US2006121046A1PendingUtilityA1

Compositions and methods for WT1 specific immunotherapy

Assignee: UNIV WASHINGTONPriority: Sep 30, 1998Filed: Jan 25, 2006Published: Jun 8, 2006
Est. expirySep 30, 2018(expired)· nominal 20-yr term from priority
A61K 38/1709C07K 14/4748A61K 2039/572A61K 2039/55522A61K 2039/5152A61K 39/0011
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Claims

Abstract

Compositions and methods for the therapy of malignant diseases, such as leukemia and cancer, are disclosed. The compositions comprise one or more of a WT1 polynucleotide, a WT1 polypeptide, an antigen-presenting cell presenting a WT1 polypeptide, an antibody that specifically binds to a WT1 polypeptide; or a T cell that specifically reacts with a WT1 polypeptide. Such compositions may be used, for example, for the prevention and treatment of metastatic diseases.

Claims

exact text as granted — not AI-modified
1 . A composition comprising a polypeptide consisting of SEQ ID NO:2 and non-specific immune response enhancer.  
     
     
         2 . A composition according to  claim 1 , wherein the non-specific immune response enhancer is an adjuvant.  
     
     
         3 . A composition comprising: 
 (a) a polypeptide consisting of SEQ ID NO:2; and    (b) a non-specific immune response enhancer that preferentially enhances a T cell response in a mammal.    
     
     
         4 . A composition according to  claim 3 , wherein the non-specific immune response enhancer is selected from the group consisting of Montanide ISA50, Seppic Montanide ISA 720, a cytokine, a microsphere, dimethyl dioctadecyl ammoniumbromide (DDA) based adjuvants, AS-1, AS-2, Ribi Adjuvant system based adjuvant, QS21, saponin based adjuvants, Syntex adjuvant in its microfluidized form, MV, ddMV, immune stimulating complex (iscom) based adjuvants, and inactivated toxins.  
     
     
         5 . The composition of  claim 4 , wherein said cytokine is selected from the group consisting of GM-CSF and Flt3-ligand.

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