STICE et al. V. STICE et al. V. STRELCHENKO et al. V. HENSEN et al. - Page 14





                F 79. Stice 577 notes that it is the use of differentiated donor cells which distinguishes the Stice                                      
                         577 invention from the prior art:                                                                                                
                                          Prior art methods have used embryonic cell types in cloning                                                     
                                 procedures. This includes work by Campbell et al (Nature, 380:64-68,1996)                                                
                                 and Stice et a] (Biol. Reprod., 54:100-110, 1996). In both of those studies,                                             
                                 embryonic cell lines were derived from embryos of less than 10 days of                                                   
                                 gestation. In both studies, the cells were maintained on a feeder layer to                                               
                                 prevent overt differentiation of the donor cell to be used in the cloning                                                
                                 procedure. The present invention uses differentiated cells.                                                              
                                          It was unexpected that cloned embryos with differentiated donor                                                 
                                 nuclei could develop to advanced embryonic and fetal stages. The scientific                                              
                                 doy-ma has been that only embryonic or undifferentiated cell Wes could                                                   
                                 direct this Me of development. It was unexpected that a large number of                                                  
                                 cloned embryos could be produced from these differentiated cell Wes. Also,                                               
                                 the fact that new transgenic embryonic cell lines could be readily derived                                               
                                 from transgenic cloned embryos was unexpected.                                                                           
                         Stice 577, col. 6,11. 12-30 (emphasis added).                                                                                    
                F 80. Stice 577 emphasizes that in the Stice cloning process differentiated cells are inserted into                                       
                         the oocyte:                                                                                                                      
                                 It is a more specific object of the invention to provide a novel method for                                              
                                 cloning mammalian cells which involves transplantation of the nucleus of a                                               
                                 differentiated mammalian cell into an enucleated oocyte of the same species.                                             
                         Strelchenko Ex. 2001, col. 3,1. 66 - col. 4,1. 2.                                                                                
                F 81. As used in the Stice 577 specification, "somatic cells" are differentiated cells.                                                   
                F 82. The Stice 577 patent does not describe reprogramming donor cells to make them totipotent                                            
                         before insertion into the enucleated oocyte.                                                                                     
                F 83. Stice 577 describes a method in which differentiated cells are used as the donor material                                           
                         without reprogramming.                                                                                                           

                ANALYSIS                                                                                                                                  
                         The University of Massachusetts has filed a motion forjudgment under 37 CFR § 1.633(a)                                           
                asserting that Strelchenko's involved claims are barred by 35 U.S.C. § 135(b)(1). Strelchenko                                             
                opposes. In opposing the motion, Strelchenko has not argued that Strelchenko's involved claims are                                        
                not directed to the same or substantially the same subj ect matter as the claims of the Stice 5 77 patent.                                
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