Ex Parte ROLLINS et al - Page 14


                   Appeal No. 2001-0869                                                                 Page 14                       
                   Application No. 08/453,347                                                                                         

                         •  Cells expressing JE/MCP-1 were created by transforming cells with                                         
                           a vector comprising murine or human JE cDNA.  No detectable                                                
                           JE/MCP-1 was produced in cells transformed with the expression                                             
                           vector alone, but “[c]onsiderable JE/MCP-1 protein was secreted by                                         
                           cell lines transfected with murine JE cDNA in the sense orientation                                        
                           . . . and human JE cDNA.”  Col. 3, line 52, to col. 4,line 17.                                             
                         •  “Transfected Chinese Hamster Ovary cell lines” containing “JE                                             
                           cDNA” did not form tumors when injected into animals.  See Table                                           
                           1 (col. 4, line 55, to col. 5, line 13).                                                                   
                         •  Co-injection of JE/MCP-1-expressing cells together with                                                   
                           untransformed, tumor-forming cells resulted in suppression of                                              
                           tumor formation; the JE/MCP-1-expressing cells (cell lines 10A-10,                                         
                           hJEC-10, and hJEC-100) were transfected with murine or human                                               
                           JE/MCP-1 cDNA.  Col. 5, lines 33-59 and Table 1.                                                           
                                                                                                                                     
                         •  For treatment of cancer, JE/MCP-1 protein can be administered                                             
                           directly (col. 6, line 67, to col. 8, line 3), or “[a]lternatively, tumor                                  
                           killing cells, such as tumor infiltrating lymphocytes (TIL cells) could                                    
                           be genetically engineered to express the JE/MCP-1 protein.  Tumor                                          
                           killing cells engineered in this way can provide synergistic local                                         
                           tumor cell killing.  The tumor killing cells could be engineered in                                        
                           vitro and administered to the vertebrate or the tumor killing cells                                        
                           could be engineered in vivo into the vertebrate’s own supply of                                            
                           tumor killing cells using methods which are known in the art.”  Col.                                       
                           8, lines 4-12.                                                                                             
                           Thus, the only JE/MCP-1-expressing cells described in the ‘078 patent are                                  
                   cells that have been genetically engineered to express JE/MCP-1.  When read in                                     
                   light of the ‘078 patent’s specification, the patent’s claims 5 and 6 must be                                      
                   interpreted to be directed to a method of suppressing tumor formation by                                           
                   administering tumor killing cells that have been genetically engineered to express                                 
                   JE/MCP-1.  Thus, instant claims 1 and 2 are directed to the same method as                                         
                   defined by the patent’s claims, properly construed, and they are not patentably                                    
                   distinguished from the claims that Appellants lost in the ‘998 interference.                                       







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