Anti-ADDL antibodies and uses thereof
View Patent ↗The present invention relates to antibodies that differentially recognize multi-dimensional conformations of Aβ-derived diffusible ligands, also known as ADDLs. The antibodies of the invention can distinguish between Alzheimer's Disease and control human brain extracts and are useful in methods of detecting ADDLs and diagnosing Alzheimer's Disease. The present antibodies also block binding of ADDLs to neurons, assembly of ADDLS, and tau phosphorylation and are there useful in methods for the preventing and treating diseases associated with soluble oligomers of amyloid β1-42.
1. An isolated antibody, or antigen binding fragment thereof, capable of differentially recognizing a multi-dimensional conformation of one or more Aβ-derived diffusible ligands, wherein
(a) the light chain variable region of the antibody or antigen binding fragment comprises,
((i) a CDR1 of SEQ ID NO: 50,
(ii) a CDR2 of SEQ ID NO: 54, and
(iii) a CDR3 of SEQ ID NO: 300; and
(b) the heavy chain variable region of the antibody or antigen binding fragment comprises,
(i) a CDR1 of SEQ ID NO: 25,
(ii) a CDR2 of SEQ ID NO: 30, and
(iii) a CDR3 of SEQ ID NO:43.
2. A kit for detecting Aβ-derived diffusible ligands comprising the isolated antibody, or antigen binding fragment thereof, of claim 1 .
3. The isolated antibody of claim 1 , wherein said antibody is a monoclonal antibody.
4. The isolated antibody of claim 3 , wherein said antibody is humanized.
5. The isolated antibody of claim 4 , wherein said antibody is affinity matured.
6. A method for attenuating binding of Aβ-derived diffusible ligands to a neuron comprising contacting the neuron with the antibody of claim 1 so that binding of Aβ-derived diffusible ligands to the neuron is attenuated.
7. A method for inhibiting assembly of Aβ-derived diffusible ligands comprising contacting a sample containing amyloid β1-42 peptides with the antibody of claim 1 thereby inhibiting assembly of Aβ-derived diffusible ligands.
8. A method for inhibiting the phosphorylation of tau protein at Ser202/Thr205 comprising contacting a sample containing a tau protein with the antibody of claim 1 thereby inhibiting the phosphorylation of tau protein at Ser202/Thr205.
9. A method for identifying a putative therapeutic agent that attenuates the binding of Aβ-derived diffusible ligands to neurons comprising
(a) contacting a composition comprising a neuron with Aβ-derived diffusible ligands in the presence of an agent;
(b) contacting the composition with an antibody of claim 1 ; and
(c) detecting the amount of antibody bound in the presence of the agent;
wherein a decrease in the amount of antibody bound in the presence of the agent as compared to the amount of antibody bound in the absence of the agent indicates that the agent is a putative therapeutic agent for attenuating binding of Aβ-derived diffusible ligands to neurons.
10. A method for detecting Aβ-derived diffusible ligands in a sample comprising contacting a sample with the antibody of claim 1 and determining the presence of a complex comprising the Aβ-derived diffusible ligands and the antibody.
11. A method for diagnosing a disease associated with Aβ-derived diffusible ligands comprising contacting a sample with the antibody of claim 1 and determining the presence of a complex comprising Aβ-derived diffusible ligands and the antibody wherein the complex is diagnostic of a disease associated with Aβ-derived diffusible ligands.
12. A pharmaceutical composition comprising the isolated antibody, or antigen binding fragment of claim 1 in admixture with a pharmaceutically acceptable carrier.
13. A method for attenuating symptoms of a disease associated with Aβ-derived diffusible ligands comprising administering an effective amount of the pharmaceutical composition of claim 12 .
14. An isolated monoclonal antibody capable of differentially recognizing a multi-dimensional conformation of one or more Aβ-derived diffusible ligands, wherein said antibody comprises heavy and light chain variable regions comprising SEQ ID NO:71 and SEQ ID NO:323, respectively.