Ex Parte Short - Page 11



          Interference No. 105,188                                                    
          Short v. Punnonnen                                                          
          the encoded protein on an immune response as compared to the                
          response prior to alteration.  The procedures described in the              
          Freeman PCT for obtaining new polynucleotides comprise the steps            
          of: a) creating a library comprising recombinant polynucleotides,           
   5      and b) screening the library to identify polynucleotides which              
          encode B7-1 and/or B7-2 variants having altered modulatory                  
          effects on an immune response, whether the effects are enhanced             
          immune responses or inhibited immune responses to a vaccine                 
          vector.  For a description of construction of a cDNA library,               
  10      see the Freeman PCT at page 18, l. 27, to page 19, l. 20 (II.               
          Isolation of mRNA and Construction of cDNA Library); page 70,               
          l. 11, to page 72, l. 4 (Example 4: Cloning, Sequencing and                 
          Expression of the B7-2 Antigen, A. Construction of cDNA Library);           
          and page 78, l. 17, page 80, l. 6 (Example 6, Cloning and                   
  15      Sequencing of the Murine B7-2 Antigen, A. Construction of cDNA              
          Library).  On consideration of more detailed instructions in the            
          Freeman PCT, we also find that the inventive procedures described           
          therein include recursive screenings for DNA encoding altered,              
          active B7-2 antigens (Exh. 2040, III. Transfection of Host Cells            
  20      and Screening for Novel B Lymphocyte Activation Antigens, p. 19,            
          l. 23, to p. 20, l. 6; emphasis added):                                     
                    The thus prepared cDNA library is then used to clone              
               the gene of interest by expression cloning techniques.                 
               . . . .                                                                
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