Combination therapies using anti-pseudomonas psl and pcrv binding molecules
US-2015023966-A1 · Jan 22, 2015 · US
US9403901B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9403901-B2 |
| Application number | US-201214125073-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 8, 2012 |
| Priority date | Jun 10, 2011 |
| Publication date | Aug 2, 2016 |
| Grant date | Aug 2, 2016 |
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The disclosure relates to an anti- Pseudomonas PSL binding molecule and uses thereof, in particular, in prevention and treatment of Pseudomonas infection. Furthermore, the disclosure provides compositions and methods for preventing and treating Pseudomonas infection.
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What is claimed is: 1. An isolated antibody or antigen-binding fragment thereof which specifically binds to Pseudomonas Psl polysaccharide, wherein the antibody or antigen-binding fragment thereof promotes opsonophagocytic killing (OPK) of P. aeruginosa , and wherein the isolated antibody or antigen-binding fragment thereof specifically binds to the same Pseudomonas Psl epitope as an antibody or antigen-binding fragment thereof comprising the heavy chain variable region (VH) and the light chain variable region (VL) of WapR-004RAD, which comprises SEQ ID NO: 74 and SEQ ID NO: 12, respectively. 2. An isolated antibody or antigen-binding fragment thereof which specifically binds to Pseudomonas Psl polysaccharide, wherein the antibody or antigen-binding fragment thereof promotes opsonophagocytic killing (OPK) of P. aeruginosa , and wherein the isolated antibody or antigen-binding fragment thereof competitively inhibits Pseudomonas Psl binding by an antibody r antigen-binding fragment comprising the heavy chain variable region (VH) and the light chain variable region (VL) of WapR-004RAD, which comprises SEQ ID NO: 74 and SEQ ID NO: 12, respectively. 3. An isolated antibody or antigen-binding fragment thereof which specifically binds to Pseudomonas Psl polysaccharide comprising a set of complementarity determining regions (CDRs) VHCDR1, VHCDR2, VHCDR3, VLCDR1, VLCDR2 and VLCDR3 comprising SEQ ID NOs: 47, 48, 75, 50, 51, and 52. 4. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof is humanized, chimeric or fully human. 5. The antibody or antigen-binding fragment thereof of claim 4 , wherein the antibody or antigen-binding fragment thereof is a Fab fragment, a Fab′ fragment, a F(ab)2 fragment or a single chain Fv (scFv). 6. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof is monoclonal. 7. The antibody or antigen-binding fragment thereof of claim 1 , further comprising a pharmaceutically acceptable carrier. 8. The antibody or antigen-binding fragment thereof of claim 3 further comprising a pharmaceutically acceptable carrier. 9. The antibody or antigen-binding fragment thereof of claim 2 , wherein the antibody or antigen-binding fragment thereof is humanized, chimeric or fully human. 10. The antibody or antigen-binding fragment thereof of claim 9 , wherein the antibody or antigen-binding fragment thereof is a Fab fragment, a Fab′ fragment, a F(ab)2 fragment or a single chain Fv (scFv). 11. The antibody or antigen-binding fragment thereof of claim 2 , wherein the antibody or antigen-binding fragment thereof is monoclonal. 12. The antibody or antigen-binding fragment thereof of claim 2 , further comprising a pharmaceutically acceptable carrier. 13. The isolated antibody or antigen-binding fragment thereof of claim 3 comprising a heavy chain variable region (VH) comprising SEQ ID NO: 74 and a light chain variable region (VL) comprising SEQ ID NO: 12. 14. The antibody or antigen-binding fragment thereof of claim 13 further comprising a pharmaceutically acceptable carrier.
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