Anti-TROP2 antibody
The present disclosure relates to antibodies, in particular monoclonal antibodies of murine, chimeric, and humanized origin, that specifically bind to the human TROP2 protein, and to the amino acid and nucleotide sequences encoding these antibodies. The disclosure also discloses the use of these antibodies as a diagnostic reagent or a drug in the diagnostic and/or therapeutic management of malignancies or any lesion related to the overexpression of the receptor.
1 . An anti-TROP2 antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, or scFv-Fc fragment thereof, comprising a heavy chain and a light chain, wherein the heavy chain comprises amino acid sequence SEQ ID NO: 13 or 17 and the light chain comprises amino acid sequence SEQ ID NO: 14 or 18, or wherein the heavy chain comprises amino acid sequence SEQ ID NO: 15 or 19 and the light chain comprises amino acid sequence SEQ ID NO: 16 or 20.
2 . The antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, or scFv-Fc fragment of claim 1 , wherein the heavy chain comprises amino acid sequence SEQ ID NO: 17 and the light chain comprises amino acid sequence SEQ ID NO: 18, or wherein the heavy chain comprises amino acid sequence SEQ ID NO: 19 and the light chain comprises amino acid sequence SEQ ID NO: 20.
3 . The antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, or scFv-Fc fragment of claim 1 , wherein the antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, or scFv-Fc fragment is a monoclonal antibody or a derivative thereof.
4 . The antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, or scFv-Fc fragment of claim 1 , wherein the antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, or scFv-Fc fragment is of murine origin.
5 . The antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, or scFv-Fc fragment of claim 1 , wherein the heavy chain comprises CDRH1, CDRH2, and CDRH3 from SEQ ID NO: 1, 2, and 3, respectively or CDRH1, CDRH2, and CDRH3 from SEQ ID NO: 4, 5, and 6 respectively.
6 . An antibody fragment or its derivative having at least one of the following sets of CDRs wherein each set of CDRs comprises an amino acid sequence of SEQ ID NO: 4-6, 7-9, or 10-12.
7 . The antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, scFv-Fc fragments of claim 2 , wherein the antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, scFv-Fc fragments comprise humanized sequences.
8 . The antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, or scFv-Fc fragment of claim 5 , wherein the light chain comprises CDRL1, CDRL2, and CDRL3 from SEQ ID NO: 7, 8, and 9 or CDRL1, CDRL2, and CDRL3 from SEQ ID NO: 10, 11, and 12.
9 . A nucleic acid sequence, comprising the nucleic acid sequence encoding the antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, scFv-Fc fragment of claim 1 .
10 . The isolated nucleic acid sequence of claim 9 , comprising the nucleic acid sequence encoding the heavy chain having SEQ ID NO: 21, 22 and 23, or SEQ ID NO: 24, 25 and 26, and the nucleic acid sequence encoding the light chain having SEQ ID NO: 27, 28, and 29 or SEQ ID NO: 30, 31, and 32.
11 . The nucleic acid sequence according to claim 10 , comprising the nucleic acid sequence having SEQ ID NO: 33 and 34, or SEQ ID NO: 35 and 36.
12 . The nucleic acid according to claim 10 , comprising the nucleic acid sequence having SEQ ID NO: 37 and 38, or SEQ ID NO: 39 and 40.
13 . An RNA, wherein the RNA sequence corresponds or is complementary to the nucleic acid sequences in claim 9 .
14 . An expression vector, comprising the nucleic acid sequences of claim 9 .
15 . A host, comprising the expression vector of claim 14 .
16 . The expression vector of claim 14 or the host of claim 15 , wherein the expression vector or the host is configured to produce the amino acid sequence SEQ ID NO: 13, 14, 15 or 16.
17 . A method for diagnosis or treating TROP2-related malignant tumors in a subject, comprising administering to the subject the antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, scFv-Fc fragment of claim 1 .
18 . An immune-conjugate, comprising the antibody or its Fv, scFv, Fab, F(ab′)2, Fab′, scFv-Fc fragment of claim 1 and a cytotoxic compound or a radioactive element.
19 . The immuno-conjugate of claim 18 , wherein the cytotoxic compound comprises an alkylating agent, an anti-metabolite, an anti-tumor drug, a mitotic inhibitor, a chromatin function inhibitor, an anti-angiogenesis agent, an anti-androgen, an anti-estrogen, an immunomodulator, or a combination thereof.