Anti-Flt-1 antibodies for treating duchenne muscular dystrophy
The present invention provides, among other things, anti-Flt-1 antibodies and methods for treating muscular dystrophy, in particular, Duchenne muscular dystrophy (DMD). In some embodiments, a method according to the present invention includes administering to an individual who is suffering from or susceptible to DMD an effective amount of an anti-Flt-1 antibody or antigen-binding protein thereof such that at least one symptom or feature of DMD is reduced in intensity, severity, or frequency, or has delayed onset.
1. An anti-Flt-I antibody or antigen-binding fragment thereof, comprising:
(a) a VL CDR1 defined by the amino acid sequence of SEQ ID NO:21, a VL CDR2 defined by the amino acid sequence of SEQ ID NO:24, a VL CDR3 defined by the amino acid sequence of SEQ ID NO: 26, a VH CDR1 defined by the amino acid sequence of SEQ ID NO: 2, a VH CDR2 defined by the amino acid sequence of SEQ ID NO: 6, and a VH CDR3 defined by the amino acid sequence of SEQ ID NO: 16;
(b) a VL CDR1 defined by the amino acid sequence of SEQ ID NO:21, a VL CDR2 defined by the amino acid sequence of SEQ ID NO:24, a VL CDR3 defined by the amino acid sequence of SEQ ID NO: 27, a VH CDR1 defined by the amino acid sequence of SEQ ID NO: 2, a VH CDR2 defined by the amino acid sequence of SEQ ID NO: 7, and a VH CDR3 defined by the amino acid sequence of SEQ ID NO: 17;
(c) a VL CDR1 defined by the amino acid sequence of SEQ ID NO:21, a VL CDR2 defined by the amino acid sequence of SEQ ID NO:24, a VL CDR3 defined by the amino acid sequence of SEQ ID NO: 26, a VH CDR1 defined by the amino acid sequence of SEQ ID NO: 3, a VH CDR2 defined by the amino acid sequence of SEQ ID NO: 12, and a VH CDR3 defined by the amino acid sequence of SEQ ID NO: 17;
(d) a VL CDR1 defined by the amino acid sequence of SEQ ID NO:21, a VL CDR2 defined by the amino acid sequence of SEQ ID NO:24, a VL CDR3 defined by the amino acid sequence of SEQ ID NO: 28, a VH CDR1 defined by the amino acid sequence of SEQ ID NO: 2, a VH CDR2 defined by the amino acid sequence of SEQ ID NO: 8, and a VH CDR3 defined by the amino acid sequence of SEQ ID NO: 17; or
(e) a VL CDR1 defined by the amino acid sequence of SEQ ID NO:21, a VL CDR2 defined by the amino acid sequence of SEQ ID NO:24, a VL CDR3 defined by the amino acid sequence of SEQ ID NO: 32, a VH CDR1 defined by the amino acid sequence of SEQ ID NO: 3, a VH CDR2 defined by the amino acid sequence of SEQ ID NO: 12, and a VH CDR3 defined by the amino acid sequence of SEQ ID NO: 17.
2. The antibody or antigen-binding fragment thereof of claim 1 , wherein the anti-Flt-1 antibody or antigen-binding fragment thereof comprises:
a VL CDR1 defined by an amino acid sequence of SEQ ID NO:21,
a VL CDR2 defined by an amino acid sequence of SEQ ID NO:24;
a VL CDR3 defined by an amino acid sequence of SEQ ID NO: 26;
a VH CDR1 defined by an amino acid sequence of SEQ ID NO: 2,
a VH CDR2 defined by an amino acid sequence of SEQ ID NO: 6, and
a VH CDR3 defined by an amino acid sequence of SEQ ID NO: 16.
3. The antibody or antigen-binding fragment thereof of claim 1 , wherein the anti-Flt-1 antibody or antigen-binding fragment thereof comprises:
a VL CDR1 defined by an amino acid sequence of SEQ ID NO:21,
a VL CDR2 defined by an amino acid sequence of SEQ ID NO:24;
a VL CDR3 defined by an amino acid sequence of SEQ ID NO: 27;
a VH CDR1 defined by an amino acid sequence of SEQ ID NO: 2,
a VH CDR2 defined by an amino acid sequence of SEQ ID NO: 7, and
a VH CDR3 defined by an amino acid sequence of SEQ ID NO: 17.
4. The antibody or antigen-binding fragment thereof of claim 1 , wherein the anti-Flt-1 antibody or antigen-binding fragment thereof comprises:
a VL CDR1 defined by an amino acid sequence of SEQ ID NO:21,
a VL CDR2 defined by an amino acid sequence of SEQ ID NO:24;
a VL CDR3 defined by an amino acid sequence of SEQ ID NO: 26;
a VH CDR1 defined by an amino acid sequence of SEQ ID NO: 3,
a VH CDR2 defined by an amino acid sequence of SEQ ID NO: 12, and
a VH CDR3 defined by an amino acid sequence of SEQ ID NO: 17.
5. The antibody or antigen-binding fragment thereof of claim 1 , wherein the anti-Flt-1 antibody or antigen-binding fragment thereof comprises:
a VL CDR1 defined by an amino acid sequence of SEQ ID NO:21,
a VL CDR2 defined by an amino acid sequence of SEQ ID NO:24;
a VL CDR3 defined by an amino acid sequence of SEQ ID NO: 28;
a VH CDR1 defined by an amino acid sequence of SEQ ID NO: 2,
a VH CDR2 defined by an amino acid sequence of SEQ ID NO: 8, and
a VH CDR3 defined by an amino acid sequence of SEQ ID NO: 17.
6. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof is selected from the group consisting of IgG, F(ab′) 2 , F(ab) 2 , Fab′, Fab, ScFvs, diabodies, triabodies and tetrabodies, optionally wherein the antibody or antigen-binding fragment thereof is IgG, optionally wherein the antibody or antigen-binding fragment thereof is IgG1.
7. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof is a monoclonal antibody,
wherein the monoclonal antibody contains a human Fc region,
wherein the Fc region contains one or more mutations that enhance the binding affinity
between the Fc region and the FcRn receptor such that the in vivo half-life of the antibody is prolonged, and
wherein the Fc region contains one or more mutations at positions corresponding to Leu 234, Leu 235 and/or Gly 237 of human IgG1.
8. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof does not bind to VEGFR2 and/or VEGFR3.
9. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof does not bind to a mouse or monkey Flt-1.
10. A pharmaceutical composition comprising the antibody or antigen-binding fragment thereof of claim 1 and a pharmaceutically acceptable carrier.
11. The antibody or antigen-binding fragment thereof of claim 1 , wherein the anti-Flt-1 antibody or antigen-binding fragment thereof comprises:
(a) a light chain variable (VL) region comprising an amino acid sequence having at least 90% identity to SEQ ID NO: 60 and a heavy chain variable (VH) region comprising an amino acid sequence having at least 90% identity SEQ ID NO: 45,
(b) a light chain comprising an amino acid sequence having at least 90% identity to of SEQ ID NO: 76 and a heavy chain comprising an amino acid sequence having at least 90% identity to SEQ ID NO: 71,
(c) a light chain comprising an amino acid sequence having at least 90% identity to SEQ ID NO: 85 and a heavy chain comprising an amino acid sequence having at least 90% identity to SEQ ID NO:72,
(d) a light chain comprising an amino acid sequence having at least 90% identity to SEQ ID NO: 84 and (ii) a heavy chain comprising an amino acid sequence having at least 90% identity to SEQ ID NO:71,
(e) a light chain comprising an amino acid sequence having at least 90% identity to SEQ ID NO: 86 and a heavy chain comprising an amino acid sequence having at least 90 0 /0 identity to SEQ ID NO:73, or
(f) a light chain comprising an amino acid sequence having at least 90% identity to SEQ ID NO: 83 and a heavy chain comprising an amino acid sequence having at least 90% identity to SEQ ID NO:70.