Patent Application
20220153853
This application incorporates by reference the material in the ASCII text file titled Amended_Sequence_Listing.txt, which was created on Dec. 15, 2021 and is 154 KB.
The present disclosure relates to human GCGR antibodies, GLP-1 peptides and mutants thereof, as well as bispecific proteins formed by the GCGR antibody fused to the GLP-1 peptide, and preparation methods and applications thereof.
The descriptions herein only provide background information about the present disclosure, and do not necessarily constitute prior art.
Diabetes (diabetes mellitus, DM) is a metabolic disease characterized by high level of blood glucose due to defect in insulin secretion and/or insulin dysfunction. The onset of the disease is mainly caused by the co-action of insulin and glucagon.
GLP-1 is one of the most important hormones affecting insulin secretion, and both GLP-1 and glucagon are derived from preproinsulin. Preproinsulin is composed of about 158 amino acids and can be cleaved into various peptide chains at different positions. The biologically active GLP-1 in the human body mainly includes two forms, GLP-1 (7-36) amide and GLP-1 (7-37). GLP-1 is secreted by small intestinal L cells, and it lowers the level of blood glucose in an organism by promoting insulin secretion mainly in a glucose concentration-dependent manner, protecting pancreatic islet f3 cells, and inhibiting glucagon secretion. At the same time, GLP-1 also has effects on inhibiting gastric emptying and reducing appetite. It is clinically useful for the treatment of type II diabetes and obesity. The natural active GLP-1 is easily to be degraded by enzyme DPPIV in an organism due to the very short half-life (less than 2 minutes) and has no clinical value.
The main direction of the research and development of GLP-1 drugs has always been prolonging the half-life. There are currently many commercially available GLP-1 agonists, such as Dulaglutide and Semaglutide. Although the efficacy of GLP-1 has been fully confirmed, though it has many side effects, mainly manifested as gastrointestinal symptoms, hypoglycemia, pancreatitis and kidney damage.
Glucagon has the opposite effect to insulin, and mainly plays a role in raising the level of blood glucose in the organism. Glucagon is a 29-amino acid peptide secreted by pancreatic islet α cells. Glucagon mainly accelerates the glycogenolysis, lipolysis and gluconeogenesis by activating the downstream cAMP/PKA pathway, and thereby increasing the level of blood glucose after binding to the receptor GCGR on the liver cell membrane.
The studies have found that GCGR-knockout mice exhibited a series of phenotypes such as increased GLP-1, decreased glycogen output, increased lipid metabolism, and decreased appetite. GCGR is one of the most popular targets for the treatment of diabetes, but currently the progress in the development of antagonistic drugs against GCGR has been slow. REMD-477, available from REMD Biotherapeutics, is currently the most cutting-edge GCGR monoclonal antibody drug, and is in clinical phase II.
GCGR antibodies have been disclosed in the prior arts, such as CN101589062A, CN101983208A, CN102482350A, CN103314011A, CN105189560A, CN107614695A, US20180273629A1 and WO2013059531A1. However, there is still a need to provide new and highly efficient GCGR antibodies and methods for the treatment of diabetes.
The present disclosure provides an anti-GCGR monoclonal antibody or antigen-binding fragment thereof. The antibody or antigen-binding fragment thereof has an ability to bind to human GCGR (or an antigen epitope comprised therein).
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a combination of a heavy chain variable region and a light chain variable region selected from the following a) or b):
a) the heavy chain variable region comprising HCDR1, HCDR2 and HCDR3 regions as shown in SEQ ID NOs: 48, 49 and 50, respectively, and the light chain variable region comprising LCDR1, LCDR2 and LCDR3 regions as shown in SEQ ID NOs: 51, 52 and 53, respectively; or
b) the heavy chain variable region comprising HCDR1, HCDR2 and HCDR3 regions as shown in SEQ ID NOs: 38, 39 and 54, respectively, and the light chain variable region comprising LCDR1, LCDR2 and LCDR3 regions as shown in SEQ ID NOs: 55, 56 and 57, respectively.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a combination of a heavy chain variable region and a light chain variable region selected from any one of the following i) to vi):
i) the heavy chain variable region comprising HCDR1, HCDR2 and HCDR3 regions as shown in SEQ ID NOs: 14, 15 and 16, respectively, and the light chain variable region comprising LCDR1, LCDR2 and LCDR3 regions as shown in SEQ ID NOs: 17, 18 and 19, respectively;
ii) the heavy chain variable region comprising HCDR1, HCDR2 and HCDR3 regions as shown in SEQ ID NOs: 20, 21 and 22, respectively, and the light chain variable region comprising LCDR1, LCDR2 and LCDR3 regions as shown in SEQ ID NOs: 23, 24 and 25, respectively;
iii) the heavy chain variable region comprising HCDR1, HCDR2 and HCDR3 regions as shown in SEQ ID NOs: 26, 27 and 28, respectively, and the light chain variable region comprising LCDR1, LCDR2 and LCDR3 regions as shown in SEQ ID NOs: 29, 30 and 31, respectively;
iv) the heavy chain variable region comprising HCDR1, HCDR2 and HCDR3 regions as shown in SEQ ID NOs: 32, 33 and 34, respectively, and the light chain variable region comprising LCDR1, LCDR2 and LCDR3 regions as shown in SEQ ID NOs: 35, 36 and 37, respectively;
v) the heavy chain variable region comprising HCDR1, HCDR2 and HCDR3 regions as shown in SEQ ID NOs: 38, 39 and 40, respectively, and the light chain variable region comprising LCDR1, LCDR2 and LCDR3 regions as shown in SEQ ID NOs: 41, 42 and 43, respectively; or
vi) the heavy chain variable region comprising HCDR1, HCDR2 and HCDR3 regions as shown in SEQ ID NOs: 38, 39 and 44, respectively, and the light chain variable region comprising LCDR1, LCDR2 and LCDR3 regions as shown in SEQ ID NOs: 45, 46 and 47, respectively.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof is a murine antibody, chimeric antibody or humanized antibody or antigen-binding fragment thereof.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof, the humanized antibody comprises framework region(s) derived from a human antibody or framework region variant thereof, and the framework region variant has at most 10 back mutations based on the light chain framework region of a human antibody, and/or the framework region variant has at most 10, at most 9, at most 8, at most 7, at most 6, at most 5, at most 4, at most 3, at most 2, at most 1 amino acid back mutation based on the heavy chain framework region of a human antibody.
In some embodiments, the framework region variant comprises:
aa) one or more amino acid back mutation(s) of 42G 44V, 71Y and 87F comprised in the light chain variable region, and/or one or more amino acid back mutation(s) of 38K, 48I, 67A, 69F, 71A, 73P, 78A and 93 comprised in the heavy chain variable region; or
ab) one or more amino acid back mutation(s) of 38L, 44V, 59S, 70E and 71Y comprised in the light chain variable region, and/or one or more amino acid back mutation(s) of 38K, 48I, 66K, 67A, 69L, 73R, 78M and 94S comprised in the heavy chain variable region. Further, the position of the back mutation site is determined according to the Kabat numbering criteria.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain variable region as shown in any one of SEQ ID NOs: 2, 61, 62, 63 and 64, or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NOs: 2, 61, 62, 63 and 64; and/or
a light chain variable region as shown in any one of SEQ ID NOs: 3, 58, 59 and 60, or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NOs: 3, 58, 59 and 60.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain variable region as shown in SEQ ID NO: 63 and a light chain variable region as shown in SEQ ID NO: 58.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain variable region as shown in SEQ ID NO: 4 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NO: 4; and/or
a light chain variable region as shown in SEQ ID NO: 5 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NO:5.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain variable region as shown in SEQ ID NO: 6 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NO: 6; and/or
a light chain variable region as shown in SEQ ID NO: 7 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NO:7.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain variable region as shown in any one of SEQ ID NOs: 8, 68, 69, 70 and 71 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NOs: 8, 68, 69, 70 and 71; and/or
a light chain variable region as shown in any one of SEQ ID NOs: 9, 65, 66 and 67 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to any one of SEQ ID NOs: 9, 65, 66 and 67.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain variable region as shown in SEQ ID NO: 71 and a light chain variable region as shown in SEQ ID NO: 67.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain variable region as shown in SEQ ID NO: 10 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NO: 10; and/or
a light chain variable region as shown in SEQ ID NO: 11 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NO:11.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain variable region as shown in SEQ ID NO: 12 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NO: 12; and/or
a light chain variable region as shown in SEQ ID NO: 13 or having at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity to SEQ ID NO:13.
In some embodiments of the anti-GCGR monoclonal antibody or antigen-binding fragment thereof, the antibody is a full-length antibody, further comprising antibody constant region(s), specifically, the heavy chain constant region of the antibody constant regions is selected from human IgG1, IgG2, IgG3 and IgG4 constant regions and the conventional variants thereof, and the light chain constant region of the antibody constant regions is selected from human antibody κ and λ chain constant regions and the conventional variants thereof, and more preferably comprising a human antibody heavy chain constant region as shown in SEQ ID NO: 72 and a human light chain constant region as shown in SEQ ID NO:73.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain and a light chain, wherein:
the heavy chain is as shown in SEQ ID NO: 74, 76 or 78 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto, and the light chain is as shown in SEQ ID NO: 75 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain and a light chain, wherein:
the heavy chain is as shown in SEQ ID NO: 74, 76 or 78 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto, and the light chain is as shown in SEQ ID NO: 77 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain and a light chain, wherein:
the heavy chain is as shown in SEQ ID NO: 74, 76 or 78 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto, and the light chain is as shown in SEQ ID NO: 79 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain and a light chain, wherein:
the heavy chain is as shown in SEQ ID NO: 80 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto, and the light chain is as shown in SEQ ID NO: 81 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain and a light chain, wherein:
the heavy chain is as shown in SEQ ID NO: 82 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto, and the light chain is as shown in SEQ ID NO: 83 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain and a light chain, wherein:
the heavy chain is as shown in SEQ ID NO: 84 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto, and the light chain is as shown in SEQ ID NO: 85 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain and a light chain, wherein:
the heavy chain is as shown in SEQ ID NO: 86 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto, and the light chain is as shown in SEQ ID NO: 87 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain and a light chain, wherein:
the heavy chain is as shown in SEQ ID NO: 88 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto, and the light chain is as shown in SEQ ID NO: 89 or has at least 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98% or 99% sequence identity thereto.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain as shown in SEQ ID NO: 78 and a light chain as shown in SEQ ID NO: 79.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a heavy chain as shown in SEQ ID NO: 84 and a light chain as shown in SEQ ID NO: 85.
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof comprises a combination of a heavy chain variable region and a light chain variable region selected from any one of the following ac) to ah):
ac) the heavy chain variable region comprising the same HCDR1, HCDR2 and HCDR3 regions as those of the heavy chain variable region as shown in SEQ ID NO: 2, and the light chain variable region comprising the same LCDR1, LCDR2 and LCDR3 regions as those of the light chain variable region as shown in SEQ ID NO: 3;
ad) the heavy chain variable region comprising the same HCDR1, HCDR2 and HCDR3 regions as those of the heavy chain variable region as shown in SEQ ID NO: 4, and the light chain variable region comprising the same LCDR1, LCDR2 and LCDR3 regions as those of the light chain variable region as shown in SEQ ID NO: 5;
ae) the heavy chain variable region comprising the same HCDR1, HCDR2 and HCDR3 regions as those of the heavy chain variable region as shown in SEQ ID NO: 6, and the light chain variable region comprising the same LCDR1, LCDR2 and LCDR3 regions as those of the light chain variable region as shown in SEQ ID NO: 7;
af) the heavy chain variable region comprising the same HCDR1, HCDR2 and HCDR3 regions as those of the heavy chain variable region as shown in SEQ ID NO: 8, and the light chain variable region comprising the same LCDR1, LCDR2 and LCDR3 regions as those of the light chain variable region as shown in SEQ ID NO: 9;
ag) the heavy chain variable region comprising the same HCDR1, HCDR2 and HCDR3 regions as those of the heavy chain variable region as shown in SEQ ID NO: 10, and the light chain variable region comprising the same LCDR1, LCDR2 and LCDR3 regions as those of the light chain variable region as shown in SEQ ID NO: 11; or
ah) the heavy chain variable region comprising the same HCDR1, HCDR2 and HCDR3 regions as those of the heavy chain variable region as shown in SEQ ID NO: 12, and the light chain variable region comprising the same LCDR1, LCDR2 and LCDR3 regions as those of the light chain variable region as shown in SEQ ID NO: 13.
In some embodiments of the anti-GCGR monoclonal antibody or antigen-binding fragment thereof, wherein the antigen-binding fragment is selected from the group consisting of Fab, Fab′, F(ab′)2, single-chain antibody, dimerized V region (diabody) and disulfide-stabilized V region (dsFv).
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof is characterized in that it competes with the monoclonal antibody or antigen-binding fragment thereof mentioned above for binding to human GCGR (or its epitope).
In some embodiments, the anti-GCGR monoclonal antibody or antigen-binding fragment thereof has at least one of the following features:
i. Antagonistic activity of blocking human GCGR to bind to human glucagon at an IC50 value of less than 500 nM, less than 450 nM, less than 400 nM, less than 350 nM, or less than 300 nM (preferably less than 300 nM);
ii. Antagonistic activity of blocking cynomolgus monkey or rhesus monkey GCGR to bind to cynomolgus monkey or rhesus monkey glucagon;
iii. Inhibition of the increase of human blood glucose concentration; and
iv. Antagonistic activity of blocking mouse GCGR to bind to mouse glucagon.
In some embodiments of the anti-GCGR monoclonal antibody or antigen-binding fragment thereof, wherein the monoclonal antibody or antigen-binding fragment thereof binds to the same antigen epitope as that of the monoclonal antibody or antigen-binding fragment thereof mentioned above.
In another aspect, the present disclosure provides a bispecific protein. In some embodiments, the bispecific protein provided herein comprises a GLP-1 peptide and a GCGR antibody, and the GLP-1 peptide is covalently linked to the polypeptide chain of the GCGR antibody via a peptide bond or a linker.
In some embodiments of the bispecific protein, wherein the carboxyl terminus of the GLP-1 peptide is linked to the amino terminus of the heavy chain variable region of the GCGR antibody via a peptide bond or a linker, or the carboxyl terminus of the GLP-1 peptide is linked to the amino terminus of the light chain variable region of the GCGR antibody via a peptide bond or a linker.
In some embodiments of the bispecific protein, the carboxyl terminus of the GLP-1 peptide is linked to the amino terminus of the heavy chain variable region of the GCGR antibody via a peptide bond or a linker.
In some embodiments of the bispecific protein, the carboxyl terminus of the GLP-1 peptide is linked to the amino terminus of the light chain variable region of the GCGR antibody via a peptide bond or a linker.
In some embodiments of the bispecific protein, the carboxyl terminus of the GLP-1 peptide is linked to the amino terminus of the heavy chain of the full-length GCGR antibody via a peptide bond or a linker.
In some embodiments of the bispecific protein, the carboxyl terminus of the GLP-1 peptide is linked to the amino terminus of the light chain of the full-length GCGR antibody via a peptide bond or a linker.
In some embodiments of the bispecific protein, the GCGR antibody is selected from the anti-GCGR monoclonal antibodies or antigen-binding fragments thereof mentioned above.
In some embodiments of the bispecific protein, the GLP-1 peptide is GLP-1A as shown in SEQ ID NO: 91, or the GLP-1 peptide is a GLP-1A peptide variant having one or more amino acid substitutions of Q17E, I23V, K28R and G30R based on GLP-1A.
In some embodiments of the bispecific protein, the GLP-1 peptide is GLP-1A as shown in SEQ ID NO: 91, or the GLP-1 peptide is a GLP-1A peptide variant having Q17E based on GLP-1A.
In some embodiments of the bispecific protein, the GLP-1 peptide is GLP-1A as shown in SEQ ID NO: 91, or the GLP-1 peptide is a GLP-1A peptide variant having Q17E and one or more amino acid substitutions of I23V, K28R and G30R based on GLP-1A.
In some embodiments of the bispecific protein, the GLP-1 peptide is GLP-1A as shown in SEQ ID NO: 91, or the GLP-1 peptide is a GLP-1A peptide variant having Q17E or both Q17E and I23V based on GLP-1A.
In some embodiments of the bispecific protein, the GLP-1A peptide variant comprises or consists of the sequence as shown in SEQ ID NO: 92, 93, 94, 95, 96, 97, 98 or 99.
In some embodiments of the bispecific protein, the GCGR antibody is selected from any one of the anti-GCGR monoclonal antibodies or antigen-binding fragments thereof mentioned above, and the GLP-1A peptide or GLP-1A peptide variant is any one as described above.
In some embodiments, the bispecific protein comprises a first polypeptide chain and a second polypeptide chain, wherein the first polypeptide chain is a polypeptide selected from the group consisting of SEQ ID NO: 100, 101, 102, 103, 104, 105, 106, 107 and 108, and the second polypeptide chain is a polypeptide as shown in SEQ ID NO: 79.
In some embodiments, the bispecific protein comprises a first polypeptide chain comprising the GCGR antibody heavy chain and a second polypeptide chain comprising the GCGR antibody light chain, wherein: the first polypeptide chain is a polypeptide as shown in SEQ ID NO: 109, and the second polypeptide chain is a polypeptide as shown in SEQ ID NO: 81;
In some embodiments, the bispecific protein comprises a first polypeptide chain comprising the GCGR antibody heavy chain and a second polypeptide chain comprising the GCGR antibody light chain, wherein: the first polypeptide chain is a polypeptide as shown in SEQ ID NO: 110, and the second polypeptide chain is a polypeptide as shown in SEQ ID NO: 83;
In some embodiments, the bispecific protein comprises a first polypeptide chain comprising the GCGR antibody heavy chain and a second polypeptide chain comprising the GCGR antibody light chain, wherein: the first polypeptide chain is a polypeptide as shown in SEQ ID NO: 111, and the second polypeptide chain is a polypeptide as shown in SEQ ID NO: 85;
In some embodiments, the bispecific protein comprises a first polypeptide chain comprising the GCGR antibody heavy chain and a second polypeptide chain comprising the GCGR antibody light chain, wherein: the first polypeptide chain is a polypeptide as shown in SEQ ID NO: 112, and the second polypeptide chain is a polypeptide as shown in SEQ ID NO: 87; or
In some embodiments, the bispecific protein comprises a first polypeptide chain comprising the GCGR antibody heavy chain and a second polypeptide chain comprising the GCGR antibody light chain, wherein: the first polypeptide chain is a polypeptide as shown in SEQ ID NO: 113, and the second polypeptide chain is a polypeptide as shown in SEQ ID NO: 89.
In another aspect, the present disclosure also provides a GLP-1 peptide variant. In some embodiments, the GLP-1 peptide variant is a mutant having one or more amino acid mutation(s) of Q17E, I23V, K28R and G30R based on GLP-1A as shown in SEQ ID NO:91.
In some embodiments, the GLP-1 peptide is GLP-1A as shown in SEQ ID NO: 91, or the GLP-1 peptide is a GLP-1A peptide variant having Q17E or both Q17E and I23V based on GLP-1A.
In some embodiments, the GLP-1 peptide variant has a sequence as shown in SEQ ID NO: 92, 93, 94, 95, 96, 97, 98 or 99.
The present disclosure also provides a pharmaceutical composition, comprising a therapeutically effective amount of the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above, or the bispecific protein as described above, or the GLP-1 peptide variant as described above, and one or more pharmaceutically acceptable carriers, diluents, buffers or excipients.
The present disclosure also provides an isolated nucleic acid molecule, which encodes the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above, or the bispecific protein as described above, or the GLP-1 peptide variant as described above.
The present disclosure provides a recombinant vector comprising the isolated nucleic acid molecule as described above.
The present disclosure provides a host cell transformed with the recombinant vector as described above, said host cell being selected from prokaryotic cells and eukaryotic cells, preferably eukaryotic cells, more preferably mammalian cells or insect cells.
The present disclosure provides a method for producing the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above, or the bispecific protein as described above, or the GLP-1 peptide variant as described above, the method comprising culturing the host cell as described above in a culture medium to generate and accumulate the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above, or the bispecific protein as described above, or the GLP-1 peptide variant as described above, and recovering the monoclonal antibody or antigen-binding fragment thereof or the bispecific protein or the GLP-1 peptide variant from the culture.
The present disclosure provides a method for detecting or measuring human GCGR in vitro, the method comprising using the monoclonal antibody or antigen-binding fragment thereof as described above.
A kit for detecting human GCGR, comprises the monoclonal antibody or antigen-binding fragment thereof as described above.
According to some embodiments, it also provides use of the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above in the preparation of medical devices (such as kits, arrays, test papers, multi-well plates, magnetic beads, coated particles), the medical device comprising the monoclonal antibody or antigen-binding fragment thereof as described above. As an example, the kit includes a multi-well plate coated with the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above.
The present disclosure provides use of the monoclonal antibody or antigen-binding fragment thereof as described above in the preparation of a reagent for detecting or measuring human GCGR.
The present disclosure provides a method for lowering the blood glucose concentration in a subject, the method comprising administering to the subject a therapeutically effective amount of the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above, or the bispecific protein as described above, or the GLP-1 peptide variant as described above, or the pharmaceutical composition as described above.
Preferably, the therapeutically effective amount is 0.1 to 3000 mg of the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above, or the bispecific protein as described above, or the GLP-1 peptide variant as described above in a unit dose of the composition.
The present disclosure provides a method for the treatment of a metabolic disorder, the method comprising administering to a subject the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above, or the bispecific protein as described above, or the GLP-1 peptide variant as described above, or the pharmaceutical composition as described above; preferably, the metabolic disorder is metabolic syndrome, obesity, impaired glucose tolerance, diabetes, diabetic ketoacidosis, hyperglycemia, hyperglycemic hyperosmolar syndrome, perioperative hyperglycemia, hyperinsulinemia, insulin resistance syndrome, impaired fasting glucose, dyslipidemia, atherosclerosis or prediabetic condition.
The present disclosure also provides a use of the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above, or the bispecific protein as described above, or the GLP-1 peptide variant as described above, or the pharmaceutical composition as described above in the preparation of a medicament for the treatment of a metabolic disorder or for lowering the blood glucose concentration in a subject;
Preferably, the metabolic disorder is metabolic syndrome, obesity, impaired glucose tolerance, diabetes, diabetic ketoacidosis, hyperglycemia, hyperglycemic hyperosmolar syndrome, perioperative hyperglycemia, hyperinsulinemia, insulin resistance syndrome, impaired fasting glucose, dyslipidemia, atherosclerosis or prediabetic condition.
The present disclosure also provides the anti-GCGR monoclonal antibody or antigen-binding fragment thereof as described above, or the bispecific protein as described above, or the GLP-1 peptide variant as described above, or the pharmaceutical composition as described above, for use as a medicament, preferably for use as a medicament for the treatment of a metabolic disorder or for lowering the blood glucose concentration in a subject.
More preferably, the metabolic disorder is metabolic syndrome, obesity, impaired glucose tolerance, diabetes, diabetic ketoacidosis, hyperglycemia, hyperglycemic hyperosmolar syndrome, perioperative hyperglycemia, hyperinsulinemia, insulin resistance syndrome, impaired fasting glucose, dyslipidemia, atherosclerosis or prediabetic condition.
Three-letter codes and one-letter codes for amino acids used in the present disclosure are as described in J. biol. chem, 243, p 3558(1968).
The term “bispecific protein” refers to a protein molecule capable of binding to two target proteins or target antigens. The bispecific protein used in the present disclosure specifically refers to a protein that is capable of binding to GCGR and GLP-1R (GLP-1 receptor), and is formed by a GLP-1 peptide fused to a polypeptide chain of a GCGR antibody (or antigen-binding fragment thereof).
“GLP-1 peptide” refers to a peptide capable of binding to and activating the GLP-1 receptor. Peptides in the prior art are described in Patent Applications WO2008/071972, WO2008/101017, WO2009/155258, WO2010/096052, WO2010/096142, WO2011/075393, WO2008/152403, WO2010/070251, WO2010/070252, WO2010/070253, WO2010/070255, WO2011/160630, WO2011/006497, WO2011/117415, WO2011/117416, WO2006/134340, WO1997046584, WO2007124461, WO2017100107, WO2007039140, CN1935261A, CN1935846A, WO2006036834, WO2005058958, WO2002046227, WO1999043705, WO1999043708, WO1999043341, CN102949730, CN104293834, CN104327187, WO2015067716, WO2015049651, WO2014096145, WO2014096148, WO2014096150, WO2014096149, the contents of which are all incorporated herein by reference. Some specific GLP-1 peptides, including GLP-1, GLP-1 analogs and GLP-1 receptor peptide agonists, are, for example, Lixisenatide/AVE0010/ZP10/Lyxumia, Exenatide/Exendin-4/Byetta/Bydureon/ITCA 650/AC-2993, liraglutide/Victoza, Semaglutide, Taspoglutide), SyncriaAlbiglutide, Dulaglutide, rExendin-4, CJC-1134-PC, PB-1023, TTP-054, Langlenatide/HM-11260C, CM-3, GLP-1 Eligen, ORMD-0901, NN-9924, NN-9926, NN-9927, Nodexen, Viador-GLP-1, CVX-096, ZYOG-1, ZYD-1, GSK-2374697, DA-3091, MAR-701, MAR709, ZP-2929, ZP-3022, TT-401, BHM-034, MOD-6030, CAM-2036, DA-15864, ARI-2651, ARI-2255, Exenatide-XTEN and Glucagon-Xten. In addition to the above GLP-1 peptides, GLP-1A as shown in SEQ ID NO: 91 and mutants thereof (as shown in SEQ ID NOs: 92-99) of the present disclosure are also included.
GPCR, i.e., G Protein-Coupled Receptor, is a type of transmembrane protein expressed on the cytoplasmic membrane. GPCR is composed of more than 800 members and is the largest membrane protein family in the mammalian genome currently known. In the human body, GPCR proteins are widely distributed in the organs and tissues such as central nervous system, immune system, heart and blood vessels and retina, and are involved in the body development and normal functioning.
The main body of the GPCR protein is composed of seven segments of a trans-cytoplasmic membrane alpha helix structure. The N-terminus and three loops are located outside the cell and are involved in the interaction between the protein and its receptor; the C-terminus and three loops are located within the cell, of which the C-terminus and the third loop plays an important role in the process of intracellular signal transduction mediated by the interaction between the GPCR protein and the downstream G protein.
“GCGR” is a glucagon receptor and a member of the GPCR family. Glucagon mainly accelerates the glycogenolysis, lipolysis and/or gluconeogenesis by activating the downstream pathway upon binding to GCGR, and thereby increasing the level of blood glucose.
The term “antibody (Ab)” includes at least one complementary determining region antigen-binding molecule (or molecule complex) that specifically binds to or interacts with (e.g., recognizes and/or binds to) a specific antigen (or epitope) (e.g., GCGR).
The term “antibody” includes immunoglobulin molecules comprising four polypeptide chains, two heavy (H) chains and two light (L) chains interconnected by disulfide bond(s), and multimers thereof (for example, IgM). Each heavy chain includes a heavy chain variable region (hereinafter abbreviated as HCVR or VH) and a heavy chain constant region (CH). This heavy chain constant region comprises three regions (domains), CH1, CH2, and CH3. Each light chain includes a light chain variable region (hereinafter abbreviated as LCVR or VL) and a light chain constant region (CL). The VH and VL regions can be further subdivided into hypervariable regions, named as complementarity determining regions (CDRs), among which interspersed with more conservative regions, named as framework regions (FRs, also named as frameworks). Each VH and VL is composed of three CDRs and four FRs, arranged from the amino terminus to the carboxyl terminus in the following order: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4.
In various embodiments of the present disclosure, the FRs of the anti-GCGR antibody (or antigen-binding fragment thereof) can be the same as those of the human germline sequence, or can be modified naturally or artificially. The antibodies can be different subclasses of antibodies, for example, IgG (e.g., IgG1, IgG2, IgG3, or IgG4 subclass), IgA1, IgA2, IgD, IgE or IgM antibody.
The term “antibody” also encompasses antigen-binding fragments of a full-length antibody molecule.
The terms “antigen-binding portion”, “antigen-binding domain”, “antigen-binding fragment” of an antibody and the like, as used herein, include any naturally occurring, enzymatically produced, synthetically or genetically engineered polypeptide or glycoprotein that specifically binds to an antigen to form a complex. Antigen-binding fragments of an antibody can be derived from, for example, a complete antibody molecule by using any suitable standard techniques, such as proteolytic digestion or recombinant genetic engineering technique involving manipulation and expression of DNAs encoding the antibody variable regions and (optionally) constant regions. The DNAs are known and/or can be easily obtained from, for example, commercially available sources, DNA database (including, for example, phage-antibody database), or can be synthesized. The DNAs can be sequenced and manipulated chemically or by molecular biotechnology, for example, arranging one or more variable and/or constant regions into a suitable configuration, introducing codons, generating cysteine residues, modifying, adding or deleting amino acids, etc.
Non-limiting examples of antigen-binding fragments include: (i) Fab fragment; (ii) F(ab′) 2 fragments; (iii) Fd fragments; (iv) Fv fragments; (v) single-chain Fv (scFv) molecules; and (vi) dAb fragments. Other engineered molecules, such as region-specific antibodies, single-domain antibodies, region-deleted antibodies, chimeric antibodies, diabodies, tribodies, tetrabodies, minibodies, nanobodies (e.g. monovalent nanobodies, bivalent nanobodies, etc.), Small Modular Immunopharmaceuticals (SMIP) and Shark Variable IgNAR Regions are also included in the term “antigen-binding fragment” as used herein.
The antigen-binding fragment will typically contain at least one variable region. The variable region can be a region of any size or amino acid composition and will generally comprise one or more CDRs adjacent to or within the framework sequences.
In some embodiments, the antigen-binding fragment of an antibody can be in any configuration of variable region and constant region, the variable region and the constant region can be connected to each other directly or through a complete or partial hinge or a linker region. The hinge region can be composed of at least 2 (for example, 5, 10, 15, 20, 40, 60 or more) amino acids, which allows a flexible and semi-flexible connection generated between the adjacent variable and/or constant region within a single polypeptide molecule.
“Murine antibody” as used herein refers to mouse- or rat-derived monoclonal antibodies prepared according to the knowledge and skills in the art. During the preparation, test subjects are injected with an antigen, and then a hybridoma expressing the antibody which possesses desired sequence or functional characteristics is isolated. When the injected test subjects are mice, the resulting antibody is a mouse-derived antibody, and when the injected test subjects are rats, the resulting antibody is a rat-derived antibody.
A “chimeric antibody” is an antibody formed by fusing antibody variable region(s) of a first species (such as mouse) to antibody constant region(s) of a second species (such as human). To establish a chimeric antibody, it is necessary to establish a hybridoma that secretes a monoclonal antibody of the first species (such as mouse), to clone the variable region(s) gene from the hybridoma cell, and then to clone the constant region gene(s) of an antibody of the second species (such as human) as needed. The variable region gene(s) of the first species is (are) connected to the constant region gene(s) of the second species to form a chimeric gene, which is then inserted into an expression vector, and finally the chimeric antibody molecule is expressed in a eukaryotic or a prokaryotic system.
In a preferable embodiment of the present disclosure, the antibody light chain of the chimeric antibody further comprises a light chain constant region of a human kappa, lambda chain or a variant thereof. The antibody heavy chain of the chimeric antibody further comprises a heavy chain constant region of human IgG1, IgG2, IgG3, IgG4 or a variant thereof, preferably comprises a heavy chain constant region of human IgG1, IgG2 or IgG4, or comprises a heavy chain constant region variant of human IgG1, IgG2 or IgG4 with amino acid mutation(s) (such as YTE mutation or back mutation, L234A and/or L235A mutation, or S228P mutation).
The term “humanized antibody”, including CDR-grafted antibody, refers to an antibody generated by grafting animal-derived antibody, e.g., murine antibody CDR sequences into human antibody variable region frameworks (i.e., framework regions). Humanized antibodies can avoid heterologous responses induced by chimeric antibodies which carry a large number of heterologous protein components. Such framework sequences can be obtained from public DNA database covering germline antibody gene sequences or published references. For example, germline DNA sequences of human heavy and light chain variable region genes can be found in “VBase” human germline sequence database (available on http://www.vbase2.org/), as well as in Kabat, E. A., et al. 1991 Sequences of Proteins of Immunological Interest, 5th Ed.
To avoid a decrease in activity caused by the decreased immunogenicity, the framework sequences in human antibody variable region can be subjected to minimal reverse mutations or back mutations to maintain the activity. The humanized antibodies of the present disclosure also comprise humanized antibodies on which CDR affinity maturation is performed by phage display.
Due to the residues contacted with an antigen, the grafting of CDR can result in a decreased affinity of an antibody or antigen binding fragment thereof to the antigen due to the framework residues contacted with the antigen. Such interactions can be resulted from highly somatic mutations. Therefore, it may still be necessary to graft the donor framework amino acids onto the humanized antibody frameworks. The amino acid residues involved in antigen binding and derived from non-human antibody or antigen binding fragment thereof can be identified by checking the sequence and structure of animal monoclonal antibody variable region. The donor CDR framework amino acid residues which are different from the germ lines can be considered as being related. If it is not possible to determine the most closely related germ line, the sequence can be compared to the common sequence shared by subtypes or the animal antibody sequence with high similarity percentage. Rare framework residues are thought to be the result of a high mutation in somatic cells, and play an important role in binding.
In an embodiment of the present disclosure, the antibody or antigen-binding fragment thereof may further comprise a light chain constant region of human or murine λ chain or variant thereof, or further comprises a heavy chain constant region of human or murine IgG1, IgG2, IgG3, IgG4 or variant thereof.
The “conventional variants” of the human antibody heavy chain constant region and the human antibody light chain constant region refer to the human heavy or light chain constant region variants disclosed in the prior art which do not change the structure and function of the antibody variable regions. Exemplary variants include IgG1, IgG2, IgG3 or IgG4 heavy chain constant region variants by site-directed modification and amino acid substitutions on the heavy chain constant region. The specific substitutions are, for example, YTE mutation, L234A and/or L235A mutations, S228P mutation, or mutations resulting in a knob-into-hole structure (making the antibody heavy chain form a combination of knob-Fc and hole-Fc), etc. These mutations have been proven to confer the antibody with new properties, without changing the function of the antibody variable region.
“Human antibody” and “antibody derived from human” can be used interchangeably, and can be antibodies derived from human or antibodies obtained from a transgenic organism which has been “engineered” and produced by any method known in the art to produce specific human antibodies in response to antigen stimulation. In some technologies, elements of human heavy and light chain loci are introduced into organism cell strains derived from embryonic stem cell lines, in which the endogenous heavy and light chain loci are targeted for disruption. Transgenic organisms can synthesize human antibodies specific for human antigens, and the organisms can be used to produce hybridomas that secrete human antibodies. A human antibody can also be such antibody in which the heavy and light chains are encoded by nucleotide sequences derived from one or more human DNA sources. Fully human antibodies can also be constructed by gene or chromosome transfection methods and phage display technology, or constructed from B cells activated in vitro, all of which are known in the art.
“Monoclonal antibody” refers to an antibody obtained from a population of substantially homogeneous antibodies, that is, the individual antibodies constituting the population are identical and/or bind to the same epitope, except for possible variant antibodies (for example, variants having naturally occurring mutations or mutations produced during the manufacture of monoclonal antibody preparations, and the mutations are usually present in minimal amounts). Unlike polyclonal antibody preparations that usually contain different antibodies directed against different determinants (epitopes), each monoclonal antibody of a monoclonal antibody preparation (formulation) is directed against a single determinant on the antigen. Therefore, the modifier “monoclonal” indicates the characteristics of the antibody obtained from a substantially homogeneous antibody population, and should not be interpreted as requiring any specific method to manufacture the antibody. For example, monoclonal antibodies used in accordance with the present disclosure can be prepared by various techniques, including but not limited to hybridoma methods, recombinant DNA methods, phage display methods, and methods by using transgenic animals having all or part of human immunoglobulin loci. Such methods, and other exemplary methods for preparing monoclonal antibodies are described herein. Monoclonal antibodies comprised in the term “monoclonal antibody or antigen-binding fragment thereof” refer to full-length antibodies.
The terms “full-length antibody”, “full antibody”, “whole antibody” and “complete antibody” are used interchangeably herein and refer to an antibody in a substantially complete form, as distinguished from antigen-binding fragments defined below. The term specifically refers to an antibody in which the heavy chain includes the VH region, the CH1 region, the hinge region and the Fc region in the order from the amino terminus to the carboxyl terminus, and the light chain includes the VL region and the CL region in the order from the amino terminus to the carboxyl terminus.
In addition, the VL domain and VH domain of the Fv fragment are encoded by two separate genes, however, they can be linked by a synthetic linker by using recombinant methods, to generate a single protein chain in which a monovalent molecular is formed by pairing the VL and VH domain (referred to as single chain Fv (scFv); see, e.g., Bird et al. (1988): 423-426; Science 242 and Huston et al (1988) Proc. Natl. Acad. Sci USA85:5879-5883). Such single chain antibodies are also intended to be included in the term of “antigen binding fragment” of an antibody. Such antibodies are obtained using conventional techniques known in the field, and are screened for functional fragments by using the same method as that for an intact antibody. Antigen binding portions can be produced by recombinant DNA technology or by enzymatic or chemical disruption of an intact immunoglobulin.
Antigen-binding fragments can also be incorporated into a single-chain molecule comprising a pair of tandem Fv fragments (VH-CH1-VH-CH1), and the pair of tandem Fv fragments form a pair of antigen-binding regions together with complementary light chain polypeptides (Zapata et al., 1995 Protein Eng. 8(10): 1057-1062; and U.S. Pat. No. 5,641,870).
Fab is an antibody fragment obtained by treating an IgG antibody molecule with a papain (which cleaves the amino acid residue at position 224 of the H chain), and the antibody fragment has a molecular weight of about 50,000 and has antigen binding activity, in which about a half of the N-terminal side of H chain and the entire L chain are bound together through disulfide bond(s).
F (ab′)2 is an antibody fragment having molecular weight of about 100,000 Da and having antigen binding activity and comprising two Fab regions which are bound at the hinge position, it can be produced by digesting the part downstream of the two disulfide bonds in the IgG hinge region with pepsin.
Fab′ is an antibody fragment having a molecular weight of about 50,000 Da and having antigen binding activity, which is obtained by cleaving the disulfide bonds at the hinge region of the above-mentioned F (ab′)2. Fab′ can be produced by treating F(ab′)2 that specifically recognizes and binds to an antigen with a reducing agent such as dithiothreitol.
Further, the Fab′ can be produced by inserting DNA encoding Fab′ of the antibody into a prokaryotic expression vector or eukaryotic expression vector and introducing the vector into a prokaryote or eukaryote to express the Fab′.
The term “single chain antibody”, “single chain Fv” or “scFv” refers to a molecule comprising antibody heavy chain variable domain (or region; VH) connected to antibody light chain variable domain (or region; VL) by a linker. Such scFv molecules have general structure of NH2-VL-linker-VH—COOH or NH2-VH-linker-VL-COOH. Suitable linkers in the prior art consist of repeated GGGGS amino acid sequence or a variant thereof, for example, a variant with 1-4 (including 1, 2, 3 or 4) repeats (Holliger et al. (1993), Proc Natl Acad Sci USA. 90: 6444-6448). Other linkers that can be used in the present disclosure are described by Alfthan et al., (1995), Protein Eng. 8:725-731, Choi et al., (2001), Eur J Immuno. 31:94-106, Hu et al., (1996), Cancer Res. 56:3055-3061, Kipriyanov et al., (1999), J Mol Biol. 293:41-56 and Roovers et al., (2001), Cancer Immunol Immunother. 50:51-59.
“Linker” refers to a connecting peptide sequence used to connect protein domains, usually with a certain degree of flexibility, and the use of linkers will not cause the protein domain to lose its original functions.
Diabody is an antibody fragment wherein the scFv is dimerized, and it is an antibody fragment having bivalent antigen binding activity. In the bivalent antigen binding activity, the two antigens can be the same or different.
dsFv is obtained by substituting one amino acid residue in each of VH and VL with a cysteine residue, and then connecting the substituted polypeptides via a disulfide bond between the two cysteine residues. The amino acid residues to be substituted with a cysteine residue can be selected based on three-dimensional structure prediction of the antibody in accordance with known methods (Protein Engineering, 7, 697 (1994)).
In some embodiments of the present disclosure, the antigen-binding fragment can be produced by the following steps: obtaining cDNAs encoding the monoclonal antibody VH and/or VL of the present disclosure that specifically recognizes and binds to the antigen, and cDNAs encoding the other domains as required; constructing DNA encoding the antigen-binding fragment; inserting the DNA into a prokaryotic or eukaryotic expression vector, and then introducing the expression vector into a prokaryote or eukaryote to express the antigen-binding fragment.
“Fc region” can be a naturally occurring sequence or a variant Fc region. The boundaries of the Fc region of an immunoglobulin heavy chain are likely to vary, however, the Fc region of a human IgG heavy chain is usually defined as being extending from the amino acid residue at position Cys226 or from Pro230 to its carboxyl terminus. The numbering of residues in the Fc region is according to the EU index numbering in Kabat. Kabat et al., Sequences of Proteins of Immunological Interest, 5th Edition Public Health Service, National Institutes of Health, Bethesda, Md., 1991. The Fc region of immunoglobulin usually has two constant domains, CH2 and CH3.
“Knob-Fc” refers to a knob-like spatial structure formed by incorporating a point mutation T366W in the Fc region of an antibody. Correspondingly, “hole-Fc” refers to a hole-like spatial structure formed by incorporating point mutations T366S, L368A, and Y407V in the Fc region of an antibody. Knob-Fc and hole-Fc are more likely to form heterodimers due to steric hindrance. In order to further promote the formation of heterodimers, point mutations S354C and Y349C can be introduced into knob-Fc and hole-Fc, respectively, to further promote the formation of heterodimers via disulfide bonds. Meanwhile, in order to eliminate or alleviate the ADCC effect caused by antibody Fc, substitution mutations of 234A and 235A can also be introduced into Fc. In a bispecific antibody, knob-Fc or hole-Fc can be used as either the Fc region of the first polypeptide chain or the Fc region of the second polypeptide chain. For a single bispecific antibody, Fc regions of the first and the second polypeptide chain can not both be knob-Fc or hole-Fc.
The term “amino acid difference” or “amino acid mutation” refers to the amino acid changes or mutations in a protein or polypeptide variant compared to the original protein or polypeptide, comprising one or more amino acid insertions, deletions or substitutions on the basis of the original protein or polypeptide.
“Variable region” of an antibody refers to an antibody light chain variable region (VL) or antibody heavy chain variable region (VH), alone or in combination. As known in the field, each of the heavy and light chain variable regions consists of three complementarity determining regions (CDRs) (also named as hypervariable regions) connected to four framework regions (FRs). The CDRs in each chain are held tightly together by FRs and contribute to the formation of an antigen binding site of the antibody together with the CDRs from the other chain. There are at least two techniques for determining CDRs: (1) a method based on cross-species sequence variability (i.e., Kabat et al. Sequences of Proteins of Immunological Interest, (5th edition, 1991, National Institutes of Health, Bethesda Md.)); and (2) a method based on the crystallographic study of antigen-antibody complexes (Al-Lazikani et al., J. Molec. Biol. 273:927-948 (1997)). As used herein, CDRs may refer to those determined by either of or the combination of the two methods.
The term “antibody framework” or “FR region” refers to a part of the variable domain, either VL or VH, which serves as a scaffold for the antigen binding loops (CDRs) of this variable domain. Essentially, it is a variable domain without CDRs.
The terms “complementary determining region” and “CDR” refer to one of the six hypervariable regions present in the antibody variable domain that mainly contribute to antigen binding. Generally, there are three CDRs (HCDR1, HCDR2, HCDR3) in each heavy chain variable region, and three CDRs (LCDR1, LCDR2, LCDR3) in each light chain variable region. The amino acid sequence boundaries of CDRs can be determined by any of a variety of well-known schemes, including the “Kabat” numbering criteria (see Kabat et al. (1991), “Sequences of Proteins of Immunological Interest”, 5th edition, Public Health Service, National Institutes of Health, Bethesda, Md.), “Chothia” numbering criteria (Al-Lazikani et al., (1997) JMB 273:927-948) and ImmunoGenTics (IMGT) numbering criteria (Lefranc M P, Immunologist, 7, 132-136 (1999); Lefranc, MP, etc., Dev. Comp. Immunol., 27, 55-77 (2003), and the like. For example, for the classical format, following the Kabat criteria, the CDR amino acid residues in the heavy chain variable domain (VH) are numbered as 31-35 (HCDR1), 50-65 (HCDR2) and 95-102 (HCDR3); and the CDR amino acid residues in the light chain variable domain (VL) are numbered as 24-34 (LCDR1), 50-56 (LCDR2), and 89-97 (LCDR3). Following the Chothia criteria, the CDR amino acid residues in VH are numbered as 26-32 (HCDR1), 52-56 (HCDR2) and 95-102 (HCDR3); and the amino acid residues in VL are numbered as 26-32 (LCDR1), 50-52 (LCDR2) and 91-96 (LCDR3). By combining both Kabat and Chothia to define CDRs, the CDRs are composed of amino acid residues 26-35 (HCDR1), 50-65 (HCDR2) and 95-102 (HCDR3) in the human VH and amino acid residues 24-34 (LCDR1), 50-56 (LCDR2) and 89-97 (LCDR3) in the human VL. Following IMGT criteria, the CDR amino acid residues in VH are roughly numbered as 26-35 (CDR1), 51-57 (CDR2) and 93-102 (CDR3), and the CDR amino acid residues in VL are roughly numbered as 27-32 (CDR1), 50-52 (CDR2) and 89-97 (CDR3). Following IMGT criteria, the CDR regions of an antibody can be determined by using IMGT/DomainGap Align Program.
“Any CDR variant thereof” in “HCDR1, HCDR2 and HCDR3 regions or any variant thereof” refers to a variant obtained by subjecting any one, or two, or three of the HCDR1, HCDR2 and HCDR3 regions to amino acid mutations.
“Antibody constant region domain” refers to the domains derived from the antibody light and heavy chain constant regions, comprising CL and CH1, CH2, CH3 and CH4 domains derived from different types of antibodies.
“Epitope” or “antigenic determinant” refers to a site on an antigen to which an immunoglobulin or antibody specifically binds. Epitopes usually include at least 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or 15 consecutive or non-contiguous amino acids in a unique spatial conformation. See, for example, Epitope Mapping Protocols in Methods in Molecular Biology, Vol. 66, GE. Morris, Ed. (1996).
The term “specifically bind to”, “selectively bind to”, “selectively binds to” or “specifically binds to” refers to the binding of an antibody to a predetermined epitope on an antigen. Typically, the antibody binds with an affinity (KD) of less than about 10−8M, for example, less than about 10−9 M, 10−10 M or 10−11M or even less.
When the term “competition” is used in the context of antigen binding proteins (e.g., neutralizing antigen binding proteins or neutralizing antibodies) that compete for the same epitope, it means that competition occurs between the antigen binding proteins, which is determined by the assays wherein an antigen binding protein to be tested (e.g., an antibody or antigen-binding fragment thereof) prevents or inhibits (e.g., reduces) the specific binding of a reference antigen binding protein (e.g., a ligand or reference antibody) to a common antigen. Numerous types of competitive binding assays are available to determine whether an antigen binding protein competes with another. These assays are, for example, solid phase direct or indirect radioimmunoassay (MA), solid phase direct or indirect enzyme immunoassay (EIA), Sandwich competition assay (see, e.g., Stahli et al, 1983, Methods in Enzymology 9: 242-253); solid phase direct biotin-avidin EIA (see, e.g., Kirkland et al, 1986, J. Immunol. 137: 3614-3619), solid phase direct labeling assay, solid phase direct labeling sandwich assay (see, e.g., Harlow and Lane, 1988, Antibodies, A Laboratory Manual, Cold Spring Harbor Press); solid phase direct labeling MA with I-125 label (see, e.g., Morel et al, 1988, Molec. Immunol. 25: 7-15); solid phase direct biotin-avidin EIA (see, e.g., Cheung, et al, 1990, Virology 176: 546-552); and direct labeling MA (Moldenhauer et al, 1990, Scand. J. Immunol. 32: 77-82). Typically, the assay involves the use of a purified antigen capable of binding to both an unlabeled test antigen binding protein and a labeled reference antigen binding protein (the antigen is located on a solid surface or cell surface). Competitive inhibition is determined by measuring the amount of a label bound to the solid surface or to the cell surface in the presence of the test antigen binding protein. Usually, the test antigen binding protein is present in excess. Antigen binding proteins identified by competitive assay (competing with the antigen binding protein) includes: antigen binding proteins that bind to the same epitope as the reference antigen binding protein; and antigen binding proteins that bind to an epitope that is sufficiently close to the epitope to which the reference antigen binding protein binds, where the two epitopes spatially interfere with each other to hinder the binding. Additional details regarding methods for determining competitive binding are provided in the Examples herein. Typically, when a competing antigen binding protein is present in excess, it will inhibit (e.g., reduce) at least 40-45%, 45-50%, 50-55%, 55-60%, 60-65%, 65-70%, 70-75% or 75% or even more of the specific binding of the reference antigen binding protein to the common antigen. In some cases, the binding is inhibited by at least 80-85%, 85-90%, 90-95%, 95-97%, or 97% or even more.
The term “affinity” refers to the strength of the interaction between an antibody and an antigen at a single epitope. Within each antigenic site, the variable region of the antibody “arm” interacts with the antigen at multiple amino acid sites via weak non-covalent forces; the greater the interaction is, the stronger the affinity is. As used herein, the term “high affinity” of an antibody or antigen-binding fragment thereof (e.g., Fab fragment) generally refers to an antibody or antigen-binding fragment with KD of 1E−9M or less (e.g., KD of 1E−10 M or less, KD of 1E−11M or less, KD of 1E−12M or less, KD of 1E−13M or less, KD of 1E−14 M or less, etc.).
The term “KD” or “KD” refers to a dissociation equilibrium constant for particular antibody-antigen interaction. Typically, the antibody binds to an antigen with a dissociation equilibrium constant (KD) of less than about 1E−8M, for example, less than about 1E−9M, 1E−1° M or 1E−11M or even less, for example, as determined by Surface Plasma Resonance (SPR) technology in Biacore instrument. The smaller the KD valuen is, the greater the affinity is.
The term “nucleic acid molecule” refers to DNA molecules and RNA molecules. The nucleic acid molecule can be single-stranded or double-stranded, but preferably is double-stranded DNA. A nucleic acid is “operably linked” when it is placed into a functional relationship with another nucleic acid sequence. For instance, a promoter or enhancer is operably linked to a coding sequence if it affects the transcription of the sequence.
The term “vector” means a construct capable of delivering one or more target genes or sequences, and preferably, expressing them in a host cell. Examples of vectors include, but are not limited to, viral vectors, naked DNA or RNA expression vectors, plasmids, cosmids or phage vectors, DNA or RNA expression vectors associated with cationic coagulants, DNA or RNA expression vectors encapsulated in liposomes, and certain eukaryotic cells such as producer cells.
Methods for producing and purifying antibodies and antigen-binding fragments are well known in the art, for example, A Laboratory Manual for Antibodies, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., chapters 5-8 and 15. For example, mice can be immunized with antigen or fragment thereof, and the resulting antibodies can then be renatured, purified, and sequenced for amino acid sequences by using conventional methods. Antigen-binding fragments can also be prepared by conventional methods. The antibodies or antigen binding fragments of the present disclosure are engineered to incorporate one or more human framework regions onto the CDR regions derived from non-human antibody. Human FR germline sequences can be obtained from website http://imgt.cines.fr, or from The Immunoglobulin Facts Book, 2001, ISBN 012441351, by aligning against IMGT human antibody variable germline gene database and MOE software.
The term “host cell” refers to a cell into which an expression vector has been introduced. Host cells may include bacterial, microbial, plant or animal cells. Bacteria suitable for transformation include members of enterobacteriaceae, such as Escherichia coli or Salmonella strains; Bacillaceae such as Bacillus subtilis; Pneumococcus; Streptococcus and Haemophilus influenzae. Suitable microorganisms include Saccharomyces cerevisiae and Pichia pastoris. Suitable animal host cell lines include CHO (Chinese Hamster Ovary cell line), HEK293 cells (non-limiting examples such as HEK293E cells), and NSO cells.
The engineered antibodies or antigen-binding fragments can be prepared and purified by conventional methods. For example, the cDNA sequences encoding the heavy and light chains can be cloned and recombined into a GS expression vector. The recombinant immunoglobulin expression vector can be stably transfected into CHO cells. As an alternative prior art, mammalian expression systems can lead to glycosylation of antibodies, especially in the highly conserved N-terminal sites of the Fc region. Stable clones were obtained by expressing an antibody specifically binding to an antigen. Positive clones can be expanded in serum-free culture medium in bioreactors for antibody production. Culture medium, into which an antibody has been secreted, can be purified by conventional techniques. For example, purification can be performed on Protein A or Protein G Sepharose FF column comprising modified buffer. The nonspecific binding components are washed out. The bound antibody is eluted by pH gradient and antibody fragments are detected by SDS-PAGE, and then pooled. The antibodies can be filtered and concentrated using common techniques. Soluble mixtures and aggregates can be effectively removed by common techniques, such as size exclusion or ion exchange. The resulting product is needed to be frozen immediately, such as at −70° C., or lyophilized.
“Administration”, “administer”, “dosing” and “treatment”, when applied to animals, humans, experimental subjects, cells, tissues, organs, or biological fluids, refer to administer exogenous pharmaceutical agents, therapeutic agents, diagnostic agents, compositions or artificial manipulations (for example, “euthanasia” as used in the examples) to the animals, humans, subjects, cells, tissues, organs, or biological fluids. “Administration” and “treatment” can refer, e.g., to therapeutic, pharmacokinetic, diagnostic, research, and experimental methods. The treatment of a cell encompasses contacting a reagent with the cell, as well as contacting a reagent with a fluid, where the fluid is in contact with the cell. “Administration” or “treatment” also means in vitro or ex vivo treatments, e.g., of a cell, with a reagent, diagnostic, binding compound, or with another cell. “Treatment”, as it applies to a human, veterinary, or research subject, refers to therapeutic treatment, prophylactic or preventative measures, research and diagnostic applications.
“Treat” means to administer a therapeutic agent, such as a composition comprising any of the compounds of the present disclosure, internally or externally to a subject having (or suspected to have or being susceptible to) one or more disease symptoms for which the agent has known therapeutic activity. Typically, the agent is administered in an amount effectively to alleviate one or more disease symptoms in the subject or population to be treated, by inducing the regression of or inhibiting the progression of such symptom(s) by any clinically measurable degree. The amount of a therapeutic agent that is effective to alleviate any particular disease symptom (also referred to as the “therapeutically effective amount”) may vary according to various factors such as the disease state, age, and body weight of the subject, and the ability of the drug to elicit a desired response in the subject. Whether a disease symptom has been alleviated can be assessed by any clinical measurement typically used by physicians or other skilled healthcare providers to assess the severity or progression status of that symptom. While the embodiment of the present disclosure (e.g., a treatment method or article of manufacture) is not effective in alleviating the target disease symptom(s) in every subject, it shall alleviate the target disease symptom(s) in a statistically significant number of subjects as determined by any statistical test known in the art such as Student's t-test, chi-square test, U-test according to Mann and Whitney, Kruskal-Wallis test (H-test), Jonckheere-Terpstra-test and Wilcoxon-test.
“Amino acid conservative modification” or “amino acid conservative substitution” means that the amino acids in a protein or polypeptide are substituted by other amino acids with similar characteristics (such as charge, side chain size, hydrophobicity/hydrophilicity, backbone conformation and rigidity, etc.), such that the changes can frequently be performed without altering the biological activity or other required characteristics (such as affinity and/or specificity to an antigen) of the protein or polypeptide. Those skilled in the art recognize that, in general, a single amino acid substitution in non-essential regions of a polypeptide does not substantially alter the biological activity (see, e.g., Watson et al. (1987) Molecular Biology of the Gene, The Benjamin/Cummings Pub. Co., p. 224 (4th Ed.)). In addition, substitutions with structurally or functionally similar amino acids are less likely to disrupt biological activity. Exemplary Amino Acid Conservative Substitutions are as follows:
“Effective amount” or “effective dose” refers to the amount of a medicament, compound, or pharmaceutical composition necessary to obtain any one or more beneficial or desired results. For prophylactic applications, beneficial or desired results include elimination or reduction of risk, reduction of severity, or delay of the onset of the disease, including the biochemical, histological, and behavioral manifestations of the condition, its complications, and intermediate pathological phenotypes during the development of the condition. For therapeutic applications, beneficial or desired results include clinical results, such as reduction of the incidence of various conditions associated with target antigen of the present disclosure or improvement of one or more symptoms of the condition, reduction of the dosage of other agents required to treat the condition, enhancement of the efficacy of another agent, and/or delay of the progression of the condition associated with the target antigen of the present disclosure in subjects.
“Exogenous” refers to substances produced outside organisms, cells, or humans according to circumstances.
“Endogenous” refers to substances produced in cells, organisms, or human bodies according to circumstances.
“Homology” and “identity” are interchangeable herein and refer to the sequence similarity between two polynucleotide sequences or between two polypeptide sequences.
When a position in both of the two sequences to be compared is occupied by the same base or amino acid monomer subunit, e.g., if a position in each of two DNA molecules is occupied by adenine, then the molecules are homologous at that position. The percentage of homology between two sequences is a function of the number of matching or homologous positions shared by the two sequences divided by the number of positions to be compared and then multiplied by 100. For example, when two sequences are optimally aligned, if 6 out of 10 positions in the two sequences are matched or homologous, then the two sequences are 60% homologous; if 95 out of 100 positions in the two sequences are matched or homologous, then the two sequences are 95% homologous. Generally, when two sequences are aligned, comparison is performed to give the maximum homology percentage. For example, the comparison can be performed by BLAST algorithm, in which the parameters of the algorithm are selected to give the maximum match between each sequence over the entire length of each reference sequence.
The following references relate to the BLAST algorithm frequently used for sequence analysis: BLAST algorithm (BLAST ALGORITHMS): Altschul, S F et al., (1990) J. Mol. Biol. 215:403-410; Gish, W. et al., (1993) Nature Genet. 3:266-272; Madden, T. L. et al., (1996) Meth. Enzymol. 266:131-141; Altschul, S. F. et al., (1997) Nucleic Acids Res. 25:3389-3402; Zhang, J. et al. (1997) Genome Res. 7:649-656. Other conventional BLAST algorithms such as those available from NCBI BLAST are also well known to those skilled in the art.
“Isolated” refers to a state of “being separated from its original environment”, and in this case means that the indicated molecule is essentially free of other non-target biomolecules. In general, the term “isolated” is not intended to mean the complete absence of these materials or the absence of water, buffers or salts, unless they are present in an amount that significantly interferes with the experimental or therapeutic use of the compound as described herein.
“Optional” or “optionally” means that the event or circumstance that follows may but does not necessarily occur, and the description includes the instances in which the event or circumstance does or does not occur.
“Pharmaceutical composition” refers to a mixture comprising one or more compounds according to the present disclosure or a physiologically/pharmaceutically acceptable salt or produg thereof and other chemical components, such as physiologically/pharmaceutically acceptable carriers and excipients. The pharmaceutical composition aims at promoting the administration to an organism, facilitating the absorption of the active ingredient and thereby exerting a biological effect.
The term “pharmaceutically acceptable carrier” refers to any inactive substance suitable for use in a formulation for the delivery of antibodies or antigen-binding fragments. The carrier can be an anti-adhesive agent, adhesive agent, coating agent, disintegrating agent, filler or diluent, preservative (such as antioxidant, antibacterial or antifungal agent), sweetener, absorption delaying agent, wetting agent, emulsifier, buffer, and the like. Examples of suitable pharmaceutically acceptable carriers include water, ethanol, polyol (such as glycerol, propylene glycol, polyethylene glycol, and the like) dextrose, vegetable oil (such as olive oil), saline, buffer, buffered saline, and isotonic agent, such as sugars, polyol, sorbitol and sodium chloride.
Specific examples of the term “metabolic disorder” are metabolic syndrome, obesity, impaired glucose tolerance, diabetes, diabetic ketoacidosis, hyperglycemia, hyperglycemic hyperosmolar syndrome, perioperative hyperglycemia, hyperinsulinemia, insulin resistance syndrome, impaired fasting glucose, dyslipidemia, atherosclerosis, and prediabetic condition.
In addition, another aspect of the present disclosure relates to methods for immunodetection or determination of target antigens, reagents for immunodetection or determination of target antigens, methods for immunodetection or determination of cells expressing target antigens, and the diagnostic agents for diagnosing diseases associated with target antigen-positive cells, comprising the monoclonal antibodies or antibody fragments of the present disclosure that specifically recognize and bind to the target antigen as active ingredients.
In the present disclosure, the method for detecting or measuring the amount of the target antigen can be any known method. For example, it includes immunoassay or immunodetection method.
The immunoassay or immunodetection method is a method of detecting or measuring the amount of an antibody or antigen with a labeled antigen or antibody. Examples of immunoassay or immunodetection methods include radioactive substance-labeled immunoantibody method (RIA), enzyme immunoassay (EIA or ELISA), fluorescence immunoassay (FIA), luminescence immunoassay, western blotting, physicochemical method, and the like.
The above-mentioned diseases related to the target antigen-positive cells can be diagnosed by detecting or measuring the target antigen-expressing cells using the antibodies or antibody fragments of the present disclosure.
Cells expressing the polypeptide can be detected by the known immunodetection methods, preferably by immunoprecipitation, fluorescent cell staining, immunotissue staining, and the like. In addition, the method such as fluorescent antibody staining method with the FMAT8100HTS system (Applied Biosystem) can be used.
In the present disclosure, living samples to be detected or measured for the target antigen are not particularly limited, as long as they are possible to contain cells expressing the target antigen, for example, tissue cells, blood, plasma, serum, pancreatic juice, urine, faeces, tissue fluid or culture medium.
Dependent on the required diagnostic method, the diagnostic agent comprising the monoclonal antibody or antibody fragment thereof of the present disclosure may also contain reagents for performing an antigen-antibody reaction or reagents for detecting the reaction. The reagents for performing an antigen-antibody reaction include buffers, salts and the like. The reagents for detection include agents commonly used in immunoassay or immunodetection methods, for example, a labeled secondary antibody that recognizes the monoclonal antibody, antibody fragment or conjugate thereof, and a substrate corresponding to the label.
The details of one or more embodiments of the present disclosure are set forth in the above specification. The preferred methods and materials are described below, although any method and material similar or identical to those described herein can be used in the practice or testing of the present disclosure. Through the specification and claims, other features, purposes and advantages of the present disclosure will become apparent. In the specification and claims, the singular forms include plural aspects unless the context clearly indicates otherwise. Unless otherwise defined explicitly herein, all technical and scientific terms used herein have the meaning commonly understood by those skilled in the art to which this disclosure belongs. All patents and publications cited in the specification are incorporated by reference. The following examples are presented to further illustrate the preferred embodiments of the present disclosure. These examples should not be construed as limiting the scope of the present disclosure in any way, and the scope of the present disclosure is defined by the claims.
1.1 Construction and Screening of Antigens
The human GCGR cDNA encoding the full-length glucagon receptor of 477 amino acids was subcloned into an expression vector (such as pcDNA3.1) and was transfected into CHO-K1 cells. After screening and single cell cloning, single clones were selected for the study of the characteristics of antigen expression and receptor-based expression on cell surface. The following GCGR antigens refer to human GCGR, unless specifically indicated.
Full-length GCGR: used for the construction of GCGR-overexpressing cell lines, or used as antigens for the immunization and for subsequent detection:
1.2 Purification of GCGR Hybridomas and Recombinant Antibodies
(1) Isolation and purification of hybridoma supernatant/Protein G affinity chromatography:
For the purification of mouse hybridoma supernatant, Protein G affinity chromatography performed was preferable. The harvested hybridoma culture was centrifuged and the supernatant was taken, and based on the volume of the supernatant, 10-15% volume of 1M Tris-HCl (pH 8.0-8.5) was added to adjust pH of the supernatant. The Protein G column was washed with 3-5× column volume of 6M guanidine hydrochloride, and then washed with 3-5× column volume of pure water; the column was equilibrated with 3-5× column volume of equilibrium buffer such as 1×PBS (pH7.4) buffer system; the cell supernatant was loaded at a low flow rate for binding, and the flow rate was controlled so that the retention time was about 1 min or longer; the column was washed with 3-5× column volume of 1×PBS (pH 7.4) until the UV absorption dropped to the baseline; The samples were eluted with 0.1M acetic acid/sodium acetate (pH3.0) buffer, the elution peaks were pooled according to UV detection. The eluted product was temporarily preserved after the pH was adjusted to 5-6 with 1M Tris-HCl (pH8.0). The eluted product can be subjected to solution replacement according to methods well-known to those skilled in the art, for example, replacing the solution with a desired buffer system by ultrafiltration-concentration with an ultrafiltration tube, or replacing the solution with a desired buffer system by using molecular exclusion such as G-25 desalting, or removing the aggregation components from the eluted product to improve the purity of the sample by using high-resolution molecular exclusion column such as Superdex 200.
(2) Extraction of Fc Tagged Bispecific Proteins or Antibodies by Protein a Affinity Chromatography:
First, the cell culture supernatant expressing containing the Fc bispecific protein or the antibody was centrifuged at a high speed to collect the supernatant. The Protein A affinity column was washed with 3-5× column volume of 6M guanidine hydrochloride, and then washed with 3-5× column volume of pure water. The column was equilibrated with 3-5× column volume of 1×PBS (pH7.4) buffer system as equilibrium buffer. The cell supernatant was loaded at a low flow rate for binding, and the flow rate was controlled so that the retention time was about 1 min or longer; after the binding was finished, the column was washed with 3-5× column volume of 1×PBS (pH 7.4) until the UV absorption dropped to the baseline The samples were eluted with 0.1M acetic acid/sodium acetate (pH3.0-3.5) buffer, the elution peak was pooled according to UV detection. The eluted product was temporarily preserved after the pH was adjusted to 5-6 with 1M Tris-HCl (pH8.0). The eluted product can be subjected to solution replacement according to methods well-known to those skilled in the art, for example, replacing the solution with a desired buffer system by ultrafiltration-concentration with an ultrafiltration tube, or replacing the solution with a desired buffer system by using molecular exclusion such as G-25 desalting, or removing the aggregation components from the eluted product to improve the purity of the sample by using high-resolution molecular exclusion column such as Superdex 200.
2.1 Immunization
(1) Mouse immunization: The anti-human GCGR monoclonal antibodies were produced by immunizing mice. SJL white mice, female, 6-8 weeks old were used for experiment (Beijing Charles River Experimental Animal Technology Co., Ltd., animal production license number: SOCK (Jing) 2012-0001). Feeding environment: SPF level. After the mice were purchased, they were adapted to the laboratory environment for 1 week, 12/12 hours light/dark cycle, at temperature of 20-25° C.; humidity of 40-60%. Then, the mice that had been adapted to the environment were immunized according to the following schemes. The antigen for immunization was CHO-K1 cells stably transfected with GCGR.
Immunization scheme: Mice were pre-immunized with the adjuvant, TiterMax® Gold Adjuvant (Sigma Cat No. T2684), by intraperitoneal injection (i.p.), 0.1 ml/mouse (first immunization). 15 min later, mice were intraperitoneally injected (i.p.) with GCGR CHO-K1 stably transfected cells, 1E7 cells per mouse. The vaccination times were on days 0, 14, 28, 42, 56, 70, 84, 98 and 112. Blood samples were collected on days 35, 63 and 91, the antibody titers in mouse serum were determined by ELISA method. After 6 to 9 immunizations, mice with a high serum antibody titer that was tending to the plateau were selected for splenocyte fusion. Three days before the splenocyte fusion, GCGR CHO-K1 stably transfected cells were injected intraperitoneally (i.p.) at 1E7 cells per mouse for booster immunization.
(2) Rat immunization: 6-8 weeks old SD rats were immunized with DNA (encoding full-length hGCGR, the coding sequence can be found in Genbank accession number: NM_000160), and the antibody titers in rat serum were determined by FACS method. After 3 to 4 immunizations, rats with a high serum antibody titer that was tending to the plateau were selected for splenocyte fusion. Booster immunization was performed 3 days before the splenocyte fusion.
2.2 Splenocyte Fusion
Hybridoma cells were obtained by fusing splenic lymphocytes with myeloma Sp2/0 cells (ATCC® CRL8287™) by using an optimized PEG-mediated fusion procedure. The fused hybridoma cells were resuspended in complete medium (IMEM medium comprising 20% FBS, 1×HAT, 1×OPI) at a density of 0.5-1E6/ml, seeded in a 96-well plate with 100 μl/well, incubated at 37° C. and 5% CO2 for 3-4 days, supplemented with 100 μl/well of HAT complete medium, and continued to be cultured for 3-4 days until clones formed. The supernatant was removed, 200 μl/well of HT complete medium (IMDM medium comprising 20% FBS, 1×HT and 1×OPI) was added to each well, incubated at 37° C., 5% CO2 for 3 days and then subjected to ELISA detection.
2.3 Screening of Hybridoma Cells
According to the growth density of hybridoma cells, the hybridoma culture supernatant was detected by cell-binding ELISA method. Cells in the wells that tested with positive were timely expanded, cryopreserved, and subcloned 2 to 3 times until a single cell clone was obtained.
Cells after each subcloning were also tested by GCGR cell binding ELISA. The hybridoma clones were screened by the assay. The antibodies were further prepared by serum-free cell culture method. The antibodies were purified according to the example of purification described in the test examples.
2.4 Sequencing of the Positive Hybridoma Clones
The procedures of cloning the sequences from the positive hybridoma were as follows. Hybridoma cells in logarithmic growth phase were collected. RNAs were extracted with Trizol (Invitrogen, Cat No. 15596-018) according to the kit's instruction and were reversely transcribed with PrimeScript™ Reverse Transcription kit (Takara, Cat No. 2680A). The cDNAs resulting from reverse transcription were amplified by PCR using mouse Ig-Primer Set (Novagen, TB326 Rev. B 0503), and were sequenced after PCR amplification.
The positive clones were obtained from the resulting DNA sequences, and the antibodies were prepared by the serum-free cell culture method. The antibodies were purified according to the purification example, and were subjected to several rounds of screening by using the cell-based GCGR binding blocking assay, thereby the murine hybridoma clones 1803, 1805, 1808, and 1810, and rat hybridoma clones 1817 and 1822 were obtained.
DYWIE
RASQDIS
NYLN
EILPGST
YSSTLHS
YTNYNEK
FKG
GLSTLMA
QQTNIFP
VDYFDY
WT
DYNMD
RASQSI
SDYLH
SID
YASQSIS
PDNG
GTIYNQK
FKG
DYYGSSS
QNGHSFP
WFAY
YT
TNGIS
RASQDIS
NYLN
EIYPRSG
YSSTLHS
NTYYNEN
FKG
SITSVIG
QQGNTFP
ADYFDY
WT
NYAIS
RASLDIS
NYLN
EIYPTSG
YTSTLHS
NTYYNEK
FKG
GVITTVV
QQGNMVP
STDYFDY
YT
SISTGGV
ADVQRPS
NTYYRDS
VKG
HTTADYF
QSYDTNI
YGIYFAL
DII
DA
NYYMA
ERSSGDI
GESYVN
SISTGGV
ADDQRPS
NTYYRDS
VKG
HTTPDYH
QSYDSSI
YGIYFAM
DIF
DA
By sequence aligning and computer simulation, it was found that the light and heavy chain CDR sequences of the murine antibodies m1803, m1805, m1808, and m1810 have higher homology, and the light and heavy chain CDR sequences of rat antibodies rat 1817 and rat1822 have higher homology. The consensus sequences thereof are shown in the following table:
The heavy and light chain variable region germline genes with high homology to murine antibodies were selected as templates by aligning against the IMGT human antibody heavy and light chain variable region germline gene database by MOE software analysis. The CDRs of the murine antibodies were grafted onto the corresponding human template to form a variable region sequence in the order of FR1-CDR1-FR2-CDR2-FR3-CDR3-FR4. As needed, some of the amino acids in the framework sequence were mutated back to the amino acids corresponding to the murine antibody to obtain the humanized anti-GCGR monoclonal antibody. The amino acid residues in the CDR regions were determined and annotated by the Kabat numbering system.
The above murine light and heavy chain variable regions were connected to the human light and heavy chain constant regions respectively to form a chimeric antibody. The chimeric antibody corresponding to clone 1803 was named as ch1803, and other antibodies were named in a similar way.
3.1 Humanization of Hybridoma Clone 1803
(1) Selection of frameworks for humanizing hybridoma clone 1803: For the murine antibody m1803, the humanization light chain templates were IGKV1-39*01 and hjk4.1, and the humanization heavy chain templates were IGHV1-3*01 and hjh6.1. The humanized variable region sequences are as follows:
EVQLVQSGAEVKKPGASVKVSCKASGYTFT
DYWIE
WVRQAPGQGLEWMG
EILPGSTYTNYNEKFKG
RVTM
TRDTSTSTVYMELSSLRSEDTAVYYCAR
GLSTLMA
VDYFDY
WGQGTTVTVSS;
DIQMTQSPSSLSASVGDRVTITC
RASQDISNYLN
WY
QQKPGKAPKLLIY
YSSTLHS
GVPSRFSGSGSGTDFT
LTISSLQPEDFATYYC
QQTNIFPWT
FGGGTKVEIK;
(2) Selection of humanization templates and design of back-mutations for the hybridoma clone 1803 are shown in the Table below:
(3) The specific humanized sequences of the hybridoma clone 1803 are as follows:
DIQMTQSPSSLSASVGDRVTITC
RASQDISNYLN
WYQQKPGKAPKLLIY
YSSTLHS
GVPSRFSGSGSGTDFTLTISSLQPEDFATYYC
QQTNIFPWT
F
GGGTKVEIK
DIQMTQSPSSLSASVGDRVTITC
RASQDISNYLN
WYQQKPGGAVKLLIY
YSSTLHS
GVPSRFSGSGSGTDYTLTISSLQPEDFATYFC
QQTNIFPWT
F
GGGTKVEIK
DIQMTQSPSSLSASVGDRVTITC
RASQDISNYLN
WYQQKPGKAVKLLIY
YSSTLHS
GVPSRFSGSGSGTDYTLTISSLQPEDFATYYC
QQTNIFPWT
F
GGGTKVEIK
EVQLVQSGAEVKKPGASVKVSCKASGYTFT
DYWIE
WVRQAPGQGLEWMG
EILPGSTYTNYNEKFKG
RVTMTRDTSTSTVYMELSSLRSEDTAVYYCAR
GLSTLMAVDYFDY
WGQGTTVTVSS
EVQLVQSGAEVKKPGASVKVSCKASGYTFT
DYWIE
WVRQAPGQGLEWMG
EILPGSTYTNYNEKFKG
RVTFTADTSTSTAYMELSSLRSEDTAVYYCAR
GLSTLMAVDYFDY
WGQGTTVTVSS
EVQLVQSGAEVKKPGASVKVSCKASGYTFT
DYWIE
WVRQAPGQGLEWIG
EILPGSTYTNYNEKFKG
RATFTADTSTSTAYMELSSLRSEDTAVYYCSR
GLSTLMAVDYFDY
WGQGTTVTVSS
EVQLVQSGAEVKKPGASVKVSCKASGYTFT
DYWIEWVKQAPGQGLEWIG
EILPGSTYTNYNEKFKG
RATFTADPSTSTAYMELSSLRSEDTAVYYCSR
GLSTLMAVDYFDY
WGQGTTVTVSS.
(4) The sequence combinations of the humanized antibody light chain variable region and heavy chain variable region of the antibody derived from hybridoma clone 1803 are as follows:
The light and heavy chain variable regions of the antibodies indicated in the above table can be connected to the corresponding antibody light and heavy chain constant region to form full-length antibodies. Unless otherwise specified in the present disclosure, for a full-length antibody, the antibody light chain is formed by the light chain variable region connected to the Kappa chain constant region as shown in SEQ ID NO: 73, and the antibody heavy chain is formed by the heavy chain variable region connected to IgG4-AA as shown in SEQ ID NO: 72.
3.2 Humanization of Hybridoma Clone 1810
(1) Selection of frameworks for humanizing hybridoma clone 1810:
For the murine antibody m1810, the humanization light chain templates were IGKV1-39*01 and hJK4.1, and the humanization heavy chain templates were IGHV1-69*02 and hJH4.1. The humanized variable region sequences are as follows:
QVQLVQSGAEVKKPGSSVKVSCKASGGTES
NYAIS
WV
RQAPGQGLEYVAIG
EIYPTSGNTYYNEKFKG
RVTITA
DKSTSTAMELSSLRSEDTAVYYCAR
GVITTVVSTDYF
DY
WGQGTLVTVSS
DIQMTQSPSSLSASVGDRVTITC
RASLDISNYLN
WYQQ
KPGKAPKLLIY
YTSTLHS
GVPSRFSGSGSGTDFTLTIS
SLQPEDFATYYC
QQGNMVPYT
FGGGTKVEIK
(2) Selection of humanization templates and design of back-mutations for the hybridoma clone 1810 are shown in the Table below:
(3) The specific humanized sequences of the hybridoma clone 1810 are as follows:
DIQMTQSPSSLSASVGDRVTITC
RASLDISNYLNW
YQQKPGKAPKLLIY
YTSTLHS
GVPSRFSGSGSGTD
FTLTISSLQPEDFATYYC
QQGNMVPYT
EGGGTKVE
IK
DIQMTQSPSSLSASVGDRVTITC
RASLDISNYLN
W
YQQKPGKAVKLLIY
YTSTLHS
GVSSRFSGSGSGTD
YTLTISSLQPEDFATYYC
QQGNMVPYT
FGGGTKVE
IK
DIQMTQSPSSLSASVGDRVTITC
RASLDISNYLN
W
YQLKPGKAVKLLIY
YTSTLHS
GVSSRFSGSGSGTE
YTLTISSLQPEDFATYYC
QQGNMVPYT
FGGGTKVE
IK
QVQLVQSGAEVKKPGSSVKVSCKASGGTFS
NYAIS
WVRQAPGQGLEWMG
EIYPTSGNTYYNEKFKG
RVTI
TADKSTSTAYMELSSLRSEDTAVYYCAR
GVITTVV
STDYFDY
WGQGTLVTVSS
QVQLVQSGAEVKKPGSSVKVSCKASGGTFS
NYAIS
WVRQAPGQGLEWMG
EIYPTSGNTYYNEKFKG
RVTI
TADRSTSTMYMELSSTRSEDTAVYYCASG
VITTVV
STDYFDY
WGQGTLVTVSS
QVQLVQSGAEVKKPGSSVKVSCKASGGTFS
NYAIS
TADRSTSTMYMELSSLRSEDTAVYYCASG
VITTVV
STDYFDY
WGQGTLVTVSS
QVQLVQSGAEVKKPGSSVKVSCKASGGTFS
NYAIS
WVKQAPGQGLEWIG
EIYPTSGNTYYNEKFKG
KATL
TADRSTSTMYMELSSLRSEDTAVYYCASG
VITTVV
STDYFDY
WGQGTLVTVSS.
(4) The sequence combinations of the humanized antibody light and heavy chain variable region of the hybridoma clone 1810 are as follows:
The light and heavy chain variable regions of the antibodies indicated in the above table can be connected to the corresponding antibody light and heavy chain constant region to form full-length antibodies. Unless otherwise specified in the present disclosure, for a full-length antibody, the antibody light chain is formed by the light chain variable region connected to the Kappa chain constant region as shown in SEQ ID NO: 73, and the antibody heavy chain is formed by the heavy chain variable region connected to IgG4-AA as shown in SEQ ID NO: 72.
Primers were designed, VH/VK gene fragment of each chimeric/humanized antibody was amplified by PCR and then inserted into the expression vector pHr (with a signal peptide and constant region gene (CH1-FC/CL) fragment) via homologous recombination to construct an expression vector for a full-length antibody VH-CH1-FC-pHr/VK-CL-pHr. The IgG4-AA antibody format can be obtained from IgG4 antibody format by simple point mutations. IgG4-AA represents mutations F234A, L235A and S228P. The mutations of F234A and L235A can reduce the binding ability of IgG4-Fc to FcγR, and further reduce ADCC/CDC. S228P indicates that the amino acid S at position 228 in the hinge region of wild-type IgG4 is mutated to P. The mutation at this position can prevent natural IgG4 antibody from mismatches caused by Fab-exchange occurring in vivo.
ch1803, ch1805, ch1808, ch1810, ch1817 and ch1822 are chimeric antibodies formed by connecting the animal-derived light and heavy chain variable regions with the human antibody kappa chain and the human antibody IgG4-AA heavy chain constant region, respectively.
Exemplary sequences of the constructed antibodies are as follows:
WFAYWGQGTLVTVSAASTKGPSVFPLAPCSRSTSE
ADYFDYWGQGTTLTVSSASTKGPSVFPLAPCSRST
QVQLVQSGAEVKKPGSSVKVSCKASGGTFS
NYAIS
WVKQAPGQGLEWIG
EIYPTSGNTYYNEKFKG
KATL
TADRSTSTMYMELSSIRSEDTAVYYCAS
GVITTVV
STDYFDY
WGQGTLVTVSSASTKGPSVFPLAPCSRS
DIQMTQSPSSLSASVGDRVTITC
RASLDISNYLNW
YQLKPGKAVKLLIY
YTSTLHS
GVSSRFSGSGSGTE
YTLTISSLQPEDFATYYCQQGNMVPYTFGGGTKVE
YGIYFALDAWGQGTSVTVSSASTKGPSVFPLAPCS
YGIYFAMDAWGQGTSVTVSSASTKGPSVFPLAPCS
Human GLP-1 peptide was used as the GLP-1 receptor agonist part of the bispecific protein, and the GCGR antibody was used as the GCGR antagonist part of the bispecific protein, to form the GLP-1/GCGR antibody bispecific protein.
Studies have found that the new GLP-1/GCGR antibody bispecific protein with amino acid mutation(s) at specific position(s) of GLP-1 (such as Q17E, I23V, K28R or G30R) has an increased in vitro stability, wherein the stability is the highest when Q at position 17 of GLP-1A is mutated to E and I at position 23 of GLP-1A is mutated to V(GLP-1C). Non-limiting exemplary sequences of GLP-1 and mutant forms thereof of the present disclosure are as follows:
The C-terminal amino acid of the GLP-1 peptide of the present disclosure was connected to the N-terminal amino acid of the GCGR antibody heavy chain through a peptide bond or a linker by using homologous recombination technology. Expression was carried out using the 293 expression system, and the structural models of the bispecific protein as shown in Table 9 were obtained:
The following proteins are formed by connecting different GLP-1 peptides to the heavy chain amino acids of different antibodies via linkers (e.g. (GGGGS)3):
DWVKQSHGRS
NGGTIYNQKF
KGKATLTVDK
SWFAYWGQGT
SWVKQRIGQG
SGNTYYNENF
KGKATLTADK
GADYFDYWGQ
VQSGAEVKKP
GSSVKVSCKA
SGGTFSNYAI
SWVKQAPGQG
LEWIG
EIYPT
SGNTYYNEKF
KG
KATLTADR
STSTMYMELS
SLRSEDTAVY
YCAS
GVITTV
VSTDYFDY
WG
QGTLVTVSSA
PEAAGGPSVF
AWVRQAPTKG
GVNTYYRDSV
KGRFTISRDN
FYGIYFALDA
Herein, preferably the linker (GGGGS)3 can be used as a linker in the bispecific protein. In other embodiments, a peptide bond or other linkers conventionally used for connection of polypeptides can also be used. The linkers for the bispecific protein of the present disclosure are not limited to the use of (GGGGS)3. Nucleotide sequences encoding the GLP-1, GCGR antibodies, and linker protein fragment ((GGGGS)3) were obtained by conventional technical means in the art. The C-terminal nucleotide of GLP-1 was linked to the N-terminal nucleotide of the GCGR antibody via a linker protein by homologous recombination technology and cloned into Phr-BsmbI vector. The recombinant GLP-1/GCGR antibody bispecific protein was expressed in 293 cells and purified by the method of Example 6. The purified protein can be used in each of the following examples.
The cell culture medium was centrifuged at high speed, the supernatant was collected, and was subjected to affinity chromatography as the first step of purification. The chromatographic medium was Protein A that interacts with Fc or a derivative filler, such as Mabselect, GE. The equilibration buffer was 1×PBS (137 mmol/L NaCl, 2.7 mmol/L KCl, 10 mmol/L Na2HPO4, 2 mmol/L KH2PO4, pH 7.4). After equilibrating the column with 5× column volume, the cell culture supernatant was loaded for binding, and the flow rate was controlled so that the retention time of the sample on the column is ≥1 min. After loading the sample, the column was washed with 1×PBS (pH 7.4) until the A280 UV absorption dropped to the baseline. Then the column was washed with 0.1M glycine (pH3.0) elution buffer, the elution peak was collected based on the A280 UV absorption peak, and the collected elution sample was neutralized with 1M Tris (pH8.5).
The neutralized elution sample was ultrafiltered and concentrated, and then subjected to size exclusion chromatography, wherein the buffer was 1×PBS, the chromatography column was XK26/60 Superdex200 (GE), the flow rate was controlled at 4 ml/min, and the loading volume was less than 5 ml. The target protein peak was pooled based on A280 UV absorption. The collected protein was identified by SEC-HPLC and the purity was greater than 95%. After LC-MS identification, the desired protein was aliquoted for use. The GLP-1/GCGR antibody bispecific proteins were obtained.
The binding ability of anti-GCGR antibodies was tested by binding assay of the antibody to CHO cells overexpressing GCGR. The human, mouse, and cynomolgus monkey GCGR full-length plasmids were transferred into CHO cells by transfection method, respectively. The expression levels of GCGR were detected after two weeks of pressure screening, After the GCGR-overexpressing cells were fixed to the bottom of 96-well plate, the antibodies were added and the signal strength was used to determine the binding activity of the antibody to GCGR overexpressing CHO cells. The binding abilities of the antibody to the three species of GCGRs were detected with the same binding assay. As an example, the binding of the GCGR antibodies to human GCGR was detected by an assay specifically described as follows:
The cells were seeded in a 96-well plate at a density of 0.9-1.0×106/ml, 100 μl/well and cultured overnight. The supernatant was discarded, the plate was washed three times with PBS, 100 μl/well of cell immune fixed solution (Beyotime, Cat No. P0098) was added and fixed for an hour at room temperature, and washed four times with PBS. The liquid was discarded, 200 μl/well blocking solution (5% skim milk (BD skim milk, Cat Wo. 232100) diluted with PBS) was added, and incubated in an incubator at 37° C. for 3 hours for blocking. After the blocking was finished, the blocking solution was discarded, the plate was washed 3 times with PBST buffer (PBS comprising 0.05% tweenW-20, pH7.4), 50 μl/well of various concentrations of each of the test antibodies (antibodies purified from hybridoma, chimeric antibodies or humanized antibodies) diluted with sample dilution solution were added, and incubated in an incubator at 37° C. for 2 hours. After the incubation was finished, the plate was washed 3 times with PBST, 50 μl/well of HRP-labeled goat anti-mouse secondary antibody (JacksoW ImmuWo Research, Cat No. 115-035-003) or goat anti-human secondary antibody (JacksoW ImmuWo Research, Cat Wo. 109-035-003) diluted with sample dilution solution was added, and incubated at 37° C. for 1 hour. The plate was washed 3 times with PBST, 50 μl/well of TMB chromogenic substrate (KPL, Cat Wo. 52-00-03) was added, incubated at room temperature for 10 min, and 50 μl/well of 1M H2SO4 was added to stop the reaction. The absorbance value was read by a microplate reader (Thermo scientific Multiskan MK3) at a wavelength of 450 nm, and the data was analyzed with GraphPad Prism 5. The binding of GCGR chimeric antibodies to GCGR-overepressing CHO cells was calculated as EC50 value.
The results show that the chimeric antibodies ch1803, ch1805, ch1808, ch1810, ch1817 and ch1822 all have favorable binding activity to human GCGR on cell surface, and also have favorable cross-affinity activity with mouse and cynomolgus monkey GCGR.
1. Purpose:
The antagonistic activities of the GCGR chimeric antibodies were evaluated by an assay of GCGR chimeric antibody blocking the binding of GCGR ligand (glucagon) to GCGR.
2. Test Principle:
The expression of luciferase gene (luciferase) downstream of CRE can be induced by the binding of cAMP to CRE. The change in luorescence signal emitted by the binding of luciferase to its substrate can reflect the inhibition efficiency. CRE was cloned upstream of the luciferase gene, and was co-transfected into CHO-K1 cells with a plasmid comprising the GCGR gene. Monoclonal cells expressing both CRE and GCGR were selected. GLP-1/GCGR antibody bispecific protein can compete with glucagon to bind to GCGR, block the signal transduction downstream of the GCGR, and affect the expression of downstream cAMP. The antagonistic activities of GLP-1/GCGR antibody bispecific proteins against GCGR can be evaluated by measuring the changes in fluorescence signal.
3. Test Samples:
Chimeric antibodies ch1803, ch1805, ch1808, ch1810, ch1817 and ch1822.
4. Experimental Procedures
a. Cell suspension was prepared with fresh cell culture medium, and was added into a 96-well cell culture plate of 80 μl culture system, 20,000 cells/well, and incubated at 5% CO2, 37° C. for 16 hours.
b. 10 μl of each of the prepared proteins to be tested was added into each well, 10 μl of the prepared glucagon was then added, and incubated at 5% CO2, 37° C. for 5 hours.
c. 100 μl of detection solution ONE Glo (Promega) was added to each well, and placed in the dark at room temperature for 7 minutes.
d. The fluorescence was detected on the microplate reader Victor3, and the IC50 value and the blocking efficiency Imax of the GCGR chimeric antibody fusion to block the binding of GCGR ligand (glucagon) to human, mouse and cynomolgus GCGRs were calculated.
The antagonistic activities of the GCGR antibodies were evaluated by assay of anti-GCGR antibody blocking the binding of GCGR ligand (glucagon) to GCGR. The experimental principle and steps are the same as Test Example 2, and the results are shown in the following table:
100%
100%
100%
100%
In Vitro Biological Evaluation
200 μg of the antibody bispecific protein to be tested was dissolved in 1 ml 1×PBS (pH 7.4) and stored in a 37° C. incubator; samples were taken at days 0 and 14 respectively, and maintenance of the intact heavy chain was detected by LC-MS with Agilent 6530 Q-TOF. The results are shown in Table 14 below. Each of the GLP-1 peptide bispecific proteins with mutations has a greatly increased stability compared to the bispecific protein comprising GLP-1A (SEQ ID NO: 91), and hu1803-9B, hu1803-9D and hu1803-9G show better stability.
The experimental principle and steps are the same as Test Example 2.
Test Samples:
1) GCGR antibodies (hu1803-9, hu1810-12)
2) Bispecific proteins: hu1803-9B and hu1803-9D.
1. Purpose:
The purpose is to evaluate the activating activity of the GLP-1 part of the GLP-1/GCGR antibody bispecific protein on GLP-1R.
2. Test Principle:
The expression of luciferase gene downstream of CRE can be induced by the binding of cAMP to CRE. The change in fluorescence signal emitted by the binding of luciferase to its substrate can reflect the inhibition efficiency. CRE was cloned upstream of the luciferase gene, and was co-transfected into CHO-K1 cells with a plasmid comprising the GLP-1R gene. Monoclonal cells highly expressing both CRE and GLP-1R were selected. Both GLP-1/GCGR antibody bispecific protein and Dulaglutide (a positive control) can bind to GLP-1R, activate the signal transduction downstream of the GLP-1R, and stimulate the expression of downstream cAMP. The agnostic activities of GLP-1/GCGR antibody bispecific proteins for GLP-1R can be evaluated by measuring the changes in fluorescence signal.
3. Test Samples:
1) Positive control: Dulaglutide
2) hu1803-9B, hu1803-9D.
4. Experimental procedures
a. Cell suspension was prepared with fresh cell culture medium, and was added into a 96-well cell culture plate of 90 μl culture system, 25000 cells/well, and incubated at 5% CO2, 37° C. for 16 hours.
b. 10 μl of each of the prepared proteins to be tested was added into each well, and incubated at 5% CO2, 37° C. for 5 hours.
c. 100 μl of detection solution ONE Glo (Promega) was added to each well, and placed in the dark at room temperature for 7 minutes.
d. The fluorescence was detected on the microplate reader Victor3, and the EC50 values of the GLP-1/GCGR antibody bispecific proteins for activating GLP-1R by binding were calculated.
Table 18 shows that all of the chimeric antibodies ch1805-D, ch1808-D and ch1817-D linked to GLP1 peptide can completely activate GLP-1R, and have comparable efficacy and EC50 (the concentration required to activate 50% of the maximum activity) to that of the positive control (Dulaglutide), indicating that the bispecific proteins formed by linking various GCGR antibodies to the GLP1 peptide in a manner as disclosed herein do not affect the biological activity of the GLP1 peptide.
Pharmacokinetic Evaluation
Four laboratory C57 mice, female, were kept at 12/12 hours light/dark cycle regulation, constant temperature of 24±3° C., humidity 50-60%, and ad libitum access to water and diet. Mice were purchased from Jiesijie Laboratory Animal Co., Ltd. On the day of the test, equimolar hu1803-9D and the positive control drug Dulaglutide were injected into tail vein of C57 mice, at a dose of 6 mg/kg and 2.35 mg/kg respectively, and at an injection volume of 10 ml/kg.
Since both the GLP-1/GCGR antibody bispecific protein of the present disclosure and the positive control Dulaglutide have cross-activity with mice, the time of drug metabolism in mice is shorter. The selected time points for blood collections were: 0h, 1h, 24h (day 2) on day 1 post-administration, and day 3. Blood was collected from the retinal vein of the mouse, 150 μl each time (1.5 μl of DPP-4 inhibitor was added to the blood collection tube before blood collection). The collected blood sample was placed at 4° C. for half an hour until coagulation, and then centrifuged at 14000×g for 5 minutes at 4° C. The supernatant (about 80 μl) was collected and stored at −80° C. immediately.
The detection process is described as follows:
a. 1 μg/mL anti-GLP1 (Novus, NBP1-05180) antibody was plated at 4° C. overnight.
b. Washed 4 times with 250 μl 1×PBST, 200 μl PBS comprising 5% milk was added, and blocked at 37° C. for 3 hours.
c. Washed 4 times with 250 μl 1×PBST, 100 μl of test drugs gradient diluted with mouse blank serum was added, and incubated at 37° C. for 2 hours.
d. Washed 3 times with 250 μl 1×PBST.
e. 100 μl horseradish peroxidase-labeled secondary antibody anti-human IgG Fc was added to each well, and incubated at 37° C. for 1 hour.
f. Washed 3 times with 250 μl 1×PBST.
g. 100 μl TMB was added to each well, incubated at room temperature for 10 minutes and then 100 μl 1M H2SO4 was added to stop the reaction.
h. Absorbance was measured at 450 nm on the microplate reader, and the data were analyzed with Graphpad Prism 5.
The results of PK analysis show that the half-life of the bispecific protein molecule hu1803-9D of the present disclosure in mice is about 23.4 h, which is twice as much as the half-life of the positive control drug.
Evaluation of In Vivo Biological Activity
1. The mouse strain used in this test was diabetic ob/ob mice and wild-type mice of the same age (Institute of Model Animals, Nanjing University). The purpose is to observe the treatment effect of the GLP-1/GCGR antibody bispecific protein on diabetes-related indicators such as blood glucose, glycosylated hemoglobin, body weight and food intake after continuous administrations in ob/ob mice.
Before the test, the animal models were divided into 6 groups according to the random and fasting weight, random and fasting blood glucose on the day of test, respectively:
Model control group, 2.84 mg/kg and 1.42 mg/kg GCGR monoclonal antibody groups (hu1803-9), 1.16 mg/kg positive control group (Dulaglutide) and 3 mg/kg and 1.5 mg/kg hu1803-9D. The mice in control group were injected subcutaneously (S.C.) with phosphate buffer, and mice in each group were injected subcutaneously once a week (9:00 AM), for a total of 4 times (Table 20).
2. Experimental Procedures
a. Fasting and random body weight were measured once a week, and food and water intake were measured once a day.
b. The blood glucose was randomly measured before the first administration and on days 1, 2, 3, and 7 after the administration, and then the blood glucose was measured once a week afterwards. The blood glucose after 6 hours of fasting was measured before the first administration and on days 3 and 7 after the administration, and then the fasting blood glucose was measured once a week.
c. On day 26 of administration, after the animals were fasted for 6 hours (8:00-14:00), a single dose of 2 g/kg glucose solution was intraperitoneally administered, and the glucose administration time was recorded as 0. The animals were tested for blood glucose at 0 min before the glucose administration, and 15, 30, 60, 90, and 120 minutes after the glucose administration. A glucose tolerance curve was drawn on the basis of the blood glucose data versus time, and the area under the curve (AUC) was calculated.
d. After the experiment, the mice were fasted for 6 hours (8:00-14:00) and then euthanized. Blood samples were taken from the heart, the whole blood was divided into two parts, one part of about 30 μl was added into a centrifuge tube pre-added with anticoagulant and stored for the determination of glycosylated hemoglobin, and the other part was allowed to rest on the bench and then centrifuged to obtain serum for the determination of TG; FFA, CHOL, HDL and LDL levels.
e. Data were analyzed by graphpad Prism 6 software, and Student-t test was used for statistical analysis of data.
3. Experimental Results:
1) Effect of Long-Term Administration on Random Blood Glucose Concentrations in Ob/Ob Mice:
As shown in
2) The Effect of Long-Term Administration on the Fasting Blood Glucose in Ob/Ob Mice:
As shown in
3) Effects of Long-Term Administration on Glycosylated Hemoglobin (HbA1c) in Ob/Ob Mice:
The results are shown in Table 21. The glycosylated hemoglobin level in each of administration groups decreased to varying degrees 30 days after once-a-week subcutaneous injection of each agent at different doses, and significantly lower than those in the model control group (P<0.05). The glycosylated hemoglobin levels in the 3 mg/kg and 1.5 mg/kg hu1803-9D groups were 5.5±0.2% and 4.7±0.1%, respectively, showing a significant dose-efficacy relationship; among them, the 3 mg/kg hu1803-9D group has a lower level than that in the equimolar 1.16 mg/kg positive control Dulaglutide and 2.84 mg/kg GCGR monoclonal antibody hu1803-9 (P<0.05).
The GCGR epitopes bound by GCGR antibodies were classified by ELISA assay, in which the competitive binding of the biotin-labeled antibodies with different concentrations of the standard antibody to GCGR-overexpressing CHO cells was detected. The method for preparing the cell plate was the same as that of Test Example 1. The following specific procedures are as follows: The antibody was labelled according to the biotin labeling kit instructions (Dojindo
Molecular Technologies, Inc. LK03). The unlabeled test antibody was diluted to a range of concentrations with sample dilution solution in a 96-well cell plate, 50 μl/well, and incubated at 37° C. for 2 hours. After the incubation was finished, the plate was washed 3 times with PBST, 50 μl/well of biotin-labeled antibody diluted with sample dilution solution was added, at a concentration of 0.1 μg/ml, incubated at 37° C. for 2 hours, the plate was washed 3 times with PBST, and HRP-labeled goat-anti-human secondary antibody (JacksoW ImmuWo Research, Cat Wo. 109-035-003) was added, and incubated at 37° C. for 1 hour. The plate was washed 3 times with PBST, 50 μl/well of TMB chromogenic substrate (KPL, Cat No. 52-00-03) was added, incubated at room temperature for 10 min, and 50 μl/well of 1M H2SO4 was added to stop the reaction. The absorbance value was read by a microplate reader (Thermo scientific Multiskan MK3) at a wavelength of 450 nm, and the data was analyzed with GraphPad Prism 5.
The lower the concentration of the biotin-labeled antibody bound to the cell plate for competition, the lower the OD value is, and vice versa. The competition efficiency was calculated according to the formula:
IC %=(test antibody highest OD450 nm−test antibody minimum OD450 nm)/(test antibody highest OD450nm−labeled antibody minimum OD450m), the results are shown in the table 22 below.
The results show that ch1817 and ch1822 have very close epitopes; ch1808, hu1803-9 and hu1810-12 have very close epitopes; while the epitopes bound by ch1808, hu1803-9 and hu1810-12 are presumed to be within the range of epitopes bound by ch1805.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201811573634.0 | Dec 2018 | CN | national |
| 201811606887.3 | Dec 2018 | CN | national |
This application is a U.S. National Phase Application of International Application No. PCT/CN2019/126903, which was filed on Dec. 20, 2019, and which claims priority to (i) Chinese Patent Application Serial No. 201811573634.0, which was filed on Dec. 21, 2018, and (ii) Chinese Patent Application Serial No. 201811606887.3, which was filed on Dec. 27, 2018. The contents of each of those applications are incorporated herein by reference in their entireties.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2019/126903 | 12/20/2019 | WO | 00 |
