US2018154013A1PendingUtilityA1
Aberrant cell-restricted immunoglobulins provided with a toxic moiety
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-modifiedWhat 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.Join the waitlist — get patent alerts
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