Ex Parte Lamb - Page 11


                 Appeal No. 2005-1511                                                                                  
                 Application No. 09/879,398                                                                            
                        It is well established that the examiner has the initial burden under § 103                    
                 to establish a prima facie case of obviousness.  In re Oetiker, 977 F.2d 1443,                        
                 1445, 24 USPQ2d 1443, 1444 (Fed. Cir. 1992); In re Piasecki, 745 F.2d 1468,                           
                 1471-72, 223 USPQ 785, 787-88 (Fed. Cir. 1984).  To that end, it is the                               
                 examiner’s responsibility to show that some objective teaching or suggestion in                       
                 the applied prior art, or knowledge generally available [in the art] would have led                   
                 one of ordinary skill in the art to combine the references to arrive at the claimed                   
                 invention.  Pro-Mold & Tool Co. v. Great Lakes Plastics, Inc., 75 F.3d 1568,                          
                 1573, 37 USPQ2d 1626, 1629 (Fed. Cir. 1996).  This the examiner has not done.                         
                        Although Falkenburg and Lamb disclose different aspects of the claimed                         
                 method of treating ALL patients, we agree with the appellants that neither these                      
                 nor any of the other cited references teaches or suggests the present invention.                      
                 Lamb discloses administering γδ+ T cells derived from an allogeneic donor to an                       
                 ALL patient, but we do not find any suggestion therein to first prime the donor                       
                 cells with irradiated leukemia cells derived from the patient.  Falkenburg                            
                 discloses irradiating leukemia cells and culturing them with CTL (cytotoxic T                         
                 cells) from a donor, but the reference does not mention the use of γδ+ T cells.                       
                 To the contrary, as pointed out by the appellant, the CTL lines taught by                             
                 Falkenburg “were phenotyped with antibodies to CD2, CD3, CD4, CD8 and                                 
                 CD56 (see page 307), indicating that they were expecting to generate αβ+ T                            
                 cells.”  Brief, p. 12.  Thus, on this record, the only suggestion we find of culturing                
                 an ALL patient’s own leukemia cells which have been irradiated ex vivo with an                        
                 enriched population of a donor γδ+ T cells and to administer said T cells said ALL                    


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