IP Library Granted Patent US 8,926,973
Granted Patent B2
US 8,926,973 · App. 13/116,830 · Granted Jan 6, 2015

Reducing the immunogenicity of fusion proteins

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Quick Facts
Patent No.
US 8,926,973
App. No.
13/116,830
Granted
Jan 6, 2015
Kind
B2
Abstract

Disclosed are compositions and methods for producing fusion proteins with reduced immunogenicity. Fusion proteins of the invention include a junction region having an amino acid change that reduces the ability of a junctional epitope to bind to MHC Class II, thereby reducing its interaction with a T-cell receptor. Methods of the invention involve analyzing, changing, or modifying one or more amino acids in the junction region of a fusion protein in order to identify a T-cell epitope and reduce its ability to interact with a T cell receptor. Compositions and methods of the invention are useful in therapy.

Claims (6)

1. A method for reducing the immunogenicity of a fusion protein, the method comprising:

i. identifying a candidate T-cell epitope within a junction region spanning a fusion junction of a fusion protein, wherein the fusion protein comprises a non-immunoglobulin protein and an immunoglobulin protein comprising an IgG region, wherein the immunoglobulin protein is fused to the non-immunoglobulin protein via the fusion junction; and,

ii. changing an LSLS amino acid sequence (amino acids 3-6 of SEQ ID NO:5) within the junction region to reduce the ability of the candidate T-cell epitope to interact with a T cell receptor.

2. A method for reducing the immunogenicity of a fusion protein, the method comprising changing a candidate T-cell epitope within a junction region spanning a fusion junction of a fusion protein, wherein the fusion protein comprises a non-immunoglobulin protein and an immunoglobulin protein fused to the non-immunoglobulin protein via the fusion junction, to reduce the ability of the candidate T-cell epitope to interact with a T-cell receptor, wherein the amino acid sequence of the junction region comprises an IgG region wherein an LSLS amino acid sequence (amino acids 3-6 of SEQ ID NO:5) is changed without generating a T-cell epitope.

3. The method of claim 1 , wherein the LSLS amino acid sequence (amino acids 3-6 of SEQ ID NO:5) is changed to an ATAT amino acid sequence (amino acids 3-6 of SEQ ID NO:6).

4. The method of claim 2 , wherein the LSLS amino acid sequence (amino acids 3-6 of SEQ ID NO:5) is changed to an ATAT amino acid sequence (amino acids 3-6 of SEQ ID NO:6).

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2013
From: GILLIES, STEPHEN D.; WAY, JEFFREY; HAMILTON, ANITA A.
To: EMD LEXIGEN RESEARCH CENTER CORP.
Reel/Frame 030484/0073 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2013
From: EMD SERONO RESEARCH CENTER, INC.
To: MERCK PATENT GMBH
Reel/Frame 030484/0169 →
CHANGE OF NAME Recorded May 24, 2013
From: EMD LEXIGEN RESEARCH CENTER CORP.
To: EMD SERONO RESEARCH CENTER, INC.
Reel/Frame 030490/0512 →