IP Library › Granted Patent US 11,365,247
Granted Patent B2
US 11,365,247 · App. 16/651,639 · Granted Jun 21, 2022

IL-5 antibody, antigen binding fragment thereof, and medical application therefor

Inventors: Hua Ying (Shanghai, CN); Jinping Shi (Shanghai, CN); Yifang Wang (Shanghai, CN); Qiyue Hu (Shanghai, CN); Hu Ge (Shanghai, CN); Weikang Tao (Shanghai, CN)
Assignees: Jiangsu Hengrui Medicine Co., Ltd.; Shanghai Hengrui Pharmaceutical Co., Ltd.
C07K16/244A61P11/06A61K2039/505C07K2317/24C07K2317/54C07K2317/55C07K2317/565C07K2317/569C07K2317/92
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Quick Facts
Patent No.
US 11,365,247
App. No.
16/651,639
Granted
Jun 21, 2022
Kind
B2
Abstract

Provided are an IL-5 antibody, an antigen binding fragment thereof, and a medical application therefor. The present invention comprises a mouse-derived antibody containing an IL-5 antibody CDR region, a chimeric antibody, a humanized antibody, and a pharmaceutical composition comprising said IL-5 antibody and said antigen binding fragment thereof, as well as the use of the pharmaceutical composition as a drug.

Claims (23)

1. A monoclonal antibody or antigen-binding fragment thereof specifically binding to human IL-5, wherein the monoclonal antibody comprises a heavy chain variable region and a light chain variable region, wherein,

(i) the heavy chain variable region comprises HCDR1, HCDR2 and HCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 16-18; and the light chain variable region comprises LCDR1, LCDR2 and LCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 19-21; or

(ii) the heavy chain variable region comprises HCDR1, HCDR2 and HCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 22-24; and the light chain variable region comprises LCDR1, LCDR2 and LCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 25-27; or

(iii) the heavy chain variable region comprises HCDR1, HCDR2 and HCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 28-30; and the light chain variable region comprises LCDR1, LCDR2 and LCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 31-33; or

(iv) the heavy chain variable region comprises HCDR1, HCDR2 and HCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 34-36; and the light chain variable region comprises LCDR1, LCDR2 and LCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 37-39; or

(v) the heavy chain variable region comprises HCDR1, HCDR2 and HCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 40-42; and the light chain variable region comprises LCDR1, LCDR2 and LCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 43-45; or

(vi) the heavy chain variable region comprises HCDR1, HCDR2 and HCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 34-36; and the light chain variable region comprises LCDR1, LCDR2 and LCDR3 region as set forth in amino acid sequences of SEQ ID NOs: 37-39.

2. The monoclonal antibody or antigen-binding fragment thereof according to claim 1 , wherein the monoclonal antibody is a recombinant antibody selected from the group consisting of murine antibody, chimeric antibody, and humanized antibody.

3. The monoclonal antibody or antigen-binding fragment thereof according to claim 2 , wherein the humanized antibody comprises a heavy chain variable region of SEQ ID NO: 49, 57, 63, 69 or 75.

4. The monoclonal antibody or antigen-binding fragment thereof according to claim 3 , further comprising a back mutation, wherein the back mutation is selected from the group consisting of S49T, V93T and K98S, or a combination thereof on the heavy chain variable region of SEQ ID NO: 49, or the back mutation is selected from the group consisting of S49T, V93T and K98T, or a combination thereof on the heavy chain variable region of SEQ ID NO: 57, or the back mutation is selected from the group consisting of R38K, M48I , R67K, V68A, M70L, R72V, T74K and L83F, or a combination thereof on the heavy chain variable region of SEQ ID NO:63, or the back mutation is selected from the group consisting of F29I , R38K, V48I , R72A, T97F on the heavy chain variable region of SEQ ID NO:69, and N55V on CDR, or a combination thereof, or the back mutation is selected from the group consisting of R38K, M48I , R67K, V68A, R72A, T74K, M81L, L83F and D89E, or a combination thereof on the heavy chain variable region of SEQ ID NO:75.

5. The monoclonal antibody or antigen-binding fragment thereof according to claim 4 , wherein the humanized antibody comprises a heavy chain variable region of SEQ ID NO:50 or 51, or comprises a heavy chain variable region of SEQ ID NO: 58 or 59, or comprises a heavy chain variable region selected from any one of SEQ ID NO: 64, 65 and 66, or comprises a heavy chain variable region of SEQ ID NO:70 or 71, or comprises a heavy chain variable region selected from any one of SEQ ID NOs: 76 to 79.

6. The monoclonal antibody or antigen-binding fragment thereof according to claim 2 , wherein the humanized antibody comprises a light chain variable region of SEQ ID NO: 46, 54, 60, 67 or 72.

7. The monoclonal antibody or antigen-binding fragment thereof according to claim 6 , further comprising a back mutation, wherein the back mutation is selected from the group consisting of A43 S, L47V, G66R, T69S, F71Y and Y87F or a combination thereof on the light chain variable region of SEQ ID NO:46; or the back mutation is selected from the group consisting of A43S, L47M, F71Y and Y87F or a combination thereof on the light chain variable region of SEQ ID NO: 54; or the back mutation is selected from the group consisting of E1D, I2T, I57V, V84T and Y86F or a combination thereof on the light chain variable region of SEQ ID NO: 60; or the back mutation is selected from the group consisting of M4L, A42S, L45P and L46W or a combination thereof on the light chain variable region of SEQ ID NO: 67; or the back mutation is selected from the group consisting of A43S, I48V and F71Y or a combination thereof on the light chain variable region of SEQ ID NO:72.

8. The monoclonal antibody or antigen-binding fragment thereof according to claim 7 , wherein the humanized antibody comprises a light chain variable region of SEQ ID NO: 47 or 48; or comprises a light chain variable region of SEQ ID NO: 55 or 56; or comprises a light chain variable region of SEQ ID NO: 61 or 62; or comprises a light chain variable region of SEQ ID NO: 68; or comprises a light chain variable region of SEQ ID NO: 73 or 74.

9. The monoclonal antibody or antigen-binding fragment thereof according to claim 1 , wherein the humanized antibody comprises:

a heavy chain variable region selected from any one of SEQ ID NOs: 49-51 and a light chain variable region selected from any one of SEQ ID NOs: 46-48; or

a heavy chain variable region selected from any one of SEQ ID NOs: 57-59 and a light chain variable region selected from any one of SEQ ID NOs: 54-56; or

a heavy chain variable region selected from any one of SEQ ID NOs: 63-66 and a light chain variable region selected from any one of SEQ ID NOs: 60-62; or

a heavy chain variable region selected from any one of SEQ ID NOs: 69-71 and a light chain variable region selected from any one of SEQ ID NOs: 67-68; or

a heavy chain variable region selected from any one of SEQ ID NOs: 75-79 and a light chain variable region selected from any one of SEQ ID NOs: 72-74.

10. The monoclonal antibody or antigen-binding fragment thereof according to claim 1 , wherein the antibody is a full length antibody, and further comprises a human antibody constant region, and wherein the full-length antibody comprises a human antibody heavy chain constant region as set forth in SEQ ID NO: 52 and a human light chain constant region as set forth in SEQ ID NO:53.

11. The monoclonal antibody or antigen-binding fragment thereof according to claim 1 , wherein the antigen-binding fragment is selected from the group consisting of Fab, Fab′, F(ab′)2, single-chain antibody (scFv), dimerized V region (diabody), and disulfide-stabilized V region (dsFv).

12. A pharmaceutical composition comprising a therapeutically effective amount of the monoclonal antibody or antigen-binding fragment thereof according to claim 1 , and one or more pharmaceutically acceptable carriers, diluents, buffers or excipients.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2020
From: YING, HUA; SHI, JINPING; WANG, YIFANG; HU, QIYUE; GE, HU; TAO, WEIKANG
To: JIANGSU HENGRUI MEDICINE CO., LTD.; SHANGHAI HENGRUI PHARMACEUTICAL CO., LTD.
Reel/Frame 052483/0780 →
Priority Claims (1)
CN 201710906068.X · Sep 29, 2017 · national
Continuity (1)
Related Publication 20200262909A1 · Aug 20, 2020
Cited By (1)
US 12,742,004