IP Library › Granted Patent US 10,385,348
Granted Patent B2
US 10,385,348 · App. 15/795,404 · Granted Aug 20, 2019

Epidermal growth factor receptor targeted/immunomodulatory fusion proteins and methods of use for them

Inventors: Nagaraj Govindappa (Karnataka, IN); Kedarnath Sastry (Karnataka, IN); Maria Melina Soares (Karnatake, IN)
Assignee: BIOCON LIMITED
C12N15/62A61K38/10A61K38/179A61K39/395A61K39/39558A61K45/06A61K48/005C07K7/08C07K14/00C07K14/495C07K14/65C07K14/70532C07K14/70596C07K14/71C07K16/2818C07K16/2863C07K16/2866C07K16/2878C07K16/2887C07K16/30C07K16/32C12N5/0018G01N33/6854A61K38/00A61K2039/505A61K2121/00C07K2317/14C07K2317/24C07K2317/31C07K2317/51C07K2317/515C07K2317/732C07K2319/00C07K2319/02C07K2319/33C12N2500/22
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Quick Facts
Patent No.
US 10,385,348
App. No.
15/795,404
Granted
Aug 20, 2019
Kind
B2
Abstract

The present invention relates generally to the field of generating fusion proteins to be used in cancer therapy, and more specifically, to nucleotide sequences encoding the fusion proteins, wherein the chimeric fusion proteins comprises at least one targeting moiety and at least one immunomodulatory moiety that counteracts the immune tolerance of cancer cells.

Claims (8)

1. A method of reducing tumor Transforming growth factor-beta (TGF-β) levels, the method comprising contacting cancer cells with a therapeutic amount of a chimeric fusion protein, wherein the chimeric fusion protein comprises a targeting moiety to target a cancer cell and an immunomodulating moiety that counteracts immune tolerance, wherein the targeting moiety and the immunomodulating moiety are linked by an amino acid spacer of sufficient length of amino acid residues so that both moieties can successfully bind to their individual targets, wherein the immunomodulating moiety is TGF-βRII consisting of an amino acid sequence of SEQ ID NO: 4, wherein the amino acid spacer is selected from SEQ ID NO: 3 or SEQ ID NO: 11; and wherein the targeting moiety is an Anti-EGFR1 antibody consisting of heavy chain of SEQ ID NO: 5 and light chain of SEQ ID NO: 6; wherein SEQ ID NO: 4 is attached via the amino acid spacer to the C-terminus of SEQ ID NO: 6.

2. The method of claim 1 , wherein the cancer cells are in a subject in need of treatment.

3. The method of claim 1 , further comprising administering the chimeric fusion protein in combination with another existing cancer treatment.

4. The method of claim 1 , wherein suppression of an immune system of the subject in the cancer cell is reduced.

5. The method of claim 1 , wherein cytotoxic lymphocytes and Natural Killer cells are activated in the subject.

6. The method of claim 1 , wherein lysis of cancer cells is increased.

7. The method of claim 1 , wherein SEQ ID NO: 4 binds to TGF-β.

8. The method of claim 1 , wherein the Anti-EGFR1 antibody binds to a cancerous tumor cell.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2024
From: GOVINDAPPA, NAGARAJ; SASTRY, KEDARNATH; SOARES, MARIA MELINA
To: BIOCON LIMITED
Reel/Frame 067766/0160 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2019
From: GOVINDAPPA, NAGARAJ; SASTRY, KEDARNATH; SOARES, MARIA MELINA
To: BIOCON LIMITED
Reel/Frame 049468/0740 →
Priority Claims (2)
IN 1689/CHE/2012 · Apr 30, 2012 · national
IN 1690/CHE/2012 · Apr 30, 2012 · national
Continuity (4)
Division 15047062 · Feb 18, 2016
Division 14458674 · Aug 13, 2014
Division 13799409 · Mar 13, 2013
Related Publication 20180066057A1 · Mar 8, 2018
Cited By (1)
US 12,351,636