Ex Parte Short - Page 7



          Interference No. 105,188                                                    
          Short v. Punnonnen                                                          
               natural ligands (e.g., CTLA4 and CD28) include a soluble               
               peptide having B7-2 binding activity but lacking the ability           
               to costimulate immune cells, antibodies that block the                 
               binding of B7-2 to its ligands and fail to deliver a co-               
   5           stimulatory signal (so called “blocking antibodies”, such as           
               blocking anti-B7-2 antibodies), B7-2-Ig fusion proteins,               
               which can be produced in accordance with the teachings of              
               the present invention, as well as soluble forms of B7-2                
               receptors, such as CTLA4Ig or CD28Ig. . . . .                          
  10                                                                                  
                    Another aspect of the invention features methods for              
               upregulating immune responses by delivery of a costimulatory           
               signal to T cells through use of a stimulatory form of B7-2            
               antigen, which include soluble, multivalent forms of B7-2              
  15           protein, such as a peptide having B7-2 activity and B7-2               
               fusion proteins.  Delivery of a stimulatory form of B7-2 in            
               conjunction with antigen may be useful prophylactically to             
               enhance the efficiency of vaccination against a variety of             
               pathogens and may also be useful therapeutically to                    
  20           upregulate an immune response against a particular pathogen            
               during an infection or against a tumor in a tumor-bearing              
               host.                                                                  
               In the Detailed Description of the Invention, the Freeman              
  25      PCT teaches:                                                                
               Costimulatory molecules within the scope of the invention              
               are referred herein as CTLA4/CD28 ligands (counter-                    
               receptors) or B lymphocyte antigens.  Novel B lymphocyte               
               antigens which provide costimulation to activated T cells              
  30           to thereby induce T cell proliferation and/or cytokine                 
               secretion include the B7-2 (human and murine) and the B7-3             
               antigens described and characterized herein.                           
          (Exh. 2040, p. 10, ll. 6-10);                                               
  35           [O]ne aspect of this invention pertains to isolated nucleic            
               acids comprising a nucleotide sequence encoding a novel                
               costimulatory molecule, such as the B lymphocyte antigen               
               B7-2, fragments of such nucleic acids, or equivalents                  
               thereof. . . . The term equivalent is intended to include              
  40           nucleotide sequences encoding functionally equivalent B                
               lymphocyte antigens or functionally equivalent peptides                
               having an activity of a novel B lymphocyte antigen, i.e.,              
                                         -7-                                          




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