Binding molecules capable of neutralizing rabies virus and uses thereof
Provided are binding molecules that specifically bind to rabies virus and are capable of neutralizing the virus. Further provided are nucleic acid molecules encoding the binding molecules, compositions comprising the binding molecules and methods of identifying or producing the binding molecules. The binding molecules can be used in the diagnosis, prophylaxis and/or treatment of a condition resulting from rabies virus. In certain embodiments, they can be used in the post-exposure prophylaxis of rabies.
1. A composition comprising first and second human monoclonal antibodies binding to a first and second epitope of a rabies virus,
wherein both the first and second human monoclonal antibodies are able to neutralize the rabies virus,
wherein the first and second epitopes are different from one another and are non-competing,
wherein either the first or second human monoclonal antibodies are CR04-098, comprising the heavy chain sequence, SEQ ID NO:335, and the light chain sequence, SEQ ID NO:337,
and wherein the antibodies have isoelectric points as measured by isoelectric focusing that differ by less than 1.5 pl units.
2. A composition comprising first and second human monoclonal antibodies binding to a first and second epitope of a rabies virus,
wherein both the first and second human monoclonal antibodies are able to neutralize the rabies virus,
wherein the first and second epitopes are different from one another and are non-competing,
wherein either the first or second human monoclonal antibodies are CR-57, comprising the heavy chain sequence, SEQ ID NO:123, and the light chain sequence, SEQ ID NO:125,
and wherein the antibodies have isoelectric points as measured by isoelectric focusing that differ by less than 1.5 pl units.
3. A composition comprising first and second human monoclonal antibodies binding to a first and second epitope of a rabies virus,
wherein both the first and second human monoclonal antibodies are able to neutralize the rabies virus,
wherein the first and second epitopes are different from one another and are non-competing,
wherein the first human monoclonal antibodies are CR04-098, comprising the heavy chain sequence, SEQ ID NO:335, and the light chain sequence, SEQ ID NO:337, and the second human monoclonal antibodies are CR-57, comprising the heavy chain sequence, SEQ ID NO:123, and the light chain sequence, SEQ ID NO:125,
and wherein the antibodies have isoelectric points as measured by isoelectric focusing that differ by less than 1.5 pl units.