Patent Application
20190112370
The present invention relates to a novel medical use of antibodies to MRAP2 or fragments thereof as, for example, therapeutic and/or preventive agents for cancer.
In recent years, a variety of antibody medicines for cancer treatment that target antigen proteins on cancer cells have come into existence. The antibody medicines used as cancer-specific therapeutic agents exhibit drug efficacy to a certain extent, and thus they have been gaining attention. However, many of target antigen proteins are also expressed on multiple normal cells. As a result of antibody administration, not only cancer cells, but also normal cells on which a target antigen has been expressed can be damaged, thereby causing a side effect, which becomes problematic. Hence, it is expected that, if it becomes possible to identify cancer antigens that are specifically expressed on the surface of a cancer cell and to use antibodies targeting such antigens as medicaments, then treatment with antibody medicines that cause fewer side effects could be realized.
Melanocortin 2 receptor accessory protein 2 (MRAP2), a type 1 or type 2 transmembrane protein, participates in the control of melanocortin receptor (MCR) activity and functions in energy metabolism in vivo (Non Patent Literature 1). Also, it has been reported that MRAP2-deficient mice become obese in spite of the absence of overeating, and it has also been reported as to humans that some severely obese patients have a mutation in the MRAP2 gene (Non Patent Literature 2). However, none of the previous reports show that the MRAP2 protein has immunity-inducing activity against cancer cells and is thereby useful for treatment or prevention of cancers.
An object of the present invention is to identify cancer antigen proteins specifically expressed on the surface of cancer cells and to provide a use of antibodies targeting such proteins as therapeutic and/or preventive agents for cancer.
As a result of intensive studies, the present inventors have now obtained cDNA encoding a protein that binds to an antibody present in the serum from a tumor-bearing organism by the SEREX method using canine testis tissue-derived cDNA libraries and sera from dogs with leukemia. With the use of the obtained canine genes and gene homologs from human, feline, and mouse, MRAP2 proteins having amino acid sequences shown in SEQ ID NO: 2, 4, 6 or 8 and antibodies against the MRAP2 proteins have now been prepared. In addition, the present inventors have now found that MRAP2 is specifically expressed in the cells of leukemia, malignant lymphoma, lung cancer, brain tumor, colorectal cancer, melanoma, neuroblastoma, pancreatic cancer, gastric cancer, liver cancer, ovary cancer, esophageal cancer, kidney cancer, mastocytoma, or perianal adenocarcinoma, and that portions of the MRAP2 proteins are specifically expressed on the surface of such cancer cells. Further, the present inventors have now found that antibodies against the MRAP2 portions expressed on cancer cell surfaces can damage cancer cells expressing MRAP2. These findings have led to the completion of the present invention.
Therefore, the present invention includes (1) to (11) below.
This description includes all or part of the contents disclosed in Japanese Patent Application No. 2016-064033, to which the present application claims the priority.
Antibodies against MRAP2 used in the present invention damage cancer cells. Therefore, such antibodies against MRAP2 are useful for treatment or prevention of cancers.
The present invention relates to a use of an antibody or fragment (preferably antigen binding fragment) thereof to an MRAP2 protein or a fragment thereof for treatment and/or prevention of cancers.
The present invention relates to a pharmaceutical composition for treatment and/or prevention of a cancer, which comprises, as an active ingredient, an antibody or fragment thereof having an immunological reactivity with an MRAP2 protein having the amino acid sequence shown in SEQ ID NO: 2, 4, 6, or 8 or an amino acid sequence having 80% or more (preferably 85% or more, more preferably 90% or more, further preferably 95% or more, and particularly preferably 99% or more, for example, 99.5% or more) sequence identity with the amino acid sequence, or with a fragment of the MRAP2 protein comprising 7 or more (7 to each full-length sequence, preferably 7 to 150 and more preferably 7 to 50) consecutive amino acids.
The present invention also relates to the pharmaceutical composition for treatment and/or prevention of a cancer, which comprises, as an active ingredient, an antibody or fragment thereof having an immunological reactivity with a partial polypeptide of an MRAP2 protein, the partial polypeptide being a polypeptide consisting of 7 or more (7 to each full-length sequence, preferably 7 to 40, more preferably 7 to 20, for example, 7 to 12 or 8 to 11) consecutive amino acids of the amino acid sequence shown in any one of the even numbered SEQ ID NOS: 10 to 24, or a polypeptide consisting of an amino acid sequence having 80% or more (preferably 85% or more, more preferably 90% or more, further preferably 95% or more, and particularly preferably 97% or more) sequence identity with the amino acid sequence.
The antitumor activity of the antibody or fragment thereof to the polypeptide consisting of the amino acid sequence shown in SEQ ID NO: 2, 4, 6, or 8 or to a fragment of the polypeptide used in the present invention can be evaluated by examining in vivo the inhibition of tumor growth in a tumor-bearing animal, or, as described below, by examining in vitro whether or not immunocyte- or complement-mediated cytotoxic activity against tumor cells expressing the polypeptide is exhibited. Likewise, the antitumor activity of the antibody or fragment thereof against the polypeptide consisting of the amino acid sequence shown in any one of the even numbered SEQ ID NOS: 10 to 24 or a fragment of the polypeptide used in the present invention can be evaluated by examining in vivo the inhibition of tumor growth in a tumor-bearing animal, or, as described below, by examining in vitro whether or not immunocyte- or complement-mediated cytotoxic activity against tumor cells expressing the polypeptide is exhibited.
In addition, the nucleotide sequences of polynucleotides encoding the proteins consisting of the amino acid sequences shown in SEQ ID NOS: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, and 24 are shown in SEQ ID NOS: 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, and 23, respectively.
The amino acid sequence shown in SEQ ID NO: 4 in the Sequence Listing disclosed according to the present invention is the amino acid sequence of the MRAP2, which was isolated, by the SEREX method using canine testis tissue-derived cDNA libraries and sera from dogs with leukemia, as a polypeptide capable of binding to antibodies specifically existing in the sera from tumor-bearing dogs; the amino acid sequence shown in SEQ ID NO: 2 is the amino acid sequence of the MRAP2 isolated as a human homolog of said dog polypeptide; the amino acid sequence shown in SEQ ID NO: 6 is the amino acid sequence of the MRAP2 isolated as a feline homolog of said dog polypeptide; and the amino acid sequence shown in SEQ ID NO: 8 is the amino acid sequence of the MRAP2 protein isolated as a mouse homolog of said dog polypeptide (see Example 1 described below).
According to the present invention, an antibody that binds to a portion expressed on cancer cell surfaces within MRAP2 protein is preferably used. Specific examples thereof include antibodies to polypeptides having the amino acid sequence shown in SEQ ID NO: 10 (human), 14 (canine), 18 (feline), or 22 (mouse), which is the N-terminal portion of the MRAP2 protein, or the amino acid sequence shown in SEQ ID NO: 12 (human), 16 (canine), 20 (feline), or 24 (mouse), which is the C-terminal portion of the MRAP2 protein, or fragments of the polypeptides (preferably, the fragments each consisting of 7 or more consecutive amino acids of any one of the amino acid sequences), or polypeptides having an amino acid sequence having 80% or more, preferably 85% or more, more preferably 90% or more, further preferably 95% or more, and particularly preferably 99% or more sequence identity to any one of these polypeptides. Antibodies of the present invention include all antibodies capable of binding to the above polypeptides and having antitumor activity.
The antibodies to MRAP2 usable in the present invention as described above may be any types thereof, as long as they can exhibit antitumor activity. Examples thereof can include monoclonal antibodies, polyclonal antibodies, synthetic antibodies, multispecific antibodies (e.g., bispecific antibodies), human antibodies, humanized antibodies, chimeric antibodies, and single-chain antibodies (scFV). The antibodies used in the present invention also include antibody fragments, for example, antigen binding fragments such as Fab and F(ab′)2. These antibodies and fragments thereof can be prepared by methods known to persons skilled in the art. In the present invention, antibodies capable of specifically binding to an MRAP2 protein or fragments thereof are desirable. Such antibodies are preferably monoclonal antibodies; however, as long as homogenous antibodies can be stably produced, polyclonal antibodies may also be used. In addition, if the subject is a human, a human antibody or a humanized antibody is desirable in order to avoid or inhibit the immunorejection.
The word “specifically binding to an MRAP2 protein or fragments thereof” as used herein means that an antibody of interest specifically binds to the MRAP2 protein or fragments thereof and does not substantially bind to other proteins.
The antitumor activity of an antibody used in the present invention can be evaluated by examining in vivo the inhibition of tumor growth in a tumor-bearing animal, or, as described below, examining in vitro whether or not the immunocyte- or complement-mediated cytotoxic activity against tumor cells expressing the polypeptide is exhibited.
Moreover, the subjects in need of treatment and/or prevention of cancer according to the present invention are mammals such as human, pet animals, livestock animals, sport animals, or experimental animals. The preferred subject is a human.
Production of antigens, production of antibodies, and pharmaceutical compositions, related to the present invention, will be explained below.
Proteins or fragments thereof used as sensitizing antigens for obtaining antibodies to MRAP2 used in the present invention are not limited in terms of their origins such as animals including, for example, humans, canines, felines, mice, bovines, horses, rats, and chickens. However, such proteins or fragments thereof are preferably selected in view of compatibility with parent cells used for cell fusion. Mammal-derived proteins are generally preferable and human-derived proteins are particularly preferable. For instance, if the MRAP2 is human MRAP2, a human MRAP2 protein, a partial polypeptide thereof, or cells capable of expressing human MRAP2 can be used.
Nucleotide sequences and amino acid sequences of human MRAP2 and homologs thereof can be obtained by, for example, accessing the website of GenBank (NCBI, USA) and using an algorithm such as BLAST or FASTA (Karlin and Altschul, Proc. Natl. Acad. Sci. USA, 90:5873-5877,1993; Altschul et al., Nucleic Acids Res. 25:3389-3402, 1997).
According to the present invention, when the nucleotide sequence (SEQ ID NO: 1) or the amino acid sequence (SEQ ID NO: 2) of human MRAP2 is used as a base sequence, targets are nucleic acids or proteins each consisting of a sequence having 70% to 100%, preferably 80% to 100%, more preferably 90% to 100%, and further preferably 95% to 100% (e.g., 97% to 100%, 98% to 100%, 99% to 100%, or 99.5% to 100%) sequence identity with the nucleotide sequence or amino acid sequence of the ORF or mature portion of the base nucleotide sequence or amino acid sequence. The term “% sequence identity” as used herein means a percentage (%) of the number of identical amino acids (or nucleotides) relative to the total number of amino acids (or nucleotides) in the case that two sequences are aligned such that maximum similarity can be achieved with or without introduction of gaps.
Fragments of an MRAP2 protein have lengths ranging from the amino acid length of an epitope (or an antigenic determinant), which is the smallest unit of an antigen recognized by an antibody, to less than the full-length of the protein. The epitope refers to a polypeptide fragment having antigenicity or immunogenicity in mammals and preferably in humans. The smallest unit of the epitope consists of approximately 7 to 12 amino acids, and for example, 8 to 11 amino acids. A specific example thereof is a polypeptide consisting of the amino acid sequence having 80% or more, preferably 85% or more, more preferably 90% or more, and further preferably 95% or more sequence identity with the amino acid sequence of an MRAP2 protein.
Polypeptides comprising the aforementioned human MRAP2 protein and partial peptides thereof can be synthesized according to chemical synthesis methods such as the Fmoc method (fluorenylmethyloxycarbonyl method) or the tBoc method (t-butyloxycarbonyl method) (the Japanese Biochemical Society (ed.), “Biochemical Experimentation Course (Seikagaku Jikken Koza) 1,” Protein Chemistry IV, Chemical Modification and Peptide Synthesis, Kagaku-dojin Publishing Company, Inc. (Japan), 1981). Also, they can be synthesized by general methods using a variety of commercially available peptide synthesizers. In addition, polypeptides of interest can be obtained by preparing polynucleotides encoding the above polypeptides, incorporating each of the polynucleotides into an expression vector and introducing the vector into a host cell, thereby allowing the host cell to produce the polypeptide, using known gene engineering methods (Sambrook et al., Molecular Cloning, 2nd edition, Current Protocols in Molecular Biology (1989), Cold Spring Harbor Laboratory Press; Ausubel et al., Short Protocols in Molecular Biology, 3rd edition, A Compendium of Methods from Current Protocols in Molecular Biology (1995), John Wiley & Sons, etc.).
Polynucleotides encoding the aforementioned polypeptides can be readily prepared by known gene engineering techniques or general methods using commercially available nucleic acid synthesizers. For example, DNA comprising the nucleotide sequence shown in SEQ ID NO: 1 can be prepared by PCR using a human chromosome DNA or cDNA library as a template and a pair of primers designed to enable the amplification of the nucleotide sequence shown in SEQ ID NO: 1. PCR conditions can be appropriately determined. For example, such conditions may comprise conducting 30 cycles of the reaction steps consisting of: 94° C., 30 seconds (denaturation); 55° C., 30 seconds to 1 minute (annealing); and 72° C., 1 minute (elongation) using a thermostable DNA polymerase (e.g., Taq polymerase) and a Mg2+-containing PCR buffer, followed by reaction at 72° C. for 7 minutes after completion of the 30 cycles. However, PCR conditions are not limited to the above-exemplified PCR conditions. PCR techniques and conditions are described in, for example, Ausubel et al., Short Protocols in Molecular Biology, 3rd edition, A Compendium of Methods from Current Protocols in Molecular Biology (1995), John Wiley & Sons (Chapter 15, in particular).
In addition, desired DNA can be isolated by preparing appropriate probes and primers based on information about the nucleotide and amino acid sequences shown in SEQ ID NOS: 1 to 8 in the Sequence Listing of the present application, and screening a cDNA library of e.g., human with the use of such probes and primers. Preferably, such cDNA library is produced from a cell, organ, or tissue in which the protein with SEQ ID NO: 2, 4, 6 or 8 is expressed. Examples of the cell or tissue include, but not limited to, cells or tissues from cancers or tumors, such as brain, leukemia, malignant lymphoma, lung cancer, brain tumor, colorectal cancer, melanoma, neuroblastoma, pancreatic cancer, gastric cancer, liver cancer, ovary cancer, esophageal cancer, kidney cancer, mastocytoma, and perianal adenocarcinoma. Operations such as preparation of probes or primers, construction of cDNA libraries, screening of cDNA libraries, and cloning of genes of interest, as described above, are known to persons skilled in the art, and they can be carried out according to, for example, the methods described in Sambrook et al., Molecular Cloning, the 2nd edition, Current Protocols in Molecular Biology (1989) and Ausbel et al. (ibid.). DNAs encoding human MRAP2 protein and partial peptides thereof can be obtained from the thus obtained DNAs.
The above-described host cells may be any cells, as long as they can express the above-described polypeptides. An example of prokaryotic host cell includes, but is not limited to, Escherichia coli. Examples of eukaryotic host cells include, but are not limited to, mammalian cells such as monkey kidney cell (COS 1), Chinese hamster ovary cell (CHO), human embryonic kidney cell line (HEK293), and mouse embryonic skin cell line (NIH3T3), yeast cells such as budding yeast and fission yeast cells, silkworm cells, and Xenopus laevis egg cells.
When prokaryotic cells are used as host cells, an expression vector preferably having an origin replicable in prokaryotic cells, a promoter, a ribosome-binding site, a multicloning site, a terminator, a drug resistance gene, an auxotrophic complementary gene, a reporter gene, or the like can be used. As expression vectors for Escherichia coli, pUC vectors, pBluescriptII, pET expression systems, pGEX expression systems, and the like can be exemplified. A DNA encoding the above polypeptide is incorporated into such an expression vector, a prokaryotic host cell is transformed with the vector, and then the thus obtained transformed cell is cultured, so that the polypeptide encoded by the DNA can be expressed in the prokaryotic host cell. At this time, the polypeptide can also be expressed as a fusion protein with another protein.
When eukaryotic cells are used as host cells, expression vectors for eukaryotic cells preferably having a promoter, a splicing region, a poly(A) addition site, or the like can be used. Examples of such expression vectors include pKA1, pCDM8, pSVK3, pMSG, pSVL, pBK-CMV, pBK-RSV, EBV vector, pRS, pcDNA3.1, pSecTag (A, B, C) and pYES2. By similar procedures to those mentioned above, a DNA encoding the aforementioned polypeptide is incorporated into such an expression vector, an eukaryotic host cell is transformed with the vector, and then the thus obtained transformed cell is cultured, so that the polypeptide encoded by the above DNA can be expressed in the eukaryotic host cell. When pIND/V5-His, pFLAG-CMV-2, pEGFP-N1, pEGFP-C1, or the like is used as an expression vector, the above polypeptide may be expressed as a fusion protein with a tag, such as His tag (e.g., (His)6 to (His)10), FLAG tag, myc tag, HA tag, or GFP.
For introduction of an expression vector into a host cell, well known methods can be employed, such as electroporation, a calcium phosphate method, a liposome method, a DEAE dextran method, microinjection, viral infection, lipofection, and binding with a cell-membrane-permeable peptide.
Isolation and purification of a polypeptide of interest from host cells can be performed using known isolation techniques in combination. Examples of isolation and purification techniques include, but are not limited to, treatment using a denaturing agent such as urea or a surfactant, ultrasonication, enzymatic digestion, salting-out, solvent fractionation and precipitation, dialysis, centrifugation, ultrafiltration, gel filtration, SDS-PAGE, isoelectric focusing electrophoresis, ion exchange chromatography, hydrophobic chromatography, affinity chromatography, and reverse phase chromatography.
In general, antibodies are heteromultimeric glycoproteins each comprising at least two heavy chains and two light chains. Meanwhile, another class of antibodies except for IgM are heterotetrameric glycoproteins (approximately 150 kDa) each comprising two identical light (L) chains and two identical heavy (H) chains. Typically, each light chain is connected to a heavy chain via a single covalent disulfide bond. However, the number of disulfide bonds between heavy chains varies among different immunoglobulin isotypes. Each of heavy chain and light chain also has an intrachain disulfide bond(s). Each heavy chain has a variable domain (VH region) at one end thereof, to which some constant regions are bound in series. Each light chain has a variable domain (VL region) at one end thereof and has a single constant region at the opposite end thereof. The constant region of a light chain is aligned with the first constant region of a heavy chain and the light-chain variable domain is aligned with the heavy-chain variable domain. A specific region of an antibody variable domain, which is called “complementarity determining region (CDR),” exhibits specific variability so as to impart binding specificity to an antibody. A relatively conserved portion in a variable region is called a “framework region (FR).” A complete heavy-chain or light-chain variable domain comprises 4 FRs connected to each other via 3 CDRs. Such CDRs are called “CDRH1,” “CDRH2,” and “CDRH3,” respectively, in such order from the N-terminus in a heavy chain. Similarly, for a light chain, they are called “CDRL1,” “CDRL2,” and “CDRL3,” respectively. CDRH3 plays the most important role in terms of antibody-antigen binding specificity. In addition, CDRs in each chain are retained by FR regions in the state that they are close to each other, and they contribute to the formation of an antigen binding site of an antibody together with CDRs in a corresponding chain. Constant regions do not directly contribute to antibody-antigen binding. However, they exhibit various effector functions such as involvement in antibody-dependent cytotoxicity (ADCC activity), phagocytosis through binding to an Fcγ receptor, half-life/clearance rate via a neonatal Fc receptor (FcRn), and complement-dependent cytotoxicity (CDC activity) via a C1q component in the complement cascade.
The term “anti-MRAP2 antibody” used in the present invention refers to an antibody having an immunological reactivity with a full-length MRAP2 protein or a fragment thereof described above.
The term “immunological reactivity” used herein indicates the characteristics of an antibody binding in vivo or in vitro to an MRAP2 antigen. The tumor- or tumor cell-damaging function (e.g., death, inhibition, or regression) can be exerted via such binding. Specifically, any type of antibody may be used in the present invention as long as the antibody can bind to an MRAP2 protein to damage a tumor, preferably a cancer expressing (or having) the MRAP2 protein on a cell surface, such as leukemia, malignant lymphoma, lung cancer, brain tumor, colorectal cancer, melanoma, neuroblastoma, pancreatic cancer, gastric cancer, liver cancer, ovary cancer, esophageal cancer, kidney cancer, mastocytoma, or perianal adenocarcinoma.
Examples of such antibodies include monoclonal antibodies, polyclonal antibodies, synthetic antibodies, multispecific antibodies (e.g., bispecific antibodies), human antibodies, humanized antibodies, chimeric antibodies, and single-chain antibodies. Examples of such antibodies also include antibody fragments (e.g., antigen binding fragments such as Fab and F(ab′)2). In addition, antibodies may be any class of immunoglobulin molecules such as IgG, IgE, IgM, IgA, IgD, and IgY, or any subclass thereof such as IgG1, IgG2, IgG3, IgG4, IgA1, and IgA2.
Antibodies may be further modified via acetylation, formylation, amidation, phosphorylation, or pegylation (PEG), in addition to glycosylation.
Production examples for a variety of antibodies are described below.
The polyclonal antibodies that can be used in the present invention can be obtained in a manner described below.
Serum is obtained by immunizing small animals such as mice, human antibody-producing mice, or rabbits with a naturally occurring MRAP2 protein, a recombinant MRAP2 protein that has been expressed as a protein fused with GST or the like in a microorganism such as Escherichia coli, or a partial peptide thereof. The serum is purified via ammonium sulfate precipitation, protein A/protein G column chromatography, DEAE ion-exchange chromatography, affinity column chromatography with a column to which an MRAP2 protein or a synthetic peptide is coupled, or the like, for preparation of polyclonal antibodies. In the Examples described below, a mouse polyclonal antibody against a domain expressed on cancer cell surfaces in an MRAP2 protein amino acid sequence was produced, and antitumor effects thereof were confirmed.
Other examples of the antibodies that can be used in the present invention include monoclonal antibodies. For example, monoclonal antibodies can be obtained in a manner described below. For example, cells expressing the MRAP2 protein on their surfaces (such as a leukemia cell line K562 or a malignant lymphoma cell line Namalwa) are administered to mice for immunization, followed by extraction of spleens from the mice. Cells are separated from each spleen and then are fused with mouse myeloma cells. Clones capable of producing an antibody having cancer cell growth inhibition action are selected from the obtained fusion cells (hybridomas). A monoclonal antibody-producing hybridoma having cancer cell growth inhibition action is isolated and cultured. An antibody of interest can be prepared via purification from the culture supernatant by a general affinity purification method.
Also, a monoclonal antibody-producing hybridoma can be produced in a manner described below, for example. First, an animal is immunized with a sensitizing antigen by a known method. In a general method, immunization is carried out by intraperitoneally or subcutaneously injecting a sensitizing antigen into a mammal. Specifically, a sensitizing antigen is diluted to an appropriate resultant amount with and suspended in PBS (Phosphate-Buffered Saline), physiological saline, or the like. If desired, an appropriate amount of a conventional adjuvant (e.g., Freund's complete adjuvant) is mixed therewith. After emulsification takes place, the resultant is administered to a mammal several times every 4 to 21 days. In addition, an adequate carrier can be used for immunization with a sensitizing antigen.
As described above, after immunization of a mammal and confirmation of an increase to a desired antibody level in serum, immunocytes are collected from the mammal and subjected to cell fusion. Particularly preferable examples of immunocytes are splenocytes.
Mammalian myeloma cells are used as relevant parent cells subjected to fusion with the above immunocytes. As the myeloma cells, the following various examples of known cell lines are preferably used: P3U1 (P3-X63Ag8U1), P3 (P3x63Ag8.653) (J. Immunol. (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. D. H. et al., Cell (1976) 8, 405-415), SP2/0 (Shulman, M. et al., Nature (1978) 276, 269-270), FO (de St. Groth, S. F. et al., J. Immunol. Methods (1980) 35, 1-21), 5194 (Trowbridge, I. S. J. Exp. Med. (1978) 148, 313-323), and R210 (Galfre, G. et al., Nature (1979) 277, 131-133).
Basically, the cell fusion of immunocytes and myeloma cells described above can be carried out according to a known method such as the method of Kohler and Milstein et al. (Kohler, G. and Milstein, C. Methods Enzymol. (1981) 73, 3-46).
More specifically, the cell fusion described above is carried out, for example, in the presence of a cell fusion promoter in a conventional nutrients-containing culture solution. Examples of a fusion promoter to be used include polyethylene glycol (PEG) and Sendai virus (HVJ: hemagglutinating virus of Japan). If desired, an auxiliary agent such as dimethylsulfoxide may be further added for improvement of fusion efficiency.
The proportion of immunocytes used relative to myeloma cells used can be arbitrarily determined. For example, the number of immunocytes used is preferably one to ten times the number of myeloma cells. Examples of a culture solution that can be used for the cell fusion described above include an RPMI1640 culture solution and an MEM culture solution adequate for growth of the above myeloma cell lines as well as other conventional culture solutions used for this kind of cell culture. Further, a serum replacement solution such as fetal calf serum (FCS) can be used in combination therewith.
For cell fusion, the above immunocytes and myeloma cells are sufficiently mixed at predetermined amounts in the culture solution. A PEG solution (e.g., average molecular weight: approximately 1000 to 6000) that has been previously heated to approximately 37° C. is added thereto at a concentration of generally 30% to 60% (w/v), followed by mixing. This results in formation of hybridomas of interest. Subsequently, sequential addition of an appropriate culture solution and removal of the supernatant via centrifugation are repeatedly carried out to remove cell fusion agent(s) and the like that are not preferable for the growth of hybridomas.
The thus obtained hybridomas are cultured in a conventional selection culture solution such as an HAT culture solution (a culture solution comprising hypoxanthine, aminopterin, and thymidine) for selection. Culture in such an HAT culture solution is continuously carried out for a sufficient time period (generally several days to several weeks) for death of cells (non-fused cells) other than hybridomas of interest. Next, a conventional limiting dilution method is employed to screen for hybridomas producing antibodies of interest and to carry out single cloning.
Further, as well as obtaining the above hybridomas via immunization of non-human animals with antigens, it is also possible to obtain hybridomas that produce human antibodies having a desired activity (e.g., cell growth inhibition activity) by sensitizing human lymphocytes (e.g., human lymphocytes infected with EB virus) in vitro with a protein, protein-expressing cells, or a lysate thereof and fusing the sensitized lymphocytes with human-derived myeloma cells having the ability to permanently divide, e.g., U266 (accession no. TIB196).
Monoclonal antibody-producing hybridomas produced as above can be passaged in a conventional culture solution. In addition, they can be preserved in liquid nitrogen for a long period of time.
Specifically, immunization is carried out using a desired antigen or cells expressing a desired antigen as sensitizing antigen(s) according to a conventional immunization method. The obtained immunocytes are fused with known parent cells by a conventional cell fusion method. Then, monoclonal antibody-producing cells (hybridomas) are screened by a conventional screening method. Thus, antibody production can be carried out.
A known human antibody-producing mouse used herein is, for example, a KM Mouse (Kirin Pharma/Medarex) or a XenoMouse (Amgen) (e.g., WO02/43478 and WO02/092812). When such mice are immunized with MRAP2 proteins or fragments thereof, complete human polyclonal antibodies can be obtained from blood. In addition, complete human monoclonal antibodies can be produced by a method of fusing splenocytes collected from immunized mice with myeloma cells.
Antigen preparation can be carried out in accordance with a method such as a method using animal cells (JP Patent Publication (Kohyo) No. 2007-530068A) or a method using a baculovirus (e.g., WO98/46777). If the immunogenicity of an antigen is low, an antigen bound to a macromolecule having immunogenicity, such as albumin, can be used for immunization.
Further, it is possible to use a genetically engineered antibody produced by cloning an antibody gene from a hybridoma, incorporating the clone into an adequate vector, introducing the vector into a host, and allowing the host to produce the antibody using a genetic engineering techniques (see, for example, Carl, A. K. Borrebaeck, James, W. Larrick, THERAPEUTIC MONOCLONAL ANTIBODIES, Published in the United Kingdom by MACMILLAN PUBLISHERS LTD, 1990). Specifically, cDNA of a variable region (V region) of an antibody is synthesized from mRNA of a hybridoma with a reverse transcriptase. After DNA encoding a V region of an antibody of interest is obtained, such DNA is ligated to desired DNA encoding an antibody constant region (C region). The resultant is incorporated into an expression vector. Alternatively, DNA encoding an antibody V region may be incorporated into an expression vector comprising DNA of an antibody C region. Such DNA is incorporated into an expression vector in a manner such that it is expressed under control of an expression control region such as an enhancer or a promoter. Next, host cells are transformed with such expression vector, thereby allowing the antibody to be expressed.
Monoclonal antibodies include human monoclonal antibodies and non-human animal monoclonal antibodies (e.g., mouse monoclonal antibodies, rat monoclonal antibodies, rabbit monoclonal antibodies, and chicken monoclonal antibodies). Monoclonal antibodies can be produced by culturing hybridomas obtained via fusion of myeloma cells and splenocytes from non-human mammals (e.g., mice or human antibody-producing mice) immunized with MRAP2 proteins or fragments thereof.
A chimeric antibody is an antibody produced by combining sequences from different animals. An example thereof is an antibody consisting of mouse antibody heavy-chain and light-chain variable regions and human antibody heavy-chain and light-chain constant regions. Such a chimeric antibody can be produced by a known method. For example, a chimeric antibody can be obtained by ligating DNA encoding an antibody V region to DNA encoding a human antibody C region, incorporating the resultant into an expression vector, introducing the vector into a host and allowing the host to produce an antibody.
Polyclonal antibodies include antibodies obtained by immunizing human antibody-producing animals (e.g., mice) with MRAP2 proteins or fragments thereof.
A humanized antibody is an engineered antibody, and it is sometimes referred to as a “reshaped human antibody.” A humanized antibody is constructed by transplanting CDRs of an immunized animal-derived antibody into complementarity determining regions of a human antibody. Also, general genetic engineering techniques therefor are known.
Specifically, a DNA sequence designed to ligate mouse antibody CDRs to framework regions (FRs) of a human antibody is synthesized by PCR method using several oligonucleotides prepared to have portions overlapping each other at their ends. A humanized antibody can be obtained by ligating the above obtained DNA to DNA encoding a human antibody constant region, incorporating the resultant into an expression vector, introducing the vector into a host and allowing the host to produce an antibody (see EP-A-239400 and WO96/02576). Human antibody FRs to be ligated to each other via CDRs are selected, provided that complementarity determining regions can form a good antigen binding site. If necessary, amino acids in framework regions of an antibody variable region may be substituted in such a manner that complementarity determining regions in a reshaped human antibody form an appropriate antigen binding site (Sato K. et al., Cancer Research 1993, 53: 851-856). In addition, the framework regions may be substituted with framework regions from various human antibodies (see WO99/51743).
After a chimeric antibody or a humanized antibody is produced, amino acids in a variable region (e.g., FR) or a constant region may be, for example, substituted with different amino acids.
Here, the amino acid substitution is a substitution of, for example, less than 15, less than 10, not more than 8, not more than 7, not more than 6, not more than 5, not more than 4, not more than 3, or not more than 2 amino acids, preferably 1 to 5 amino acids, and more preferably 1 or 2 amino acids. A substituted antibody should be functionally equivalent to an unsubstituted antibody. The substitution is preferably a conservative amino acid substitution, which is a substitution between amino acids having similar characteristics in terms of charge, side chains, polarity, aromaticity, and the like. For example, amino acids having similar characteristics can be classified into the following types: basic amino acids (arginine, lysine, and histidine); acidic amino acids (aspartic acid and glutamic acid); uncharged polar amino acids (glycine, asparagine, glutamine, serine, threonine, cysteine, and tyrosine); nonpolar amino acids (leucine, isoleucine, alanine, valine, proline, phenylalanine, tryptophan, and methionine); branched-chain amino acids (threonine, valine, isoleucine); and aromatic amino acids (phenylalanine, tyrosine, tryptophan, and histidine).
Antibodies of the present invention may be modified antibodies. An example of a modified antibody is an antibody bound to a molecule such as polyethylene glycol (PEG). Regarding modified antibody of the present invention, substances that bind to an antibody are not limited. Such a modified antibody can be obtained by chemically modifying an obtained antibody. A method of such modification has been already established in the field related to the present invention.
The expression “functionally equivalent” used herein indicates a situation in which an antibody of interest has biological or biochemical activity similar to that of an antibody of the present invention. Specifically, such antibody has a function of damaging tumors and causes essentially no rejection reaction when applied to humans. An example of such activity is cell growth inhibition activity or binding activity.
A known method for preparing a polypeptide functionally equivalent to a given polypeptide that is well known to persons skilled in the art is a method comprising introducing a mutation into the polypeptide. For instance, a person skilled in the art can adequately introduce a mutation into an antibody of the present invention using a site-specific mutagenesis method (Hashimoto-Gotoh, T. et al., (1995) Gene 152, 271-275; Zoller, M J., and Smith, M. (1983) Methods Enzymol. 100, 468-500; Kramer, W. et al., (1984) Nucleic Acids Res. 12, 9441-9456; Kramer, W. and Fritz, H J., (1987) Methods Enzymol. 154, 350-367; Kunkel, T A., (1985) Proc. Natl. Acad. Sci. USA. 82, 488-492; or Kunkel (1988) Methods Enzymol. 85, 2763-2766) or the like. Thus, an antibody functionally equivalent to the antibody of the present invention can be prepared.
An antibody capable of recognizing an epitope of an MRAP2 protein recognized by the aforementioned anti-MRAP2 antibody can be obtained by a method known to persons skilled in the art. For example, it can be obtained by: a method comprising determining an epitope of an MRAP2 protein recognized by the anti-MRAP2 antibody by a general method (e.g., epitope mapping) and producing an antibody using a polypeptide having an amino acid sequence contained in the epitope as an immunogen; or a method comprising determining an epitope of a produced antibody by a general method and selecting an antibody having an epitope identical to an epitope of the anti-MRAP2 antibody. Here, the term “epitope” refers to a polypeptide fragment having antigenicity or immunogenicity in mammals and preferably in humans. The smallest unit thereof consists of approximately 7 to 12 amino acids and preferably 8 to 11 amino acids.
The affinity constant Ka (kon/koff) of an antibody of the present invention is preferably at least 107 M−1, at least 108 M−1, at least 5×108 M−1, at least 109 M−1, at least 5×109 M−1, at least 1010 M−1, at least 5×1010 M−1, at least 1011 M−1, at least 5×1011 M−1, at least 1012 M−1, or at least 1013 M−1.
An antibody of the present invention can be conjugated with an antitumor agent. Binding between an antibody and an antitumor agent can be carried out via a spacer having a group reactive to an amino group, a carboxyl group, a hydroxy group, a thiol group, or the like (e.g., an imidyl succinate group, a formyl group, a 2-pyridyldithio group, a maleimidyl group, an alkoxycarbonyl group, or a hydroxy group).
Examples of antitumor agents include the following antitumor agents known in references or the like: paclitaxel, doxorubicin, daunorubicin, cyclophosphamide, methotrexate, 5-fluorouracil, thiotepa, busulfan, improsulfan, piposulfan, benzodopa, carboquone, meturedopa, uredopa, altretamine, triethylenemelamine, triethylenephosphoramide, triethilenethiophosphoramide, trimethylolomelamine, bullatacin, bullatacinone, camptothecin, bryostatin, callystatin, cryptophycin 1, cryptophycin 8, dolastatin, duocarmycin, eleutherobin, pancratistatin, sarcodictyin, spongistatin, chlorambucil, chlornaphazine, cholophosphamide, estramustine, ifosfamide, mechlorethamine, mechlorethamine oxide hydrochloride, melphalan, novembichin, phenesterine, prednimustine, trofosfamide, uracil mustard, carmustine, chlorozotocin, fotemustine, lomustine, nimustine, ranimustine, calicheamicin, dynemicin, clodronate, esperamicin, aclacinomycin, actinomycin, authramycin, azaserine, bleomycin, cactinomycin, carabicin, carminomycin, carzinophilin, chromomycin, dactinomycin, detorbicin, 6-diazo-5-oxo-L-norleucine, ADRIAMYCIN, epirubicin, esorubicin, idarubicin, marcellomycin, mitomycin C, mycophenolic acid, nogalamycin, olivomycin, peplomycin, potfiromycin, puromycin, quelamycin, rodorubicin, streptonigrin, streptozocin, tubercidin, ubenimex, zinostatin, zorubicin, denopterin, pteropterin, trimetrexate, fludarabine, 6-mercaptopurine, thiamiprine, thioguanine, ancitabine, azacitidine, 6-azauridine, carmofur, cytarabine, dideoxyuridine, doxifluridine, enocitabine, floxuridine, androgens such as calusterone, dromostanolone propionate, epitiostanol, mepitiostane, testolactone, aminoglutethimide, mitotane, trilostane, frolinic acid, aceglatone, aldophosphamide glycoside, aminolevulinic acid, eniluracil, amsacrine, bestrabucil, bisantrene, edatraxate, defofamine, demecolcine, diaziquone, elfornithine, elliptinium acetate, epothilone, etoglucid, lentinan, lonidamine, maytansine, ansamitocine, mitoguazone, mitoxantrone, mopidanmol, nitraerine, pentostatin, phenamet, pirarubicin, losoxantrone, podophyllinic acid, 2-ethylhydrazide, procarbazine, razoxane, rhizoxin, schizophyllan, spirogermanium, tenuazonic acid, triaziquone, roridine A, anguidine, urethane, vindesine, dacarbazine, mannomustine, mitobronitol, mitolactol, pipobroman, gacytosine, docetaxel, chlorambucil, gemcitabine, 6-thioguanine, mercaptopurine, cisplatin, oxaliplatin, carboplatin, vinblastine, etoposide, ifosfamide, mitoxantrone, vincristine, vinorelbine, novantrone, teniposide, edatrexate, daunomycin, aminopterin, xeloda, ibandronate, irinotecan, topoisomerase inhibitor, difluoromethylornithine (DMFO), retinoic acid, capecitabine, and pharmacologically acceptable salts or derivatives thereof.
Alternatively, it is also possible to bind a radioactive isotope such as 211At, 131I, 125I, 90Y, 186Re, 88Re, 153Sm, 212Bi, 32P, 175Lu, or 176Lu known in references and the like to an antibody of the present invention. It is desirable for such radioactive isotopes to be effective for tumor treatment or diagnosis.
An antibody of the present invention is preferably an antibody having an immunological reactivity with MRAP2 or an antibody capable of specifically recognizing MRAP2. Such an antibody should be an antibody having a structure that allows a subject animal to which the antibody is administered to completely or almost completely avoid a rejection reaction. If the subject animal is a human, examples of such antibodies include human antibodies, humanized antibodies, chimeric antibodies (e.g., human-mouse chimeric antibodies), single-chain antibodies, and bispecific antibodies. Such an antibody is a recombinant antibody having human antibody-derived heavy-chain and light-chain variable regions, a recombinant antibody having heavy-chain and light-chain variable regions each consisting of non-human animal antibody-derived complementarity determining regions (CDR1, CDR2, and CDR3) and human antibody-derived framework regions, or a recombinant antibody having non-human animal antibody-derived heavy-chain and light-chain variable regions and human antibody-derived heavy-chain and light-chain constant regions. The first two antibodies are preferable.
The above recombinant antibody can be produced in the manner described below. DNA encoding a monoclonal antibody against human MRAP2 (e.g., a human monoclonal antibody, a mouse monoclonal antibody, a rat monoclonal antibody, a rabbit monoclonal antibody, or a chicken monoclonal antibody) is cloned from an antibody-producing cell such as a hybridoma. DNAs encoding a light-chain variable region and a heavy-chain variable region of the antibody are produced by an RT-PCR method or the like using the obtained clone as a template. Then, the sequences of a light-chain variable region and a heavy-chain variable region or the sequences of CDR1, CDR2, and CDR3 are determined by the Kabat EU numbering system (Kabat et al., Sequences of Proteins of Immunological Interest, 5th Ed. Public Health Service, National Institute of Health, Bethesda, Md. (1991)).
Further, such DNAs encoding variable regions or DNAs encoding CDRs are produced by genetic engineering techniques (Sambrook et al., Molecular Cloning A Laboratory Manual, Cold Spring Harbor Laboratory Press (1989)) or a DNA synthesizer. Here, the above human monoclonal antibody-producing hybridoma can be produced by immunizing a human antibody-producing animal (e.g., a mouse) with human MRAP2 and fusing splenocytes removed from the animal with myeloma cells. In addition to the above, if necessary, DNAs encoding human antibody-derived light-chain or heavy-chain variable regions and constant regions are produced by genetic engineering techniques or a DNA synthesizer.
In the case of a humanized antibody, DNA in which the CDR coding sequences in a DNA encoding a human antibody-derived light-chain or heavy-chain variable region have been substituted with corresponding CDR coding sequences of an antibody from a non-human animal (e.g., a mouse, a rat, or a chicken) is produced. The DNA obtained as above is ligated to the DNA encoding a constant region of a human antibody-derived light chain or heavy chain. Thus, DNA encoding a humanized antibody can be produced.
In the case of a chimeric antibody, DNA encoding an antibody light-chain or heavy-chain variable region from a non-human animal (e.g., a mouse, a rat, or a chicken) is ligated to the DNA encoding a human antibody-derived light-chain or heavy-chain constant region. Thus, DNA encoding a chimeric antibody can be produced.
A single-chain antibody is an antibody in which a heavy-chain variable region and a light-chain variable region are linearly ligated to each other via a linker. DNA encoding a single-chain antibody can be produced by ligating DNA encoding a heavy-chain variable region, DNA encoding a linker, and a DNA encoding a light-chain variable region together. Here, a heavy-chain variable region and a light-chain variable region are those from a human antibody or those from a human antibody in which CDRs alone have been substituted with CDRs of an antibody from a non-human animal (e.g., a mouse, a rat, or a chicken). In addition, the linker consists of 12 to 19 amino acids. An example thereof is (G4S)3 consisting of 15 amino acids (G.-B. Kim et al., Protein Engineering Design and Selection 2007, 20 (9): 425-432).
A bispecific antibody (diabody) is an antibody capable of specifically binding to two different epitopes. DNA encoding a bispecific antibody can be produced by, for example, ligating DNA encoding a heavy-chain variable region A, DNA encoding a light-chain variable region B, DNA encoding a heavy-chain variable region B, and DNA encoding a light-chain variable region A together in such order (provided that DNA encoding a light-chain variable region B and DNA encoding a heavy-chain variable region B are ligated to each other via DNA encoding a linker described above). Here, both a heavy-chain variable region and a light-chain variable region are those from a human antibody or those from a human antibody in which CDRs alone have been substituted with CDRs of an antibody from a non-human animal (e.g., a mouse, a rat, or a chicken).
Recombinant DNA produced as above is incorporated into one or a plurality of appropriate vector(s). Each such vector is introduced into a host cell (e.g., a mammal cell, a yeast cell, or an insect cell) for (co)expression. Thus, a recombinant antibody can be produced. See, P. J. Delves., ANTIBODY PRODUCTION ESSENTIAL TECHNIQUES., 1997 WILEY, P. Shepherd and C. Dean., Monoclonal Antibodies., 2000 OXFORD UNIVERSITY PRESS; J. W. Goding, Monoclonal Antibodies: Principles and Practice., 1993 ACADEMIC PRESS.
The above antibodies preferably have cytotoxic activity, thereby exhibiting antitumor effects.
In addition, a hybridoma capable of producing a different human antibody or a non-human animal antibody (e.g., a mouse antibody) against human MRAP2 is produced. A monoclonal antibody produced by the hybridoma is collected. Then, it is determined whether or not the obtained antibody is an antibody of interest using, as indicators, immunological binding activity to human MRAP2 and cytotoxic activity. Thus, a monoclonal antibody-producing hybridoma of interest is identified. Thereafter, as described above, DNAs encoding heavy-chain and light-chain variable regions of an antibody of interest are produced from the hybridoma and sequenced. The DNAs are used for production of different antibodies.
Further, the above antibody of the present invention may have a substitution, deletion, or addition of one or several (and preferably, 1 or 2) amino acid(s), particularly in a framework region sequence and/or a constant region sequence, as long as it has the specificity of specifically recognizing MRAP2. Here, the term “several amino acids” indicates 2 to 5 and preferably 2 or 3 amino acids.
Furthermore, according to the present invention, DNA encoding the above antibody of the present invention, DNA encoding a heavy chain or light chain of the antibody, or DNA encoding a heavy-chain or light-chain variable region of the antibody is also provided.
Complementarity determining regions (CDRs) encoded by DNAs of the above sequences are regions that determine antibody specificity. Therefore, sequences encoding the other regions (i.e., constant regions and framework regions) in an antibody may be sequences from a different antibody. Here, different antibodies include antibodies from non-human organisms. However, in view of reduction of side effects, human-derived antibodies are preferable. That is to say, in the above DNA, regions encoding framework regions and constant regions of heavy and light chains preferably comprise nucleotide sequences encoding the relevant amino acid sequences from a human antibody.
DNA of the present invention can be obtained by, for example, the aforementioned methods or the following methods. First, total RNA is prepared from a hybridoma associated with an antibody of the present invention using a commercially available RNA extraction kit. Then, cDNA is synthesized with a reverse transcriptase using random primers or the like. Next, cDNA encoding an antibody is amplified by a PCR method using, as primers, oligonucleotides having sequences conserved in variable regions of known mouse antibody heavy-chain and light-chain genes. Sequences encoding constant regions can be obtained by amplifying known sequences by a PCR method. The nucleotide sequence of the DNA can be determined by a general method involving, for example, incorporation into a plasmid or phage for sequence determination.
It is thought that antitumor effects of an anti-MRAP2 antibody used in the present invention upon MRAP2-expressing cancer cells are exhibited through effector cell-mediated antibody-dependent cellular cytotoxicity (ADCC) activity against MRAP2-expressing cells or complement-dependent cytotoxicity (CDC) activity against MRAP2-expressing cells.
Accordingly, the activity of an anti-MRAP2 antibody used in the present invention can be evaluated via in vitro determination of ADCC activity or CDC activity to MRAP2-expressing cancer cells as specifically described in the Examples mentioned below.
An anti-MRAP2 antibody used in the present invention binds to an MRAP2-protein on a cancer cell and exhibits antitumor effects based on the above activity. Therefore, such antibody is believed to be useful for cancer treatment or prevention. Specifically, according to the present invention, a pharmaceutical composition for treatment and/or prevention of cancer that comprises, as an active ingredient, an anti-MRAP2 antibody, is provided. When an anti-MRAP2 antibody is used for the purpose of administering the antibody to humans (antibody treatment), it is preferably used in the form of a human antibody or a humanized antibody in order to reduce immunogenicity.
In addition, as the binding affinity between an anti-MRAP2 antibody and an MRAP2 protein on a cancer cell surface becomes higher, stronger antitumor activity can be exhibited by an anti-MRAP2 antibody. Therefore, if an anti-MRAP2 antibody having high binding affinity to an MRAP2 protein can be obtained, even stronger antitumor effects can be expected to be exhibited. Accordingly, it becomes possible to use such antibody as a pharmaceutical composition for treatment and/or prevention of cancer. As described above, for high binding affinity, the affinity constant Ka (kon/koff) is preferably at least 107 M−1, at least 108 M−1, at least 5×108 M−1, at least 109 M−1, at least 5×109 M−1, at least 1010 M−1, at least 5×1010 M−1, at least 1011 M−1, at least 5×1011 M−1, at least 1012 M−1, or at least 1013 M−1.
The capacity of an antibody to bind to MRAP2 can be determined via binding assay using, for example, ELISA, a Western blot method, immunofluorescence, or flowcytometry analysis as described in the Examples.
An antibody that recognizes MRAP2 can be tested in terms of reactivity with MRAP2 by an immunohistochemical method well-known to persons skilled in the art using a frozen tissue section fixed with paraformaldehyde or acetone or a paraffin-embedded tissue section fixed with paraformaldehyde. Such section is prepared from a tissue obtained from a patient during surgery, a bone marrow tissue, lymph node, peripheral blood cells, or bone marrow cells of a patient, or a tissue obtained from an animal carrying xenograft tissue that has been inoculated with a cell line that expresses MRAP2 naturally or after transfection thereof.
For immunohistochemical staining, an antibody immunologically reactive to MRAP2 can be stained by a variety of methods. For example, it can be visualized by reacting with a horseradish peroxidase-conjugated goat anti-mouse antibody or goat anti-rabbit antibody.
The present invention provides a pharmaceutical composition (or medicament) comprising an antibody of the present invention, i.e., an antibody against MRAP2 or fragment (preferably antigen binding fragment) thereof described above. The pharmaceutical composition (or medicament) of the present invention usually comprises an effective amount of the antibody against MRAP2 or fragment (preferably antigen binding fragment) thereof described above.
A target of the pharmaceutical composition for treatment and/or prevention of a cancer of the present invention is not particularly limited as long as the target is a cancer (cell) expressing the MRAP2 gene (usually, on a cell surface).
Both the terms “tumor” and “cancer” used herein refer to malignant neoplasm, and thus they are used in an exchangeable manner.
A cancer that can be a target in the present invention is a cancer expressing a gene encoding a polypeptide comprising the amino acid sequence of SEQ ID NO: 2, 4, 6, or 8 or a partial sequence consisting of 7 or more consecutive amino acids of said amino acid sequence, and is preferably a cancer expressing such polypeptide on a cell surface. The cancer that can be a target in the present invention is preferably leukemia, malignant lymphoma, lung cancer, brain tumor, colorectal cancer, melanoma, neuroblastoma, pancreatic cancer, gastric cancer, liver cancer, ovary cancer, esophageal cancer, kidney cancer, mastocytoma, or perianal adenocarcinoma. Specific examples of these cancers include, but are not limited to, acute non-lymphocytic leukemia, chronic lymphocytic leukemia, acute granulocytic leukemia, chronic granulocytic leukemia, acute promyelocytic leukemia, adult T-cell leukemia, aleukemic leukemia, leukocythemic leukemia, basophilic leukemia, blastic leukemia, bovine leukemia, chronic myeloleukemia, leukemia cutis, embryonal leukemia, eosinophilic leukemia, Gross leukemia, Rieder cell leukemia, Schilling's leukemia, stem cell leukemia, subleukemic leukemia, undifferentiated cell leukemia, hairy cell leukemia, hemoblastic leukemia, hemocytoblastic leukemia, histiocytic leukemia, stem cell leukemia, acute monocytic leukemia, leukopenic leukemia, lymphatic leukemia, lymphoblastic leukemia, lymphocytic leukemia, lymphotropic leukemia, lymphoid leukemia, lymphosarcoma cell leukemia, mast cell leukemia, megakaryocytic leukemia, micromyeloblastic leukemia, monocytic leukemia, myeloblastic leukemia, myeloleukemia, myeloid granulocytic leukemia, myelomonocytic leukemia, Naegeli leukemia, plasma cell leukemia, plasmacytic leukemia, promyelocytic leukemia, non-Hodgkin lymphoma (Burkitt lymphoma (BL), small lymphocytic lymphoma/chronic lymphocytic leukemia (SLL/CLL), mantle cell lymphoma (MCL), follicular lymphoma (FL), diffuse large B-cell lymphoma (DLCL), marginal zone lymphoma (MZL), hairy cell leukemia (HCL), lymphoplasmacytic leukemia (LPL), extranodal marginal zone B cell lymphoma of mucosa-associated lymphoid tissue (MALT), mediastinal large cell lymphoma, intravascular large cell lymphoma, primary effusion lymphoma, precursor B-cell lymphoblastic leukemia/lymphoma, precursor T-cell and NK-cell lymphoma (precursor T-cell lymphoblastic lymphoma, NK-cell lymphoblastic lymphoma), mature T- and NK-cell neoplasms (including peripheral T-cell lymphoma and leukemia (PTL)), adult T-cell leukemia/T-cell lymphoma and large granular lymphocytic leukemia, chronic T-cell lymphocytic leukemia/prolymphocytic leukemia, T-cell large granular lymphocytic leukemia, aggressive NK-cell leukemia, extranodal T-/NK-cell lymphoma, enteropathy-type T-cell lymphoma, hepatosplenic T-cell lymphoma, anaplastic large cell lymphoma (ALCL), angiocentric and angioimmunoblastic T-cell lymphoma, mycosis fungoides/Sezary's syndrome, cutaneous T-cell lymphoma (CTCL)), Hodgkin lymphoma, non-small cell lung cancer, squamous cell carcinoma (epidermoid cancer), lung adenocarcinoma, large cell lung cancer, small cell lung cancer, glioma, astrocytoma, brainstem glioma, ependymoma, oligodendroglioma, nonglial tumor, acoustic neurilemoma, craniopharyngioma, medulloblastoma, meningioma, pineocytoma, pineoblastoma, primary brain lymphoma, germ cell tumor, superficial colorectal cancer, protuberant colorectal cancer, ulcerative infiltrative colorectal cancer, diffuse infiltrative colorectal cancer, basal cell cancer, prickle cell cancer, melanoma, superficial spreading melanoma, nodular melanoma, malignant lentigo melanoma, acral lentiginous melanoma, neuroblastoma, ganglioneuroblastoma, ganglioma, insulinoma, gastrinoma, glucagonoma, VIPoma, somatostatin-secreting tumor, carcinoid, islet cell tumor, protuberant gastric cancer, ulcerative localized gastric cancer, ulcerative infiltrative gastric cancer, diffuse infiltrative gastric cancer, hepatocellular cancer and hepatoblastoma, epithelial ovarian cancer, borderline tumor, germ cell tumor, stromal tumor, serous adenocarcinoma, clear cell adenocarcinoma, endometrioid adenocarcinoma, transitional cell cancer, mucous adenocarcinoma, mixed ovary cancer, squamous cell carcinoma, esophageal adenocarcinoma, renal cell cancer, kidney adenocarcinoma, hypernephroma, renal fibrosarcoma, transitional cell cancer (renal pelvis and/or uterer), mastocytoma, perianal adenoma, and perianal adenocarcinoma.
In addition, the subject animal of the present invention is a mammal. Examples thereof include mammals such as primates, pet animals, livestock animals, sport animals, and experimental animals. Humans, dogs, and cats are particularly preferable.
When an antibody used in the present invention is used in a pharmaceutical composition, it can be formulated by a method known to persons skilled in the art. For instance, it can be parenterally used in the form of an injection being an aseptic solution or suspension liquid in water or other pharmacologically acceptable solution. For example, in one possible case, it can be formulated with the combined use of a pharmacologically acceptable carrier or medium or additive and specifically sterilized water, physiological saline, plant oil, an emulsifier, a suspending agent, a surfactant, a stabilizer, a flavoring agent, an excipient, a vehicle, a preservative, a binder or the like in an appropriate manner by mixing in a unit dosage form required for a generally acceptable pharmaceutical formulation. The amount of an active ingredient in a formulation is determined such that an appropriate dosage within the indicated range can be achieved.
An aseptic composition for injection purposes can be formulated in accordance with general formulation practice using a vehicle such as distilled water for injection purposes.
Examples of an aqueous solution for injection purposes include physiological saline and isotonic solutions comprising glucose and other auxiliary agents, such as D-sorbitol, D-mannose, D-mannitol, and sodium chloride. Such solution may be used together with an appropriate solubilizing agent, for example, alcohols such as ethanol and polyalcohol (e.g., propylene glycol, polyethylene glycol), and nonion surfactants such as polysorbate 80TM and HCO-60.
Examples of oil liquid include sesame oil and soybean oil. Such oil liquid may be used in combination with benzyl benzoate or benzyl alcohol as a solubilizing agent. In addition, it may be mixed with a buffering agent such as a phosphate buffer solution, a sodium acetate buffer solution, a soothing agent such as procaine hydrochloride, a stabilizer such as benzyl alcohol, phenol, and/or an antioxidant. In general, a formulated injection solution is introduced into an adequate ample.
The administration is performed orally or parenterally, and preferably parenterally. Specific examples of dosage forms include injectable dosage forms, intranasal dosage form, transpulmonary dosage form, and percutaneous dosage form. For example, injectable dosage form can be systemically or locally administered via intravenous injection, intramuscular injection, intraperitoneal injection, or subcutaneous injection. Alternatively, an antibody of the present invention may be administered directly to a tumor by local administration, such as injection, infusion, or implantation of a sustained-release formation, to the tumor.
In addition, the administration method can be appropriately determined depending on e.g., patient age, weight, gender, and/or symptoms. For example, a single dose of a pharmaceutical composition comprising the antibody or a polynucleotide encoding the antibody can be selected within a range of 0.0001 mg to 1,000 mg per kg of body weight. Alternatively, the dose can be selected, for example, within a range of 0.001 to 100,000 mg per patient's body; however, it is not necessarily limited thereto. The dose and the administration method vary depending on e.g., patient age, weight, gender, and symptoms. However, persons skilled in the art can appropriately select the dose and the method.
The cancer described above, particularly, a cancer expressing MRAP2 on a cell surface, preferably leukemia, malignant lymphoma, lung cancer, brain tumor, colorectal cancer, melanoma, neuroblastoma, pancreatic cancer, gastric cancer, liver cancer, ovary cancer, esophageal cancer, kidney cancer, mastocytoma, or perianal adenocarcinoma can be treated and/or prevented by administering an antibody of the present invention or fragment thereof, or the pharmaceutical composition comprising the same to a subject.
Further, a method for treating and/or preventing a cancer, which comprises administering, to a subject, the pharmaceutical composition (or medicament) of the present invention in combination with an antitumor agent as listed above or a pharmaceutical composition (or medicament) comprising the antitumor agent, is also included in the present invention. A target cancer is the same as above. The antibody or fragment thereof according to the present invention and the antitumor agent can be administered concurrently or separately to the subject. In the case of separately administering them, either of the pharmaceutical compositions can be administered first or later, and their dosing intervals, doses, administration routes, and the number of doses can be appropriately selected by a specialist physician. In the case of concurrently administering them, for example, a pharmaceutical composition in a dosage form obtained by mixing the antibody or fragment thereof according to the present invention and the antitumor agent in a pharmacologically acceptable carrier (or medium) for formulation is also included in the present invention. The description about prescription, formulation, administration routes, doses, cancers, etc. regarding pharmaceutical compositions and dosage forms containing antibodies of the present invention is applicable to all of the pharmaceutical compositions and dosage forms containing antitumor agents.
Accordingly, the present invention also provides a pharmaceutical combination for treatment and/or prevention of a cancer, which comprises the pharmaceutical composition of the present invention and a pharmaceutical composition comprising an antitumor agent as listed above, and a method for treating and/or preventing a cancer, which comprises administering the same. In addition, the present invention also provides a pharmaceutical composition for treatment and/or prevention of a cancer, which comprises an antibody or fragment thereof according to the present invention and an antitumor agent together with a pharmacologically acceptable carrier and/or additive.
The present invention is hereafter described in greater detail with reference to the following examples, although the scope of the present invention is not limited thereto.
(1) Construction of cDNA Library
Total RNA was extracted from a testis tissue of a healthy dog by an Acid guanidium-Phenol-Chloroform method and then a polyA RNA was purified according to protocols included with an Oligotex-dT30 mRNA purification Kit (Takara Shuzo Co., Ltd.).
A canine testis cDNA phage library was synthesized using the thus obtained mRNA (5 μg). The cDNA phage library was constructed using a cDNA Synthesis Kit, a ZAP-cDNA Synthesis Kit, and a ZAP-cDNA GigapackIII Gold Cloning Kit (STRATAGENE) according to protocols included with the kits. The size of the thus constructed cDNA phage library was 1×106 pfu/ml.
(2) Screening of cDNA Library Using Serum
Immunoscreening was performed using the above constructed canine testis cDNA phage library. Specifically, host Escherichia coli (XL1-Blue MRF′) was infected with the phage on an NZY agarose plate (Φ90×15 mm) so as to obtain approximately 2500 clones. E. coli cells were cultured at 42° C. for 3 to 4 hours to form plaques. The plate was covered with a nitrocellulose membrane (Hybond C Extra: GE Healthcare Bio-Science) impregnated with IPTG (isopropyl-β-D-thiogalactoside) at 37° C. for 4 hours, so that the protein was induced, expressed, and then transferred to the membrane. Subsequently, the membrane was taken and then immersed in TBS (10 mM Tris-HCl, 150 mM NaCl, and pH 7.5) containing 0.5% powdered skim milk, followed by overnight shaking at 4° C., thereby suppressing nonspecific reaction. The filter was reacted with a 500-fold diluted serum of a canine patient at room temperature for 2 to 3 hours.
As the above serum of a canine patient, a serum collected from a canine patient with leukemia was used. These sera were stored at −80° C. and then subjected to pre-treatment immediately before use. A method for pretreatment of serum is as follows. Specifically, host Escherichia coli (XL1-Blue MRF) was infected with a X ZAP Express phage in which no foreign gene had been inserted and then cultured overnight on a NZY plate medium at 37° C. Subsequently, buffer (0.2 M NaHCO3 and pH 8.3) containing 0.5 M NaCl was added to the plate, the plate was left to stand at 4° C. for 15 hours, and then a supernatant was collected as an Escherichia coli/phage extract. Next, the thus collected Escherichia coli/phage extract was applied to an NHS-column (GE Healthcare Bio-Science), so that an Escherichia coli.phage-derived protein was immobilized. The serum of a canine patient was applied to the protein-immobilized column for reaction and then antibodies adsorbed to the Escherichia coli and phage were removed from the serum. The serum fraction that had passed through the column was diluted 500-fold with TBS containing 0.5% powdered skim milk. The resultant was used as an immuno screening material.
The above membrane onto which the treated serum and the protein had been blotted was washed 4 times with TBS-T (0.05% Tween20/TBS) and then caused to react with goat anti-dog IgG (Goat anti-Dog IgG-h+L HRP conjugated (BETHYL Laboratories)) diluted 5000-fold with TBS containing 0.5% powdered skim milk as a secondary antibody for 1 hour at room temperature. Detection was performed via an enzyme coloring reaction using an NBT/BCIP reaction solution (Roche). Colonies that matched sites positive for a coloring reaction were collected from the NZY agarose plate (Φ90×15 mm) and then lysed in 500 μl of an SM buffer (100 mM NaCl, 10 mM MgClSO4, 50 mM Tris-HCl, 0.01% gelatin, and pH 7.5). Until colonies positive for coloring reaction were unified, secondary screening and tertiary screening were repeated so that approximately 10,000 phage clones reacting with serum IgG were screened for by a method similar to the above. Thus, 1 positive clone was isolated.
For nucleotide sequence analysis of the 1 positive clone isolated by the above method, a procedure for conversion from phage vectors to plasmid vectors was performed. Specifically, 200 μl of a solution was prepared to contain host Escherichia coli (XL1-Blue MRF) so that absorbance OD600 was 1.0. The solution was mixed with 100 μl of a purified phage solution and then with 1 μl of an ExAssist helper phage (STRATAGENE), followed by 15 minutes of reaction at 37° C. Three (3) ml of LB medium was added and then culture was performed at 37° C. for 2.5 to 3 hours. Immediately after culture, the temperature of the solution was kept at 70° C. by water bath for 20 minutes, centrifugation was performed at 4° C. and 1000×g for 15 minutes, and then the supernatant was collected as a phagemid solution. Subsequently, 200 μl of a solution was prepared to contain phagemid host Escherichia coli (SOLR) so that absorbance OD600 was 1.0. The solution was mixed with 10 μl of a purified phage solution, followed by 15 minutes of reaction at 37° C. The solution (50 μl) was seeded on LB agar medium containing ampicillin (final concentration of 50 μg/ml) and then cultured overnight at 37° C. Transformed SOLR single colony was collected and then cultured in LB medium containing ampicillin (final concentration: 50 μg/ml) at 37° C. A plasmid DNA containing the insert of interest was purified using a QIAGEN plasmid Miniprep Kit (QIAGEN).
The purified plasmid was subjected to analysis of the full-length insert sequence by a primer walking method using the T3 primer of SEQ ID NO: 25 and the T7 primer of SEQ ID NO: 26. As a result of sequence analysis, the gene sequence of SEQ ID NO: 3 was obtained. A sequence identity search program, BLAST search (http://www.ncbi.nlm.nih.gov/BLAST/), was performed using the nucleotide sequence of the gene and the amino acid sequence thereof. As a result of this sequence identity search with known genes, it was revealed that the obtained gene was MRAP2 gene. The sequence identity with human MRAP2, a human homolog of canine MRAP2, was 91% in terms of nucleotide sequence and 94% in terms of amino acid sequence. The sequence identity with feline MRAP2 was 95% in terms of nucleotide sequence and 96% in terms of amino acid sequence. The sequence identity with mouse MRAP2, a mouse homolog of canine MRAP2, was 84% in terms of nucleotide sequence and 88% in terms of amino acid sequence. The nucleotide sequence of human MRAP2 is shown in SEQ ID NO: 1 and the amino acid sequence of the same is shown in SEQ ID NO: 2. The nucleotide sequence of feline MRAP2 is shown in SEQ ID NO: 5 and the amino acid sequence of the same is shown in SEQ ID NO: 6. The nucleotide sequence of mouse MRAP2 is shown in SEQ ID NO: 7 and the amino acid sequence of the same is shown in SEQ ID NO: 8.
Expression of the gene obtained by the above method in canine, human, and mouse various normal tissues, various tumor tissues, and various cancer cell lines was examined by an RT-PCR (reverse transcription-PCR) method. A reverse transcription reaction was performed as follows. Specifically, total RNA was extracted from each tissue (50 mg to 100 mg) and each cell line (5 to 10×106 cells) using a TRIZOL reagent (Thermo Fisher Scientific) according to protocols included therewith. cDNA was synthesized using the total RNA and Superscript First-Strand Synthesis System for RT-PCR ((Thermo Fisher Scientific) according to protocols included with the kit. Gene Pool cDNA (Thermo Fisher Scientific), QUICK-Clone cDNA (Clontech Laboratories, Inc.), and Large-Insert cDNA Library (Clontech Laboratories, Inc.) were used as cDNAs from human normal tissues (brain, testis, colon, and placenta). PCR was performed as follows using primers specific to the obtained gene (canine primers: SEQ ID NOS: 27 and 28, human primers: SEQ ID NOS: 29 and 30, mouse primers: SEQ ID NOS: 31 and 32). Specifically, PCR was performed by repeating 30 times a cycle of 94° C./30 seconds, 55° C./30 seconds, and 72° C./1 minute using a Thermal Cycler (BIO RAD) and a reaction solution adjusted to a total amount of 25 μl through addition of each reagent and an attached buffer (0.25 μl of the cDNA sample prepared by reverse transcription reaction, the above primers (2 μM each), dNTP (0.2 mM each), and 0.65 U of ExTaq polymerase (Takara Shuzo)). As a result, as shown in
(1) Cloning of Full-Length cDNA Encoding Human MRAP2, and cDNA Encoding Extracellular Region of Human MRAP2 (Hereinafter, Referred to as hN-Terminal Portion of MRAP2 or hC-Terminal Portion of MRAP2, Respectively)
Full-length cDNA encoding human MRAP2 was cloned by the following method based on the gene of SEQ ID NO: 1 obtained in Example 1. PCR was performed by repeating 30 times a cycle of 98° C./10 seconds, 55° C./15 seconds, and 72° C./1 minute using a Thermal Cycler (BIO RAD) and a reaction solution adjusted to a total amount of 50 μl through addition of each reagent and an attached buffer (1 μl of cDNA (which was from a variety of tis sue/cell-derived cDNAs prepared in Example 1 and observed for their expression by RT-PCR), 2 types of primers (0.4 μM each; SEQ ID NOS: 33 and 34) containing EcoRI and NotI restriction enzyme cleavage sequences, 0.2 mM dNTP, 1.25 U PrimeSTAR HS polymerase (Takara Shuzo). The above 2 types of primers were used to amplify the region encoding the full-length amino acid sequence of SEQ ID NO: 2. After PCR, the thus amplified DNA was subjected to 1% agarose gel electrophoresis and then a DNA fragment of approximately 0.6 kbp was purified using a QIAquick Gel Extraction Kit (QIAGEN). The thus obtained PCR amplification product was inserted into pcDNA3.1 (Thermo Fisher Scientific) (hereinafter, the resultant is referred to as human MRAP2/pcDNA3.1). The amplification product was also confirmed, by sequencing using a DNA sequencer, to have a cDNA sequence encoding human MRAP2. The sequence shown in SEQ ID NO: 1 is the nucleotide sequence of the human MRAP2 gene, and the sequence shown in SEQ ID NO: 2 is the amino acid sequence of the human MRAP2 protein.
Further, PCR was performed based on SEQ ID NO: 1 by repeating 30 times a cycle of 98° C./10 seconds, 55° C./15 seconds, and 72° C./30 seconds using a Thermal Cycler (BIO RAD) and a reaction solution adjusted to a total amount of 50 μl through addition of each reagent and an attached buffer (2 types of primers (0.4 μM each; SEQ ID NOS: 35 and 36) containing KpnI and EcoRI restriction enzyme cleavage sequences, 0.2 mM dNTP, 1.25 U PrimeSTAR HS polymerase (Takara Shuzo)). The above 2 types of primers were used to amplify the region encoding the amino acid sequence (SEQ ID NO: 10) of the extracellular region (N-terminal) of the MRAP2 protein, in SEQ ID NO: 1. After PCR, the thus amplified DNA was subjected to 1% agarose gel electrophoresis and then a DNA fragment of approximately 130 bp was purified using a QIAquick Gel Extraction Kit (QIAGEN). The thus obtained PCR amplification product was ligated to pSecTagB (Thermo Fisher Scientific) having an insert of cDNA encoding the mouse IgG2a Fc protein to prepare an expression vector encoding a human N-terminal MRAP2 extracellular region/mouse IgG2a Fc fusion protein (hereinafter, referred to as hN-terminal MRAP2-mIgG2aFc) (hereinafter, the obtained expression vector is referred to as pSecB-hN-terminal MRAP2-mIgG2aFc). The amplification product was also confirmed, by sequencing using a DNA sequencer, to have a cDNA sequence encoding hN-terminal MRAP2-mIgG2aFc. The sequence shown in SEQ ID NO: 37 is the nucleotide sequence encoding hN-terminal MRAP2-mIgG2aFc, and the sequence shown in SEQ ID NO: 38 is the amino acid sequence of hN-terminal MRAP2-mIgG2aFc.
Further, PCR was performed based on SEQ ID NO: 1 by repeating 30 times a cycle of 98° C./10 seconds, 55° C./15 seconds, and 72° C./30 seconds using a Thermal Cycler (BIO RAD) and a reaction solution adjusted to a total amount of 50 μl through addition of each reagent and an attached buffer (2 types of primers (0.4 μM each; SEQ ID NOS: 39 and 40) containing KpnI and EcoRI restriction enzyme cleavage sequences, 0.2 mM dNTP, 1.25 U PrimeSTAR HS polymerase (Takara Shuzo)). The above 2 types of primers were used to amplify the region encoding the amino acid sequence (SEQ ID NO: 12) of the extracellular region (C-terminal) of the MRAP2 protein, in SEQ ID NO: 1. After PCR, the thus amplified DNA was subjected to 1% agarose gel electrophoresis and then a DNA fragment of approximately 400 bp was purified using a QIAquick Gel Extraction Kit (QIAGEN). The thus obtained PCR amplification product was ligated to pSecTagB (Thermo Fisher Scientific) having an insert of cDNA encoding the mouse IgG2a Fc protein to prepare an expression vector encoding a human C-terminal MRAP2 extracellular region/mouse IgG2a Fc fusion protein (hereinafter, referred to as hC-terminal MRAP2-mIgG2aFc) (hereinafter, the obtained expression vector is referred to as pSecB-hC-terminal MRAP2-mIgG2aFc). The amplification product was also confirmed, by sequencing using a DNA sequencer, to have a cDNA sequence encoding hC-terminal MRAP2-mIgG2aFc. The sequence shown in SEQ ID NO: 41 is the nucleotide sequence encoding hC-terminal MRAP2-mIgG2aFc, and the sequence shown in SEQ ID NO: 42 is the amino acid sequence of hC-terminal MRAP2-mIgG2aFc.
(2) Preparation of hN-Terminal MRAP2-mIgG2aFc
hN-terminal MRAP2-mIgG2aFc was prepared as an immunizing antigen for preparing antibodies to MRAP2.
The expression vector pSecB-hN-terminal MRAP2-mIgG2aFc was introduced by the lipofection method into human embryonic kidney cell line HEK293 cells and purification of hN-terminal MRAP2-mIgG2aFc was carried out from a culture supernatant obtained 7 days after introduction. The culture supernatant was applied to a Hi Trap Protein A HP column (GE Healthcare Bio-Science), which was then washed with a binding buffer (20 mM sodium phosphate (pH 7.0)), followed by elution with an elution buffer (0.1 M glycine-HCl (pH 2.7)). Eluates were immediately neutralized by elution into a tube supplemented with a neutralization buffer (1 M Tris-HCl (pH 9.0)). Next, the buffer in the eluates obtained by the above method was replaced with physiological phosphate buffer (Nissui Pharmaceutical Co., Ltd.) using ultrafiltration NANOSEP 10K OMEGA (PALL). Sterilized filtration was performed using 0.22-μm HT Tuffryn Acrodisc (PALL) and then the resultants were used for the following experiments.
(3) Preparation of hC-Terminal MRAP2-mIgG2aFc
hC-terminal MRAP2-mIgG2aFc was prepared as an immunizing antigen for preparing antibodies to MRAP2.
The expression vector pSecB-hC-terminal MRAP2-mIgG2aFc was introduced by the lipofection method into human embryonic kidney cell line HEK293 cells and purification of hC-terminal MRAP2-mIgG2aFc was carried out from a culture supernatant obtained 7 days after introduction. The culture supernatant was applied to a Hi Trap Protein A HP column (GE Healthcare Bio-Science), which was then washed with a binding buffer (20 mM sodium phosphate (pH 7.0)), followed by elution with an elution buffer (0.1 M glycine-HCl (pH 2.7)). Eluates were immediately neutralized by elution into a tube supplemented with a neutralization buffer (1 M Tris-HCl (pH 9.0)). Next, the buffer in the eluates obtained by the above method was replaced with physiological phosphate buffer (Nissui Pharmaceutical Co., Ltd.) using ultrafiltration NANOSEP 10K OMEGA (PALL). Sterilized filtration was performed using 0.22-μm HT Tuffryn Acrodisc (PALL) and then the resultants were used for the following experiments.
To obtain an antibody binding to the N-terminal extracellular region of MRAP2, hN-terminal MRAP2-mIgG2aFc (0.1 mg) prepared as described above as an antigen was mixed with a complete Freund's adjuvant (CFA) solution in an amount equivalent thereto. The mixture was subcutaneously administered to a mouse 4 times every 2 weeks. Subsequently, blood was collected, so that an antiserum containing a polyclonal antibody was obtained. Furthermore, the antiserum was purified using a protein G carrier (GE Healthcare Bio-Sciences) and then a polyclonal antibody against hN-terminal MRAP2-mIgG2aFc was obtained. In addition, an antibody obtained by purifying serum of mice to which no antigen had been administered with the use of a protein G carrier in the manner described above was designated as a control antibody.
To obtain an antibody binding to the C-terminal extracellular region of MRAP2, hC-terminal MRAP2-mIgG2aFc (0.1 mg) prepared as described above as an antigen was mixed with a complete Freund's adjuvant (CFA) solution in an amount equivalent thereto. The mixture was subcutaneously administered to a mouse 4 times every 2 weeks. Subsequently, blood was collected, so that an antiserum containing a polyclonal antibody was obtained. Furthermore, the antiserum was purified using a protein G carrier (GE Healthcare Bio-Sciences) and then a polyclonal antibody against hC-terminal MRAP2-mIgG2aFc was obtained. In addition, an antibody obtained by purifying serum of mice to which no antigen had been administered with the use of a protein G carrier in the manner described above was designated as a control antibody.
Human MRAP2/pcDNA3.1 prepared as described above was introduced by the lipofection method into CHO-K1 cells (ATCC) and then selection was performed using 500 μg/ml G418 (Nacalai Tesque, Inc.) to establish a CHO cell line stably expressing full-length human MRAP2 (CHO-human MRAP2). Cells obtained by introducing an expression vector (hereinafter, referred to as emp/pcDNA3.1) having no insert of cDNA encoding MRAP2 and then performing selection in the manner described above was designated as control cells (hereinafter, referred to as CHO-emp).
It was examined whether or not the polyclonal antibody prepared in (1) above specifically reacted with MRAP2 expressed on the surfaces of the full-length human MRAP2-stably expressing cells established in (3) above. The CHO-human MRAP2 cells or the CHO-emp cells (106 cells each) were centrifuged in a 1.5-ml microcentrifugal tube. The polyclonal antibody against N-terminal portion of MRAP2 (2 μg in 5 μl) prepared in (1) above was added thereto. The resultant was further suspended in PBS containing 0.1% fetal bovine serum (95 μl) and then left to stand on ice for 1 hour. After washing with PBS, the resultant was suspended in PBS containing an FITC-labeled goat anti-mouse IgG antibody (Santa Cruz Biotechnology, Inc.) (5 μl) and 0.1% fetal bovine serum (FBS) (95 μl) and then left to stand on ice for 1 hour. After washing with PBS, fluorescence intensity was measured using FACSCalibur (Becton, Dickinson and Company). Meanwhile, a procedure similar to the above was performed using the control antibody prepared in (1) above instead of the polyclonal antibody against MRAP2, so that a control was prepared. As a result, 215% increase in fluorescence intensity was found in the CHO-human MRAP2 cells to which the anti-N-terminal portion of MRAP2 polyclonal antibody had been added, as compared with the control. Meanwhile, a procedure similar to the above was performed for the CHO-emp cells. As a result, 0% increase in fluorescence intensity was found in the CHO-emp cells to which the anti-N-terminal portion of MRAP2 polyclonal antibody had been added, as compared with the control. Based on the above, it was revealed that the anti-N-terminal portion of MRAP2 polyclonal antibody was capable of specifically binding to the MRAP2 protein expressed on the cell membrane surfaces. In addition, the rate of increase in fluorescence intensity is represented by the rate of increase in mean fluorescence intensity (MFI value) in cells. It was calculated by the following equation.
Rate of increase in mean fluorescence intensity (rate of increase in fluorescence intensity) (%)=((MFI value of cells reacted with an anti-human MRAP2 antibody)−(control MFI value))/(control MFI value)×100
Next, it was examined whether or not the polyclonal antibody prepared in (2) above specifically reacted with MRAP2 expressed on the surfaces of the full-length human MRAP2-stably expressing cells established in (3) above. The CHO-human MRAP2 cells or the CHO-emp cells (106 cells each) were centrifuged in a 1.5-ml microcentrifugal tube. The polyclonal antibody against C-terminal portion of MRAP2 (2 μg in 5 μl) prepared in (2) above was added thereto. The resultant was further suspended in PBS containing 0.1% fetal bovine serum (95 μl) and then left to stand on ice for 1 hour. After washing with PBS, the resultant was suspended in PBS containing an FITC-labeled goat anti-mouse IgG antibody (Santa Cruz Biotechnology, Inc.) (5 μl) and 0.1% fetal bovine serum (FBS) (95 μl) and then left to stand on ice for 1 hour. After washing with PBS, fluorescence intensity was measured using FACSCalibur (Becton, Dickinson and Company). Meanwhile, a procedure similar to the above was performed using the control antibody prepared in (2) above instead of the polyclonal antibody against MRAP2, so that a control was prepared. As a result, 223% increase in fluorescence intensity was found in the CHO-human MRAP2 cells to which the anti-C-terminal portion of MRAP2 polyclonal antibody had been added, as compared with the control. Meanwhile, a procedure similar to the above was performed for the CHO-emp cells. As a result, 0% increase in fluorescence intensity was found in the CHO-emp cells to which the anti-C-terminal portion of MRAP2 polyclonal antibody had been added, as compared with the control. Based on the above, it was revealed that the anti-C-terminal portion of MRAP2 polyclonal antibody was capable of specifically binding to the MRAP2 protein expressed on the cell membrane surfaces. In addition, the rate of increase in fluorescence intensity is represented by the rate of increase in mean fluorescence intensity (MFI value) in cells. It was calculated by the following equation.
Rate of increase in mean fluorescence intensity (rate of increase in fluorescence intensity) (%)=((MFI value of cells reacted with an anti-human MRAP2 antibody)−(control MFI value))/(control MFI value)×100
Next, it was examined whether or not the MRAP2 protein was expressed on cell surfaces of 2 types of leukemia cell lines (K562 and THP-1) and a malignant lymphoma cell line (Namalwa) in which MRAP2 gene expression had been strongly observed. Each human cell line (106 cells) in which gene expression had been observed as described above was centrifuged in a 1.5-ml microcentrifugal tube. The polyclonal antibody against C-terminal portion of MRAP2 (2 μg in 5 μl) prepared in (2) above was added thereto. The resultant was further suspended in PBS containing 0.1% fetal bovine serum (95 μl) and then left to stand on ice for 1 hour. After washing with PBS, the resultant was suspended in PBS containing an FITC-labeled goat anti-mouse IgG antibody (Santa Cruz Biotechnology, Inc.) (5 μl) and 0.1% fetal bovine serum (FBS) (95 μl) and then left to stand on ice for 1 hour. After washing with PBS, fluorescence intensity was measured using FACSCalibur (Becton, Dickinson and Company). Meanwhile, a procedure similar to the above was performed using the control antibody prepared in (2) above instead of the polyclonal antibody against C-terminal portion of MRAP2, so that a control was prepared. As a result, fluorescence intensity was found to be at least 30% stronger in all cells to which the anti-C-terminal portion of MRAP2 polyclonal antibody had been added than that in control cells. Specifically, the following increases in fluorescence intensity were observed: K562: 197%, THP-1: 123%, and Namalwa: 104%. Based on the above, it was revealed that the MRAP2 protein was expressed on the cell membrane surfaces of the above human cancer cell lines. In addition, the rate of increase in fluorescence intensity is represented by the rate of increase in mean fluorescence intensity (MFI value) in cells. It was calculated by the following equation.
Rate of increase in mean fluorescence intensity (rate of increase in fluorescence intensity) (%)=((MFI value of cells reacted with an anti-human MRAP2 antibody)−(control MFI value))/(control MFI value)×100
Next, it was examined whether or not a polyclonal antibody against MRAP2 would be able to damage MRAP2-expressing tumor cells. Evaluation was carried out using the polyclonal antibody against human N-terminal portion of MRAP2 or human C-terminal portion of MRAP2 prepared in Example 3. A human leukemia cell line K562 or a human malignant lymphoma cell line Namalwa (106 cells), in which MRAP2 expression had been confirmed, were separately collected into a 50-ml centrifugal tube. Chromium 51 (100 μCi) was added thereto, followed by incubation at 37° C. for 2 hours. Thereafter, cells were washed 3 times with an RPMI1640 medium containing 10% fetal bovine serum and added to wells (103 cells per well) in 96-well V-bottom plates. The above each polyclonal antibody against human MRAP2 was added thereto (1 μg per well). Further, lymphocytes separated from mouse peripheral blood were added thereto (2×105 cells per well), followed by culture under conditions of 37° C. and 5% CO2 for 4 hours. After culture, the level of chromium (Cr) 51 released from damaged tumor cells in each culture supernatant was determined. Then, the ADCC activity of the polyclonal antibody against human N-terminal portion of MRAP2 or human C-terminal portion of MRAP2 to cancer cells was calculated. As a result, ADCC activities against the K562 cells (15.7% and 16.3%, respectively) and the Namalwa cells (14.8% and 14.0%, respectively) were observed (see
In addition, for cytotoxic activity (ADCC activity) in
Cytotoxic activity (%)=[(the level of chromium 51 released from K562 to which an antibody against MRAP2 and mouse lymphocytes were added)/(the level of chromium 51 released from target cells to which 1 N hydrochloric acid was added)]×100 *Equation:
The antibodies of the present invention are useful for treatment and/or prevention of cancers.
All publications, patents, and patent applications cited herein are incorporated herein by reference in their entirety.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2016-064033 | Mar 2016 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2017/012263 | 3/27/2017 | WO | 00 |
