ex Parte 5854038 et al - Page 7

                   Appeal No. 2006-0735                                                                                             
                   Reexamination Control No. 90/006,036                                                                             

                           The complete paper that was presented at the 1991 meeting is not relied upon by                          
                   the examiner in making the rejection and does not appear to be before us.1                                       
                   25.  The copy of the one page abstract on the record before us is not dated, however,                            
                       there appears to be no dispute that the publication date of the article is such that it                      
                       qualifies as prior art under 35 U.S.C. § 102(b).                                                             
                   26.  The entirety of the Dropulic abstract is set out below:                                                     
                           Ribozymes are catalytic RNA molecules that display specific cleavage reactions                           
                           to complementary RNAs.  They are potentially useful as therapeutic agents                                
                           against HIV.  We have designed ribozymes targeted to various regions of the                              
                           HIV-1 genomic RNA.  When T-cells that are chronically infected with HIV-1 are                            
                           co-cultured with cloned packaging cells producing amphotropic ribozyme-                                  
                           containing retrovirus, a suppression of HIV-1 replication is seen.  We have also                         
                           generated two types of ribozymes that have been integrated into the HIV genome                           
                           at the nef gene.   These two types of ribozymes are a cis self cleaving RNA                              
                           sequence and a RNA sequence that is capable of cleaving in trans the HIV-1 U5                            
                           RNA.  In both cases, replication of the ribozyme-containing HIV-1 was                                    
                           dramatically reduced.  These results suggest that catalytic RNAs can be designed                         
                           to specifically destroy HIV-1 RNA.                                                                       
                   27.  The examiner notes that Dropulic reference teaches the incorporation of a nucleic                           
                       acid therapeutic agent (i.e., a ribozyme) into the nef coding region of the HIV-1                            
                       genome.  (Answer at 4).                                                                                      
                   28.  The examiner argues that “[t]he HIV-1 genome inherently contains an RNA                                     
                       packaging/encapsidation signal (ψ) that localizes the viral genome to the inner surface                      
                       of the cytoplasmic cell membrane prior to encapsidation into the virion..”  (Answer at                       
                       4).                                                                                                          

                                                                                                                                    
                   1  Patentee has submitted a paper that it says “disclose[s] the details of the Dropulic                          
                   abstract”, i.e., Dropulic et al., Journal of Virology, 66:1432 (1992). but has provided no                       
                   evidence that this is the paper presented at the 1991 meeting. (Brief at 15).  In any event,                     
                   the examiner has not rejected the claims over the complete paper-only over an abstract of                        
                   the paper presented at the meeting.                                                                              

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