US 9879080 B2 - Anti-transthyretin Antibodies - The Lens - Free & Open Patent and Scholarly Search

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US 9879080 B2

Anti-transthyretin Antibodies

Published: Jan 30, 2018
Earliest Priority: Jan 28 2015
Family: 3
Cited Works: 49
Cited by: 1
Cites: 13
Sequences: 63
Additional Info: Cited Works Full text Sequence

Abstract

The invention provides antibodies that specifically bind to transthyretin (TTR). The antibodies can be used for treating or effecting prophylaxis of diseases or disorders associated with TTR accumulation or accumulation of TTR deposits (e.g., TTR amyloidosis). The antibodies can also be used for diagnosing TTR amyloidosis and inhibiting or reducing aggregation of TTR, among other applications.

Claims

A monoclonal antibody that specifically binds transthyretin comprising three heavy chain CDRs and three light chain CDRs of SEQ ID NOS. 1 and 13 respectively.
The antibody of claim 1 comprising three Kabat heavy chain CDRs designated SEQ ID NOS: 10-12, respectively and three light CDRs designated SEQ ID NOS: 18-20, respectively.
The antibody of claim 1, wherein the sequence of heavy chain CDR-H1 is SEQ ID NO: 63.
The antibody of claim 1 that is a chimeric, humanized, or veneered antibody.
The antibody of claim 1, wherein the antibody is a human IgG1 isotype.
The antibody of claim 1 wherein the antibody has a human IgG2 or IgG4 isotype.
The antibody of claim 1, that is a humanized or chimeric antibody.
The humanized antibody of claim 7 comprising a humanized mature heavy chain variable region having an amino acid sequence at least 90% identical to SEQ ID NO:9 and a humanized mature light chain variable region having an amino acid sequence at least 90% identical to SEQ ID NO:17.
The humanized antibody of claim 8, provided position H77 is occupied by T.
The humanized antibody of claim 9, provided position H49 is occupied by A.
The humanized antibody of claim 9, provided positions H19, H44, H83, and H89 are occupied by K, R, K, and M, respectively.
The humanized antibody of claim 11, provided position H49 is occupied by A.
The humanized antibody of claim 9, provided position L45 is occupied by K.
The humanized antibody of claim 8, comprising a mature heavy chain variable region having an amino acid sequence at least 95% identical to SEQ ID NO:9 and a mature light chain variable region having an amino acid sequence at least 95% identical to SEQ ID NO:17.
The humanized antibody of claim 14, comprising a mature heavy chain variable region having an amino acid sequence at least 98% identical to SEQ ID NO:9 and a mature light chain variable region having an amino acid sequence at least 98% identical to SEQ ID NO:17.
The humanized antibody of claim 9, wherein the mature heavy chain variable region has the amino acid sequence of SEQ ID NO: 9.
The humanized antibody of claim 16, wherein the mature light chain variable region has the amino acid sequence of SEQ ID NO: 17.
The antibody of claim 1, wherein the antibody is an intact antibody.
The antibody of claim 1, wherein the antibody is a binding fragment.
The antibody of claim 19, wherein the binding fragment is a single-chain antibody, Fab, or Fab′2 fragment.
The humanized antibody of claim 8, wherein the mature light chain variable region is fused to a light chain constant region and the mature heavy chain variable region is fused to a heavy chain constant region.
The humanized antibody of claim 21, wherein the heavy chain constant region is a mutant form of a natural human heavy chain constant region which has reduced binding to a Fcγ receptor relative to the natural human heavy chain constant region.
The humanized antibody of claim 21, wherein the heavy chain constant region is of IgG1 isotype.
The humanized antibody of claim 21, wherein the mature heavy chain variable region is fused to a heavy chain constant region having the sequence of SEQ ID NO:26 and/or the mature light chain variable region is fused to a light chain constant region having the sequence of SEQ ID NO:28.
A pharmaceutical composition comprising the antibody of claim 1 and a pharmaceutically acceptable carrier.
A nucleic acid or nucleic acids encoding the heavy chain and light chain of the antibody of claim 1.
A recombinant expression vector comprising the nucleic acid of claim 26.
A host cell transformed with the recombinant expression vector of claim 27.
A method of humanizing an antibody, the method comprising: (a) selecting an acceptor antibody; (b) identifying the amino acid residues of the mouse antibody to be retained; (c) synthesizing a nucleic acid encoding a humanized heavy chain comprising CDRs of the mouse antibody heavy chain and a nucleic acid encoding a humanized light chain comprising CDRs of the mouse antibody light chain; and (d) expressing the nucleic acids in a host cell to produce a humanized antibody; wherein the mouse antibody comprises a heavy chain variable region having the amino acid sequence of SEQ ID NO:1 and a light chain variable region having the amino acid sequence of SEQ ID NO:13.
A method of producing a humanized, chimeric, or veneered antibody, the method comprising: (a) culturing cells transformed with nucleic acids encoding the heavy and light chains of the antibody, so that the cells secrete the antibody; and (b) purifying the antibody from cell culture media; wherein the antibody is a humanized, chimeric, or veneered form of the antibody of claim 1.
A method of producing a cell line producing a humanized, chimeric, or veneered antibody, the method comprising: (a) introducing a vector encoding heavy and light chains of an antibody and a selectable marker into cells; (b) propagating the cells under conditions to select for cells having increased copy number of the vector; (c) isolating single cells from the selected cells; and (d) banking cells cloned from a single cell selected based on yield of antibody; wherein the antibody is a humanized, chimeric, or veneered form of the antibody of claim 1.
A method of inhibiting or reducing aggregation of transthyretin in a subject having or at risk of developing a transthyretin-mediated amyloidosis, comprising administering to the subject an effective regime of the antibody of claim 1, thereby inhibiting or reducing aggregation of transthyretin in the subject.
A method of inhibiting or reducing transthyretin fibril formation in a subject having or at risk of developing a transthyretin-mediated amyloidosis, comprising administering to the subject an effective regime of the antibody of claim 1, thereby inhibiting or reducing transthyretin accumulation in the subject.
A method of reducing transthyretin deposits in a subject having or at risk of developing a transthyretin-mediated amyloidosis, comprising administering to the subject an effective regime of the antibody of claim 1, thereby reducing transthyretin deposits in the subject.
A method of clearing aggregated transthyretin in a subject having or at risk of developing a transthyretin-mediated amyloidosis, comprising administering to the subject an effective regime of the antibody of claim 1, thereby clearing aggregated transthyretin from the subject relative to a subject having or at risk of developing a transthyretin-mediated amyloidosis who has not received the antibody.
A method of detecting the presence or absence of transthyretin deposits in a subject, comprising contacting a biological sample from the subject suspected of comprising the amyloid accumulation with an effective amount of the antibody of claim 1.

Owners (US)

Prothena Biosciences Inc (Jul 20 2016)
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Prothena Biosciences Limited (Jul 20 2016)
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University Health Network (Jul 14 2016)
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Applicants

Prothena Biosciences Ltd
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Univ Health Network
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Inventors

Nijjar Tarlochan S
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Chakrabartty Avijit
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Higaki Jeffrey N
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CPC Classifications

C07K16/18
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A61K2039/505
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C07K2317/24
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C07K2317/34
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C07K2317/565
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C07K2317/567
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C07K2317/76
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C07K2317/92
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G01N33/6893
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G01N33/6896
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G01N2800/28
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G01N2800/32
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IPC Classifications

G01N33/68
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A61K39/00
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C07K14/575
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C07K16/18
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C07K16/26
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G01N33/74
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Document History

Publication: Jan 30, 2018
US 9879080 B2
Application: Jul 2, 2016
US 201615201416 A
Priority: Jul 2, 2016
US 201615201416 A
Priority: Jan 28, 2016
US 201615009666 A
Priority: Dec 11, 2015
US 201562266557 P
Priority: Jan 28, 2015
US 201562109001 P

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