US2019233515A1PendingUtilityA1

Methods for Manipulating Phagocytosis Mediated by CD47

Assignee: UNIV LELAND STANFORD JUNIORPriority: Jan 15, 2008Filed: Mar 22, 2019Published: Aug 1, 2019
Est. expiryJan 15, 2028(~1.5 yrs left)· nominal 20-yr term from priority
A61P 35/02A61P 35/00A61P 43/00A61P 25/00A61P 13/10A61P 15/00G01N 33/57505C07K 16/3069A61K 47/6863C07K 16/2803A61K 47/6869A61K 47/6861A61K 2039/505A61K 47/6865A61K 47/6867C07K 16/3053C07K 16/3038C07K 2317/73A61K 47/6851A61K 2039/507C07K 16/3046A61K 39/39558C07K 2317/76C07K 16/30C07K 16/2896C07K 16/18C07K 16/3061C07K 2317/31G01N 2500/04C12N 5/0694C12N 5/0093C07K 2317/24C12Q 2600/136C07K 16/28C07K 2317/75C12Q 1/6886G01N 33/5011C12Q 2600/112
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Claims

Abstract

Methods are provided to manipulate phagocytosis of cells, including hematopoietic cells, e.g. circulating hematopoietic cells, bone marrow cells, acute leukemia cells, etc.; and solid tumor cells. In some embodiments of the invention the circulating cells are hematopoietic stem cells, or hematopoietic progenitor cells, particularly in a transplantation context, where protection from phagocytosis is desirable. In other embodiments the circulating cells are leukemia cells, particularly acute myeloid leukemia (AML), where increased phagocytosis is desirable.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of treating a human subject for myelodysplastic syndrome (MDS), the method comprising:
 administering to a human subject in need thereof an antibody that disrupts the binding of CD47 with SIRPα, at a dose that achieves a depletion in MDS tumor cells by increasing phagocytosis of MDS tumor cells.   
     
     
         2 . The method of  claim 1 , wherein the antibody that disrupts the binding of CD47 with SIRPα specifically binds to CD47. 
     
     
         3 . The method of  claim 1 , wherein the antibody is a humanized or chimeric monoclonal antibody. 
     
     
         4 . The method of  claim 1 , wherein the MDS is a preleukemia.

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