ISOFORM-SELECTIVE TGFB1 INHIBITORS AND USE THEREOF
Disclosed herein are monoclonal antibodies and antigen-binding fragments thereof capable of selectively inhibiting TGFβ1 with high potency. Related compositions, methods and therapeutic use are also disclosed.
1 .- 31 . (canceled)
32 . A polynucleotide encoding an antibody, or an antigen-binding fragment thereof, that binds pro-transforming growth factor beta 1 (proTGFβ1), comprising:
a first nucleic acid sequence encoding a heavy chain variable domain comprising:
a heavy chain complementarity determining region 1 (H-CDR1) having an amino acid sequence set forth in SEQ ID NO: 107;
a heavy chain complementarity determining region 2 (H-CDR2) having an amino acid sequence set forth in SEQ ID NO: 103; and
a heavy chain complementarity determining region 3 (H-CDR3) having an amino acid sequence set forth in SEQ ID NO: 6; and/or
a second nucleic acid sequence encoding a light chain variable domain comprising:
a light chain complementarity determining region 1 (L-CDR1) having an amino acid sequence set forth in SEQ ID NO: 105;
a light chain complementarity determining region 2 (L-CDR2) having an amino acid sequence set forth in SEQ ID NO: 106; and,
a light chain complementarity determining region 3 (L-CDR3) having an amino acid sequence set forth in SEQ ID NO: 12.
33 . The polynucleotide of claim 32 , wherein:
the first nucleic acid sequence encoding the heavy chain variable domain comprises SEQ ID NO: 14; and/or
the second nucleic acid sequence encoding the light chain variable domain comprises SEQ ID NO: 16.
34 . The polynucleotide of claim 32 , wherein:
the first nucleic acid sequence encodes a heavy chain domain as set forth in SEQ ID NO 18; and/or
the second nucleic acid sequence encodes a light chain domain as set forth in SEQ ID NO 20.
35 . The polynucleotide of claim 32 , which is a DNA, an RNA or a cDNA.
36 . The polynucleotide of claim 32 , further comprising one or more regulatory elements.
37 . The polynucleotide of claim 36 , wherein the one or more regulatory elements are selected from the group consisting of a promoter, an enhancer, a transcription termination signal, a leader sequence, a fusion protein and combinations thereof.
38 . The polynucleotide of claim 37 , wherein:
the promoter is selected from the group consisting of a PL promoter, a lac promoter, a Trp promoter, a Tac promoter, an AOX1 promoter, a GAL1 promoter, a CMV promoter, an SV40 promoter and an RSV promoter;
the enhancer is selected from the group consisting of a CMV-enhancer, an SV40-enhancer and a globin intron; and/or
the transcription termination signal comprises a poly-A signal.
39 . The polynucleotide of claim 32 , wherein the first nucleic acid sequence encoding the heavy chain variable domain and the second nucleic acid sequence encoding the light chain variable domain are under the control of the same promoter.
40 . The polynucleotide of claim 32 , wherein the first nucleic acid sequence encoding the heavy chain variable domain and the second nucleic acid sequence encoding the light chain variable domain are under the control of different promoters.
41 . A vector comprising the polynucleotide of claim 32 .
42 . A host cell comprising the polynucleotide of claim 32 .
43 . The host cell of claim 42 , which is a bacterial cell, an insect cell, a fungal cell, a plant cell, a mammalian cell or a human cell.
44 . The host cell of claim 43 , wherein
the bacterial cell is selected from the group consisting of an E. coli cell, an S. typhimurium cell, a Serratia marcescens cell, and a Bacillus subtilis cell;
the fungal cell is a Saccharomyces cerevisiae cell; or
the mammalian cell is selected from the group consisting of a CHO cell, a 293 cell, an MDCK cell, and an NSO cell.
45 . A host cell comprising the vector of claim 41 .
46 . A host cell expressing an antibody, or an antigen-binding fragment thereof, that binds pro-transforming growth factor beta 1 (proTGFβ1), wherein the host cell comprises:
a first polynucleotide encoding a heavy chain variable domain comprising:
a heavy chain complementarity determining region 1 (H-CDR1) having an amino acid sequence set forth in SEQ ID NO: 107;
a heavy chain complementarity determining region 2 (H-CDR2) having an amino acid sequence set forth in SEQ ID NO: 103; and
a heavy chain complementarity determining region 3 (H-CDR3) having an amino acid sequence set forth in SEQ ID NO: 6; and/or
a second polynucleotide encoding a light chain variable domain comprising:
a light chain complementarity determining region 1 (L-CDR1) having an amino acid sequence set forth in SEQ ID NO: 105;
a light chain complementarity determining region 2 (L-CDR2) having an amino acid sequence set forth in SEQ ID NO: 106; and,
a light chain complementarity determining region 3 (L-CDR3) having an amino acid sequence set forth in SEQ ID NO: 12.
47 . The host cell of claim 46 , wherein:
the first polynucleotide encodes a heavy chain variable domain as set forth in SEQ ID NO: 14; and/or
the second polynucleotide encodes a light chain variable domain as set forth in SEQ ID NO: 16.
48 . The host cell of claim 46 , wherein the first polynucleotide and the second polynucleotide are under the control of the same promoter.
49 . The host cell of claim 46 , wherein the first polynucleotide and the second polynucleotide are under the control of different promoters.
50 . The host cell of claim 46 , wherein:
the first polynucleotide encodes a heavy chain domain as set forth in SEQ ID NO 18; and/or
the second polynucleotide encodes a light chain domain as set forth in SEQ ID NO 20.