US2018154013A1PendingUtilityA1

Aberrant cell-restricted immunoglobulins provided with a toxic moiety

Assignee: APO T B VPriority: Jan 13, 2012Filed: Dec 28, 2017Published: Jun 7, 2018
Est. expiryJan 13, 2032(~5.5 yrs left)· nominal 20-yr term from priority
C07K 16/32C07K 2317/76C07K 16/3069C07K 2317/569C07K 16/2833C07K 16/3092A61K 47/6813A61P 35/00C07K 2317/34C07K 2317/32C07K 16/2884C07K 16/40A61K 47/6851C07K 16/30A61K 47/6883C07K 2319/33C07K 16/085C07K 16/084A61K 47/6849A61K 47/6809A61K 2039/505
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Claims

Abstract

Described are immunoglobulins provided with a toxic moiety, comprising at least an immunoglobulin variable region that specifically binds to an MHC-peptide complex preferentially associated with aberrant cells. These immunoglobulins provided with a toxic moiety are preferably used in selectively modulating biological processes. The provided immunoglobulins provided with a toxic moiety are of particular use in pharmaceutical compositions for the treatment of diseases related to cellular aberrancies, such as cancers and autoimmune diseases.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . An immunoglobulin provided with a toxic moiety, comprising at least an immunoglobulin variable region that specifically binds to an MHC-peptide complex preferentially associated with aberrant cells. 
     
     
         2 . The immunoglobulin according to  claim 1 , wherein said immunoglobulin variable region is a Vh or Vhh. 
     
     
         3 . The immunoglobulin according to  claim 2 , wherein said immunoglobulin variable region further comprises a Vl. 
     
     
         4 . The immunoglobulin according to  claim 3 , which is a human IgG. 
     
     
         5 . The immunoglobulin of  claim 1 , wherein the MHC-peptide complex is specific for aberrant cells. 
     
     
         6 . The immunoglobulin of  claim 1 , wherein the toxic moiety is chemically linked to the immunoglobulin. 
     
     
         7 . The immunoglobulin of  claim 1 , wherein the toxic moiety is a fusion protein, fused to the immunoglobulin at the DNA level. 
     
     
         8 . A pharmaceutical composition comprising:
 the immunoglobulin of  claim 1 , and   suitable diluents and/or excipients.   
     
     
         9 . A method of treating a host suffering from a disease associated with aberrant cells, the method comprising:
 utilizing an immunoglobulin provided with a toxic moiety of  claim 1 , for the treatment of the host suffering from a disease associated with aberrant cells.   
     
     
         10 . The method according to  claim 9 , wherein the toxic moiety is internalized into the aberrant cell. 
     
     
         11 . A method of treating a subject determined to be suffering from cancer, the method comprising:
 utilizing the immunoglobulin of  claim 1  to treat cancer.   
     
     
         12 . The method according to  claim 11 , wherein at least the toxic moiety is internalized into an aberrant cell of the subject. 
     
     
         13 . An immunoglobulin provided with a toxic moiety according to  FIG. 5B . 
     
     
         14 . The immunoglobulin of  claim 5 , wherein the MHC-peptide complex is specific for aberrant cells through a peptide derived from MAGE. 
     
     
         15 . The immunoglobulin of  claim 14 , wherein the MAGE is MAGE-A. 
     
     
         16 . The immunoglobulin of  claim 7 , wherein the toxic moiety is a fusion protein fused to the immunoglobulin at the DNA level through a linking sequence. 
     
     
         17 . An immunoglobulin chemically linked with a toxic moiety comprising:
 at least a Vh or Vhh immunoglobulin variable region that specifically binds to an MHC-peptide complex, which is derived from MAGE, preferentially associated with aberrant cells,   wherein the immunoglobulin is a human IgG.   
     
     
         18 . The immunoglobulin of  claim 17  wherein the immunoglobulin variable region is a Vl. 
     
     
         19 . The immunoglobulin of  claim 17 , wherein the MAGE is MAGE-A. 
     
     
         20 . The immunoglobulin of  claim 1 , wherein the toxic moiety is a fusion protein fused to the immunoglobulin at the DNA level through a linking sequence.

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