Crispr/cas-related methods and compositions for knocking out c5
US-2024415980-A1 · Dec 19, 2024 · US
US8940272B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-8940272-B2 |
| Application number | US-201113271118-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 11, 2011 |
| Priority date | Oct 11, 2010 |
| Publication date | Jan 27, 2015 |
| Grant date | Jan 27, 2015 |
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Provided are novel human tau-specific antibodies as well as fragments, derivatives and variants thereof as well as methods related thereto. Assays, kits, and solid supports related to antibodies specific for tau are also disclosed. The antibody, immunoglobulin chain(s), as well as binding fragments, derivatives and variants thereof can be used in pharmaceutical and diagnostic compositions for tau targeted immunotherapy and diagnosis, respectively.
Opening claim text (preview).
What is claimed is: 1. A human monoclonal anti-tau antibody or tau binding fragment thereof comprising a heavy chain variable region (VH) and a light chain variable region (VL) wherein: (a) the VH comprises a heavy chain CDR1, CDR2, and CDR3 comprising the amino acid sequences of SEQ ID NO: 23, 24, and 25, respectively; and (b) the VL comprises a light chain CDR1, CDR2, and CDR3 comprising the amino acid sequences of SEQ ID NO: 26, 27, and 28, respectively; wherein the VH does not comprise an asparagine at Kabat numbering position 30. 2. The antibody or tau binding fragment thereof of claim 1 , which is selected from the group consisting of a single chain Fv fragment (scFv), an F(ab′) fragment, an F(ab) fragment, and an F(ab′)2 fragment. 3. The anti-tau antibody or tau binding fragment thereof of claim 1 , which is (a) detectably labeled wherein the detectable label is selected from the group consisting of an enzyme, a radioisotope, a fluorophore and a heavy metal; or (b) which is attached to a drug. 4. The anti-tau antibody or tau binding fragment thereof of claim 1 wherein the VH comprises a glutamine at Kabat numbering position 30. 5. A composition comprising the anti-tau antibody or tau binding fragment thereof of claim 1 , wherein the composition is (i) a pharmaceutical composition further comprising a pharmaceutically acceptable carrier; or (ii) a diagnostic composition further comprising one or more reagents conventionally used in immuno or nucleic acid based diagnostic methods. 6. The composition of claim 5 further comprising an additional agent which can treat a neurodegenerative tauopathy. 7. A kit comprising the antibody or tau binding fragment thereof of claim 1 , with reagents or instructions for use. 8. A human monoclonal anti-tau antibody or tau binding fragment thereof comprising a heavy chain variable region (VH) and a light chain variable region (VL), wherein (a) the VH comprises a heavy chain CDR1, CDR2, and CDR3 comprising the amino acid sequences of SEQ ID NO: 23, 24, and 25, respectively; (b) the VL comprises a light chain CDR1, CDR2, and CDR3 comprising the amino acid sequences of SEQ ID NO: 26, 27, and 28, respectively; and (c) the antibody is a non-naturally occurring variant of a monoclonal antibody comprising the VH of SEQ ID NO:9 and VL of SEQ ID NO:11. 9. A human monoclonal anti-tau antibody or tau binding fragment thereof comprising (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 93, and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 11.
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variable (Fv) region, i.e. VH and/or VL · CPC title
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