WO2014073292A1 - 癌治療のための抗adam28抗体 - Google Patents
癌治療のための抗adam28抗体 Download PDFInfo
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- C07K16/40—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against enzymes
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
- C07K16/2896—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against molecules with a "CD"-designation, not provided for elsewhere
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- C07K2317/34—Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
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- C07K2317/00—Immunoglobulins specific features
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- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
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- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
- C07K2317/565—Complementarity determining region [CDR]
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- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
Definitions
- the present invention relates to an anti-human ADAM28 antibody and its pharmaceutical use.
- ADAM proteins are multifunctional proteins involved in ectodomain shedding, cell adhesion and invasion of transmembrane proteins (Non-patent Documents 1 and 2).
- the human genome contains 25 ADAMs including 4 pseudogenes, and 21 ADAMs consist of 13 proteolytic ADAMs and 8 non-proteolytic ADAMs that exhibit proteolytic activity. (Non-Patent Documents 1 and 3).
- Proteolytic ADAMs share the metalloproteinase domain of matrix metalloproteinases (MMPs), and typical proteolytic ADAMs are propeptides, metalloproteinases, disintegrin-like, cysteine-rich, epidermal growth factor-like, transmembrane and Many proteolytic ADAMs, including intracellular domains (Non-Patent Documents 3-9), including ADAM8, ADAM9, ADAM12, ADAM15, ADAM17, ADAM19 and ADAM28, are overexpressed in human cancer, It is related to progress (Non-Patent Documents 5 and 9).
- MMPs matrix metalloproteinases
- ADAM28 ADAM metallopeptidase domain 28
- ADAM28m prototype membrane anchor type
- ADAM28s short secreted form
- Non-Patent Documents 12 and 13 have also been shown to be expressed in large amounts in human non-small cell lung cancer and breast cancer.
- the present inventors have found that ADAM28 is preferentially expressed in cancer cells contained in cancer tissue, and that the expression level of ADAM28 mRNA is high in breast cancer cells.
- Non-patent Document 13 It was shown to be related to proliferation (Non-patent Document 13) and to non-small cell lung cancer, both related to cancer cell proliferation and invasion (Non-patent Document 12).
- Non-patent Document 14 serum ADAM27 levels increase in patients with non-small cell lung cancer with tumor progression, lymph node metastasis, and cancer recurrence.
- IGF-1 insulin-like growth factor-I
- IGFBP-3 complex IGF binding protein-3
- Phage display method is one of the display technologies that achieve high-speed in vitro selection by having one-to-one correspondence between functional peptides and proteins and DNA encoding them in the form of phage particles.
- This phage display method is applied to antibody selection, and many drug developments of antibodies obtained by this method have been carried out (Non-patent Document 16).
- Non-patent Document 16 methods for obtaining specific antibodies by combining a human artificial antibody library and a phage display method have also been established, and these methods have been put into practical use by several companies including MorphoSys' HuCAL (Human Combined Antibody Library). It has been advanced.
- An object of the present invention is to provide an anti-human ADAM28 antibody useful for preventing or treating cancer or inhibiting cancer metastasis.
- the present inventors produced a plurality of anti-ADAM28 antibodies that bind to human ADAM28.
- the prepared anti-human ADAM28 antibody inhibits the enzyme activity of ADAM28 and exhibits an excellent cancer cell growth inhibitory effect and cancer metastasis inhibitory effect in an in vivo model.
- the present invention relates to the following.
- the light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 5, CDR2 having the amino acid sequence represented by SEQ ID NO: 6, and CDR3 having the amino acid sequence represented by SEQ ID NO: 7.
- the heavy chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 8, CDR2 having the amino acid sequence represented by SEQ ID NO: 9 and CDR3 having the amino acid sequence represented by SEQ ID NO: 10;
- the light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 5, CDR2 having the amino acid sequence represented by SEQ ID NO: 6 and CDR3 having the amino acid sequence represented by SEQ ID NO: 7.
- the heavy chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 8, CDR2 having the amino acid sequence represented by SEQ ID NO: 9, and CDR3 having the amino acid sequence represented by SEQ ID NO: 10 ( However, at least one amino acid sequence selected from the group consisting of the amino acid sequences represented by SEQ ID NOs: 5, 6 and 7 has 1 to 3 amino acids substituted, deleted, inserted and / or added.
- the light chain variable region includes CDR1 having the amino acid sequence represented by SEQ ID NO: 11, CDR2 having the amino acid sequence represented by SEQ ID NO: 12, and CDR3 having the amino acid sequence represented by SEQ ID NO: 13.
- the heavy chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 14, CDR2 having the amino acid sequence represented by SEQ ID NO: 15 and CDR3 having the amino acid sequence represented by SEQ ID NO: 16;
- the light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 11, CDR2 having the amino acid sequence represented by SEQ ID NO: 12, and CDR3 having the amino acid sequence represented by SEQ ID NO: 13.
- the heavy chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 14, CDR2 having the amino acid sequence represented by SEQ ID NO: 15, and CDR3 having the amino acid sequence represented by SEQ ID NO: 16 ( However, at least one amino acid sequence selected from the group consisting of the amino acid sequences represented by SEQ ID NOs: 11, 12, and 13 has 1 to 3 amino acids substituted, deleted, inserted, and / or added.
- the light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 24, CDR2 having the amino acid sequence represented by SEQ ID NO: 25, and CDR3 having the amino acid sequence represented by SEQ ID NO: 26
- the heavy chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 27, CDR2 having the amino acid sequence represented by SEQ ID NO: 28, and CDR3 having the amino acid sequence represented by SEQ ID NO: 29;
- a CDR1 having the amino acid sequence represented by SEQ ID NO: 27, and the heavy chain variable region represented by SEQ ID NO: 27 CDR2 having a non-acid sequence and CDR3 having an amino acid sequence represented by SEQ ID NO: 29 (however, in at least one amino acid sequence selected from the group consisting of amino acid sequences represented by SEQ ID NOs: 24, 25 and 26) 1 to 3 amino acids are substituted, deleted, inserted, and / or added, and / or 1 to 3 amino acids are substituted, deleted, inserted and / or added in at least one amino acid sequence selected from the group consisting of the amino acid sequences represented by SEQ ID NOs: 27, 28 and 29); [1] The antibody according to [1].
- the light chain variable region comprises the amino acid sequence represented by SEQ ID NO: 17, and the heavy chain variable region comprises the amino acid sequence represented by SEQ ID NO: 18; (3 ′) the light chain variable region comprises the amino acid sequence represented by SEQ ID NO: 19, and the heavy chain variable region comprises the amino acid sequence represented by SEQ ID NO: 20, or (5 ′) the light chain
- a pharmaceutical composition comprising the antibody according to any one of [1] to [4].
- a preventive or therapeutic agent for cancer comprising the antibody according to any one of [1] to [4].
- a cancer metastasis inhibitor comprising the antibody according to any one of [1] to [4].
- a method for preventing or treating cancer in a mammal comprising administering an effective amount of the antibody according to any one of [1] to [4] to the mammal.
- the method of [8], wherein the mammal is a human.
- a method for inhibiting cancer metastasis in a mammal comprising administering an effective amount of the antibody according to any one of [1] to [4] to the mammal.
- the method of [10] wherein the mammal is a human.
- an anti-human ADAM28 antibody useful for prevention or treatment of cancer or inhibition of cancer metastasis is provided.
- Enzyme activity inhibitory effect of anti-human ADAM28 antibody In vitro cancer cell growth inhibitory effect of anti-human ADAM28 antibody. In vivo cancer cell growth inhibitory effect of anti-human ADAM28 antibody. In vivo cancer cell metastasis inhibitory effect of anti-human ADAM28 antibody. In vivo cancer cell metastasis inhibitory effect of anti-human ADAM28 antibody.
- the present invention provides an antibody having a specific binding activity to human ADAM28 and an activity inhibiting the enzymatic activity of human ADAM28.
- ADAM28 is a known protein, and its amino acid sequence and cDNA sequence are also known. There are two types of ADAM28, a prototype membrane anchor type (ADAM28m) and a short secretion type (ADAM28s), both of which are included in ADAM28 in the present invention.
- the representative amino acid sequence of human ADAM28m is SEQ ID NO: 2
- the representative cDNA sequence of human ADAM28m is SEQ ID NO: 1
- the representative amino acid sequence of human ADAM28s is SEQ ID NO: 4
- the representative cDNA sequence of human ADAM28s is Are shown in SEQ ID NO: 3, respectively.
- the antibody of the present invention has specific binding activity for human ADAM28.
- “Human ADAM28” means that the amino acid sequence or nucleotide sequence of ADAM28 has the same or substantially the same amino acid sequence or nucleotide sequence as the amino acid sequence or nucleotide sequence of ADAM28 naturally expressed in humans. . “Substantially the same” means that the focused amino acid sequence or nucleotide sequence is 70% or more (preferably 80% or more, more preferably 90% or more) with the amino acid sequence or nucleotide sequence of ADAM28 that is naturally expressed in humans. And more preferably 95% or more, most preferably 99% or more), and has the function of human ADAM28. The same applies to biological species other than humans, and proteins, genes, and fragments other than ADAM28.
- Specific binding to an antigen X by an antibody means that the binding affinity of the antibody to the antigen X in the antigen-antibody reaction is more than the binding affinity to a non-specific antigen (eg, bovine serum albumin (BSA)). Means high.
- BSA bovine serum albumin
- the antibody of the present invention has an activity of inhibiting the enzyme activity of human ADAM28.
- the enzyme activity of human ADAM28 specifically means the activity of human ADAM28 cleaving human IGFBP-3 (Insulin-like Growth Factor Binding Protein-3).
- the activity of human ADAM28 cleaving human IGFBP-3 can be evaluated by, for example, zymography analysis described in CancerCanRes 2006; 66 (20): 9913-9920.
- antibody is used to include a full-length antibody and any antigen-binding fragment thereof (ie, “antigen-binding portion”) or a single chain thereof.
- Antibody refers to a glycoprotein or antigen-binding portion thereof comprising at least two heavy chains (H) and two light chains (L) linked by disulfide bonds.
- Each heavy chain is composed of a heavy chain variable region (abbreviated as V H in the text) and a heavy chain constant region.
- the heavy chain constant region is comprised of three domains, C H 1, C H 2 and C H 3.
- Each light chain is composed of a light chain variable region (abbreviated herein as VL ) and a light chain constant region.
- the light chain constant region is comprised of one domain C L.
- VH and VL regions are further subdivided into highly variable regions called complementarity determining regions (CDRs), which are called framework regions (FR) and are more conserved The area is scattered.
- CDRs complementarity determining regions
- FR framework regions
- Each V H and V L is composed of 3 CDRs and 4 FRs, arranged in the following order: FR1, CDR1, FR2, CDR2, FR3, CDR3, FR4 from the amino terminus to the carboxy terminus.
- the variable regions of the heavy and light chains contain a binding domain that interacts with an antigen.
- the constant region of an antibody can mediate binding of immunoglobulins to host tissues or factors, including various cells of the immune system (eg, effector cells) and the first component of the traditional complement system (C1q). It is.
- antigen-binding portion of an antibody is used to refer to one or more fragments of an antibody that retain the ability to specifically bind to an antigen (eg, human ADAM28). It has been shown that the antigen binding function of an antibody is performed by fragments of a full-length antibody.
- binding fragments included in the term “antigen-binding portion” of an antibody include: (i) a Fab fragment that is a monovalent fragment composed of V L , V H , C L and C H1 domains; (ii) hinge F (ab ′) 2 fragment which is a bivalent fragment containing two Fab fragments linked by disulfide bridge in the region, (iii) Fab ′ fragment which is a native Fab having a hinge region part (FUNDAMENTAL IMMUNOLOGY (Paul ed., 3. sup.rd ed.
- single chain Fv single chain Fv
- antigen-binding portion of an antibody
- these antibody fragments are known to those skilled in the art. It obtained using conventional techniques, and the fragments are screened for utility in the same manner as are intact antibodies.
- the antibody of the present invention is preferably a monoclonal antibody.
- “Monoclonal antibody” refers to a preparation of antibody molecules of single molecular composition.
- a monoclonal antibody composition displays a single binding specificity and affinity for a particular epitope.
- the antibody of the present invention is preferably a human antibody or a humanized antibody.
- Human antibody refers to an antibody having variable regions derived from human germline immunoglobulin sequences in both the framework and CDR regions. Furthermore, if the antibody contains a constant region, this constant region is also derived from a human germline immunoglobulin sequence.
- human antibody includes amino acid residues that are not encoded by human germline immunoglobulin sequences (eg, mutations introduced by random or site-directed mutagenesis in vitro or somatic mutation in vivo). Embodiments are also included.
- the “humanized antibody” refers to an antibody in which a CDR sequence derived from a germ line of a non-human animal species such as a mouse is fused on a human framework sequence.
- human antibodies include “reconstituted human antibodies”.
- the reshaped human antibody refers to a modified antibody in which at least one CDR contained in the first human donor antibody is used in place of the CDR of the second human acceptor antibody in the second human acceptor antibody. Preferably all six CDRs are replaced. More preferably, the entire antigen binding region (eg, Fv, Fab or F (ab ′) 2) of the first human donor antibody is used in place of the corresponding region in the second human acceptor antibody. More preferably, the Fab region of the first human donor antibody is operably linked to an appropriate constant region of the second human acceptor antibody to form a full length antibody.
- Reconstituted human antibodies can be produced using general gene recombination techniques disclosed in, for example, EP 125023, WO 96/02576, Reference 16 above. Specifically, for example, a DNA sequence designed to link a target CDR in a donor human antibody and a target framework region (FR) in an acceptor human antibody overlaps with the terminal regions of both the CDR and FR. Using several oligonucleotides prepared so as to have a part to be synthesized as primers, the DNA is synthesized by the PCR method (see the method described in WO 98/13388).
- the reconstructed human antibody can be obtained by ligating the obtained DNA with DNA encoding a human antibody constant region or a human antibody constant region variant, then incorporating the DNA into an expression vector, introducing it into a host and producing it. (See EP 125023, WO 96/02576).
- artificial human antibody is included in the human antibody.
- the artificial human antibody can be produced, for example, using a general gene recombination technique disclosed in the above-mentioned document 16 or the like.
- the antibody of the present invention includes a fusion protein in which the above-described antibody is fused with another peptide or protein.
- a polynucleotide encoding an antibody of the present invention and a polynucleotide encoding another peptide or polypeptide are linked so that the frames coincide with each other, introduced into an expression vector, and expressed in a host. Any technique known to those skilled in the art can be used.
- Other peptides subjected to fusion with the antibody of the present invention include, for example, FLAG (Hopp, T. P.
- polypeptides to be subjected to fusion with the antibody of the present invention examples include GST (glutathione-S-transferase), HA (influenza agglutinin), immunoglobulin constant region, ⁇ -galactosidase, MBP (maltose). Binding protein) and the like. Preparing a fusion polypeptide by fusing a commercially available polynucleotide encoding the peptide or polypeptide with a polynucleotide encoding the antibody of the present invention and expressing the fusion polynucleotide prepared thereby. Can do.
- the antibody of the present invention may be a conjugated antibody bound to various molecules such as a polymer such as polyethylene glycol (PEG) or hyaluronic acid, a radioactive substance, a fluorescent substance, a luminescent substance, an enzyme, or a toxin.
- a conjugated antibody can be obtained by chemically modifying the obtained antibody.
- the modification method of an antibody has already been established in this field (for example, US5057313, US5156840).
- the antibody of the present invention is preferably isolated or purified. “Isolated or purified” means that an operation for removing components other than the target component from a naturally occurring state has been performed.
- the purity (the ratio of the weight of the antibody of the present invention to the total protein weight) of the isolated or purified antibody of the present invention is usually 50% or more, preferably 70% or more, more preferably 90% or more, most preferably 95% or more (for example, substantially 100%).
- the antibody of the present invention binds to human ADAM28 at an epitope comprising the amino acid sequence represented by SEQ ID NO: 21, 22 or 23.
- the epitope containing the amino acid sequence represented by SEQ ID NO: 21 is a continuous partial sequence of the amino acid sequence represented by SEQ ID NO: 4, and the amino acid sequence represented by SEQ ID NO: 21 And an epitope consisting of a partial sequence of preferably 20 amino acids or less, more preferably 12 amino acids or less.
- an epitope including the amino acid sequence represented by SEQ ID NO: 21 an epitope comprising the amino acid sequence represented by SEQ ID NO: 21, an epitope comprising the amino acid sequence represented by SEQ ID NO: 32 (FTLENFSKWRGS), and The epitope which consists of an amino acid sequence (ENFSKWRGSVLS) represented by sequence number 33 can be mentioned.
- the epitope containing the amino acid sequence represented by SEQ ID NO: 22 is a continuous partial sequence of the amino acid sequence represented by SEQ ID NO: 4, and the amino acid sequence represented by SEQ ID NO: 22 And an epitope consisting of a partial sequence of preferably 20 amino acids or less, more preferably 12 amino acids or less.
- Specific examples of the epitope including the amino acid sequence represented by SEQ ID NO: 22 include an epitope consisting of the amino acid sequence represented by SEQ ID NO: 22.
- the epitope including the amino acid sequence represented by SEQ ID NO: 23 is a continuous partial sequence of the amino acid sequence represented by SEQ ID NO: 4, and the amino acid sequence represented by SEQ ID NO: 23 And an epitope consisting of a partial sequence of preferably 20 amino acids or less, more preferably 12 amino acids or less.
- an epitope including the amino acid sequence represented by SEQ ID NO: 23 an epitope consisting of the amino acid sequence represented by SEQ ID NO: 23, an epitope consisting of the amino acid sequence represented by SEQ ID NO: 34 (LSNCLFNAPLPT), and The epitope which consists of an amino acid sequence (CLFNAPLPTDII) represented by sequence number 35 can be mentioned.
- Preferred embodiments of the antibody of the present invention include the antibodies described in the following (1) to (4): (1) comprising a light chain variable region and a heavy chain variable region,
- the light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 5, CDR2 having the amino acid sequence represented by SEQ ID NO: 6 and CDR3 having the amino acid sequence represented by SEQ ID NO: 7, and
- the light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 5, CDR2 having the amino acid sequence represented by SEQ ID NO: 6 and CDR3 having the amino acid sequence represented by SEQ ID NO: 7, and
- An antibody wherein the heavy chain variable region comprises CDR1 having the amino acid
- the light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 11, CDR2 having the amino acid sequence represented by SEQ ID NO: 12, and CDR3 having the amino acid sequence represented by SEQ ID NO: 13, and An antibody in which the heavy chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 14, CDR2 having the amino acid sequence represented by SEQ ID NO: 15 and CDR3 having the amino acid sequence represented by SEQ ID NO: 16; (4) comprising a light chain variable region and a heavy chain variable region, The light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 11, CDR2 having the amino acid sequence represented by SEQ ID NO: 12, and CDR3 having the amino acid sequence represented by SEQ ID NO:
- the light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 24, CDR2 having the amino acid sequence represented by SEQ ID NO: 25, and CDR3 having the amino acid sequence represented by SEQ ID NO: 26, and An antibody in which the heavy chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 27, CDR2 having the amino acid sequence represented by SEQ ID NO: 28, and CDR3 having the amino acid sequence represented by SEQ ID NO: 29; (6) comprising a light chain variable region and a heavy chain variable region, The light chain variable region comprises CDR1 having the amino acid sequence represented by SEQ ID NO: 24, CDR2 having the amino acid sequence represented by SEQ ID NO: 25, and CDR3 having the amino acid sequence represented by SEQ ID NO:
- the number of substitutions, deletions, insertions and / or additions is such that the antibody has specific binding activity for human ADAM28 and human ADAM28 Although it does not specifically limit as long as it has the activity which inhibits the enzyme activity of this, Preferably it is less than 2 amino acids per one CDR sequence, More preferably, it is 1 amino acid. Further, the number of CDR sequences in which amino acids are substituted, deleted, inserted and / or added is particularly limited as long as the antibody has a specific binding activity to human ADAM28 and an activity to inhibit the enzymatic activity of human ADAM28.
- Examples of a method for substituting one or more amino acid residues with other amino acids of interest include, for example, site-directed mutagenesis (Hashimoto-Gotoh, T, Mizuno, T, Ogasahara, Y, and Nakagawa, M. (1995). ) An oligodeoxyribonucleotide-directed dual amber method for site-directed mutagenesis. Gene 152, 271-275, Zoller, MJ, and Smith, M. (1983) Oligonucleotide-directed mutagenesis of DNA fragments cloned into M13 vectors.M ths Enzymol.
- the framework region (FR) of the antibody linked to the CDR is selected so that the CDR forms a favorable antigen binding site.
- the FR used in the antibody of the present invention is not particularly limited, and any FR may be used, but it is preferable to use a human antibody FR.
- the FR of a human antibody may be a FR having a natural sequence, and if necessary, one or more amino acids in a framework region having a natural sequence are substituted so that the CDR forms an appropriate antigen-binding site. , Deletion, addition and / or insertion.
- a mutant FR sequence having a desired property can be selected by measuring and evaluating the antigen-binding activity of an antibody using FRs substituted with amino acids (Sato, K. et al., Cancer Res. (1993). 53, 851-856).
- the human antibody Vk1 (Kabat database) FR is preferably used for the light chain, and the human antibody VH5 (Kabat database) FR is preferably used for the heavy chain. It is done.
- the human antibody Vk2 (Kabat database) FR is preferably used for the light chain, and the human antibody VH6 (Kabat database) FR is preferably used for the heavy chain. It is done.
- the human antibody Vk2 (Kabat database) FR is preferably used for the light chain
- the human antibody VH3 (Kabat database) FR is preferably used for the heavy chain. It is done.
- the constant region used in the antibody of the present invention is not particularly limited, and any constant region may be used.
- the constant region used in the antibody of the present invention include human antibody constant regions (such as IgG1, IgG2, IgG3, IgG4, IgA, and IgM-derived constant regions).
- C ⁇ 1, C ⁇ 2, C ⁇ 3, C ⁇ 4, C ⁇ , C ⁇ , C ⁇ 1, C ⁇ 2, and C ⁇ can be used for the H chain, and C ⁇ and C ⁇ can be used for the L chain.
- the C ⁇ constant region of a human antibody is preferably used for the light chain, and the C ⁇ 1 constant region of the human antibody is preferably used for the heavy chain.
- the C ⁇ constant region of a human antibody is preferably used for the light chain, and the C ⁇ 1 constant region of the human antibody is preferably used for the heavy chain.
- Preferred antibodies of the present invention include the following: (1 ′) an amino acid comprising a light chain variable region and a heavy chain variable region, wherein the light chain variable region comprises an amino acid sequence represented by SEQ ID NO: 17, and wherein the heavy chain variable region is represented by SEQ ID NO: 18 An antibody comprising a sequence; (3 ′) an amino acid comprising a light chain variable region and a heavy chain variable region, the light chain variable region comprising the amino acid sequence represented by SEQ ID NO: 19, and the heavy chain variable region represented by SEQ ID NO: 20 An antibody comprising a sequence; and (5 ′) a light chain variable region and a heavy chain variable region, wherein the light chain variable region comprises the amino acid sequence represented by SEQ ID NO: 30, and the heavy chain variable region is a sequence An antibody comprising the amino acid sequence represented by No. 31.
- the antibody (1 ') corresponds to the preferred embodiment of the antibody (1), and the antibody (3') corresponds to the preferred embodiment of the antibody (3).
- the antibody (5 ') corresponds to a preferred embodiment of the antibody (5).
- the present invention also provides a polynucleotide comprising a nucleotide sequence encoding the antibody of the present invention.
- the polynucleotide may be DNA or RNA, or may be a DNA / RNA chimera.
- the polynucleotide may be double-stranded or single-stranded. In the case of a double strand, it may be a double-stranded DNA, a double-stranded RNA or a DNA: RNA hybrid.
- the polynucleotide of the present invention includes a polynucleotide comprising a nucleotide sequence encoding both the heavy chain variable region and the light chain variable region of the antibody of the present invention, and a polynucleotide comprising a nucleotide sequence encoding the heavy chain variable region. And a polynucleotide comprising a nucleotide sequence encoding a light chain variable region is included.
- the polynucleotide of the present invention can be easily produced by utilizing a known gene recombination technique based on the amino acid sequence information of the antibody of the present invention, known sequence information, or sequence information described in the sequence listing of the present specification. can do. For example, by designing an appropriate primer based on the sequence information, amplifying DNA encoding the component constituting the antibody of the present invention by PCR reaction, and ligating the DNA fragment using an appropriate enzyme such as ligase, The polynucleotide of the present invention can be produced. Alternatively, a polynucleotide encoding each component may be synthesized by a polynucleotide synthesizer based on the amino acid sequence information of the antibody of the present invention.
- the obtained polynucleotide encoding the antibody of the present invention can be used as it is or after digestion with a restriction enzyme or adding a linker, if desired.
- the polynucleotide may have ATG as a translation initiation codon on the 5 'end side, and may have TAA, TGA or TAG as a translation stop codon on the 3' end side. These translation initiation codon and translation termination codon can be added using an appropriate synthetic DNA adapter.
- the polynucleotide of the present invention is preferably isolated or purified.
- the purity of the isolated or purified polynucleotide of the present invention is usually 50% or more, preferably 70% or more, more preferably 90% or more, Most preferably, it is 95% or more (for example, substantially 100%).
- the present invention provides a vector containing the polynucleotide of the present invention.
- the vector of the present invention includes a vector comprising a polynucleotide comprising a nucleotide sequence encoding both the heavy chain variable region and the light chain variable region of the antibody of the present invention, and a polynucleotide comprising a nucleotide sequence encoding the heavy chain variable region And a vector comprising a polynucleotide comprising a nucleotide sequence encoding a light chain variable region.
- the vector is preferably isolated or purified. Examples of the vector include an expression vector and a cloning vector, and can be selected according to the purpose. Preferably, the vector is an expression vector.
- the expression vector can express the antibody of the present invention.
- the expression vector can be produced by operably linking the polynucleotide of the present invention downstream of a promoter in an appropriate expression vector.
- Examples of the vector include plasmid vectors and virus vectors, and can be appropriately selected depending on the host to be used.
- hosts include Escherichia (Escherichia coli, etc.), Bacillus (Bacillus subtilis, etc.), yeast (Saccharomyces cerevisiae, night, etc.). Larvae-derived cell lines (Spodoptera frugiperda cells; Sf cells), insects (larvae of silkworms), mammalian cells (rat neurons, monkey cells (COS-7, etc.), Chinese hamster cells (CHO cells, etc.) Etc.) is used.
- mammals include, for example, laboratory animals such as rodents and rabbits such as mice, rats, hamsters, and guinea pigs, domestic animals such as pigs, cows, goats, horses, sheep and minks, pets such as dogs and cats, humans, Examples include, but are not limited to, primates such as monkeys, cynomolgus monkeys, rhesus monkeys, marmosets, orangutans and chimpanzees.
- plasmid vectors derived from E. coli (eg, pBR322, pBR325, pUC12, pUC13), plasmid vectors derived from Bacillus subtilis (eg, pUB110, pTP5, pC194), yeast-derived plasmid vectors (eg, pSH19, pSH15), etc. And can be appropriately selected depending on the type of host used and the purpose of use.
- the type of virus vector can be appropriately selected according to the type of host used and the purpose of use. For example, when insect cells are used as the host, baculovirus vectors can be used. When mammalian cells are used as hosts, Moloney murine leukemia virus vectors, lentivirus vectors, Sindbis virus vectors and other retrovirus vectors, adenovirus vectors, herpes virus vectors, adeno-associated virus vectors, parvovirus vectors, Vaccinia virus vectors, Sendai virus vectors and the like can be used.
- a promoter that can start transcription in the host can be selected according to the type of host to be used. For example, when the host is Escherichia, trp promoter, lac promoter, T7 promoter and the like are preferable. When the host is Bacillus, SPO1 promoter, SPO2 promoter, penP promoter and the like are preferable. When the host is yeast, PHO5 promoter, PGK promoter and the like are preferable. When the host is an insect cell, a polyhedrin promoter, a P10 promoter and the like are preferable. When the host is a mammalian cell, a subgenomic (26S) promoter, CMV promoter, SR ⁇ promoter and the like are preferable.
- the vector of the present invention may contain a signal sequence for antibody secretion.
- a signal sequence for antibody secretion the pelB signal sequence (Lei, SP et al. J. Bacteriol. (1987) 169, 4379) may be used in the case of production in the periplasm of E. coli.
- the vector of the present invention may contain an enhancer, a splicing signal, a poly A addition signal, a selection marker, an SV40 replication origin (hereinafter sometimes abbreviated as SV40ori) and the like in a functional manner, if desired.
- selectable markers include dihydrofolate reductase (hereinafter sometimes abbreviated as dhfr) gene [methotrexate (MTX) resistance], ampicillin resistance gene (sometimes abbreviated as Amp r ), neomycin resistance gene (Neo). G418 resistance) which may be abbreviated as r ).
- the above-described vector of the present invention is prepared according to a gene transfer method known per se (for example, lipofection method, calcium phosphate method, microinjection method, proplast fusion method, electroporation method, DEAE dextran method, Gene Gun gene transfer method, etc.) By introducing it into a host, a transformant introduced with the vector (transformant of the present invention) can be produced. By using an expression vector as the introduced vector, the transformant can express the antibody of the present invention.
- the transformant of the present invention is useful for producing the antibody of the present invention.
- the antibody of the present invention can be produced by culturing the transformant of the present invention by a method known per se according to the type of host and isolating the antibody of the present invention from the culture.
- the transformant whose host is Escherichia is cultured in an appropriate medium such as LB medium or M9 medium, usually at about 15 to 43 ° C. for about 3 to 24 hours.
- the transformant whose host is Bacillus is cultured in an appropriate medium, usually at about 30 to 40 ° C. for about 6 to 24 hours.
- Cultivation of the transformant whose host is yeast is usually carried out at about 20 ° C. to 35 ° C. for about 24 to 72 hours in a suitable medium such as a Burkholder medium.
- Incubation of transformants whose hosts are insect cells or insects is usually performed at about 27 ° C. for about 3 to 5 days in a suitable medium such as Grace's Insect medium supplemented with about 10% bovine serum. .
- a suitable medium such as Grace's Insect medium supplemented with about 10% bovine serum.
- the transformant whose host is an animal cell is cultured in an appropriate medium such as a MEM medium supplemented with about 10% bovine serum, usually at about 30 ° C. to 40 ° C. for about 15 to 60 hours. In any culture, aeration and agitation may be performed as necessary.
- Separation and purification of the antibody of the present invention from the culture may be carried out by any separation or purification method used in normal antibody purification, and is not limited in any way.
- any separation or purification method used in normal antibody purification and is not limited in any way.
- chromatography column, filter, ultrafiltration, salting out, solvent precipitation, solvent extraction, distillation, immunoprecipitation, SDS-polyacrylamide gel electrophoresis, isoelectric focusing, dialysis, recrystallization, etc. are appropriately selected.
- antibodies can be separated and purified.
- chromatography examples include affinity chromatography, ion exchange chromatography, hydrophobic chromatography, gel filtration, reverse phase chromatography, adsorption chromatography, and the like (Strates for Protein and Purification: Charactorization: A Laboratory Course Manual. Ed Dan. R. Marshak et al., Cold Spring Harbor or Laboratory Press, 1996). These chromatography can be performed using liquid phase chromatography, for example, liquid phase chromatography, such as HPLC and FPLC. Examples of columns used for affinity chromatography include a protein A column and a protein G column. For example, Hyper D, POROS, Sepharose FF (GE Amersham Biosciences) etc. are mentioned as a column using protein A. The present invention also encompasses antibodies highly purified using these purification methods.
- the present invention also provides a pharmaceutical composition containing the antibody of the present invention as an active ingredient.
- the pharmaceutical composition of the present invention is useful as a preventive or therapeutic agent for cancer; a cancer growth inhibitor; a cancer metastasis inhibitor;
- the type of cancer is not particularly limited as long as it can achieve the effect of preventing or treating cancer by the antibody of the present invention; the effect of inhibiting the growth of cancer; or the effect of inhibiting cancer metastasis, but it is not limited to liver cancer, colon cancer, kidney cancer, melanoma, Pancreatic cancer, thyroid cancer, gastric cancer, lung cancer (small cell lung cancer, non-small cell lung cancer), brain tumor, uterine cancer, breast cancer, multiple osteosarcoma, ovarian cancer, chronic leukemia, prostate cancer, acute lymphocytic leukemia, germ cell tumor, acute Examples include myeloid leukemia, malignant lymphoma, ciliary cancer, childhood malignant tumor, gallbladder / bile duct cancer and the like.
- ADAM28 inhibits the formation of IGF-1 / IGFBP-3 complex by degrading IGFBP-3 and promotes the proliferation of cancer cells by IGF-1.
- the antibody of the present invention inhibits the growth of cancer cells by IGF-1 by inhibiting the degradation of IGFBP-3 by ADAM28. Therefore, in one embodiment, the cancer to which the antibody of the present invention is applied is an IGF-1-sensitive cancer (that is, a cancer that exhibits IGF-1-dependent growth promotion). Whether or not the cancer is IGF-1 sensitive can be evaluated by analyzing the expression of the IGF-1 receptor in the cancer by Western blotting, RT-PCR or the like.
- ADAM28 inhibits cancer cell apoptosis induction by vWF by degrading von Willebrand factor (vWF).
- the antibody of the present invention inhibits the degradation of vWF by ADAM28, thereby promoting the induction of apoptosis of cancer cells by vWF and consequently suppressing the growth and metastasis of cancer. Therefore, in one embodiment, the cancer to which the present invention is applied is a vWF-sensitive cancer (that is, a cancer in which apoptosis is induced by vWF).
- Whether cancer is vWF-sensitive can be determined by culturing cancer cells on a vWF-coated plate and analyzing DNA fragmentation by the method described in J Natl Cancer Inst 2012; 104: 906-922, for example. It can be evaluated by doing.
- “Containing the antibody of the present invention as an active ingredient” means containing the antibody of the present invention as at least one of the active ingredients, and does not limit the content rate. Moreover, the pharmaceutical composition of the present invention may contain other active ingredients in combination with the antibody of the present invention.
- the antibody of the present invention can be formulated in accordance with a conventional method (for example, Remington's Pharmaceutical Science, latest edition, Mark Publishing Company, Easton, USA).
- a pharmaceutically acceptable carrier and / or additive may be included as necessary.
- surfactants PEG, Tween, etc.
- excipients antioxidants (ascorbic acid, etc.)
- coloring agents flavoring agents, preservatives, stabilizers, buffering agents (phosphoric acid, citric acid, other organic acids) Etc.), chelating agents (EDTA, etc.), suspending agents, tonicity agents, binders, disintegrating agents, lubricants, fluidity promoters, flavoring agents and the like.
- the pharmaceutical composition of the present invention is not limited to these and may contain other conventional carriers as appropriate. Specifically, light anhydrous silicic acid, lactose, crystalline cellulose, mannitol, starch, carmellose calcium, carmellose sodium, hydroxypropylcellulose, hydroxypropylmethylcellulose, polyvinylacetal diethylaminoacetate, polyvinylpyrrolidone, gelatin, medium chain fatty acid triglyceride, Examples thereof include polyoxyethylene hydrogenated castor oil 60, sucrose, carboxymethylcellulose, corn starch, and inorganic salts. It may also contain other low molecular weight polypeptides, proteins such as serum albumin, gelatin and immunoglobulins, and amino acids.
- the antibody of the present invention is dissolved in an isotonic solution containing, for example, physiological saline, glucose or other adjuvants.
- the adjuvant include D-sorbitol, D-mannose, D-mannitol, sodium chloride, and further suitable solubilizers such as alcohol (ethanol etc.), polyalcohol (propylene glycol, PEG etc.), A nonionic surfactant (polysorbate 80, HCO-50) or the like may be used in combination.
- polypeptides can be encapsulated in microcapsules (microcapsules such as hydroxymethylcellulose, gelatin, poly [methylmethacrylic acid]) or colloid drug delivery systems (liposomes, albumin microspheres, microemulsions, nanoparticles and nanoparticles). Capsules etc.) (see Remington's Pharmaceutical Science 16th edition &, Oslo Ed. (1980), etc.).
- a method of making a drug a sustained-release drug is also known and can be applied to a polypeptide (Langer et al., J. Biomed. Mater. Res. (1981) 15: 167-277; Langer, Chem. Tech. (1982) 12: 98-105; U.S.
- the content of the antibody of the present invention in the pharmaceutical composition is, for example, about 0.01 to 100% by weight, preferably 0.1 to 99.9% of the whole pharmaceutical composition.
- the pharmaceutical composition of the present invention can be administered either orally or parenterally, but is preferably administered parenterally. Specifically, it is administered to a patient by injection and transdermal administration.
- the injection form it can be administered systemically or locally by, for example, intravenous injection, intramuscular injection or subcutaneous injection. Local injections, particularly intramuscular injections, may be made at or around the treatment site.
- transdermal dosage forms include ointments, gels, creams, poultices, patches, and the like, which can be administered systemically or locally.
- the administration method can be appropriately selected depending on the age and symptoms of the patient.
- the dose can be selected in the range of 0.5 mg to 10 mg of the antibody of the present invention per kg body weight per time, for example.
- the pharmaceutical composition of the present invention is not limited to these doses.
- the rhADAM28 immobilized beads were added to the phage library to bind the antigen-specific antibody. After collecting the magnetic beads and washing several times, the phage was eluted from the magnetic beads. The eluted phages were infected with E. coli and cultured overnight at 37 ° C. In addition, the phage rescue operation from phage-infected Escherichia coli followed a general method (Molecular cloning third. Ed. Cold Spring Harbor Lab. Press, 2001). The selection round described above was repeated a plurality of times, and the operation of concentrating phages displaying antigen-specific antibodies was performed.
- IgG expression vector (heavy chain constant region is IgG1) was constructed by subcloning the obtained two clone Fab antibody genes. These expression vectors were transfected into HEK293T cells according to the standard method of Lipofectamine (manufactured by Invitrogen), and the culture supernatant after 72 hours of culture was collected. As the medium, DMEM (Sigma) supplemented with Ultra Low IgG FBS (manufactured by Invitrogen) at 10% was used.
- an IgG antibody was purified by a standard method using rProtein A Sepharose Fast Flow (manufactured by GE healthcare). The purified protein was confirmed to be a single band by SDS-PAGE, and the concentration was determined using BCA Protein Assay Kit (PIERCE).
- Example 2 Anti-human ADAM28 antibody human ADAM28 enzyme activity inhibitory effect rhADAM28 and anti-ADAM28 antibody were incubated for 2 hours at the weight ratio shown in the figure, then IGFBP-3 (100 ng) was added and incubated at 37 ° C for 24 hours, and 5 mM EDTA The reaction was terminated with SDS-sample buffer containing. Thereafter, the reaction product was subjected to SDS-PAGE (10% acrylamide gel), and the degree of IGFBP-3 degradation was detected by immunoblotting using an anti-IGFBP-3 antibody (Santa Cruz Biotechnology, Inc., Santa Cruz, Calif.). (FIG. 1). Both antibodies 211-14 and 211-12 inhibited the degradation of IGFBP-3 by human ADAM28.
- Example 3 Proliferation inhibitory effect of anti-human ADAM28 antibody on breast cancer cell line 5-GF-2-deoxy-uridine (BrdUrd) Labeling and Detection Kit according to the manufacturer's instructions on the mitogenic effect of IGF-I on MDA-MB231 cells Measurements were made using III (Roche Molecular Biochemicals, Basel, Switzerland). After synchronization and growth arrest, cells were treated with 1 ⁇ g / ml IGF-1 in DMEM containing 1% FBS. After 6 hours, BrdUrd (10 ⁇ mol / L) was added to the medium, and the cells were further cultured for 42 hours.
- Anti-human ADAM28 antibody suppresses cancer cell proliferation in vivo ADAM28 high-expressing breast cancer cell line MDA-MB231 ffLuc-cp156 that constitutively expresses luciferase using a lentiviral vector was prepared, and NOD / SCID mice (Six-week-old male , Charles River Laboratories International Inc, Washington, MA). After transplantation, anti-ADAM28 antibody (2 mg / kg / mice) was locally injected 5 times at 2-day intervals, and the effect of suppressing tumor growth was examined.
- Example 5 Inhibitory effect of anti-human ADAM28 antibody on metastasis of cancer cells in vivo PC-9 ffLuc-cp156 cells in the tail vein of male NOD / SCID mice (6 weeks old) (Charles River Laboratories International, Inc., Wilmington, Mass. ) 1 ⁇ 10 6 ) were injected in 300 ⁇ l of PBS. Lung metastases were monitored by bioluminescence imaging using an In Vivo Imaging System (IVIS) -100 camera system (Xenogen Co., Alameda, Calif.) For detection of luciferase activity according to the manufacturer's instructions.
- IVIS In Vivo Imaging System
- mice were anesthetized with isoflurane and D-luciferin (150 mg / kg; Promega Co., Madison, Wis.) was injected intraperitoneally and 1 minute later, photons from the whole animal were counted.
- D-luciferin 150 mg / kg; Promega Co., Madison, Wis.
- Example 6 In Example 4, RT-PCR was performed from RNA extracted from each mouse organ 6 weeks after transplantation of cancer cells using luciferase-specific primers to confirm the presence or absence of tumor-derived gene expression. The presence or absence of natural metastasis was examined (FIG. 5). Both antibodies 211-14 and 211-12 suppressed micrometastasis of cancer cells.
- Example 7 From the cDNA of the hybridoma producing the mouse anti-human ADAM28 monoclonal antibody 297-2F3 obtained in Example 1 (7) above, the variable region of the antibody was PCR amplified, sub-cloned into a cloning vector, and the base of the region The sequence was analyzed. Table 2 shows the amino acid sequence of CDR (complementarity determining region). The full-length amino acid sequences of the light chain and heavy chain variable regions are shown in SEQ ID NOs: 146 and 147, respectively.
- each CDR of the mouse anti-human ADAM28 monoclonal antibody 297-2F3 was grafted to a human antibody frame for humanization.
- the resulting full-length amino acid sequences of the light chain and heavy chain variable regions of humanized 297-2F3 are shown in SEQ ID NOs: 30 and 31, respectively.
- Example 9 Epitope identification (1) Epitope mapping was performed for anti-human ADAM28 antibodies 211-12 and 297-2F3 using a peptide array in which a partial peptide of human ADAM28s was immobilized. Specifically, as shown in the table below, a peptide comprising a peptide group having 12 amino acid residues and 3 amino acid residues offset with respect to a sequence covering from the protease domain of human ADAM28s to the C-terminus. An array was made. HRP-labeled anti-human ADAM28s antibody was reacted with the peptide array.
- 211-12 specifically bound to the peptides # 25 and # 26. From this result, it was suggested that the epitope of 211-12 includes the amino acid sequence (ENFSKWRGS) represented by SEQ ID NO: 21 common to peptides # 25 and # 26.
- ENFSKWRGS amino acid sequence represented by SEQ ID NO: 21 common to peptides # 25 and # 26.
- 297-2F3 specifically bound to the peptides # 65 and # 66.
- the epitope of 297-2F3 contains the amino acid sequence represented by SEQ ID NO: 23 (LFNAPLPT) was included.
- 297-2F3 specifically recognizes SEQ ID NO: 23 as an epitope by dot blot using Escherichia coli lysate forcibly expressing a fusion protein in which the amino acid sequence represented by SEQ ID NO: 23 is added to the C-terminus of MBP It was confirmed.
- Epitope identification (2) A fusion protein in which a partial sequence of the following region of human ADAM28s (SEQ ID NO: 4) was added to the C-terminus of MBP was prepared. 399-540, 399-497, 491-540, 491-510, 501-220, 511-530, 521-540, 513-522, 515-524, 517-526, 519-528 As a control, a fusion protein was prepared by adding a partial sequence of the following region of human ADAM28m (SEQ ID NO: 2) to the C-terminus of MBP. 517-526 (human ADAM28m, as control)
- the reactivity of the anti-human ADAM28 antibody 211-14 to the fusion protein was evaluated by Western blotting. As a result, 211-14 strongly bound to a fusion protein containing partial sequences of the regions 399-540, 491-540, 511-530, and 517-526 of human ADAM28s. From this result, it was suggested that the epitope of 211-14 includes the region 517-526 of human ADAM28s (TELWGPGRRT, SEQ ID NO: 22).
- an anti-human ADAM28 antibody applicable to cancer prevention or treatment is provided.
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Abstract
Description
[1]ヒトADAM28に特異的に結合し、且つヒトADAM28の酵素活性を阻害する活性を有する、抗体。
[2]配列番号21、22又は23で表されるアミノ酸配列を含むエピトープにおいて、ヒトADAM28に結合する、[1]に記載の抗体。
[3]軽鎖可変領域及び重鎖可変領域を含み、
(1)該軽鎖可変領域が、配列番号5で表されるアミノ酸配列を有するCDR1、配列番号6で表されるアミノ酸配列を有するCDR2及び配列番号7で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号8で表されるアミノ酸配列を有するCDR1、配列番号9で表されるアミノ酸配列を有するCDR2及び配列番号10で表されるアミノ酸配列を有するCDR3を含む;
(2)該軽鎖可変領域が、配列番号5で表されるアミノ酸配列を有するCDR1、配列番号6で表されるアミノ酸配列を有するCDR2及び配列番号7で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号8で表されるアミノ酸配列を有するCDR1、配列番号9で表されるアミノ酸配列を有するCDR2及び配列番号10で表されるアミノ酸配列を有するCDR3を含む
(但し、配列番号5、6及び7で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加しており、且つ/或いは、
配列番号8、9及び10で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加している);
(3)該軽鎖可変領域が、配列番号11で表されるアミノ酸配列を有するCDR1、配列番号12で表されるアミノ酸配列を有するCDR2及び配列番号13で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号14で表されるアミノ酸配列を有するCDR1、配列番号15で表されるアミノ酸配列を有するCDR2及び配列番号16で表されるアミノ酸配列を有するCDR3を含む;
(4)該軽鎖可変領域が、配列番号11で表されるアミノ酸配列を有するCDR1、配列番号12で表されるアミノ酸配列を有するCDR2及び配列番号13で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号14で表されるアミノ酸配列を有するCDR1、配列番号15で表されるアミノ酸配列を有するCDR2及び配列番号16で表されるアミノ酸配列を有するCDR3を含む
(但し、配列番号11、12及び13で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加しており、且つ/或いは、
配列番号14、15及び16で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加している);
(5)該軽鎖可変領域が、配列番号24で表されるアミノ酸配列を有するCDR1、配列番号25で表されるアミノ酸配列を有するCDR2及び配列番号26で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号27で表されるアミノ酸配列を有するCDR1、配列番号28で表されるアミノ酸配列を有するCDR2及び配列番号29で表されるアミノ酸配列を有するCDR3を含む;又は
(6)該軽鎖可変領域が、配列番号24で表されるアミノ酸配列を有するCDR1、配列番号25で表されるアミノ酸配列を有するCDR2及び配列番号26で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号27で表されるアミノ酸配列を有するCDR1、配列番号28で表されるアミノ酸配列を有するCDR2及び配列番号29で表されるアミノ酸配列を有するCDR3を含む
(但し、配列番号24、25及び26で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加しており、且つ/或いは、
配列番号27、28及び29で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加している);
ことを特徴とする[1]に記載の抗体。
[4](1’)該軽鎖可変領域が配列番号17で表されるアミノ酸配列を含み、且つ、該重鎖可変領域が配列番号18で表されるアミノ酸配列を含む;
(3’)該軽鎖可変領域が配列番号19で表されるアミノ酸配列を含み、且つ、該重鎖可変領域が配列番号20で表されるアミノ酸配列を含む、又は
(5’)該軽鎖可変領域が配列番号30で表されるアミノ酸配列を含み、且つ、該重鎖可変領域が配列番号31で表されるアミノ酸配列を含む、[3]に記載の抗体。
[5][1]~[4]のいずれかに記載の抗体を含む医薬組成物。
[6][1]~[4]のいずれかに記載の抗体を含む、癌の予防又は治療剤。
[7][1]~[4]のいずれかに記載の抗体を含む、癌転移阻害剤。
[8]哺乳動物へ有効量の[1]~[4]のいずれかに記載の抗体を投与することを含む、該哺乳動物における癌の予防又は治療方法。
[9]哺乳動物がヒトである、[8]記載の方法。
[10]哺乳動物へ有効量の[1]~[4]のいずれかに記載の抗体を投与することを含む、該哺乳動物における癌転移阻害方法。
[11]哺乳動物がヒトである、[10]記載の方法。
[12]癌の予防又は治療において使用するための、[1]~[4]のいずれかに記載の抗体。
[13]癌転移阻害において使用するための、[1]~[4]のいずれかに記載の抗体。
[14]癌の予防又は治療剤の製造のための、[1]~[4]のいずれかに記載の抗体の使用。
[15]癌転移阻害剤の製造のための、[1]~[4]のいずれかに記載の抗体の使用。
[16][1]~[4]のいずれかに記載の抗体をコードするポリヌクレオチド。
[17][16]に記載のポリヌクレオチドを含むベクター。
[18][17]に記載のベクターを含む形質転換体。
(1)軽鎖可変領域及び重鎖可変領域を含み、
該軽鎖可変領域が、配列番号5で表されるアミノ酸配列を有するCDR1、配列番号6で表されるアミノ酸配列を有するCDR2及び配列番号7で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号8で表されるアミノ酸配列を有するCDR1、配列番号9で表されるアミノ酸配列を有するCDR2及び配列番号10で表されるアミノ酸配列を有するCDR3を含む、抗体;
(2)軽鎖可変領域及び重鎖可変領域を含み、
該軽鎖可変領域が、配列番号5で表されるアミノ酸配列を有するCDR1、配列番号6で表されるアミノ酸配列を有するCDR2及び配列番号7で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号8で表されるアミノ酸配列を有するCDR1、配列番号9で表されるアミノ酸配列を有するCDR2及び配列番号10で表されるアミノ酸配列を有するCDR3を含む、抗体
(但し、配列番号5、6及び7で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加しており、且つ/或いは、
配列番号8、9及び10で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加している)。
(3)軽鎖可変領域及び重鎖可変領域を含み、
該軽鎖可変領域が、配列番号11で表されるアミノ酸配列を有するCDR1、配列番号12で表されるアミノ酸配列を有するCDR2及び配列番号13で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号14で表されるアミノ酸配列を有するCDR1、配列番号15で表されるアミノ酸配列を有するCDR2及び配列番号16で表されるアミノ酸配列を有するCDR3を含む、抗体;
(4)軽鎖可変領域及び重鎖可変領域を含み、
該軽鎖可変領域が、配列番号11で表されるアミノ酸配列を有するCDR1、配列番号12で表されるアミノ酸配列を有するCDR2及び配列番号13で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号14で表されるアミノ酸配列を有するCDR1、配列番号15で表されるアミノ酸配列を有するCDR2及び配列番号16で表されるアミノ酸配列を有するCDR3を含む、抗体
(但し、配列番号11、12及び13で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加しており、且つ/或いは、
配列番号14、15及び16で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加している);
(5)軽鎖可変領域及び重鎖可変領域を含み、
該軽鎖可変領域が、配列番号24で表されるアミノ酸配列を有するCDR1、配列番号25で表されるアミノ酸配列を有するCDR2及び配列番号26で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号27で表されるアミノ酸配列を有するCDR1、配列番号28で表されるアミノ酸配列を有するCDR2及び配列番号29で表されるアミノ酸配列を有するCDR3を含む、抗体;及び
(6)軽鎖可変領域及び重鎖可変領域を含み、
該軽鎖可変領域が、配列番号24で表されるアミノ酸配列を有するCDR1、配列番号25で表されるアミノ酸配列を有するCDR2及び配列番号26で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号27で表されるアミノ酸配列を有するCDR1、配列番号28で表されるアミノ酸配列を有するCDR2及び配列番号29で表されるアミノ酸配列を有するCDR3を含む、抗体
(但し、配列番号24、25及び26で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加しており、且つ/或いは、
配列番号27、28及び29で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加している)。
(3)及び(4)の抗体においては、軽鎖については、好ましくはヒト抗体のVk2(Kabat database)のFRが、重鎖については、好ましくはヒト抗体のVH6(Kabat database)のFRが用いられる。
(5)及び(6)の抗体においては、軽鎖については、好ましくはヒト抗体のVk2(Kabat database)のFRが、重鎖については、好ましくはヒト抗体のVH3(Kabat database)のFRが用いられる。
(5)及び(6)の抗体においては、軽鎖については、好ましくはヒト抗体のCκの定常領域が、重鎖については、好ましくはヒト抗体のCγ1の定常領域が用いられる。
(1’)軽鎖可変領域及び重鎖可変領域を含み、該軽鎖可変領域が配列番号17で表されるアミノ酸配列を含み、且つ、該重鎖可変領域が配列番号18で表されるアミノ酸配列を含む、抗体;
(3’)軽鎖可変領域及び重鎖可変領域を含み、該軽鎖可変領域が配列番号19で表されるアミノ酸配列を含み、且つ、該重鎖可変領域が配列番号20で表されるアミノ酸配列を含む、抗体;及び
(5’)軽鎖可変領域及び重鎖可変領域を含み、該軽鎖可変領域が配列番号30で表されるアミノ酸配列を含み、且つ、該重鎖可変領域が配列番号31で表されるアミノ酸配列を含む、抗体。
抗原および抗体作製
(1)ヒトADAM28組み換えタンパク質(rhADAM28)の作製
完全長rhADAM28は、Biochem Biophys Res Commun. 2004; 315: 79-84に記載の方法にしたがって、作製および精製された。
精製したrhADAM28は、EZ-Link NHS-PEO4-Biotin(Thermo Scientific)の標準プロトコールに従ってビオチン化し、BCA Protein Assay Kit(PIERCE社製)を用いて濃度を決定した。
ビオチン化したrhADAM28は、ストレプトアビジンコート磁性体ビーズ(Dynabeads MyOne Streptavidin T1 磁性体ビーズ、Invitrogen社製)100μlに4℃、1時間固相化し、1mlのPBST(0.05% Tween 20含有PBS)で5回洗浄した。ヒト抗体ファージライブラリーにはHuCAL GOLD(MorphoSys社製)を用い、WO2007/042309及びWO2006/122797等に記載された方法に従って抗体選択を行った。ファージライブラリーにrhADAM28固相化ビーズを加えて抗原特異的抗体を結合させた。磁性体ビーズを回収し、数回洗浄を行った後、ファージを磁性体ビーズから溶出させた。溶出したファージは、大腸菌に感染させ、37℃で一晩培養した。尚、ファージ感染大腸菌からのファージレスキュー操作は一般的な方法に従った(Molecular cloning third. Ed. Cold Spring Harbor Lab. Press, 2001)。以上に記載した選択ラウンドを複数回繰り返して抗原特異的抗体を提示するファージの濃縮操作を行った。
濃縮操作後に得られたFab遺伝子のプールを大腸菌発現ベクターにサブクローニングした。WO2006/122797等に記載の手法に従って、Fab抗体を発現させ、ELISA法により抗原特異的抗体のスクリーニングを行った。Fab抗体は大腸菌破砕液の可溶性画分よりStrep-Tactinカラム(IBA社製)の標準法に従い精製を行った。また、SDS-PAGEによって精製抗体の純度を確認し、BCA Protein Assay Kit(PIERCE社製)を用いて濃度を決定した。
得られた2クローン(211-12、211-14)の大腸菌を培養し、プラスミドを回収(QIAprep Spin MiniPrep kit:QIAGEN社製)して塩基配列解析に使用した。表1に、それぞれのクローンのCDR(相補性決定領域)のアミノ酸配列を示す。また、各クローンの可変領域の全長アミノ酸配列を配列番号17~20に示す。
得られた2クローンのFab抗体遺伝子をサブクローニングすることでIgG発現ベクター(重鎖の定常領域はIgG1)を構築した。これらの発現ベクターをLipofectamine(Invitrogen社製)の標準方法に従ってHEK293T細胞にトランスフェクションし、72時間培養後の培養上清を回収した。尚、培地にはUltra Low IgG FBS(Invitrogen社製)を10%で添加したDMEM(Sigma)を用いた。この培養上清からrProteinA Sepharose Fast Flow(GE healthcare社製)を用いた標準方法によってIgG抗体を精製した。精製後のタンパク質はSDS-PAGEによって単一バンドであることを確認し、BCA Protein Assay Kit(PIERCE社製)を用いて濃度を決定した。
精製したrhADAM28を抗原として用いて、ヒトADAM28タンパク質に対するモノクローナル抗体を樹立した。rhADAM28を用いたELISAによりまず5つのクローン選抜し、クローン297-2F3をヒトADAM28に対する抗体の候補として選択した。モノクローナル抗体(297-2F3)の単一反応性を、組み換え型ヒトADAM28のイムノブロッティングにより決定した。
抗ヒトADAM28抗体のヒトADAM28酵素活性抑制効果
rhADAM28と抗ADAM28抗体を、図中に示す重量比で2時間インキュベート後、IGFBP-3(100ng)を加えて37℃で24時間インキュベートし、5mMのEDTAを含むSDS-sample bufferで反応を終了させた。その後、反応産物をSDS-PAGE(10% アクリルアミドゲル)し、抗IGFBP-3抗体(Santa Cruz Biotechnology, Inc., Santa Cruz, CA)を用いたイムノブロット法によりIGFBP-3分解の程度を検出した(図1)。211-14及び211-12のいずれの抗体も、ヒトADAM28によるIGFBP-3の分解を抑制した。
乳癌細胞株に対する抗ヒトADAM28抗体の増殖抑制効果
MDA-MB231細胞に対するIGF-Iの細胞分裂促進効果を、製造者の指示書に従い、5-bromo-2’deoxy-uridine (BrdUrd) Labeling and Detection Kit III (Roche Molecular Biochemicals, Basel, Switzerland)を用いて測定した。同期化及び増殖停止の後、細胞を1%FBSを含有するDMEM中の1μg/mlのIGF-1により処理した。6時間後、BrdUrd(10μmol/L)を培地へ添加し、更に42時間培養した。IGF-Iの細胞分裂促進効果へのADAM28活性の寄与を調べるため、細胞をIGF-I処理の30分前に、1又は5μg/mlの抗ADAM28抗体とともにインキュベートし、次に、IGF-Iの存在下で、42時間、BrdUrdと反応させた(図2)。211-14、211-12及び297-2F3のいずれの抗体もMDA-MB231細胞のインビトロ増殖を抑制した。
抗ヒトADAM28抗体のインビボにおける癌細胞増殖抑制効果
レンチウイルスベクターによりルシフェラーゼを恒常的に発現するADAM28高発現乳癌細胞株MDA-MB231 ffLuc-cp156を作製し、NOD/SCIDマウス(Six-week-old male, Charles River Laboratories International Inc, Washington, MA)の乳房皮下組織に移植(2 x 10e6個)した。移植後、抗ADAM28抗体(2mg/kg/mice)を2日間隔で5回局所注射し、腫瘍増殖の抑制効果を検討した。D-ルシフェリン(150mg/Kg)(Promega Co, Madison, MI)を腹腔内投与後in vivo imaging system (IVIS)-100 (Xenogen Co., Alameda, CA)にて発光を検出した(図3)。211-14及び211-12のいずれの抗体も、インビボにおけるMDA-MB231 ffLuc-cp156の増殖を抑制した。
抗ヒトADAM28抗体のインビボにおける癌細胞転移抑制効果
雄のNOD/SCIDマウス(6週齢)(Charles River Laboratories International, Inc., Wilmington, MA)の尾静脈中に、PC-9ffLuc-cp156細胞(300μlのPBS中に、1x106個)を注射した。製造者の指示書に従い、肺転移を、ルシフェラーゼ活性の検出のためのIn Vivo Imaging System (IVIS)-100カメラシステム(Xenogen Co., Alameda, CA)を用いた生物発光イメージングによりモニターした。イメージングの間、マウスを、イソフルランで麻酔し、D-ルシフェリン(150 mg/kg; Promega Co., Madison, WI)を腹腔内へ注射し、1分後、動物全身からの光子をカウントした。抗ADAM28中和抗体の、肺転移への効果を調べるため、PC-9ffLuc-cp156細胞を5μg/mlのマウス抗ヒトADAM28モノクローナル抗体(297-2F3)、又は5μg/mlの非免疫IgGとともに2時間、4℃にてインキュベートし、マウスへ静注した(1群あたりn = 9匹)(図4)。297-2F3投与によって癌転移が抑制された。
また、実施例4において、癌細胞移植後6週間後のマウスの各臓器から抽出したRNAから、ルシフェラーゼ特異的なプライマーを用いてRT-PCRを行い、腫瘍由来の遺伝子発現の有無を確認し、自然転移の有無を検討した(図5)。211-14及び211-12のいずれの抗体も、癌細胞の微小転移を抑制した。
上記実施例1(7)において得られた、マウス抗ヒトADAM28モノクローナル抗体297-2F3を産生するハイブリドーマのcDNAより、当該抗体の可変領域をPCR増幅し、クローニングベクターへサブローニングし、当該領域の塩基配列を解析した。表2に、CDR(相補性決定領域)のアミノ酸配列を示す。また、軽鎖及び重鎖可変領域の全長アミノ酸配列を配列番号146及び147にそれぞれ示す。
次に、WO98/13388に記載の方法を参照しつつ、マウス抗ヒトADAM28モノクローナル抗体297-2F3の各CDRを、ヒト抗体フレームにグラフティングし、ヒト化を行った。この結果得られたヒト化297-2F3の軽鎖及び重鎖可変領域の全長アミノ酸配列を配列番号30及び31にそれぞれ示す。
エピトープの同定(1)
ヒトADAM28sの部分ペプチドを固定化したペプチドアレイを用いて、抗ヒトADAM28抗体211-12及び297-2F3について、エピトープマッピングを行った。具体的には、下記の表のように、ヒトADAM28sのプロテアーゼドメインからC末端までをカバーする配列に対して、残基数が12アミノ酸残基でオフセットが3アミノ酸残基のペプチド群からなるペプチドアレイを作製した。HRP標識した抗ヒトADAM28s抗体をペプチドアレイと反応させた。
エピトープの同定(2)
MBPのC末端に、ヒトADAM28s(配列番号4)の以下の領域の部分配列を付加した融合タンパク質を、それぞれ調製した。
399-540、399-497、491-540、491-510、501-520、511-530、521-540、513-522、515-524、517-526、519-528
また、コントロールとして、MBPのC末端に、ヒトADAM28m(配列番号2)の以下の領域の部分配列を付加した融合タンパク質を調製した。
517-526(ヒトADAM28m、コントロールとして)
Claims (18)
- ヒトADAM28に特異的に結合し、且つヒトADAM28の酵素活性を阻害する活性を有する、抗体。
- 配列番号21、22又は23で表されるアミノ酸配列を含むエピトープにおいて、ヒトADAM28に結合する、請求項1記載の抗体。
- 軽鎖可変領域及び重鎖可変領域を含み、
(1)該軽鎖可変領域が、配列番号5で表されるアミノ酸配列を有するCDR1、配列番号6で表されるアミノ酸配列を有するCDR2及び配列番号7で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号8で表されるアミノ酸配列を有するCDR1、配列番号9で表されるアミノ酸配列を有するCDR2及び配列番号10で表されるアミノ酸配列を有するCDR3を含む;
(2)該軽鎖可変領域が、配列番号5で表されるアミノ酸配列を有するCDR1、配列番号6で表されるアミノ酸配列を有するCDR2及び配列番号7で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号8で表されるアミノ酸配列を有するCDR1、配列番号9で表されるアミノ酸配列を有するCDR2及び配列番号10で表されるアミノ酸配列を有するCDR3を含む
(但し、配列番号5、6及び7で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加しており、且つ/或いは、
配列番号8、9及び10で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加している);
(3)該軽鎖可変領域が、配列番号11で表されるアミノ酸配列を有するCDR1、配列番号12で表されるアミノ酸配列を有するCDR2及び配列番号13で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号14で表されるアミノ酸配列を有するCDR1、配列番号15で表されるアミノ酸配列を有するCDR2及び配列番号16で表されるアミノ酸配列を有するCDR3を含む;
(4)該軽鎖可変領域が、配列番号11で表されるアミノ酸配列を有するCDR1、配列番号12で表されるアミノ酸配列を有するCDR2及び配列番号13で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号14で表されるアミノ酸配列を有するCDR1、配列番号15で表されるアミノ酸配列を有するCDR2及び配列番号16で表されるアミノ酸配列を有するCDR3を含む
(但し、配列番号11、12及び13で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加しており、且つ/或いは、
配列番号14、15及び16で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加している);
(5)該軽鎖可変領域が、配列番号24で表されるアミノ酸配列を有するCDR1、配列番号25で表されるアミノ酸配列を有するCDR2及び配列番号26で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号27で表されるアミノ酸配列を有するCDR1、配列番号28で表されるアミノ酸配列を有するCDR2及び配列番号29で表されるアミノ酸配列を有するCDR3を含む;又は
(6)該軽鎖可変領域が、配列番号24で表されるアミノ酸配列を有するCDR1、配列番号25で表されるアミノ酸配列を有するCDR2及び配列番号26で表されるアミノ酸配列を有するCDR3を含み、且つ
該重鎖可変領域が、配列番号27で表されるアミノ酸配列を有するCDR1、配列番号28で表されるアミノ酸配列を有するCDR2及び配列番号29で表されるアミノ酸配列を有するCDR3を含む
(但し、配列番号24、25及び26で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加しており、且つ/或いは、
配列番号27、28及び29で表されるアミノ酸配列からなる群から選択される少なくとも1つのアミノ酸配列において、1~3個のアミノ酸が置換、欠失、挿入、及び/又は付加している);
ことを特徴とする請求項1に記載の抗体。 - (1’)該軽鎖可変領域が配列番号17で表されるアミノ酸配列を含み、且つ、該重鎖可変領域が配列番号18で表されるアミノ酸配列を含む;
(3’)該軽鎖可変領域が配列番号19で表されるアミノ酸配列を含み、且つ、該重鎖可変領域が配列番号20で表されるアミノ酸配列を含む;又は
(5’)該軽鎖可変領域が配列番号30で表されるアミノ酸配列を含み、且つ、該重鎖可変領域が配列番号31で表されるアミノ酸配列を含む請求項3に記載の抗体。 - 請求項1~4のいずれか1項に記載の抗体を含む医薬組成物。
- 請求項1~4のいずれか1項に記載の抗体を含む、癌の予防又は治療剤。
- 請求項1~4のいずれか1項に記載の抗体を含む、癌転移阻害剤。
- 哺乳動物へ有効量の請求項1~4のいずれか1項に記載の抗体を投与することを含む、該哺乳動物における癌の予防又は治療方法。
- 哺乳動物がヒトである、請求項8記載の方法。
- 哺乳動物へ有効量の請求項1~4のいずれか1項に記載の抗体を投与することを含む、該哺乳動物における癌転移阻害方法。
- 哺乳動物がヒトである、請求項10記載の方法。
- 癌の予防又は治療において使用するための、請求項1~4のいずれか1項に記載の抗体。
- 癌転移阻害において使用するための、請求項1~4のいずれか1項に記載の抗体。
- 癌の予防又は治療剤の製造のための、請求項1~4のいずれか1項に記載の抗体の使用。
- 癌転移阻害剤の製造のための、請求項1~4のいずれか1項に記載の抗体の使用。
- 請求項1~4のいずれか1項に記載の抗体をコードするポリヌクレオチド。
- 請求項16記載のポリヌクレオチドを含むベクター。
- 請求項17記載のベクターを含む形質転換体。
Priority Applications (9)
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US14/440,391 US9845364B2 (en) | 2012-11-09 | 2013-10-01 | Anti-ADAM28 antibody for treating cancer |
CN201380058516.5A CN104937099B (zh) | 2012-11-09 | 2013-10-01 | 用于治疗癌症的抗adam28抗体 |
AU2013342779A AU2013342779B2 (en) | 2012-11-09 | 2013-10-01 | Anti-ADAM28 antibody for treating cancer |
CA2890862A CA2890862C (en) | 2012-11-09 | 2013-10-01 | Anti-adam28 antibody for treating cancer |
JP2014545609A JP6361003B2 (ja) | 2012-11-09 | 2013-10-01 | 癌治療のための抗adam28抗体 |
EP13853016.7A EP2918678B1 (en) | 2012-11-09 | 2013-10-01 | Anti-adam28 antibody for treating cancer |
EP18211128.6A EP3473718A1 (en) | 2012-11-09 | 2013-10-01 | Anti-adam28 antibody for treating cancer |
ZA2015/04169A ZA201504169B (en) | 2012-11-09 | 2015-06-09 | Anti-adam28 antibody for treating cancer |
US15/815,148 US10556967B2 (en) | 2012-11-09 | 2017-11-16 | Anti-ADAM28 antibody for treating cancer |
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US201261724484P | 2012-11-09 | 2012-11-09 | |
US61/724,484 | 2012-11-09 |
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US14/440,391 A-371-Of-International US9845364B2 (en) | 2012-11-09 | 2013-10-01 | Anti-ADAM28 antibody for treating cancer |
US15/815,148 Continuation US10556967B2 (en) | 2012-11-09 | 2017-11-16 | Anti-ADAM28 antibody for treating cancer |
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EP (2) | EP3473718A1 (ja) |
JP (2) | JP6361003B2 (ja) |
CN (2) | CN108424453B (ja) |
AU (1) | AU2013342779B2 (ja) |
CA (2) | CA2890862C (ja) |
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WO2016143702A1 (ja) * | 2015-03-06 | 2016-09-15 | ジーンフロンティア株式会社 | 抗ヒト膜型adam28抗体 |
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CN114569709B (zh) * | 2022-05-05 | 2022-07-12 | 苏州慧疗生物医药科技有限公司 | 高表达adam-28的黑色素瘤自体肿瘤疫苗的制备方法及其应用 |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3773919A (en) | 1969-10-23 | 1973-11-20 | Du Pont | Polylactide-drug mixtures |
EP0058481A1 (en) | 1981-02-16 | 1982-08-25 | Zeneca Limited | Continuous release pharmaceutical compositions |
EP0125023A1 (en) | 1983-04-08 | 1984-11-14 | Genentech, Inc. | Recombinant immunoglobulin preparations, methods for their preparation, DNA sequences, expression vectors and recombinant host cells therefor |
EP0133988A2 (de) | 1983-08-02 | 1985-03-13 | Hoechst Aktiengesellschaft | Regulatorische Peptide enthaltende pharmazeutische Präparate mit protrahierter Freisetzung und Verfahren zu deren Herstellung |
US5057313A (en) | 1986-02-25 | 1991-10-15 | The Center For Molecular Medicine And Immunology | Diagnostic and therapeutic antibody conjugates |
US5156840A (en) | 1982-03-09 | 1992-10-20 | Cytogen Corporation | Amine-containing porphyrin derivatives |
WO1996002576A1 (fr) | 1994-07-13 | 1996-02-01 | Chugai Seiyaku Kabushiki Kaisha | Anticorps humain reconstitue contre l'interleukine-8 humaine |
WO1998013388A1 (fr) | 1996-09-26 | 1998-04-02 | Chugai Seiyaku Kabushiki Kaisha | Anticorps contre les peptides lies a la parathormone humaine |
WO2004078140A2 (en) | 2003-03-05 | 2004-09-16 | Halozyme, Inc. | SOLUBLE HYALURONIDASE GLYCOPROTEIN (sHASEGP), PROCESS FOR PREPARING THE SAME, USES AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEREOF |
US20060122377A1 (en) | 2004-02-19 | 2006-06-08 | Genentech, Inc. | CDR-repaired antibodies |
WO2006122797A2 (en) | 2005-05-18 | 2006-11-23 | Morphosys Ag | Anti-gm-csf antibodies and uses therefor |
WO2007042309A2 (en) | 2005-10-12 | 2007-04-19 | Morphosys Ag | Generation and profiling of fully human hucal gold-derived therapeutic antibodies specific for human cd38 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5530101A (en) * | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
FI20061156A0 (fi) * | 2006-12-27 | 2006-12-27 | Elina Kivi | Uusia peptidejä |
EP2373692A4 (en) * | 2008-12-04 | 2013-11-20 | Abbvie Inc | IMMUNOGLOBULINE WITH DOUBLE VARIABLE DOMAIN AND ITS USE |
JP5808349B2 (ja) * | 2010-03-01 | 2015-11-10 | カリス ライフ サイエンシズ スウィッツァーランド ホールディングスゲーエムベーハー | セラノーシスのためのバイオマーカー |
-
2013
- 2013-10-01 EP EP18211128.6A patent/EP3473718A1/en not_active Withdrawn
- 2013-10-01 CN CN201810155252.XA patent/CN108424453B/zh not_active Expired - Fee Related
- 2013-10-01 AU AU2013342779A patent/AU2013342779B2/en not_active Ceased
- 2013-10-01 EP EP13853016.7A patent/EP2918678B1/en not_active Not-in-force
- 2013-10-01 JP JP2014545609A patent/JP6361003B2/ja not_active Expired - Fee Related
- 2013-10-01 WO PCT/JP2013/076745 patent/WO2014073292A1/ja active Application Filing
- 2013-10-01 CN CN201380058516.5A patent/CN104937099B/zh not_active Expired - Fee Related
- 2013-10-01 CA CA2890862A patent/CA2890862C/en not_active Expired - Fee Related
- 2013-10-01 US US14/440,391 patent/US9845364B2/en active Active
- 2013-10-01 CA CA3126108A patent/CA3126108A1/en not_active Abandoned
-
2015
- 2015-06-09 ZA ZA2015/04169A patent/ZA201504169B/en unknown
-
2017
- 2017-11-16 US US15/815,148 patent/US10556967B2/en not_active Expired - Fee Related
-
2018
- 2018-05-16 JP JP2018094616A patent/JP6656521B2/ja not_active Expired - Fee Related
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3773919A (en) | 1969-10-23 | 1973-11-20 | Du Pont | Polylactide-drug mixtures |
EP0058481A1 (en) | 1981-02-16 | 1982-08-25 | Zeneca Limited | Continuous release pharmaceutical compositions |
US5156840A (en) | 1982-03-09 | 1992-10-20 | Cytogen Corporation | Amine-containing porphyrin derivatives |
EP0125023A1 (en) | 1983-04-08 | 1984-11-14 | Genentech, Inc. | Recombinant immunoglobulin preparations, methods for their preparation, DNA sequences, expression vectors and recombinant host cells therefor |
EP0133988A2 (de) | 1983-08-02 | 1985-03-13 | Hoechst Aktiengesellschaft | Regulatorische Peptide enthaltende pharmazeutische Präparate mit protrahierter Freisetzung und Verfahren zu deren Herstellung |
US5057313A (en) | 1986-02-25 | 1991-10-15 | The Center For Molecular Medicine And Immunology | Diagnostic and therapeutic antibody conjugates |
WO1996002576A1 (fr) | 1994-07-13 | 1996-02-01 | Chugai Seiyaku Kabushiki Kaisha | Anticorps humain reconstitue contre l'interleukine-8 humaine |
WO1998013388A1 (fr) | 1996-09-26 | 1998-04-02 | Chugai Seiyaku Kabushiki Kaisha | Anticorps contre les peptides lies a la parathormone humaine |
WO2004078140A2 (en) | 2003-03-05 | 2004-09-16 | Halozyme, Inc. | SOLUBLE HYALURONIDASE GLYCOPROTEIN (sHASEGP), PROCESS FOR PREPARING THE SAME, USES AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEREOF |
US20060122377A1 (en) | 2004-02-19 | 2006-06-08 | Genentech, Inc. | CDR-repaired antibodies |
WO2006122797A2 (en) | 2005-05-18 | 2006-11-23 | Morphosys Ag | Anti-gm-csf antibodies and uses therefor |
WO2007042309A2 (en) | 2005-10-12 | 2007-04-19 | Morphosys Ag | Generation and profiling of fully human hucal gold-derived therapeutic antibodies specific for human cd38 |
Non-Patent Citations (53)
Title |
---|
"FUNDAMENTAL IMMUNOLOGY", 1993 |
"Kelley's Textbook of Rheumatology", 2009, ELSEVIER SAUNDERS, pages: 115 - 134 |
"Molecular cloning", 2001, COLD SPRING HARBOR LAB. PRESS |
"Remington's Pharmaceutical Science", 1980 |
"Remington's Pharmaceutical Science", MARK PUBLISHING COMPANY |
"Strategies for Protein Purification and Characterization: A Laboratory Course Manual", 1996, COLD SPRING HARBOR LABORATORY PRESS |
BETTER, M.; HORWITZ, A. H., METHODS ENZYMOL., vol. 178, 1989, pages 476 - 496 |
BIOCHEM BIOPHYS RES COMMUN., vol. 315, 2004, pages 79 - 84 |
BIOCHEM IOPHYS RES COMMUN., vol. 402, no. 4, 2010, pages 651 - 657 |
BIRD ET AL., SCIENCE, vol. 242, 1988, pages 423 - 426 |
BIRD, R. .; WALKER, B. W., TRENDS BIOTECHNOL., vol. 9, 1991, pages 132 - 137 |
CANCER RES, vol. 66, no. 20, 2006, pages 9913 - 9920 |
CANCER RES., vol. 66, no. 20, 2006, pages 9913 - 9920 |
CANCER SCI., vol. 98, no. 5, 2007, pages 621 - 628 |
CO, M. S. ET AL., J. IMMUNOL., vol. 152, 1994, pages 2968 - 2976 |
CURR OPIN CELL BIOL., vol. 15, no. 5, 2003, pages 598 - 606 |
CURR PHARM DES., vol. 15, no. 20, 2009, pages 2349 - 2358 |
GENES DEV., vol. 17, no. 1, 2003, pages 7 - 30 |
HASHIMOTO-GOTOH, T; MIZUNO, T; OGASAHARA, Y; NAKAGAWA, M: "An oligodeoxyribonucleotide-directed dual amber method for site-directed mutagenesis", GENE, vol. 152, 1995, pages 271 - 275, XP004042690, DOI: doi:10.1016/0378-1119(94)00750-M |
HOPP, T.P. ET AL., BIOTECHNOLOGY, vol. 6, 1988, pages 1204 - 1210 |
HUSTON ET AL., PROC. NATL. ACAD. SCI. USA, vol. 85, 1988, pages 5879 - 5883 |
INT J CANCER, vol. 118, no. 2, 2006, pages 263 - 273 |
IRIT J CANCER, vol. 127, no. 8, 2010, pages 1844 - 1856 |
J BIOL CHEM., vol. 274, no. 41, 1999, pages 29251 - 29259 |
J NATL CANCER INST, vol. 104, 2012, pages 906 - 922 |
KRAMER W; FRITZ HJ: "Oligonucleotide-directed construction of mutations via gapped duplex DNA Methods", ENZYMOL, vol. 154, 1987, pages 350 - 367 |
KRAMER, W; DRUTSA, V; JANSEN, HW; KRAMER, B; PFLUGFELDER, M; FRITZ, HJ: "The gapped duplex DNA approach to ligonucleotide-directed mutation construction", NUCLEIC ACIDS RES., vol. 12, 1984, pages 9441 - 9456, XP002026371 |
KUNKEL, TA: "Rapid and efficient site-specific mutagenesis without phenotypic selection", PROC NATL ACAD SCI U S A., vol. 82, 1985, pages 488 - 492, XP002052322, DOI: doi:10.1073/pnas.82.2.488 |
KURODA H. ET AL.: "ADAM28 is a serological and histochemical marker for non-small-cell lung cancers", INT. J. CANCER, vol. 127, no. 8, 2010, pages 1844 - 1856, XP055255305 * |
LAMOYI, E., METHODS ENZYMOL., vol. 121, 1986, pages 652 - 663 |
LANGER ET AL., J. BIOMED. MATER. RES., vol. 15, 1981, pages 167 - 277 |
LANGER, CHEM. TECH., vol. 12, 1982, pages 98 - 105 |
LEI, S. P. ET AL., J. BACTERIOL., vol. 169, 1987, pages 4379 |
MITSUI Y. ET AL.: "ADAM28 is overexpressed in human breast carcinomas: implications for carcinoma cell proliferation through cleavage of insulin-like growth factor binding protein- 3", CANCER RES., vol. 66, no. 20, 2006, pages 9913 - 9920, XP055255298 * |
MOCHIZUKI S. ET AL.: "ADAMs in cancer cell proliferation and progression", CANCER SCI., vol. 98, no. 5, 2007, pages 621 - 628, XP055255304 * |
MOCHIZUKI S. ET AL.: "Connective tissue growth factor is a substrate of ADAM28", BIOCHEM. BIOPHYS. RES. COMMUN., vol. 402, no. 4, 2010, pages 651 - 657, XP027516836 * |
MOCHIZUKI S. ET AL.: "Effect of ADAM28 on carcinoma cell metastasis by cleavage of von Willebrand factor", J. NATL. CANCER INST., vol. 104, no. 12, 2012, pages 906 - 922, XP055255303 * |
MOL ASPECTS MED., vol. 29, no. 5, 2008, pages 258 - 289 |
MOL IMMUNOL., vol. 44, no. 11, April 2007 (2007-04-01), pages 3049 - 60 |
NAT REV CANCER., vol. 8, no. 12, 2008, pages 929 - 941 |
NAT REV MOL CELL BIOL., vol. 6, no. 1, 2005, pages 32 - 43 |
OHTSUKA T. ET AL.: "ADAM28 is overexpressed in human non-small cell lung carcinomas and correlates with cell proliferation and lymph node metastasis", INT. J. CANCER, vol. 118, no. 2, 2006, pages 263 - 273, XP055009343 * |
PATHOL INT., vol. 60, no. 7, 2010, pages 477 - 496 |
PLUCKTHUN, A.; SKERRA, A., METHODS ENZYMOL., vol. 178, 1989, pages 497 - 515 |
ROTHE C. ET AL.: "The human combinatorial antibody library HuCAL GOLD combines diversification of all six CDRs according to the natural immune system with a novel display method for efficient selection of high-affinity antibodies", J. MOL. BIOL., vol. 376, no. 4, 2008, pages 1182 - 1200, XP027363305 * |
ROTHE, C ET AL., J. MOL. BIOL., vol. 376, 2008, pages 1182 - 1200 |
ROUSSEAUX, J. ET AL., METHODS ENZYMOL., vol. 121, 1986, pages 663 - 669 |
SATO, K. ET AL., CANCER RES., vol. 53, 1993, pages 851 - 856 |
See also references of EP2918678A4 * |
SEMIN CELL DEV BIOL., vol. 20, no. 2, 2009, pages 138 - 145 |
SIDMAN ET AL., BIOPOLYMERS, vol. 22, 1983, pages 547 - 56 |
WARD ET AL., NATURE, vol. 341, 1989, pages 544 - 546 |
ZOLLER, MJ; SMITH, M.: "Oligonucleotide-directed mutagenesis of DNA fragments cloned into M13 vectors", METHODS ENZYMOL., vol. 100, 1983, pages 468 - 500, XP001088749, DOI: doi:10.1016/0076-6879(83)00074-9 |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016143702A1 (ja) * | 2015-03-06 | 2016-09-15 | ジーンフロンティア株式会社 | 抗ヒト膜型adam28抗体 |
CN107614527A (zh) * | 2015-03-06 | 2018-01-19 | 基因先端领域株式会社 | 抗人膜类型adam28抗体 |
EP3266799A4 (en) * | 2015-03-06 | 2018-09-12 | GeneFrontier Corporation | Anti-human membrane-type adam28 antibody |
US10329358B2 (en) | 2015-03-06 | 2019-06-25 | Genefrontier Corporation | Anti-human membrane-type ADAM28 antibody |
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CA2890862A1 (en) | 2014-05-15 |
EP2918678A4 (en) | 2016-07-06 |
US20150274840A1 (en) | 2015-10-01 |
CA2890862C (en) | 2021-10-12 |
EP2918678A1 (en) | 2015-09-16 |
CA3126108A1 (en) | 2014-05-15 |
EP3473718A1 (en) | 2019-04-24 |
EP2918678B1 (en) | 2019-01-30 |
JP6361003B2 (ja) | 2018-07-25 |
US10556967B2 (en) | 2020-02-11 |
JP6656521B2 (ja) | 2020-03-04 |
AU2013342779B2 (en) | 2019-09-26 |
AU2013342779A8 (en) | 2015-08-20 |
CN104937099B (zh) | 2018-03-30 |
US20180155448A1 (en) | 2018-06-07 |
AU2013342779A1 (en) | 2015-07-02 |
CN108424453B (zh) | 2021-08-06 |
CN108424453A (zh) | 2018-08-21 |
JP2018148910A (ja) | 2018-09-27 |
US9845364B2 (en) | 2017-12-19 |
JPWO2014073292A1 (ja) | 2016-09-08 |
ZA201504169B (en) | 2020-12-23 |
CN104937099A (zh) | 2015-09-23 |
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