US2016051675A1PendingUtilityA1

B7-h4 expression on tumor vasculature

Assignee: MAYO FOUNDATIONPriority: Mar 20, 2006Filed: Aug 31, 2015Published: Feb 25, 2016
Est. expiryMar 20, 2026(expired)· nominal 20-yr term from priority
G01N 33/5759G01N 33/5758C12N 2310/11C07K 16/2827A61K 38/39A61K 38/484C12N 2310/14A61K 39/39558A61K 45/06G01N 2333/70532C12N 15/1138C12N 2320/30C07K 2317/76A61K 38/19G01N 33/57492
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Claims

Abstract

Methods of evaluating patients by assessing expression of B7-H4 in the vasculature are described.

Claims

exact text as granted — not AI-modified
1 - 25 . (canceled) 
     
     
         26 . A method of treating a cancer patient, said method comprising:
 (a) identifying a patient as having a tumor that is B7-H4 negative but that exhibits B7-H4 expression in the tumor vasculature; and   (b) delivering to said patient an agent that reduces B7-H4 activity.   
     
     
         27 . The method of  claim 26 , wherein said agent comprises an antibody or a fragment thereof. 
     
     
         28 . The method of  claim 27 , wherein said antibody fragment is selected from the group consisting of an Fab′ fragment, an F(ab′)2 fragment, or a single chain Fv fragment. 
     
     
         29 . The method of  claim 26 , wherein said agent binds to B7-H4. 
     
     
         30 . The method of  claim 26 , wherein said B7-H4 activity is decreased CD4+ and CD8+ T cell proliferation. 
     
     
         31 . The method of  claim 26 , further comprising delivering to said patient one or more immunomodulatory cytokines, growth factors, or anti-angiogenic factors. 
     
     
         32 . The method of  claim 31 , wherein said one or more immunomodulatory cytokines, growth factors, or anti-angiogenic factors are selected from the group consisting of interleukin (IL)-1 to IL-25, interferon-alpha (IFN-α), interferon-beta (IFN-(β), interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), granulocyte macrophage colony stimulating factor (GM-CSF), endostatin, angiostatin, and thrombospondin. 
     
     
         33 . The method of  claim 26 , wherein said patient has a cancer selected from the group consisting of hematological cancer, neurological cancer, melanoma, breast cancer, lung cancer, head and neck cancer, gastrointestinal cancer, liver cancer, pancreatic cancer, renal cancer, genitourinary cancer, bone cancer, and vascular cancer. 
     
     
         34 . The method of  claim 33 , wherein said cancer is a renal cell carcinoma. 
     
     
         35 . The method of  claim 26 , wherein said agent is an antisense oligonucleotide that hybridizes to a B7-H4 transcript. 
     
     
         36 . The method of  claim 26 , wherein said agent is an interference RNA (RNAi). 
     
     
         37 . A method of increasing CD4+ and CD8+ T cell proliferation in a cancer patient, said method comprising:
 (a) identifying a patient as having a tumor that is B7-H4 negative but that exhibits B7-H4 expression in the tumor vasculature; and   (b) delivering to said patient an agent that reduces B7-H4 activity.   
     
     
         38 . The method of  claim 37 , wherein said agent comprises an antibody or a fragment thereof. 
     
     
         39 . The method of  claim 38 , wherein said antibody fragment is selected from the group consisting of an Fab′ fragment, an F(ab′)2 fragment, or a single chain Fv fragment. 
     
     
         40 . The method of  claim 37 , wherein said agent binds to B7-H4. 
     
     
         41 . The method of  claim 37 , further comprising delivering to said patient one or more immunomodulatory cytokines, growth factors, or anti-angiogenic factors. 
     
     
         42 . The method of  claim 41 , wherein said one or more immunomodulatory cytokines, growth factors, or anti-angiogenic factors are selected from the group consisting of IL-1 to IL-25, IFN-α, IFN-β, IFN-γ, TNF-α, GM-CSF, endostatin, angiostatin, and thrombospondin. 
     
     
         43 . The method of  claim 37 , wherein said patient has a cancer selected from the group consisting of hematological cancer, neurological cancer, melanoma, breast cancer, lung cancer, head and neck cancer, gastrointestinal cancer, liver cancer, pancreatic cancer, renal cancer, genitourinary cancer, bone cancer, and vascular cancer. 
     
     
         44 . The method of  claim 43 , wherein said cancer is a renal cell carcinoma. 
     
     
         45 . The method of  claim 37 , wherein said agent is an antisense oligonucleotide that hybridizes to a B7-H4 transcript. 
     
     
         46 . The method of  claim 37 , wherein said agent is an RNAi.

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