Human cytomegalovirus neutralizing antibodies and use thereof
The invention relates to neutralising antibodies which are specific for human cytomegalovirus and bind with high affinity as well as immortalised B cells that produce such antibodies. The invention also relates to the epitopes that the antibodies bind to as well as the use of the antibodies and the epitopes in screening methods as well as the diagnosis and therapy of disease.
1. An isolated antibody, or an antigen binding fragment thereof, that inhibits hCMV infection, comprising the heavy chain CDR1, CDR2, and CDR3 sequences as set forth in SEQ ID NO: 1, SEQ ID NO: 2, and SEQ ID NO: 3, respectively, and the light chain CDR1, CDR2, and CDR3 sequences as set forth in SEQ ID NO: 4, SEQ ID NO: 5, and SEQ ID NO: 6, respectively.
2. An isolated antibody, or an antigen binding fragment thereof, that inhibits hCMV infection, wherein the antibody comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 7 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 8.
3. The antibody or fragment of claim 2 , wherein the antibody is human monoclonal antibody 1F11.
4. The antibody or fragment of claim 1 or 2 , wherein the antibody is a human antibody, a monoclonal antibody, a human monoclonal antibody, a single chain antibody, Fab, Fab′, F(ab′) 2 , Fv or scFv.
5. An isolated antibody, or an antigen binding fragment thereof, that binds to the same epitope as an antibody having a heavy and light chain variable region comprising the amino acid sequence of SEQ ID NO: 7 and SEQ ID NO: 8, respectively, wherein the antibody or fragment inhibits hCMV infection.
6. An isolated nucleic acid molecule comprising a nucleotide sequence encoding the antibody or fragment of claim 1 , 2 or 5 .
7. The nucleic acid molecule of claim 6 comprising a nucleotide sequence that is at least 95% identical to any one of SEQ ID NOs: 9, 10, or 21-26.
8. An isolated cell expressing the antibody or fragment of claim 1 , 2 or 5 .
9. A pharmaceutical composition comprising the antibody or fragment of claim 1 , 2 or 5 , and a pharmaceutically acceptable diluent or carrier.
10. A pharmaceutical composition comprising the nucleic acid of claim 6 , and a pharmaceutically acceptable diluent or carrier.
11. A pharmaceutical composition comprising the antibody or fragment of claim 1 , 2 or 5 , and a second antibody, or antigen binding fragment thereof, which inhibits hCMV infection.
12. The antibody or fragment of claim 1 , 2 or 5 , that is specific for a complex comprising hCMV proteins UL130 and UL131A and inhibits infection of endothelial cells, retinal cells, or dendritic cells by human cytomegalovirus (hCMV), wherein the concentration of antibody required for 50% inhibition of hCMV is 0.3 μg/ml or less.
13. The antibody or fragment of claim 12 , wherein the concentration of antibody required for 50% inhibition of hCMV is 0.01 μg/ml or less.
14. The antibody or fragment of claim 12 wherein the concentration of antibody required for 50% neutralisation of hCMV is 0.003 μg/ml or less.
15. The antibody or fragment of claim 12 which binds a conformational epitope formed by the two proteins.