Ex Parte SMITH - Page 10



              Appeal No. 2002-2209                                                              Page 10                
              Application No. 08/137,168                                                                               

                     A second approach is to mix monospecific antisera, each produced in                               
                     separate animals.  This method maximizes the possible number of                                   
                     available antibody-producing cells and, in theory, should provide a wider                         
                     range of specific antibodies.  However, because these antisera are then                           
                     mixed, a dilution effect is produced, the magnitude of which is dependent                         
                     on the number of monospecific antisera included in the product.  Such                             
                     dilution should, in theory, reduce the effectiveness of such a product, but                       
                     because many venoms are highly cross-reactive (for the reasons given                              
                     above) the dilution effects are again much reduced.  Experiments to                               
                     monitor the ability of both poly-, monospecific and mixed monospecific                            
                     antivenoms to neutralize the phospholipase activity of crotalid venoms                            
                     have shown that, as anticipated, monospecific products often offer the                            
                     best protection, while mixed monospecific antivenoms are in general                               
                     better than polyspecific antivenoms (Fig. 6.2).                                                   
              Id., page 124.  Figure 6.2 of Theakston appears to be a duplicate of Figure 2 of this                    
              application.  In other words, the conclusion reached by Theakston in this portion of the                 
              document appears to be based upon the same data present in this application that is                      
              graphically depicted in Figure 2.  This is not surprising since, as noted above, present                 
              appellant D.C. Smith is a co-author of the Theakston article.                                            
                     These portions of Theakston are of interest since they state in a positive manner                 
              that “a second approach is to mix monospecific antisera.”  This is all that claim 37 on                  
              appeal requires.  Turning to Christensen, the source document relied upon for this prior                 
              art knowledge, we find that Christensen acknowledges that “[s]ome laboratories prepare                   
              polyvalent sera by blending several monovalent sera.“ While Christensen does state                       
              that “others, including ourselves, prefer to immunize the horses with all the antigens,”                 
              the fact remains that Christensen acknowledges that as of 1966 it was not novel to                       
              blend “several monovalent sera.”  Again, this is all that claim 37 on appeal                             









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