US2021283169A1PendingUtilityA1

Beta-glucan methods and compositions that affect the tumor microenvironment

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Assignee: HIBERCELL INCPriority: Nov 6, 2014Filed: Mar 29, 2021Published: Sep 16, 2021
Est. expiryNov 6, 2034(~8.3 yrs left)· nominal 20-yr term from priority
C12N 5/0645C12N 5/0639C12N 5/0636C07K 16/2818C07K 2317/24C12N 2501/24C07K 16/3038C07K 16/3061A61P 35/00C07K 2317/76A61K 39/3955C07K 16/2863C12N 2501/2304C07K 16/3053A61K 2039/505C07K 16/3015C12N 2501/052C07K 16/2827C12N 2501/51C12N 2502/1114C12N 2500/34C12N 2501/22C07K 16/3046C07K 16/303A61K 31/716C07K 16/3023
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Claims

Abstract

This disclosure relates to the combination of soluble β-glucan and immune suppression-relieving agents that affect the tumor microenvironment. Soluble β-glucan promotes an immunostimulatory environment, which allows enhanced effectiveness of anti-angiogenics, checkpoint inhibitors including non-tumor targeting antibodies.

Claims

exact text as granted — not AI-modified
1 . A method of treating a subject having cancer, the method comprising administering soluble β-glucan and nivolumab or pembrolizumab. 
     
     
         2 . The method according to  claim 1 , wherein the cancer is melanoma, renal cell carcinoma, or lung cancer. 
     
     
         3 . The method according to  claim 1 , wherein the cancer is selected from the group consisting of breast cancer, pancreatic cancer, colon cancer, and B cell lymphoma. 
     
     
         4 . The method according to  claim 1 , wherein the soluble β-glucan and nivolumab or pembrolizumab are in a single formulation. 
     
     
         5 . The method according to  claim 1 , wherein the soluble β-glucan and nivolumab or pembrolizumab are in separate formulations. 
     
     
         6 . The method according to  claim 1 , wherein the soluble β-glucan is derived from yeast. 
     
     
         7 . The method according to  claim 6 , wherein the yeast is  Saccharomyces cerevisiae.    
     
     
         8 . The method according to  claim 1 , wherein the soluble β-glucan stimulates the subject's immune system. 
     
     
         9 . (canceled) 
     
     
         10 . (canceled) 
     
     
         11 . (canceled) 
     
     
         12 . (canceled) 
     
     
         13 . (canceled) 
     
     
         14 . The method according to  claim 1 , wherein the method further comprises administration of a tumor targeting antibody. 
     
     
         15 . The method according to  claim 1 , wherein the method does not include IL-2 administration. 
     
     
         16 . A method of stimulating a subject's immune system against cancer cells, the method comprising administering soluble β-glucan and nivolumab or pembrolizumab. 
     
     
         17 . The method according to  claim 16 , wherein the immune stimulation comprises activation of M1 macrophages, N1 neutrophils, NK cells, T cells, B cells or dendritic cells. 
     
     
         18 . The method according to  claim 16 , wherein the immune stimulation comprises activation of interleukin-12, interferon-γ, tumor-necrosis factor α, or a combination thereof. 
     
     
         19 . A method of removing immune suppression in a tumor microenvironment, the method comprising administering soluble β-glucan and nivolumab or pembrolizumab. 
     
     
         20 . The method according to  claim 19 , wherein the method comprises suppression of M2 macrophages, N2 neutrophils, myeloid-derived suppressor cells, or a combination thereof.

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