IP Library Granted Patent US 10,214,593
Granted Patent B2
US 10,214,593 · App. 14/243,751 · Granted Feb 26, 2019

Anti-idiotype antibody against anti-c-MET antibody

Inventors: Soo Yeon Jung (Seongnam-si, KR); Yun Jeong Song (Seongnam-si, KR); Mi Young Cho (Seoul, KR); Han Na Choi (Seoul, KR)
Assignee: SAMSUNG ELECTRONICS CO., LTD.
C07K16/4258G01N33/6806G01N33/686C07K16/2863C07K2317/24C07K2317/53C07K2317/565C07K2317/622C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 10,214,593
App. No.
14/243,751
Granted
Feb 26, 2019
Kind
B2
Abstract

Disclosed are an anti-idiotype antibody that specifically binds to an idiotope site of an anti-c-Met antibody, the use of the anti-idiotype antibody for detecting the anti-c-Met antibody, and methods, polypeptides, polynucleotides, compositions, and vaccines related thereto.

Claims (34)

1. An anti-idiotype antibody or antigen-binding fragment thereof that specifically binds to an idiotype of an anti-c-Met antibody comprising:

(a) a CDR-H1 comprising the amino acid sequence of SEP ID NO: 116, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 126, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 140, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 156, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 173, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 189;

(b) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 115, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 125, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 139, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 155, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 172, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 188;

(c) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 117, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 127, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 141, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 157, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 174, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 190;

(d) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 118, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 128, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 142, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 158, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 175, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 191;

(e) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 117, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 129, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 143, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 159, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 176, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 192;

(f) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 118, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 130, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 144, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 160, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 177, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 193;

(g) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 115, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 131, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 145, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 161, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 178, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 191;

(h) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 116, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 132, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 146, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 162, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 178, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 194;

(i) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 119, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 133, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 147, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 163, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 179, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 189;

(j) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 119, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 134, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 148, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 164, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 180, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 195; or

(k) a CDR-H1 comprising the amino acid sequence of SEQ ID NO: 120, a CDR-H2 comprising the amino acid sequence of SEQ ID NO: 126, a CDR-H3 comprising the amino acid sequence of SEQ ID NO: 149, a CDR-L1 comprising the amino acid sequence of SEQ ID NO: 165, a CDR-L2 comprising the amino acid sequence of SEQ ID NO: 181, and a CDR-L3 comprising the amino acid sequence of SEQ ID NO: 196.

2. The anti-idiotype antibody or antigen-binding fragment thereof according to claim 1 , wherein the anti-idiotype antibody comprises:

a heavy chain variable region of SEQ ID NO: 202 and a light chain variable region of SEQ ID NO: 236;

a heavy chain variable region of SEQ ID NO: 203 and a light chain variable region of SEQ ID NO: 237;

a heavy chain variable region of SEQ ID NO: 204 and a light chain variable region of SEQ ID NO: 238;

a heavy chain variable region of SEQ ID NO: 205 and a light chain variable region of SEQ ID NO: 239;

a heavy chain variable region of SEQ ID NO: 206 and a light chain variable region of SEQ ID NO: 240;

a heavy chain variable region of SEQ ID NO: 207 and a light chain variable region of SEQ ID NO: 241;

a heavy chain variable region of SEQ ID NO: 208 and a light chain variable region of SEQ ID NO: 242;

a heavy chain variable region of SEQ ID NO: 209 and a light chain variable region of SEQ ID NO: 243;

a heavy chain variable region of SEQ ID NO: 210 and a light chain variable region of SEQ ID NO: 244;

a heavy chain variable region of SEQ ID NO: 211 and a light chain variable region of SEQ ID NO: 245; or

a heavy chain variable region of SEQ ID NO: 212 and a light chain variable region of SEQ ID NO: 246.

3. The anti-idiotype antibody or antigen-binding fragment thereof according to claim 1 , wherein the anti-idiotype antibody is a mouse antibody, a mouse-human chimeric antibody, a humanized antibody, or a human antibody.

4. The anti-idiotype antibody or antibody fragment thereof according to claim 1 , wherein the anti-idiotype antibody or antibody fragment thereof is an antigen-binding fragment selected from the group consisting of scFv, (scFv) 2 , Fab, Fab′, and F(ab′) 2 .

5. A composition comprising an anti-idiotype antibody or antigen-binding fragment thereof according to claim 1 and a carrier.

6. A method for detecting an anti-c-Met antibody comprising:

contacting a biological sample with an anti-idiotype antibody or antigen-binding fragment thereof according to claim 1 ; and

determining the presence or absence of an antigen-antibody reaction.

7. The method according to claim 6 , wherein the biological sample comprises serum isolated from a subject.

8. A method for analyzing an anti-drug antibody, the method comprising measuring the absorption of a serum isolated from a patient to whom a test drug has been intravenously administered; and

comparing the obtained absorption results with the absorption change of the anti-idiotype antibody or antigen-binding fragment thereof according to claim 1 in a serum isolated from a patient to whom an anti-c-Met antibody has been administered.

9. The anti-idiotype antibody or antigen-binding fragment thereof of claim 1 , wherein the anti-idiotype antibody or antigen-binding fragment thereof has an affinity (K d ) to an anti-c-Met antibody or antibody fragment of about 50 nM or less.

Assignments (2)
NUNC PRO TUNC ASSIGNMENT Recorded Mar 11, 2026
From: SAMSUNG ELECTRONICS CO., LTD.
To: SAMSUNG BIOLOGICS CO., LTD.
Reel/Frame 074033/0938 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2014
From: JUNG, SOO YEON; SONG, YUN JEONG; CHO, MI YOUNG; CHOI, HAN NA
To: SAMSUNG ELECTRONICS CO., LTD.
Reel/Frame 032759/0237 →
Priority Claims (2)
KR 10-2013-0036053 · Apr 2, 2013 · national
KR 10-2014-0037574 · Mar 31, 2014 · national
Continuity (1)
Related Publication 20140302517A1 · Oct 9, 2014
Cited By (2)
US 12,545,735 US 12,605,473