IP Library Granted Patent US 12661402
Granted Patent B2
US 12661402 · App. 18/259,205 · Granted Jun 23, 2026

Polypeptide specific for mucin 1 and use thereof

Inventors: Ji Hyun Lee (Daejeon, KR); Hae Youn Lee (Daejeon, KR); Yoon Aa Choi (Daejeon, KR); Dae Gwan Yi (Daejeon, KR); Jungwon Choi (Daejeon, KR); Areum Park (Daejeon, KR); Saem Jung (Daejeon, KR); Eu Rim Song (Daejeon, KR); Kyubong Na (Daejeon, KR); Min Jeong Park (Daejeon, KR); Eun Ji Jeun (Daejeon, KR); Kyuhong Choe (Daejeon, KR); Hyoju Yi (Daejeon, KR); Hee Jung Yang (Daejeon, KR); Sung Woong Jang (Daejeon, KR)
Assignee: LG CHEM, LTD.
A61K40/4257A61K35/17A61K40/11A61K40/31A61P35/00C07K14/7051C07K14/70517C07K14/70521C07K16/3092C12N5/0636C12N15/86A61K2239/13A61K2239/17A61K2239/21A61K2239/31A61K2239/38A61K2239/49A61K2239/54C07K2317/53C07K2317/565C07K2317/622C07K2319/02C07K2319/03C12N2510/00C12N2740/15043
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Quick Facts
Patent No.
US 12661402
App. No.
18/259,205
Granted
Jun 23, 2026
Kind
B2
Abstract

The present invention relates to a polypeptide binding to mucin 1, an isolated polynucleotide encoding same, a vector carrying the polynucleotide, and a cell including the vector. In addition, the present invention relates to a chimeric antigen receptor including the polypeptide binding to mucin 1, an isolated polynucleotide encoding the chimeric antigen receptor, a vector carrying the polynucleotide, an immune cell expressing the chimeric antigen receptor, a composition comprising same for treatment of cancer, and a method for treatment of cancer.

Claims (51)

1 . An antibody or an antigen-binding fragment thereof binding to mucin1, the antibody or antigen-binding fragment thereof comprising a pair of a heavy chain variable (VH) region and a light chain variable (VL) region selected from the following VH and VL regions:

a VH region comprising complementarity-determining region (CDR) 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 1, SEQ ID NO: 2, and SEQ ID NO: 3, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 4, SEQ ID NO: 5, and SEQ ID NO: 6, respectively;

a VH region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 11, SEQ ID NO: 12, and SEQ ID NO: 13, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 14, SEQ ID NO: 15, and SEQ ID NO: 16, respectively;

a VH region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 21, SEQ ID NO: 22, and SEQ ID NO: 23, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 24, SEQ ID NO: 25, and SEQ ID NO: 26, respectively;

a VH region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 31, SEQ ID NO: 32, and SEQ ID NO: 33, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 34, SEQ ID NO: 35, and SEQ ID NO: 36, respectively;

a VH region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 41, SEQ ID NO: 42, and SEQ ID NO: 43, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 44, SEQ ID NO: 45, and SEQ ID NO: 46, respectively;

a VH region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 51, SEQ ID NO: 52, and SEQ ID NO: 53, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 54, SEQ ID NO: 55, and SEQ ID NO: 56, respectively;

a VH region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 61, SEQ ID NO: 62, and SEQ ID NO: 63, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 64, SEQ ID NO: 65, and SEQ ID NO: 66, respectively;

a VH region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 71, SEQ ID NO: 72, and SEQ ID NO: 73, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 74, SEQ ID NO: 75, and SEQ ID NO: 76, respectively;

a VH region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 81, SEQ ID NO: 82, and SEQ ID NO: 83, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 84, SEQ ID NO: 85, and SEQ ID NO: 86, respectively; or

a VH region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 91, SEQ ID NO: 92, and SEQ ID NO: 93, respectively, and a VL region comprising CDR 1, CDR 2, and CDR 3 comprising amino acid sequences of SEQ ID NO: 94, SEQ ID NO: 95, and SEQ ID NO: 96, respectively.

2 . The antibody or antigen-binding fragment thereof of claim 1 , comprising a pair of a heavy chain variable (VH) region and a light chain variable (VL) region selected from the following VH and VL regions:

a VH region comprising an amino acid sequence of SEQ ID NO: 7 and a VL region comprising an amino acid sequence of SEQ ID NO: 8;

a VH region comprising an amino acid sequence of SEQ ID NO: 17 and a VL region comprising an amino acid sequence of SEQ ID NO: 18;

a VH region comprising an amino acid sequence of SEQ ID NO: 27 and a VL region comprising an amino acid sequence of SEQ ID NO: 28;

a VH region comprising an amino acid sequence of SEQ ID NO: 37 and a VL region comprising an amino acid sequence of SEQ ID NO: 38;

a VH region comprising an amino acid sequence of SEQ ID NO: 47 and a VL region comprising an amino acid sequence of SEQ ID NO: 48;

a VH region comprising an amino acid sequence of SEQ ID NO: 57 and a VL region comprising an amino acid sequence of SEQ ID NO: 58;

a VH region comprising an amino acid sequence of SEQ ID NO: 67 and a VL region comprising an amino acid sequence of SEQ ID NO: 68;

a VH region comprising an amino acid sequence of SEQ ID NO: 77 and a VL region comprising an amino acid sequence of SEQ ID NO: 78;

a VH region comprising an amino acid sequence of SEQ ID NO: 87 and a VL region comprising an amino acid sequence of SEQ ID NO: 88; or

a VH region comprising an amino acid sequence of SEQ ID NO: 97 and a VL region comprising an amino acid sequence of SEQ ID NO: 98.

3 . The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof is a single chain variable fragment (scFv), a peptibody, a fragment antigen binding (Fab), a monoclonal antibody, a bispecific antibody, a minibody, a domain antibody, a synthetic antibody, a chimeric antibody, a humanized antibody, a human antibody, or an antibody fusion protein.

4 . The antibody or antigen-binding fragment thereof of claim 1 , wherein the VH region and the VL region are linked to each other via a linker.

5 . The antibody or antigen-binding fragment thereof of claim 4 , wherein an amino acid sequence of the linker is GGGGSGGGGSGGGAS of SEQ ID NO: 116.

6 . The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof is a single chain variable fragment (scFv) and the scFv includes an amino acid sequence selected from the group consisting of SEQ ID NO: 9, SEQ ID NO: 19, SEQ ID NO: 29, SEQ ID NO: 39, SEQ ID NO: 49, SEQ ID NO: 59, SEQ ID NO: 69, SEQ ID NO: 79, SEQ ID NO: 89, and SEQ ID NO: 99.

7 . An isolated polynucleotide encoding the antibody or antigen-binding fragment of claim 1 .

8 . A vector comprising the polynucleotide of claim 7 .

9 . A cell comprising the vector of claim 8 .

10 . A chimeric antigen receptor comprising the antibody or antigen-binding fragment of claim 1 .

11 . The chimeric antigen receptor of claim 10 , comprising an extracellular domain comprising the antibody or antigen-binding fragment; a transmembrane domain; and an intracellular signaling domain.

12 . The chimeric antigen receptor of claim 11 , wherein the extracellular domain further comprises a spacer region between the antibody or antigen-binding fragment and the transmembrane domain.

13 . The chimeric antigen receptor of claim 12 , wherein the spacer region comprises a hinge region of CD8α or CD28, or all or part of a constant region of an immunoglobulin (IgG).

14 . The chimeric antigen receptor of claim 11 , wherein the transmembrane domain is a transmembrane domain of CD28 or CD8.

15 . The chimeric antigen receptor of claim 11 , wherein the intracellular signaling domain is a CD3 zeta signaling domain.

16 . The chimeric antigen receptor of claim 11 , further comprising at least one co-stimulatory domain.

17 . The chimeric antigen receptor of claim 16 , wherein the at least one co-stimulatory domain is placed between the transmembrane domain and the intracellular signaling domain.

18 . The chimeric antigen receptor of claim 16 , wherein the at least one co-stimulatory domain is a signaling domain of CD28, OX-40, 4-1BB (CD137), CD27, or ICOS.

19 . An isolated polynucleotide encoding the chimeric antigen receptor of claim 10 .

20 . A vector comprising the polynucleotide of claim 19 .

21 . An immune cell expressing a chimeric antigen receptor comprising the polynucleotide according to claim 19 .

22 . The immune cell of claim 21 , wherein the immune cell is a T cell, a tumor infiltrating lymphocyte (TIL), a natural killer (NK) cell, a TCR-expressing cell, a dendritic cell, or an NK-T cell.

23 . The immune cell of claim 21 , wherein the immune cell is an autologous T cell or an allogenic T cell.

24 . A composition comprising the antibody or antigen-binding fragment of claim 1 .

25 . A composition comprising the isolated polynucleotide according to claim 7 .

26 . A composition comprising the vector according to claim 8 .

27 . A composition comprising the cell according to claim 9 .

28 . A composition comprising the chimeric antigen receptor according to claim 10 .

29 . A composition comprising the isolated polynucleotide according to claim 19 .

30 . A composition comprising the vector according to claim 20 .

31 . A composition comprising the immune cell according to claim 21 .