JP4987117B2 - A blood MMP-3 concentration reducing agent comprising an IL-6 antagonist as an active ingredient - Google Patents

Description

  The present invention relates to a blood MMP-3 concentration lowering agent, a cartilage destruction inhibitor, and the like, which contain an interleukin-6 (IL-6) antagonist as an active ingredient.

  IL-6 is a cytokine also called B cell stimulating factor 2 (BSF2) or interferon β2. IL-6 was discovered as a differentiation factor involved in the activation of B lymphoid cells (Hirano, T. et al., Nature (1986) 324, 73-76) and subsequently affected the function of various cells. (Akira, S. et al., Adv. In Immunology (1993) 54, 1-78). IL-6 has been reported to induce maturation of T lymphoid cells (Lotz, M. et al., J. Exp. Med. (1988) 167, 1253-1258).

  IL-6 transmits its biological activity through two proteins on the cell. One is the IL-6 receptor, a ligand-binding protein with a molecular weight of about 80 kD to which IL-6 binds (Taga, T. et al., J. Exp. Med. (1987) 166, 967-981, Yamasaki, K. et al., Science (1987) 241, 825-828). IL-6 receptor exists as a soluble IL-6 receptor mainly composed of the extracellular region in addition to the membrane-bound type that penetrates the cell membrane and is expressed on the cell membrane.

  The other is a membrane protein gp130 with a molecular weight of about 130 kD involved in non-ligand binding signaling. IL-6 and IL-6 receptor form an IL-6 / IL-6 receptor complex, and then bind to gp130, thereby transmitting the biological activity of IL-6 into the cell (Taga , T. et al., Cell (1989) 58, 573-581).

  An IL-6 antagonist is a substance that inhibits the transmission of the biological activity of IL-6. So far, antibodies against IL-6 (anti-IL-6 antibody), antibodies against IL-6 receptor (anti-IL-6 receptor antibody), antibodies against gp130 (anti-gp130 antibody), IL-6 variants, IL -6 or IL-6 receptor partial peptide and the like are known.

  There are several reports on anti-IL-6 receptor antibodies (Novick, D. et al., Hybridoma (1991) 10, 137-146, Huang, YW et al., Hybridoma (1993) 12, 621- 630, international patent application publication number WO 95-09873, French patent application publication number FR 2694767, US patent number US 521628). One of them, mouse antibody PM-1 (Hirata, Y. et al., J. Immunol. (1989) 143, 2900-2906) transplantation of complementarity determining region (CDR) to human antibody A humanized PM-1 antibody obtained by doing so is known (International Patent Application Publication No. WO 92-19759).

  Articular cartilage destruction due to rheumatoid arthritis (RA) and osteoarthritis (OA) is caused by the combined action of various factors: 1) chondrocyte death, 2) enhanced degradation of extracellular matrix (ECM), 3 It progresses by the occurrence of reduced cartilage ECM production. In recent years, MMP has attracted particular attention among proteolytic enzymes that promote the degradation of ECM.

  MMP is an important ECM degrading enzyme together with neutrophil elastase and cathepsin G, and about 20 kinds of molecular species have been reported so far as the MMP gene family. These MMPs are collagenase group (MMP-1, MMP-8, MMP-13), gelatinase group (MMP-2, MMP-9), stromalysin group (MMP-3, MMP-10), membrane MMP group ( MMP-14, MMP-15, MMP-16, MMP-17) and other MMPs (MMP-7, MMP-11, MMP-12, MMP-19, MMP-20, etc.). Here, the stromelysin group (MMP-3, MMP-10) degrades proteoglycan, type III, type IV, type IX collagen, laminin, fibronectin, etc., and has the widest substrate specificity among MMPs.

  High levels of MMP-1, 2, 3, 8, 9 are present in the RA fluid of RA patients, and MMP-1, 2, 3, and 9 are present in RA joint synovial cells and non-pannus articular cartilage tissue. 9, MT1-MMP expression is observed. These data indicate that ECM degradation by MMP plays an important role in articular cartilage destruction especially in RA. However, in contrast, RA synovium is known not to be a target tissue of MMP.

  In addition, the fact that most OA articular cartilage is MMP-3 positive, and that MMP-3 activity secreted by culturing OA articular cartilage tissue is significantly higher than that of normal cartilage group. MMP-3 is also considered to play an important role. In addition, MMP-3 is thought to play an important role in juvenile rheumatoid arthritis, adult-type still disease, etc., and suppression of the action of MMP-3 is thought to improve the symptoms of these diseases .

  It is widely known that MMP-3 itself degrades cartilage proteoglycan (aggrecan) from many reports, and it is said that MMP-3 has the strongest degradation activity of aggrecan core protein among MMPs. Furthermore, MMP exists as latent MMP and is known to be converted to active MMP by cleavage of the propeptide. Active MMP-3 converts latent MMP-1, 7, 8, 9 It is also attracting attention because it has the function of activating to a complete level. MMP-3 is expressed in RA and OA joint tissues, but the amount of RA produced is higher in RA than in OA. In RA with multiple joints, elevated MMP-3 levels in blood are differentiated from OA. It is known to be useful. That is, the level of serum MMP-3 is an indicator of RA synovitis.

  MMP-3 expression is induced by IL-1, TNF-α, EGF, bFGF, etc. and is known to be suppressed by retinoic acid, glucocorticoid, TGF-β, etc. There is no report about.

  IL-6 antagonists such as anti-IL-6 receptor antibodies have been reported to improve rheumatic symptoms by suppressing abnormal proliferation of synovial cells (WO96 / 11020), but IL-6 antagonists, particularly It has not been known that anti-IL-6 receptor antibody decreases the blood concentration of MMP-3, which is a major enzyme of cartilage destruction, in rheumatic patients.

  The present invention intends to provide a blood MMP-3 concentration reducing agent and a cartilage destruction inhibitor, and a method for detecting, evaluating and judging the effect of the reducing agent and / or the inhibitor, and a reagent used therefor. To do.

  The inventor found that IL-6 antagonists such as anti-IL-6 receptor antibodies reduce blood levels of MMP-3, MMP-1, and Tissue Inhibitor of Metalloproteinases-1 (TIMP-1), especially MMP-3 As a result, the present invention has been completed.

That is, the present invention provides (1) a blood MMP-3 concentration-lowering agent and a cartilage destruction inhibitor containing an IL-6 antagonist as an active ingredient.
The present invention also provides (2) a blood MMP-3 concentration-lowering agent and a cartilage destruction inhibitor containing an antibody against IL-6 receptor as an active ingredient.

The present invention also provides (3) a blood MMP-3 concentration-lowering agent and a cartilage destruction inhibitor containing a monoclonal antibody against IL-6 receptor as an active ingredient.
The present invention also provides (4) a blood MMP-3 concentration-lowering agent and a cartilage destruction inhibitor containing a monoclonal antibody against human IL-6 receptor as an active ingredient. The monoclonal antibody against human IL-6 receptor is preferably PM-1 antibody.

  The present invention also provides (5) a blood MMP-3 concentration-lowering agent and a cartilage destruction-inhibiting agent containing a monoclonal antibody against mouse IL-6 receptor as an active ingredient. The monoclonal antibody against mouse IL-6 receptor is preferably MR16-1 antibody.

  The present invention also provides (6) a blood MMP-3 concentration-lowering agent and a cartilage destruction-inhibiting agent comprising a recombinant antibody against IL-6 receptor as an active ingredient. The recombinant antibody against IL-6 receptor preferably has a human antibody constant region (C region).

The present invention also provides (7) a blood MMP-3 concentration-lowering agent and a cartilage destruction inhibitor containing a chimeric antibody or humanized antibody against IL-6 receptor as an active ingredient.
The present invention also provides (8) a blood MMP-3 concentration-lowering agent and a cartilage destruction inhibitor containing humanized PM-1 antibody as an active ingredient.
The present invention also provides a therapeutic agent for osteoarthritis containing an interleukin-6 (IL-6) antagonist as an active ingredient.

  The present invention also relates to an IL-6 antagonist, which is selected from the group consisting of MMP-3, MMP-1 and TIMP-1, but using IL-6 antagonist as an indicator, particularly the in vivo concentration of MMP-3, for example, blood concentration. A method of detecting, evaluating, or judging an effect (for example, therapeutic effect) of a drug as an active ingredient, such as a cartilage destruction inhibitor or an osteoarthritis therapeutic agent containing an IL-6 antagonist as an active ingredient And reagents used therein.

FIG. 1 is a graph showing the time course of blood MMP-1 after administration of humanized IL-6 receptor antibody in 8 rheumatic patients. FIG. 2 is a graph showing the time course of blood MMP-3 after administration of humanized IL-6 receptor antibody in 8 rheumatic patients. FIG. 3 is a graph showing the time course of blood TIMP-1 after administration of humanized IL-6 receptor antibody in 8 rheumatic patients.

FIG. 4 is a graph showing the time course of blood MMP-1 after administration of humanized IL-6 receptor antibody in 5 CD patients. FIG. 5 is a graph showing the time course of blood MMP-3 after administration of humanized IL-6 receptor antibody in 5 CD patients. FIG. 6 is a graph showing the time course of blood TIMP-1 after administration of humanized IL-6 receptor antibody in 5 CD patients.

The IL-6 antagonist used in the present invention may be of any origin, type, and shape as long as it exhibits a blood MMP-3 concentration lowering effect and / or a cartilage destruction inhibiting effect.
An IL-6 antagonist is a substance that blocks IL-6 signaling and inhibits IL-6 biological activity. The IL-6 antagonist is preferably a substance having an inhibitory action on the binding of any of IL-6, IL-6 receptor and gp130. Examples of IL-6 antagonists include anti-IL-6 antibody, anti-IL-6 receptor antibody, anti-gp130 antibody, IL-6 variant, soluble IL-6 receptor variant or IL-6 or IL-6 receptor And low molecular weight substances exhibiting the same activity as these partial peptides.

  The anti-IL-6 antibody used in the present invention can be obtained as a polyclonal or monoclonal antibody using known means. As the anti-IL-6 antibody used in the present invention, a monoclonal antibody derived from a mammal is particularly preferable. Mammal-derived monoclonal antibodies include those produced by hybridomas and those produced by hosts transformed with expression vectors containing antibody genes by genetic engineering techniques. This antibody binds to IL-6, thereby blocking the binding of IL-6 to the IL-6 receptor and blocking the transmission of IL-6 biological activity into the cell.

  Examples of such antibodies include MH166 (Matsuda, T. et al., Eur. J. Immunol. (1988) 18, 951-956) and SK2 antibody (Sato, K. et al., 21st Japan Immunological Society). General meeting, academic records (1991) 21, 166).

  An anti-IL-6 antibody-producing hybridoma can be basically produced using a known technique as follows. That is, using IL-6 as a sensitizing antigen, immunizing it according to a normal immunization method, fusing the resulting immune cells with a known parent cell by a normal cell fusion method, by a normal screening method, It can be produced by screening monoclonal antibody-producing cells.

  Specifically, the anti-IL-6 antibody can be prepared as follows. For example, human IL-6 used as a sensitizing antigen for antibody acquisition is Eur. J. Biochem (1987) 168, 543-550, J. Immunol. (1988) 140, 1534-1541, or Agr. Biol. It is obtained by using the IL-6 gene / amino acid sequence disclosed in Chem. (1990) 54, 2685-2688.

  After inserting the gene sequence of IL-6 into a known expression vector system and transforming an appropriate host cell, the target IL-6 protein is purified from the host cell or culture supernatant by a known method. The purified IL-6 protein may be used as a sensitizing antigen. Further, a fusion protein of IL-6 protein and another protein may be used as a sensitizing antigen.

  The anti-IL-6 receptor antibody used in the present invention can be obtained as a polyclonal or monoclonal antibody using a known means. As the anti-IL-6 receptor antibody used in the present invention, a monoclonal antibody derived from a mammal is particularly preferable. Mammal-derived monoclonal antibodies include those produced by hybridomas and those produced by hosts transformed with expression vectors containing antibody genes by genetic engineering techniques. This antibody binds to the IL-6 receptor, thereby blocking the binding of IL-6 to the IL-6 receptor and blocking the transmission of IL-6 biological activity into the cell.

  Examples of such antibodies include MR16-1 antibody (Tamura, T. et al. Proc. Natl. Acad. Sci. USA (1993) 90, 11924-11928), PM-1 antibody (Hirata, Y. et al. , J. Immunol. (1989) 143, 2900-2906), AUK12-20 antibody, AUK64-7 antibody or AUK146-15 antibody (International Patent Application Publication No. WO 92-19759). Among these, PM-1 antibody is mentioned as a particularly preferable antibody.

  The PM-1 antibody-producing hybridoma cell line was designated as PM-1 at the Institute of Biotechnology, Institute of Industrial Science and Technology (1-3 Higashi 1-3, Tsukuba City, Ibaraki Prefecture) on July 10, 1990. BP-2998 is deposited internationally based on the Budapest Treaty. The MR16-1 antibody-producing hybridoma cell line was established as Rat-mouse hybridoma MR16-1 at the Institute of Biotechnology, Tsukuba City, Ibaraki Pref. Every day, it has been deposited internationally under the Budapest Treaty as FERM BP-5875.

  An anti-IL-6 receptor monoclonal antibody-producing hybridoma can be basically produced using a known technique as follows. That is, IL-6 receptor is used as a sensitizing antigen, immunized according to a normal immunization method, and the obtained immune cells are fused with a known parent cell by a normal cell fusion method. Can be prepared by screening monoclonal antibody-producing cells.

  Specifically, an anti-IL-6 receptor antibody can be produced as follows. For example, a human IL-6 receptor used as a sensitizing antigen for obtaining an antibody was disclosed in European Patent Application Publication No. EP 325474, and a mouse IL-6 receptor was disclosed in Japanese Patent Application Publication No. JP-A-3-155795. It is obtained by using IL-6 receptor gene / amino acid sequence.

  IL-6 receptor protein is expressed on the cell membrane and detached from the cell membrane (soluble IL-6 receptor) (Yasukawa, K. et al., J. Biochem. (1990) 108, 673-676). Soluble IL-6 receptor antibody is composed essentially of the extracellular region of IL-6 receptor bound to the cell membrane, and lacks the transmembrane region or the transmembrane region and the intracellular region. Different from membrane-bound IL-6 receptor. Any IL-6 receptor may be used as the IL-6 receptor protein as long as it can be used as a sensitizing antigen for producing the anti-IL-6 receptor antibody used in the present invention.

  After inserting the gene sequence of IL-6 receptor into a known expression vector system and transforming an appropriate host cell, the target IL-6 receptor protein is known from the host cell or culture supernatant. The purified IL-6 receptor protein may be used as a sensitizing antigen. Further, cells expressing IL-6 receptor or fusion proteins of IL-6 receptor protein and other proteins may be used as the sensitizing antigen.

  E. coli containing the plasmid pIBIBSF2R containing cDNA encoding the human IL-6 receptor was inaugurated by the National Institute of Biotechnology, National Institute of Advanced Industrial Science and Technology on January 9, 1989. pIBIBSF2R is deposited internationally under the Budapest Treaty under the deposit number FERM BP-2232.

  The anti-gp130 antibody used in the present invention can be obtained as a polyclonal or monoclonal antibody using known means. As the anti-gp130 antibody used in the present invention, a monoclonal antibody derived from a mammal is particularly preferable. Mammal-derived monoclonal antibodies include those produced by hybridomas and those produced by hosts transformed with expression vectors containing antibody genes by genetic engineering techniques. This antibody binds to gp130, thereby blocking the binding of IL-6 / IL-6 receptor complex to gp130 and blocking the transmission of IL-6 biological activity into cells.

Examples of such antibodies include AM64 antibody (JP-A-3-219894), 4B11 antibody and 2H4 antibody (US 5571513) B-S12 antibody and B-P8 antibody (JP-A-8-291199).
An anti-gp130 monoclonal antibody-producing hybridoma can be basically produced using a known technique as follows. That is, gp130 is used as a sensitizing antigen and immunized according to a normal immunization method. The obtained immune cells are fused with a known parent cell by a normal cell fusion method, and a monoclonal antibody is obtained by a normal screening method. It can be produced by screening production cells.

  Specifically, the monoclonal antibody can be produced as follows. For example, gp130 used as a sensitizing antigen for obtaining antibodies can be obtained by using the gp130 gene / amino acid sequence disclosed in European Patent Application Publication No. EP 411946.

After inserting the gene sequence of gp130 into a known expression vector system and transforming an appropriate host cell, the target gp130 protein is purified from the host cell or the culture supernatant by a known method. A gp130 receptor protein may be used as a sensitizing antigen. Further, a cell expressing gp130 or a fusion protein of gp130 protein and another protein may be used as a sensitizing antigen.
The mammal to be immunized with the sensitizing antigen is not particularly limited, but is preferably selected in consideration of compatibility with the parent cell used for cell fusion. Animals such as mice, rats, hamsters and the like are used.

  In order to immunize an animal with a sensitizing antigen, a known method is performed. For example, as a general method, a sensitizing antigen is injected into a mammal intraperitoneally or subcutaneously. Specifically, the sensitized antigen is diluted to an appropriate amount with PBS (Phosphate-Buffered Saline) or physiological saline, etc. and mixed with an appropriate amount of a normal adjuvant, for example, Freund's complete adjuvant, if necessary, and emulsified. Preferably, it is administered to mammals several times every 4-21 days. In addition, an appropriate carrier can be used during immunization with the sensitizing antigen.

  After immunizing in this way and confirming that the desired antibody level rises in the serum, immune cells are removed from the mammal and subjected to cell fusion. Spleen cells are particularly preferred as preferable immune cells to be subjected to cell fusion.

  Mammalian myeloma cells as the other parental cells to be fused with the immune cells are already known in various cell lines such as P3X63Ag8.653 (Kearney, JF et al. J. Immnol. (1979) 123, 1548-1550), P3X63Ag8U.1 (Current Topics in Microbiology and Immunology (1978) 81, 1-7), NS-1 (Kohler. G. and Milstein, C. Eur. J. Immunol. (1976) 6, 511 -519), MPC-11 (Margulies. DH et al., Cell (1976) 8, 405-415), SP2 / 0 (Shulman, M. et al., Nature (1978) 276, 269-270), FO (De St. Groth, SF et al., J. Immunol. Methods (1980) 35, 1-21), S194 (Trowbridge, ISJ Exp. Med. (1978) 148, 313-323), R210 (Galfre, G et al., Nature (1979) 277, 131-133) are used as appropriate.

  The cell fusion between the immunocytes and myeloma cells is basically performed by a known method such as the method of Milstein et al. (Kohler. G. and Milstein, C., Methods Enzymol. (1981) 73, 3-46). It can be done according to this.

  More specifically, the cell fusion is performed, for example, in a normal nutrient culture medium in the presence of a cell fusion promoter. For example, polyethylene glycol (PEG), Sendai virus (HVJ) or the like is used as a fusion promoter, and an auxiliary agent such as dimethyl sulfoxide can be added and used to increase the fusion efficiency as desired.

  The usage ratio of immune cells and myeloma cells is preferably, for example, 1-10 times that of immune cells relative to myeloma cells. As the culture medium used for the cell fusion, for example, RPMI1640 culture medium suitable for growth of the myeloma cell line, MEM culture medium, and other normal culture liquids used for this type of cell culture can be used. Serum supplements such as fetal calf serum (FCS) can be used in combination.

  For cell fusion, a predetermined amount of the immune cells and myeloma cells are mixed well in the culture solution, and a PEG solution pre-warmed to about 37 ° C., for example, a PEG solution having an average molecular weight of about 1000-6000 is usually used. The target fused cell (hybridoma) is formed by adding and mixing at a concentration of 30-60% (w / v). Subsequently, cell fusion agents and the like that are undesirable for the growth of the hybridoma can be removed by adding an appropriate culture solution successively and centrifuging to remove the supernatant.

  The hybridoma is selected by culturing in a normal selective culture solution, for example, a HAT culture solution (a culture solution containing hypoxanthine, aminopterin and thymidine). Culturing with the HAT culture solution is continued for a time sufficient for the cells other than the target hybridoma (non-fused cells) to die, usually several days to several weeks. Subsequently, a normal limiting dilution method is performed, and screening and cloning of the hybridoma producing the target antibody are performed.

  In addition to immunizing a non-human animal with an antigen to obtain the above hybridoma, human lymphocytes are sensitized with a desired antigen protein or antigen-expressing cells in vitro, and sensitized B lymphocytes are human myeloma cells such as U266. And a desired human antibody having binding activity to a desired antigen or antigen-expressing cell can be obtained (see Japanese Patent Publication No. 1-59878). Further, antigens or antigen-expressing cells may be administered to a transgenic animal having a repertoire of human antibody genes, and a desired human antibody may be obtained according to the aforementioned method (International Patent Application Publication Nos. WO 93/12227, WO 92 / 03918, WO 94/02602, WO 94/25585, WO 96/34096, WO 96/33735).

  The hybridoma producing the monoclonal antibody thus produced can be subcultured in a normal culture solution, and can be stored for a long time in liquid nitrogen.

  In order to obtain a monoclonal antibody from the hybridoma, the hybridoma is cultured according to a usual method and obtained as a culture supernatant thereof, or the hybridoma is administered to a mammal compatible therewith to proliferate, and its ascites The method obtained as follows is adopted. The former method is suitable for obtaining highly pure antibodies, while the latter method is suitable for mass production of antibodies.

  For example, the production of an anti-IL-6 receptor antibody-producing hybridoma can be performed by the method disclosed in JP-A-3-139293. PM-1 antibody production deposited internationally under the Budapest Treaty as FERM BP-2998 on July 10, 1990 at the Institute of Biotechnology, Institute of Industrial Science and Technology (1-3 East, Tsukuba City, Ibaraki Prefecture) Hybridomas are injected into the peritoneal cavity of BALB / c mice to obtain ascites, and PM-1 antibody is purified from the ascites, or the hybridoma is treated with an appropriate medium such as 10% fetal bovine serum, 5% BM-Condimed. Culture in HMI (Boehringer Mannheim) -containing RPMI1640 medium, hybridoma SFM medium (GIBCO-BRL), PFHM-II medium (GIBCO-BRL), etc., and purify PM-1 antibody from the culture supernatant be able to.

  In the present invention, as a monoclonal antibody, a recombinant antibody produced by cloning an antibody gene from a hybridoma, incorporating it into an appropriate vector, introducing it into a host, and producing it using a gene recombination technique can be used. (See, for example, Borrebaeck CAK and Larrick JW THERAPEUTIC MONOCLONAL ANTIBODIES, Published in the United Kingdom by MACMILLAN PUBLISHERS LTD, 1990).

  Specifically, mRNA encoding the variable (V) region of the antibody is isolated from cells producing the antibody of interest, such as a hybridoma. Isolation of mRNA is performed by a known method such as guanidine ultracentrifugation (Chirgwin, JM et al., Biochemistry (1979) 18, 5294-5299), AGPC (Chomczynski, P. et al., Anal. Biochem. (1987) 162, 156-159) etc., and then prepare mRNA using mRNA Purification Kit (manufactured by Pharmacia) etc. Alternatively, mRNA can be directly prepared by using QuickPrep mRNA Purification Kit (manufactured by Pharmacia).

  From the obtained mRNA, cDNA of the antibody V region is synthesized using reverse transcriptase. cDNA synthesis can be performed using AMV Reverse Transcriptase First-strand cDNA Synthesis Kit or the like. In addition, 5'-Ampli FINDER RACE Kit (Clontech) and 5'-RACE method using PCR (Frohman, MA et al., Proc. Natl. Acad. Sci. USA ( 1988) 85, 8998-9002; Belyavsky, A. et al., Nucleic Acids Res. (1989) 17, 2919-2932). The desired DNA fragment is purified from the obtained PCR product and ligated with vector DNA. Further, a recombinant vector is prepared from this, introduced into Escherichia coli, etc., and colonies are selected to prepare a desired recombinant vector. The base sequence of the target DNA is confirmed by a known method such as the deoxy method.

If DNA encoding the V region of the target antibody is obtained, it is ligated with DNA encoding the desired antibody constant region (C region) and incorporated into an expression vector. Alternatively, DNA encoding the V region of the antibody may be incorporated into an expression vector containing DNA of the antibody C region.
In order to produce the antibody used in the present invention, the antibody gene is incorporated into an expression vector so as to be expressed under the control of an expression control region, for example, an enhancer or a promoter, as described later. Next, host cells can be transformed with this expression vector to express the antibody.

  In the present invention, a recombinant antibody that has been artificially modified for the purpose of reducing the heterologous antigenicity to humans, for example, a chimeric antibody or a humanized antibody can be used. These modified antibodies can be produced using known methods.

A chimeric antibody can be obtained by ligating the DNA encoding the antibody V region obtained as described above with DNA encoding the human antibody C region, incorporating it into an expression vector, introducing it into a host, and producing it (Europe). (See Patent Application Publication No. EP 125023, International Patent Application Publication No. WO 92-19759). Using this known method, a chimeric antibody useful in the present invention can be obtained.
For example, plasmids containing DNA encoding the V regions of the L chain and H chain of the chimeric PM-1 antibody are named pPM-k3 and pPM-h1, respectively, and Escherichia coli having this plasmid is National Collections of Industrial and Marine. It was deposited with Bacteria Limited internationally on February 11, 1991 as NCIMB 40366 and NCIMB40362, respectively, under the Budapest Treaty.

  A humanized antibody is also referred to as a reshaped human antibody, and is obtained by transplanting the complementarity determining region (CDR) of a non-human mammal such as a mouse antibody into the complementarity determining region of a human antibody. General gene recombination techniques are also known (see European Patent Application Publication No. EP 125023, International Patent Application Publication No. WO 92-19759).

  Specifically, several oligo oligonucleotides were prepared so that the DNA sequence designed to link the CDR of the mouse antibody and the framework region (FR) of the human antibody had an overlapping portion at the end. Synthesize from nucleotides by PCR. The obtained DNA is ligated with DNA encoding the human antibody C region, then incorporated into an expression vector, and introduced into a host for production (European Patent Application Publication Number EP 239400, International Patent Application Publication Number). See WO 92-19759).

  As the FR of the human antibody to be ligated via CDR, the one in which the complementarity determining region forms a favorable antigen binding site is selected. If necessary, amino acid in the framework region of the variable region of the antibody may be substituted so that the complementarity determining region of the reshaped human antibody forms an appropriate antigen binding site (Sato, K. et al., Cancer Res. (1993) 53, 851-856).

  The human antibody C region is used for the chimeric antibody and the humanized antibody. Examples of the human antibody C region include Cγ, and for example, Cγ1, Cγ2, Cγ3, or Cγ4 can be used. In addition, the human antibody C region may be modified in order to improve the stability of the antibody or its production.

  A chimeric antibody is composed of a variable region of a non-human mammal-derived antibody and a C region derived from a human antibody, and a humanized antibody is a complementarity determining region of a non-human mammal-derived antibody, a framework region derived from a human antibody, and a C region. Since it consists of regions and has reduced antigenicity in the human body, it is useful as an antibody used in the present invention.

  Preferable specific examples of humanized antibodies used in the present invention include humanized PM-1 antibodies (see International Patent Application Publication No. WO 92-19759).

  The antibody gene constructed as described above can be expressed and obtained by a known method. In the case of a mammalian cell, it can be expressed by a commonly used useful promoter, an antibody gene to be expressed, a DNA operably linked with a poly A signal at the 3 ′ downstream thereof, or a vector containing the same. For example, examples of promoter / enhancer include human cytomegalovirus immediate early promoter / enhancer.

In addition, other promoters / enhancers that can be used for expression of antibodies used in the present invention include retrovirus, polyoma virus, adenovirus, simian virus 40 (SV 40) and other promoters / enhancers and human elongation factor 1 α ( A promoter / enhancer derived from mammalian cells such as HEF1α) may be used.
For example, when the SV 40 promoter / enhancer is used, the method of Mulligan et al. (Mulligan, RC et al., Nature (1979) 277, 108-114), and when the HEF1α promoter / enhancer is used, the method of Mizushima et al. (Mizushima, S. and Nagata, S. Nucleic Acids Res. (1990) 18, 5322).

  In the case of Escherichia coli, it can be expressed by functionally combining a commonly used useful promoter, a signal sequence for antibody secretion, and an antibody gene to be expressed. For example, examples of the promoter include lacZ promoter and araB promoter. When using the lacZ promoter, the method of Ward et al. (Ward, ES et al., Nature (1989) 341, 544-546; Ward, ES et al. FASEB J. (1992) 6, 2422-2427), araB promoter Can be used according to the method of Better et al. (Better, M. et al. Science (1988) 240, 1041-1043).

  As a signal sequence for antibody secretion, the pelB signal sequence (Lei, S. P. et al J. Bacteriol. (1987) 169, 4379-4383) may be used when the periplasm of E. coli is produced. After separating the antibody produced in the periplasm, the structure of the antibody is appropriately refolded and used (see, for example, WO96 / 30394).

  As the origin of replication, those derived from SV40, polyoma virus, adenovirus, bovine papilloma virus (BPV), etc. can be used. Furthermore, the expression vector serves as a selection marker for gene copy number amplification in the host cell system. Aminoglycoside phosphotransferase (APH) gene, thymidine kinase (TK) gene, E. coli xanthine guanine phosphoribosyltransferase (Ecogpt) gene, dihydrofolate reductase (dhfr) gene and the like.

  Any production system can be used for the production of the antibodies used in the present invention. Production systems for antibody production include in vitro and in vivo production systems. Examples of in vitro production systems include production systems that use eukaryotic cells and production systems that use prokaryotic cells.

  When eukaryotic cells are used, there are production systems using animal cells, plant cells, or fungal cells. Animal cells include: (1) mammalian cells, such as CHO, COS, myeloma, BHK (baby hamster kidney), HeLa, Vero, etc., (2) amphibian cells, such as Xenopus oocytes, or (3) insects Cells such as sf9, sf21, Tn5 are known. As plant cells, cells derived from Nicotiana tabacum are known, and these may be cultured in callus. As fungal cells, yeasts such as the genus Saccharomyces, such as Saccharomyces cerevisiae, and fungi such as the genus Aspergillus, such as Aspergillus niger, are known.

  When prokaryotic cells are used, there are production systems using bacterial cells. Known bacterial cells include E. coli and Bacillus subtilis.

  An antibody can be obtained by introducing a desired antibody gene into these cells by transformation and culturing the transformed cells in vitro. Culture is performed according to a known method. For example, DMEM, MEM, RPMI1640, IMDM can be used as a culture solution, and serum supplements such as fetal calf serum (FCS) can be used in combination. Alternatively, antibodies may be produced in vivo by transferring cells into which the antibody gene has been introduced to the abdominal cavity of an animal.

  On the other hand, examples of in vivo production systems include production systems using animals and production systems using plants. When animals are used, there are production systems using mammals and insects.

  As mammals, goats, pigs, sheep, mice, cows and the like can be used (Vicki Glaser, SPECTRUM Biotechnology Applications, 1993). In addition, silkworms can be used as insects. When using a plant, for example, tobacco can be used.

  An antibody gene is introduced into these animals or plants, and antibodies are produced in the body of the animals or plants and recovered. For example, an antibody gene is inserted into the middle of a gene encoding a protein inherently produced in milk such as goat β casein to prepare a fusion gene. A DNA fragment containing the fusion gene into which the antibody gene has been inserted is injected into a goat embryo and the embryo is introduced into a female goat. The desired antibody is obtained from the milk produced by the transgenic goat born from the goat that received the embryo or its progeny. In order to increase the amount of milk containing the desired antibody produced from the transgenic goat, hormones may be used in the transgenic goat as appropriate. (Ebert, K.M. et al., Bio / Technology (1994) 12, 699-702).

  When silkworms are used, silkworms are infected with baculovirus into which the antibody gene of interest is inserted, and desired antibodies are obtained from the body fluids of these silkworms (Maeda, S. et al., Nature (1985) 315, 592-594). ). Further, when tobacco is used, the target antibody gene is inserted into a plant expression vector such as pMON 530, and this vector is introduced into a bacterium such as Agrobacterium tumefaciens. This bacterium is infected with tobacco, for example Nicotiana tabacum, and the desired antibody is obtained from the leaves of this tobacco (Julian, K.-C. Ma et al., Eur. J. Immunol. (1994) 24, 131-138) .

As described above, when an antibody is produced in an in vitro or in vivo production system, DNAs encoding the antibody heavy chain (H chain) or light chain (L chain) are separately incorporated into an expression vector to simultaneously transform the host. Alternatively, the host may be transformed by incorporating DNAs encoding H and L chains into a single expression vector (see International Patent Application Publication No. WO 94-11523).
The antibody used in the present invention may be an antibody fragment or a modified product thereof as long as it can be suitably used in the present invention. For example, antibody fragments include Fab, F (ab ') 2, Fv, or single chain Fv (scFv) in which H chain and L chain Fv are linked by an appropriate linker.

  Specifically, the antibody is treated with an enzyme such as papain or pepsin to generate antibody fragments, or a gene encoding these antibody fragments is constructed and introduced into an expression vector, and then an appropriate host cell. (E.g., Co, MS et al., J. Immunol. (1994) 152, 2968-2976, Better, M. & Horwitz, AH Methods in Enzymology (1989) 178, 476-496, Plueckthun, A. & Skerra, A. Methods in Enzymology (1989) 178, 476-496, Lamoyi, E., Methods in Enzymology (1989) 121, 652-663, Rousseaux, J. et al., Methods in Enzymology (1989) 121, 663-669, Bird, RE et al., TIBTECH (1991) 9, 132-137).

  scFv can be obtained by linking the H chain V region and L chain V region of an antibody. In this scFv, the H chain V region and the L chain V region are linked via a linker, preferably a peptide linker (Huston, JS et al., Proc. Natl. Acad. Sci. USA (1988) 85, 5879. -5883). The H chain V region and L chain V region in scFv may be derived from any of those described as the above antibody. As the peptide linker that links the V regions, for example, any single chain peptide consisting of amino acid residues 12-19 is used.

  The scFv-encoding DNA is a DNA sequence encoding the H chain or H chain V region of the antibody and a DNA encoding the L chain or L chain V region, and a desired amino acid sequence of those sequences. The DNA part encoding the DNA is amplified by PCR using a primer pair that defines both ends of the DNA, and then the DNA that encodes the peptide linker part and both ends thereof are ligated to the H and L chains, respectively. Obtained by combining and amplifying primer pairs.

  Moreover, once a DNA encoding scFv is prepared, an expression vector containing them and a host transformed with the expression vector can be obtained according to a conventional method, and the host is used according to a conventional method. , ScFv can be obtained.

  These antibody fragments can be produced by the host by obtaining and expressing the gene in the same manner as described above. The term “antibody” as used in the claims of the present application encompasses these antibody fragments.

  As a modified antibody, an antibody conjugated with various molecules such as polyethylene glycol (PEG) can also be used. The “antibody” referred to in the claims of the present application includes these modified antibodies. In order to obtain such a modified antibody, it can be obtained by chemically modifying the obtained antibody. These methods are already established in this field.

  The antibody produced and expressed as described above can be isolated from the inside and outside of the cell and from the host and purified to homogeneity. Separation and purification of the antibody used in the present invention can be performed by affinity chromatography. Examples of the column used for affinity chromatography include a protein A column and a protein G column. Examples of the carrier used for the protein A column include Hyper D, POROS, Sepharose F.F. In addition, it is only necessary to use a separation and purification method used in ordinary proteins, and the method is not limited at all.

  For example, the antibody used in the present invention can be separated and purified by appropriately selecting and combining chromatography other than the affinity chromatography, filter, ultrafiltration, salting out, dialysis and the like. Examples of chromatography include ion exchange chromatography, hydrophobic chromatography, gel filtration, and the like. These chromatographies can be applied to high performance liquid chromatography (HPLC). Moreover, you may use reverse phase HPLC (reverse phase HPLC).

  The concentration of the antibody obtained above can be measured by measuring absorbance or ELISA. That is, in the case of measuring absorbance, after appropriately diluting with PBS (-), the absorbance at 280 nm is measured, and 1 mg / ml is calculated as 1.35 OD. When using ELISA, the measurement can be performed as follows. That is, 100 μl of goat anti-human IgG (manufactured by TAGO) diluted to 1 μg / ml with 0.1 M bicarbonate buffer (pH 9.6) was added to a 96-well plate (manufactured by Nunc), and incubated at 4 ° C. overnight. Solidify. After blocking, 100 μl of appropriately diluted antibody used in the present invention or a sample containing the antibody, or human IgG (manufactured by CAPPEL) as a sample is added and incubated at room temperature for 1 hour.

  After washing, add 100 μl of alkaline phosphatase-labeled anti-human IgG (BIO SOURCE) diluted 5000 times and incubate at room temperature for 1 hour. After washing, the substrate solution is added, and after incubation, the absorbance at 405 nm is measured using MICROPLATE READER Model 3550 (manufactured by Bio-Rad) to calculate the concentration of the target antibody.

The IL-6 variant used in the present invention is a substance that has a binding activity to the IL-6 receptor and does not transmit the biological activity of IL-6. That is, the IL-6 variant competitively binds IL-6 to the IL-6 receptor, but does not transmit IL-6 biological activity, and therefore blocks signal transduction by IL-6.
IL-6 variants are produced by introducing mutations by substituting amino acid residues in the amino acid sequence of IL-6. The origin of IL-6, which is a variant of IL-6, does not matter, but human IL-6 is preferred in consideration of antigenicity and the like.

  Specifically, the secondary structure of the amino acid sequence of IL-6 is predicted using a known molecular modeling program such as WHATIF (Vriend et al., J. Mol. Graphics (1990) 8, 52-56). Further, it is performed by evaluating the influence on the whole of the amino acid residue to be substituted. After determining the appropriate substitution amino acid residue, IL- is introduced by introducing a mutation so that the amino acid is substituted by a usual PCR method using a vector containing a nucleotide sequence encoding the human IL-6 gene as a template. 6 Gene encoding the variant is obtained. This is incorporated into an appropriate expression vector as necessary, and an IL-6 variant can be obtained according to the expression, production and purification methods of the recombinant antibody.

  Specific examples of IL-6 variants include Brakenhoff et al., J. Biol. Chem. (1994) 269, 86-93, and Savino et al., EMBO J. (1994) 13, 1357-1367, WO 96-18648, WO96-17869.

  The IL-6 partial peptide or IL-6 receptor partial peptide used in the present invention has a binding activity to IL-6 receptor or IL-6, respectively, and transmits the biological activity of IL-6. It is a substance that does not. That is, IL-6 partial peptide or IL-6 receptor partial peptide binds to IL-6 receptor or IL-6, and captures these to specifically bind IL-6 to IL-6 receptor. To inhibit. As a result, it does not transmit the biological activity of IL-6, and therefore blocks signal transduction by IL-6.

  IL-6 partial peptide or IL-6 receptor partial peptide is a part or all of amino acids in the region related to the binding of IL-6 and IL-6 receptor in the amino acid sequence of IL-6 or IL-6 receptor A peptide consisting of a sequence. Such a peptide usually consists of 10 to 80, preferably 20 to 50, more preferably 20 to 40 amino acid residues.

  IL-6 partial peptide or IL-6 receptor partial peptide specifies the region involved in the binding of IL-6 and IL-6 receptor in the amino acid sequence of IL-6 or IL-6 receptor. Part or all of the amino acid sequences can be prepared by a generally known method such as a genetic engineering method or a peptide synthesis method.

  In order to prepare an IL-6 partial peptide or IL-6 receptor partial peptide by genetic engineering techniques, a DNA sequence encoding the desired peptide is incorporated into an expression vector, and the recombinant antibody is expressed, produced and purified. It can obtain according to.

  In order to prepare an IL-6 partial peptide or IL-6 receptor partial peptide by peptide synthesis, a method generally used in peptide synthesis, for example, a solid phase synthesis method or a liquid phase synthesis method can be used.

  Specifically, it may be carried out in accordance with the method described in the 1991 follow-up drug development volume 14 peptide synthesis supervision Yajima Haruaki Yodogawa Shoten 1991. As the solid-phase synthesis method, for example, an amino acid corresponding to the C terminus of the peptide to be synthesized is bound to a support that is insoluble in an organic solvent, and the α-amino group and the side chain functional group are protected with an appropriate protecting group. By alternately repeating the reaction of condensing amino acids one by one in the order from the C-terminal to the N-terminal and the reaction of removing the protecting group of the amino acid or peptide α-amino group bound on the resin, A method of stretching is used. Solid phase peptide synthesis methods are roughly classified into Boc method and Fmoc method according to the type of protecting group used.

  After synthesizing the target peptide in this way, deprotection reaction and cleavage reaction from the support of the peptide chain are performed. For the cleavage reaction with the peptide chain, hydrogen fluoride or trifluoromethanesulfonic acid can be usually used in the Boc method, and TFA can be usually used in the Fmoc method. In the Boc method, for example, the protected peptide resin is treated in hydrogen fluoride in the presence of anisole. Next, the peptide is recovered by removing the protecting group and cleaving from the support. This is freeze-dried to obtain a crude peptide. On the other hand, in the Fmoc method, for example, the deprotection reaction and the cleavage reaction from the support of the peptide chain can be performed in the same manner as described above in TFA.

  The obtained crude peptide can be separated and purified by application to HPLC. For the elution, a water-acetonitrile solvent usually used for protein purification may be used under optimum conditions. The fraction corresponding to the peak of the obtained chromatographic profile is collected and lyophilized. The peptide fraction thus purified is identified by molecular weight analysis by mass spectrum analysis, amino acid composition analysis, amino acid sequence analysis or the like.

  Specific examples of IL-6 partial peptide and IL-6 receptor partial peptide are disclosed in JP-A-2-188600, JP-A-7-324097, JP-A-8-311098 and US Pat.

The IL-6 signaling inhibitory activity of the IL-6 antagonist used in the present invention can be evaluated by a commonly used method. Specifically, an IL-6-dependent human myeloma line (S6B45, KPMM2), a human Rennelt T lymphoma cell line KT3, or an IL-6-dependent cell MH60.BSF2 is cultured, and IL-6 is added thereto. At the same time, the incorporation of ³ H-thymidine in IL-6-dependent cells may be measured by coexisting with an IL-6 antagonist. Further, by culturing U266 is IL-6 receptor-expressing cells, ¹²⁵ was added I-labeled IL-6, by the addition of IL-6 antagonist at the same time, ¹²⁵ I-labeled IL bound to IL-6 receptor-expressing cells -6 is measured. In the above assay system, there is a negative control group that does not contain IL-6 antagonist in addition to the group in which IL-6 antagonist is present, and the IL-6 inhibitory activity of IL-6 antagonist can be evaluated by comparing the results obtained with both. can do.

  As shown in the Examples below, administration of anti-IL-6 receptor antibody resulted in a decrease in the blood concentration of MMP-3 in rheumatic patients. It was suggested that IL-6 antagonist has a blood MMP-3 concentration lowering effect, and thereby has a cartilage destruction inhibiting action.

  The subject of treatment in the present invention is a mammal. The mammal to be treated is preferably a human.

  The blood MMP-3 concentration reducing agent and cartilage destruction inhibitor of the present invention can be administered orally or parenterally systemically or locally. For example, intravenous injection such as infusion, intramuscular injection, intraperitoneal injection, subcutaneous injection, suppository, enema, oral enteric solvent, etc. can be selected, and the administration method should be selected appropriately depending on the age and symptoms of the patient Can do. The effective dose is selected in the range of 0.01 mg to 100 mg per kg body weight. Alternatively, a dose of 1-1000 mg, preferably 5-50 mg per patient can be selected. For example, in the case of an anti-IL-6 receptor antibody, a preferable dose and administration method are effective doses in such an amount that free antibodies are present in the blood. 0.5 mg to 40 mg, preferably 1 mg to 20 mg per month (4 weeks) divided into 1 to several times, for example, 2 times / week, 1 time / week, 1 time / 2 weeks, 1 time / 4 weeks, etc. For example, the administration schedule may be intravenous injection such as infusion or subcutaneous injection.

  The blood MMP-3 concentration-lowering agent and cartilage destruction inhibitor of the present invention may contain both pharmaceutically acceptable carriers and additives depending on the administration route. Examples of such carriers and additives include water, pharmaceutically acceptable organic solvents, collagen, polyvinyl alcohol, polyvinyl pyrrolidone, carboxyvinyl polymer, sodium carboxymethylcellulose, sodium polyacrylate, sodium alginate, water soluble dextran, Sodium carboxymethyl starch, pectin, methylcellulose, ethylcellulose, xanthan gum, gum arabic, casein, gelatin, agar, diglycerin, propylene glycol, polyethylene glycol, petroleum jelly, paraffin, stearyl alcohol, stearic acid, human serum albumin (HSA), mannitol, Examples include sorbitol, lactose, and surfactants acceptable as pharmaceutical additives. The additive to be used is selected appropriately or in combination from the above depending on the dosage form, but is not limited thereto.

  In the present invention, due to the action of an IL-6 antagonist such as an anti-IL-6 receptor antibody, the concentration in the body of a substance selected from the group consisting of MMP-3, MMP-1 and TIMP-1 such as blood concentration is decreased. Therefore, by using the blood concentration of MMP-3 or the like as an indicator, drugs containing IL-6 antagonist as an active ingredient, for example, inhibiting cartilage destruction using IL-6 antagonist as an active ingredient A method for detecting, evaluating, and / or determining an effect (for example, a therapeutic effect) of an agent or a treatment for osteoarthritis, or a reagent used in the method is useful. It will be understood that it is.

  Regarding MMP-3, MMP-1 and TIMP-1, methods for measuring them in vivo or in vitro or reagents for the measurement are widely known in the art. From among the known methods and reagents, It can select suitably and can be used for the objective of this invention.

  MMP-3, MMP-1 or TIMP-1 in a sample can be measured using an anti-MMP antibody, an MMP inhibitor, or a compound having an inhibitory activity against the MMP family (including synthetic compounds), but preferably Is an antibody such as a monoclonal antibody against MMP-3 [wherein the term “antibody” may be used in a broad sense, and may be a single monoclonal antibody against a desired substance or various kinds of antibodies. It may be an antibody composition with specificity for an epitope, including monovalent or multivalent antibodies and polyclonal and monoclonal antibodies, and also representing intact molecules and fragments and derivatives thereof Including fragments such as F (ab ') 2, Fab' and Fab, and having at least two antigen or epitope binding sites. Chimeric antibodies or hybrid antibodies, or bispecific recombinant antibodies such as quadrome, triome, interspecific hybrid antibodies, anti-idiotype antibodies, and chemically modified or processed Applying known cell fusion or hybridoma technology and antibody engineering, antibodies obtained using synthetic or semi-synthetic technology, and conventional technologies known from the viewpoint of antibody production Or antibodies prepared using DNA recombination techniques, antibodies having neutralizing properties or binding properties with respect to the target antigenic substance or target epitope described and defined herein, or antibodies having binding properties. Immunization using an antibody such as a monoclonal antibody against MMP-1 or an antibody such as a monoclonal antibody against TIMP-1. It can be carried out by measurement method. In addition, various methods including biochemical techniques such as measuring enzyme activity or inhibitory activity may be used.

  The immunoassay may be any of competitive or non-competitive binding assays, direct and indirect sandwich assays, and immunoprecipitation assays, as well as enzyme immunoassays, radioimmunoassays, fluorescent immunoassays, and other biotin-avidins. Any assay using a label known in the art, such as a system, metal particles such as gold colloid, a coloring substance, a magnetic substance, etc.

  According to the measurement method of the present invention, for example, a labeled antibody reagent such as a monoclonal antibody in which a substance to be measured is labeled with an enzyme and an antibody bound to a carrier are reacted sequentially or simultaneously. You can also. The order in which reagents are added depends on the type of carrier system selected. If sensitized plastic beads or wells are used, a labeled antibody reagent such as a monoclonal antibody labeled with an enzyme or the like is first put together with a specimen sample containing the substance to be measured in a suitable test tube. And then adding the sensitized beads such as plastic or placing them in the well.

  As a sample to be measured by the measurement method of the present invention, any form of solution, colloidal solution, non-fluid sample, etc. can be used, but preferably a sample derived from a living organism such as thymus, testis, intestine, kidney, brain, breast cancer. Ovarian cancer, colorectal cancer, blood, serum, plasma, joint fluid, cerebrospinal fluid, saliva, amniotic fluid, urine, other body fluids, cell culture fluid, tissue culture fluid, tissue homodulate, biopsy sample, tissue, cell Etc.

When various analysis / quantification methods including these individual immunological measurement methods are applied to the measurement method of the present invention, special conditions, operations, and the like are not required to be set. A measurement system related to the target substance of the present invention or a substance having substantially the same activity may be constructed by adding ordinary technical considerations to those skilled in the art to the normal conditions and operation methods in each method. .
MMP-3 measurement is described in, for example, Matrix, (1990) 10, 285-291, or Japanese Patent Application Laid-Open No. 4-237499. In particular, as a technique suitable for measuring MMP-3 in a specimen, for example, a technique described in JP-A-4-237499 is mentioned.

  MMP-1 measurement is described in, for example, Clin. Chim. Acta (1993) 219, 1-14 or Res. Commun. Mol. Pathol. Pharmacol. (1997) 95, 115-128. In particular, examples of techniques suitable for measuring MMP-1 in a specimen include those described in Clin. Chim. Acta (1993) 219, 1-14.

  TIMP-1 measurement is described in, for example, J. Immunol. Methods (1990) 127, 103-108, Matrix (1989) 9, 1-6, or Japanese Patent Laid-Open No. 63-210665. In particular, as a technique suitable for measuring TIMP-1 in a specimen, for example, a technique described in JP-A-63-210665 and the like can be mentioned.

  Protease activity or inhibitor activity can be measured according to the usual measurement method, for example, referring to the method shown in Biochemistry (1993) 32,4330-4337. Various labels, buffer systems, and other suitable reagents can also be used. In carrying out the method, MMPs or the like can be treated with an activator such as aminophenylmercuric acetate, or a precursor or latent type thereof can be converted into an active type in advance. For each measurement, an appropriate measurement system may be constructed by adding ordinary technical considerations to those skilled in the art to the normal conditions and operation methods in each method.

  EXAMPLES Hereinafter, although an Example, a reference example, and an experiment example demonstrate this invention concretely, this invention is not limited to these.

Example : Treatment with humanized anti-IL-6 receptor antibody (humanized PM-1 antibody; composed of L chain version a and H chain version f described in WO92 / 19759) for 2 months or more 8 patients with rheumatoid arthritis and 5 patients with Multicentric Castleman's Disease (CD) were treated with MMP-1, -2, -3, -7, -8 and -13 and TIMP-1 and -2 Changes in blood concentration were examined. The antibody was dissolved in 100 ml of physiological saline and increased to 1 mg, 10 mg and 50 mg while confirming safety, and was used by intravenous infusion at a rate of 50 mg / body twice a week or 100 mg / body once a week.

  The values at the 6th month were also examined for 4 patients with rheumatism and 2 patients with CD who had continued treatment for the previous value, 2 months after the start of treatment, and 6 months. ELISA kits (Fuji Pharmaceutical Co., Ltd.) were used to measure the blood concentrations of MMP-1, -2, -3, -7, -8 and -13 and TIMP-1 and -2. As a result, it was shown that humanized anti-IL-6 receptor antibody decreases the blood concentration of MMP-1, MMP-3 and TIMP-1 in rheumatic patients and Castleman disease patients (FIGS. 1 to 6). ).

  From the above, it was shown that anti-IL-6 receptor antibody decreases the blood MMP-3 concentration and can be a cartilage destruction inhibitor and osteoarthritis therapeutic agent.

Reference Example 1 Preparation of human soluble IL-6 receptor
Soluble by PCR using plasmid pBSF2R.236 containing cDNA encoding IL-6 receptor obtained according to the method of Yamasaki et al. (Yamasaki, K. et al., Science (1988) 241, 825-828) IL-6 receptor was created. Plasmid pBSF2R.236 was digested with restriction enzyme Sph I to obtain IL-6 receptor cDNA, which was inserted into mp18 (Amersham). Using a synthetic oligo primer designed to introduce a stop codon into the IL-6 receptor cDNA, a mutation was introduced into the IL-6 receptor cDNA by PCR using an in vitro mutagenesis system (manufactured by Amersham). By this operation, a stop codon was introduced at the position of amino acid 345, and a cDNA encoding a soluble IL-6 receptor was obtained.

  In order to express soluble IL-6 receptor cDNA in CHO cells, it was ligated with plasmid pSV (manufactured by Pharmacia) to obtain plasmid pSVL344. The soluble IL-6 receptor cDNA cleaved with Hind III-Sal I was inserted into the plasmid pECEdhfr containing the dhfr cDNA to obtain the CHO cell expression plasmid pECEdhfr344.

  10 μg of plasmid pECEdhfr344 was transferred to dhfr-CHO cell line DXB-11 (Urlaub, G. et al., Proc. Natl. Acad. Sci. USA (1980) 77, 4216-4220) by calcium phosphate precipitation (Chen, C et al., Mol. Cell. Biol. (1987) 7, 2745-2751). Transfected CHO cells were cultured for 3 weeks in a nucleoside-free αMEM selective culture medium containing 1 mM glutamine, 10% dialyzed FCS, 100 U / ml penicillin and 100 μ / ml streptomycin.

  Selected CHO cells were screened by limiting dilution to obtain a single CHO cell clone. This CHO cell clone was amplified with methotrexate at a concentration of 20 nM to 200 nM to obtain a human soluble IL-6 receptor-producing CHO cell line 5E27. CHO cell line 5E27 was cultured in Iscove modified Dulbecco medium (IMDM, Gibco) containing 5% FBS. The culture supernatant was collected, and the concentration of soluble IL-6 receptor in the culture supernatant was measured by ELISA. As a result, it was confirmed that soluble IL-6 receptor was present in the culture supernatant.

Reference Example 2 Preparation of anti-human IL-6 antibody
10 μg of recombinant IL-6 (Hirano, T. et al., Immunol. Lett. (1988) 17, 41) was immunized with Freund's complete adjuvant in BALB / c mice, and anti-IL-6 antibody was found in the serum. This was continued every week until detected. Immune cells were removed from local lymph nodes and fused with myeloma cell line P3U1 using polyethylene glycol 1500. Hybridomas were selected according to the method of Oi et al. Using a HAT culture solution (Selective Methods in Cellular Immunology, WHFreeman and Co., San Francisco, 351, 1980) to establish hybridomas producing anti-human IL-6 antibodies.

  Hybridomas producing anti-human IL-6 antibodies were subjected to IL-6 binding assay as follows. Specifically, a 96-well microplate made of flexible polyvinyl (Dynatech Laboratories, Inc., Alexandria, VA) was washed with 100 μl of goat anti-mouse Ig (10 μl / ml, 0.1 M carbonate-hydrogen carbonate buffer (pH 9.6)). Cooper Biomedical, Inc. Malvern, PA) and coated overnight at 4 ° C. The plates were then treated with 100 μl of 1% bovine serum albumin (BSA) in PBS for 2 hours at room temperature.

After washing with PBS, 100 μl of hybridoma culture supernatant was added to each well and incubated at 4 ° C. overnight. The plate was washed and ¹²⁵ I-labeled recombinant IL-6 was added to each well to 2000 cpm / 0.5 ng / well. After washing, the radioactivity in each well was measured using a gamma counter (Beckman Gamma 9000, Beckman Instruments , Fullerton, CA). Of the 216 hybridoma clones, 32 hybridoma clones were positive by IL-6 binding assay. Of these clones, stable MH166.BSF2 was finally obtained. The anti-IL-6 antibody MH166 produced by the hybridoma has an IgG1κ type subtype.

Subsequently, the neutralizing activity of the MH166 antibody on the growth of the hybridoma was examined using the IL-6-dependent mouse hybridoma clone MH60.BSF2. MH60.BSF2 cells dispensed so minute a 1 × 10 ⁴ / 200μl / well, to which was added a sample containing MH166 antibody were cultured for 48 hours, 0.5 [mu] Ci / well of ³ H-thymidine (New England Nuclear, Boston , MA) was added, and the culture was further continued for 6 hours. Cells were placed on glass filter paper and treated with an automatic harvester (Labo Mash Science Co., Tokyo, Japan). Rabbit anti-IL-6 antibody was used as a control.

As a result, MH166 antibody inhibited uptake of ³ H thymidine in MH60.BSF2 cells induced by IL-6 in a dose-dependent manner. This revealed that MH166 antibody neutralizes IL-6 activity.

Reference Example 3 Preparation of anti-human IL-6 receptor antibody
Sepharose 4B (manufactured by Pharmacia Fine Chemicals) in which anti-IL-6 receptor antibody MT18 prepared by the method of Hirata et al. (Hirata, Y. et al. J. Immunol. (1989) 143, 2900-2906) was activated by CNBr. And IL-6 receptor (Yamasaki, K. et al., Science (1988) 241, 825-828). Human myeloma cell line U266 was converted to 1% digitonin (manufactured by Wako Chemicals), 1 mM p-paraaminophenylmethanesulfonyl fluoride hydrochloride (manufactured by Wako Chemicals) containing 10 mM triethanolamine (pH 7.8) and 0.15 M NaCl (digitonin buffer) And mixed with MT18 antibody conjugated with Sepharose 4B beads. Thereafter, the beads were washed 6 times with digitonin buffer to obtain partially purified IL-6 receptor for immunization.

BALB / c mice were immunized 4 times every 10 days with the partially purified IL-6 receptor obtained from 3 × 10 ⁹ U266 cells, and then a hybridoma was prepared by a conventional method. The hybridoma culture supernatant from the positive growth hole was examined for binding activity to IL-6 receptor by the following method. 5 × 10 ⁷ U266 cells were labeled with ³⁵ S-methionine (2.5 mCi) and solubilized with the above digitonin buffer. Solubilized U266 cells were mixed with MT18 antibody conjugated to 0.04 ml volume of Sepharose 4B beads, then washed 6 times with digitonin buffer and ³⁵ S-methionine with 0.25 ml digitonin buffer (pH 3.4). The labeled IL-6 receptor was drained and neutralized with 0.025 ml of 1M Tris (pH 7.4).

0.05 ml of the hybridoma culture supernatant was mixed with 0.01 ml of Protein G Sepharose (manufactured by Pharmacia). After washing, Sepharose was incubated with 0.005 ml of ³⁵ S-labeled IL-6 receptor solution prepared above. Immunoprecipitates were analyzed by SDS-PAGE to examine hybridoma culture supernatants that react with IL-6 receptor. As a result, a reaction positive hybridoma clone PM-1 (FERM BP-2998) was established. The antibody produced from hybridoma PM-1 has an IgG1κ type subtype.

The inhibitory activity of IL-6 binding to the human IL-6 receptor of the antibody produced by hybridoma PM-1 was examined using the human myeloma cell line U266. Recombinant human IL-6 was prepared from E. coli (Hirano, T. et al., Immunol. Lett. (1988) 17, 41-45) and ¹²⁵ by Bolton-Hunter reagent (New England Nuclear, Boston, MA). I-labeled (Taga, T. et al., J. Exp. Med. (1987) 166, 967-981).

4 × 10 ⁵ U266 cells were cultured for 1 hour with 70% (v / v) hybridoma PM-1 culture supernatant and 14000 cpm of ¹²⁵ I-labeled IL-6. 70 μl of the sample was layered on 300 μl of FCS in a 400 μl microfuge polyethylene tube, and after centrifugation, the radioactivity on the cells was measured.
As a result, it was revealed that the antibody produced by hybridoma PM-1 inhibits the binding of IL-6 to the IL-6 receptor.

Reference Example 4 Preparation of anti-mouse IL-6 receptor antibody
A monoclonal antibody against mouse IL-6 receptor was prepared by the method described in Saito, T. et al., J. Immunol. (1991) 147, 168-173.
CHO cells producing mouse soluble IL-6 receptor are cultured in IMDM medium containing 10% FCS, and anti-mouse IL-6 receptor antibody RS12 (see Saito, T. et al above) is cultured from the culture supernatant. Mouse soluble IL-6 receptor was purified using an affinity column immobilized on Affigel 10 gel (Biorad).

The obtained mouse soluble IL-6 receptor (50 μg) was mixed with Freund's complete adjuvant and injected into the abdomen of Wistar rats. Two weeks later, booster immunization was performed with Freund's incomplete adjuvant. On day 45, rat spleen cells were collected, and 2 x 10 ⁸ cells were fused with 1 x 10 ⁷ mouse myeloma cells P3U1 and 50% PEG1500 (manufactured by Boehringer Mannheim) in a conventional manner. Hybridomas were screened in the medium.

  Hybridoma culture supernatant was added to a plate coated with rabbit anti-rat IgG antibody (Cappel), and then mouse soluble IL-6 receptor was reacted. Subsequently, hybridomas producing antibodies against mouse soluble IL-6 receptor were screened by ELISA using rabbit anti-mouse IL-6 receptor antibody and alkaline phosphatase-labeled sheep anti-rabbit IgG. Hybridoma clones in which antibody production was confirmed were sub-screened twice to obtain a single hybridoma clone. This clone was named MR16-1.

The neutralizing activity of the antibody produced by this hybridoma in the signal transduction of mouse IL-6 was measured by ³ H using MH60.BSF2 cells (Matsuda, T. et al., J. Immunol. (1988) 18, 951-956). Investigated by thymidine incorporation. MH60.BSF2 cells were prepared in a 96-well plate at 1 × 10 ⁴ cells / 200 μl / well. The plate 10 pg / ml of mouse IL-6 and MR16-1 antibody or RS12 antibody 12.3~1000ng / ml addition 37 ° C., after incubation for 44 hours at 5% CO2, was added ³ H-thymidine 1 [mu] Ci / well . After 4 hours, ³ H thymidine incorporation was measured. As a result, MR16-1 antibody suppressed ³ H thymidine incorporation in MH60.BSF2 cells.

  Therefore, it was revealed that the antibody produced by the hybridoma MR16-1 (FERM BP-5875) inhibits the binding of IL-6 to the IL-6 receptor.

EFFECT OF THE INVENTION According to the present invention, it was shown that IL-6 antagonists such as anti-IL-6 receptor antibodies have a blood MMP-3 concentration lowering effect. Therefore, it has been clarified that IL-6 antagonist is useful as a blood MMP-3 concentration lowering agent, a cartilage destruction inhibitor and / or an osteoarthritis therapeutic agent.

References to the microorganisms deposited under Rule 13-2 of the Patent Cooperation Treaty and Depositary Organizations Depositary Organizations Name: National Institute of Biotechnology, National Institute of Advanced Industrial Science and Technology
Address: 1-3, East 1-3 Tsukuba, Ibaraki, Japan
Microorganism (1) Name: PM-1
Deposit number: FERM BP-2998
Deposit date: July 12, 1989
(2) Name: Rat-mouse hybridoma MR16-1
Deposit number: FERM BP-5875
Deposit date: March 13, 1997
(3) Name: HB-101-pIBIBSF2R
Deposit number: FERM BP-2232
Deposit date: January 9, 1989

Depositary: National Collections of Industrial, Food and Marine Bacteria Limited
Address: 23 St Macher Drive, Aberdeen AB2 IRY, UNITED KINGDOM
(4) Name: E.coli DH5α pPM-k3
Deposit number: MCIMB 40366
Deposit date: February 12, 1991
(5) Name: E.coli DH5α pPM-h1
Deposit number: MCIMB 40362
Deposit date: February 12, 1991

Summary of disclosure A blood matrix metalloproteinase-3 (MMP-3) concentration reducing agent comprising an interleukin-6 (IL-6) antagonist as an active ingredient.
2. The agent for reducing blood MMP-3 level according to claim 1, wherein the IL-6 antagonist is an antibody against IL-6 receptor.

3. 3. The blood MMP-3 concentration reducing agent according to item 2, wherein the antibody against IL-6 receptor is a monoclonal antibody against IL-6 receptor.
4). 4. The blood MMP-3 concentration reducing agent according to item 3, wherein the antibody to IL-6 receptor is a monoclonal antibody to human IL-6 receptor.
5. 4. The blood MMP-3 concentration reducing agent according to item 3, wherein the antibody to IL-6 receptor is a monoclonal antibody to mouse IL-6 receptor.

6). 6. The blood MMP-3 concentration reducing agent according to any one of items 2 to 5, wherein the antibody against IL-6 receptor is a recombinant antibody.
7). 5. The blood MMP-3 concentration reducing agent according to item 4, wherein the monoclonal antibody against human IL-6 receptor is PM-1 antibody.
8). 6. The blood MMP-3 concentration reducing agent according to item 5, wherein the monoclonal antibody against mouse IL-6 receptor is MR16-1 antibody.

9. 5. The blood MMP-3 concentration reducing agent according to any one of items 2 to 4, wherein the antibody to IL-6 receptor is a chimeric antibody or a humanized antibody to IL-6 receptor.
Ten. 10. The blood MMP-3 concentration reducing agent according to item 9, wherein the humanized antibody against IL-6 receptor is a humanized PM-1 antibody.

11． A cartilage destruction inhibitor containing an interleukin-6 (IL-6) antagonist as an active ingredient.
12． Item 12. The cartilage destruction inhibitor according to Item 11, wherein the IL-6 antagonist is an antibody against IL-6 receptor.
13. Item 13. The cartilage destruction inhibitor according to Item 12, wherein the antibody to IL-6 receptor is a monoclonal antibody to IL-6 receptor.

14. Item 14. The inhibitor of cartilage destruction according to item 13, wherein the antibody to IL-6 receptor is a monoclonal antibody to human IL-6 receptor.
15． Item 14. The cartilage destruction inhibitor according to Item 13, wherein the antibody to IL-6 receptor is a monoclonal antibody to mouse IL-6 receptor.
16． 16. The cartilage destruction inhibitor according to any one of items 12 to 15, wherein the antibody to IL-6 receptor is a recombinant antibody.

17． 15. The cartilage destruction inhibitor according to item 14, wherein the monoclonal antibody against human IL-6 receptor is PM-1 antibody.
18． Item 16. The inhibitor of cartilage destruction according to Item 15, wherein the monoclonal antibody against mouse IL-6 receptor is MR16-1 antibody.
19. 15. The cartilage destruction inhibitor according to any one of items 12 to 14, wherein the antibody to IL-6 receptor is a chimeric antibody or a humanized antibody to IL-6 receptor.

20． Item 20. The inhibitor of cartilage destruction according to Item 19, wherein the humanized antibody to IL-6 receptor is a humanized PM-1 antibody.
twenty one. A therapeutic agent for osteoarthritis containing an interleukin-6 (IL-6) antagonist as an active ingredient.

twenty two. (1) Using MMP-3 concentration in the specimen as an index, and (2) (a) a drug containing an IL-6 antagonist as an active ingredient, (b) a cartilage destruction inhibitor containing an IL-6 antagonist as an active ingredient, or (C) A method for detecting, evaluating and determining the effect of a therapeutic agent for osteoarthritis comprising an IL-6 antagonist as an active ingredient.

twenty three. To detect, evaluate, and determine (1) the effect of inhibiting the destruction of cartilage by an agent containing an IL-6 antagonist as an active ingredient, or (2) the therapeutic effect of osteoarthritis of an agent containing an IL-6 antagonist as an active ingredient A reagent for measuring MMP-3 concentration in a specimen, characterized by being used.
twenty four. 24. The reagent according to item 23, which contains an anti-MMP-3 antibody.

Claims (4)

(1) MMP-3 concentration in the sample as an index, and (2) ( a ) a cartilage destruction inhibitor containing an antibody against IL-6 receptor as an active ingredient, or ( b ) an antibody against IL-6 receptor A method for detecting, evaluating, and judging the effect of a therapeutic agent for osteoarthritis as an active ingredient.   The detection / evaluation / determination method according to claim 1, wherein the cartilage destruction inhibitor is a therapeutic agent for rheumatism. Containing anti-MMP-3 antibody, (1) anti- cartilage destruction inhibitory action of drug containing IL-6 receptor antibody as active ingredient, or (2) modification of drug containing IL-6 receptor antibody as active ingredient A reagent for measuring the concentration of MMP-3 in a specimen, characterized by being used for detecting, evaluating and judging the therapeutic effect of osteoarthritis.   The reagent for measuring MMP-3 concentration according to claim 3, wherein the cartilage destruction inhibiting action is a rheumatic treatment effect.

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