Patent Grant
7964767
This application is the National Stage of International Application No. PCT/JP2005/006298, filed on Mar. 31, 2005, which claims the benefit of Japanese Patent Application Serial No. 2004-107669, filed on Mar. 31, 2004. The contents of both of the foregoing applications are hereby incorporated by reference in their entireties.
The present invention relates to systems and such for antibody production in which animals are immunized with immunogens comprising, other than target antigens, background antigens to produce antibodies specific to the target antigens, and particularly relates to systems and such in which immunized animals carry genes encoding soluble forms of membrane proteins so that immunotolerance against the background antigens comprising the membrane proteins is induced in the immunized animals.
Antibody production is very difficult when it is difficult to express and purify the target antigens necessary to produce the antibodies. This tendency is pronounced for membrane proteins. Therefore, a technique has been developed which uses proteins that are difficult to express or purify, such as seven-transmembrane proteins, as antigens by expressing the antigenic proteins on the membrane surface of the Autographa californica nuclear polyhedrosis virus (AcNPV), which belongs to Baculovirus (Non-Patent Document 1).
However, although baculovirus expression systems are useful as expression systems for various proteins comprising membrane proteins, there are many gp64 membrane proteins (Non-Patent Documents 2 and 3) on the surface of baculoviruses, and these contaminate the expression products obtained from baculovirus expression systems. gp64 is a 64-kDa protein, a major component of the surface of budding viruses, and known to be a protein involved in envelope fusion at low pH. This gp64 is more easily recognized as non-self than human-derived antigenic proteins, and when gp64 contaminates immunogens, antibodies are produced more readily against gp64 than against the target antigens. Therefore, when preparing immunogens using a baculovirus expression system, it is difficult to produce and obtain specific antibodies against antigenic proteins (Non-Patent Document 4). As a means to solve this problem, the present inventors generated gp64 transgenic mice (hereinafter referred to as “Tgm”). Before their immune system develops, these Tgm (hereinafter referred to as “gp64Tgm”) carry an exogenous gp64 in the same way as the endogenous genes. Therefore, these Tgm show immunotolerance against gp64, just as they do for the endogenous genes. Thus they recognize target antigenic proteins expressed using baculovirus, enabling the advantageous production of specific antibodies (Patent Document 1).
However, the gp64Tgm showed a phenotype with no testes development nor sperm formation. Therefore, the maintenance of the strain was restricted to females, and although the strain could be maintained, efficient breeding was not possible. In addition, there were some difficulties when producing crossbred animals by crossing with other knockout mice or Tgm.
As described above, the aforementioned gp64Tgm are useful as animals to be immunized for producing specific antibodies against proteins expressed using baculoviruses, but gp64Tgm had a problem of being infertile. Therefore, an objective of the present invention is to generate even more useful Tgm without unfavorable phenotypes such as inhibited testes development, and to provide methods and such for producing antibodies using these novel Tgm, so that the expression and maintenance of such exogenous membrane proteins in transgenic animals are enabled.
The present inventors predicted that the inhibition of testes development is caused by gp64 expression on cell membranes in the testes. Soluble gp64 (hereinafter referred to as “sgp64”), produced by deleting the transmembrane region from (full-length) gp64, was linked to the pCAGGS vector (Gene, vol. 108, 193-200, 1991) to construct an sgp64 expression vector (hereinafter referred to as “pCAG-sgp64 vector”). When sgp64Tgm were produced by introducing this vector into mice, male Tgm maintained their fertility, and the present inventors successfully overcame the conventional problem of inhibited testes development. These sgp64Tgm and control non-transgenic mice were immunized using a budding baculovirus, sera were collected, and the presence of immunotolerance against gp64 was examined. As a result, antibodies against gp64 were produced in control non-transgenic mice, but were hardly detected in sgp64Tgm. In other words, the present inventors were able to avoid the male infertility observed in conventional gp64Tgm by using sgp64, and were able to establish transgenic mice effective for producing antibodies using antigens expressed in baculovirus. The present invention is based on these findings, and more specifically, relates to the following:
immunizing the nonhuman animal of any one of (1) to (10) with an immunogen comprising a target antigen; and
obtaining an antibody against the target antigen or a gene encoding such an antibody;
To facilitate the understanding of the present invention, the meaning of some of the presupposed terms are explained.
In the present invention, the term “target antigen” denotes antigens recognized by subject antibodies. The target antigens can be selected from any substance having antigenicity. Specifically, proteins, sugar chains, lipids, inorganic substances, or such are known as substances showing antigenicity. The target antigens may be naturally occurring or artificially synthesized. The artificially synthesized target antigens comprise recombinant proteins prepared by genetic engineering technology, and many kinds of chemically-synthesized organic compounds.
The term “background antigen” denotes substances comprising antigenic determinants for which antibody generation is not desired, or denotes the antigenic determinants themselves. For example, any antigenic substance that is not a target antigen, but which contaminates the target antigen, is a background antigen. Typical background antigens are proteins contaminated within crudely purified target antigens. More specifically, host cell-derived proteins in a recombinant protein are examples of background antigens. The term “background antigen” may also be defined to mean antigens that are comprised within an immunogen for inducing subject antibody generation, and that induce production of a non-subject antibody. Generally, a background antigen is thought to indicate an antigenic substance other than a target antigen. In the present invention, however, antigenic determinants present on target antigen molecules may also be comprised in the background antigens. For example, if an antigenic determinant for which antibody generation is undesired is present on a target antigen molecule, the antigenic determinant is comprised in the background antigens of the present invention.
The term “immunotolerance” denotes a condition in which an immune response, specific to an antigen that is an immunotolerance target (an immunotolerance antigen), is lost or decreased. When the level of a subject's immune response to an immunotolerance antigen is reduced compared to that of a normal immunized animal, the subject can be regarded to comprise immunotolerance against the immunotolerance antigen. For example, when the amount of an antibody generated against an immunotolerance antigen is decreased in response to the administration of an immunotolerance antigen, the level of immune response is then considered to be low.
FIG. 1-a shows the nucleotide sequence of the soluble gp64 gene used in the Examples. Nucleotides 1 to 720 are shown.
FIG. 1-b shows the nucleotide sequence of the soluble gp64 gene used in the Examples. Nucleotides 721 to 1486 are shown.
The present invention provides transgenic animals useful for producing antibodies against target antigens when using immunogens that have, other than the target antigens, membrane proteins contaminating as background antigens, and also provides methods and systems for antibody production using such transgenic animals.
As described above, in the present invention, the background antigens are membrane proteins. Examples of cases where membrane proteins contaminate as background antigens comprise the contamination of membrane proteins derived from host organisms used to prepare target antigens, and the contamination of membrane proteins derived from viruses used for the expression systems. For example, when the target antigen is expressed together with viral vector-derived membrane proteins, such as the case in which a baculovirus expression system is used to prepare a membrane protein as a target antigen, large quantities of vector-derived membrane proteins contaminate as background antigens.
Herein, “membrane protein” ordinarily means a protein that constitutes a biological membrane, and for example, it refers to a protein embedded in a biological membrane; however, in the present invention, it also comprises proteins linked to a cell membrane surface via an anchor and the like, such as GPI-anchored proteins. Moreover, virus-derived membrane proteins ordinarily refer to proteins that constitute the envelope of budding viruses. For example, in baculoviruses, a protein called gp64 corresponds to a membrane protein. The structure of many of these membrane proteins comprises a region embedded in the cell membrane (transmembrane region), a region exposed on the outer side of the cell membrane (extracellular region), and a region positioned on the inner side of the cell membrane (intracellular region). Functionally, membrane proteins comprise proteins constituting membranes, receptors, proteins involved in signal transduction and the like such as transporters, and proteins such as membrane enzymes that perform specific reactions. Therefore, when such an exogenous membrane protein is introduced into an animal to be immunized, its expression in any biological membrane of the animal to be immunized will not only induce immunotolerance, but may also confer other unfavorable characteristics. For example, the problem of male infertility arises in mice into which the baculovirus-derived membrane protein gp64 has been introduced.
In the nonhuman animals of the systems for antibody production of the present invention, immunotolerance is induced against virus-derived membrane proteins that may be contaminating immunogens as the aforementioned background antigens. For example, nonhuman animals in which immunotolerance against baculovirus-derived membrane protein gp64 has been induced are used as the immunized animals when using immunogens prepared with the baculovirus expression systems. In the past, methods where immunized animals carry a gene encoding a full-length membrane protein, which is a background antigen, had been developed as methods for inducing immunotolerance; however, in the present invention, nonhuman animals carry a gene encoding a solubilized membrane protein (hereinafter referred to as a “soluble protein”).
A “soluble protein” (also referred to as “soluble form protein” in the present application) refers to a membrane protein originally expressed on a biological membrane (insoluble protein) that has been modified so that it may be expressed outside a biological membrane. As described above, since membrane proteins comprise those that function as receptors or transporters that may be involved in signal transduction and those that function as switches in the living body, such as membrane enzymes, when such membrane proteins are expressed in the biological membranes of the animals to be immunized, they not only induce immunotolerance against background antigens in the animals to be immunized but can also confer unfavorable characteristics to the animals. To avoid such inconveniences, in the present invention, the membrane proteins are converted to soluble forms so that they may be expressed outside biological membranes. In addition, compared to conventional methods that use full-length membrane proteins and express them on biological membranes, which are localized sites, the present invention allows membrane proteins to be expressed systemically in the cytoplasm in their soluble form; therefore, the efficiency of immunotolerance induction is expected to improve.
In the present invention, genetic engineering methods for modifying genes encoding membrane proteins are used to modify the membrane proteins into soluble forms. An example of a genetic engineering method for solubilizing membrane proteins is the deletion of a transmembrane region. The degree of transmembrane region deletion may be deletion of a portion of the transmembrane region, or deletion of the entire transmembrane region, so long as the membrane protein can be expressed extracellularly. Since transmembrane regions generally form an α-helical structure comprising 20 to 30 amino acids, proteins can also be solubilized by introducing mutations to change this structure.
As regions other than the transmembrane region, there are the intracellular region and the extracellular region; however, when modifying membrane proteins into soluble proteins, the intracellular region is not necessary, and soluble proteins may be limited to the extracellular region alone, which is equipped with antigenic determinants that can induce immunotolerance. Moreover, the extracellular region may also be limited to regions that may induce immunotolerance, such as regions that maintain antigenicity and are equipped with antigenic determinants capable of inducing immunotolerance against membrane proteins.
In addition to deleting the transmembrane region and such from membrane proteins and such, the aforementioned soluble proteins may comprise a chimeric protein into which other peptides and such have been added or inserted. The peptides added/inserted to the chimeric proteins may be antigenic determinants of other background antigens (these “other background antigens” may or may not be membrane proteins). Thus, immunotolerance against multiple background antigens can be induced by equipping a single protein with antigenic determinants against multiple background antigens.
As an example of the construction of a soluble protein, the case of baculovirus membrane protein gp64 will be used and explained. gp64 is encoded by the DNA sequence of SEQ ID NO: 1; its transmembrane region is encoded by nucleotides 1465 to 1515, and its extracellular region is encoded by nucleotides 1 to 1464. Therefore, to solubilize gp64, the aforementioned transmembrane region can be deleted, the sequence encoding the amino acids responsible for the α-helix structure can be substituted with that of other amino acids, or so forth. Also, the entire protein, comprising 488 amino acid residues that are encoded by nucleotides 1 to 1464 shown in SEQ ID NO: 3, may be used for the aforementioned extracellular region, or the length of the extracellular region can be shortened to within a range that can maintain cross-reactivity with gp64 and induce immunotolerance against gp64. Furthermore, one or more modifications such as amino acid deletion, substitution, addition, or insertion can be made to the amino acid sequence of the extracellular region of gp64 (amino acid residues 1 to 488 in the amino acid sequences of SEQ ID NOs: 1 to 3), within a range that allows the induction of immunotolerance against gp64 in the immunized animals described below.
In the present invention, immunotolerance is induced by making nonhuman animals carry genes encoding such soluble proteins. Nonhuman animals that can be used in the present invention comprise, for example, monkeys, pigs, dogs, rats, mice, and rabbits. For example, rodents such as rats, mice, and hamsters are preferable as nonhuman animals. To induce immunotolerance by preparing transgenic animals, it is advantageous to use nonhuman animals which mature fast and for which gene manipulation technologies have been established, such as rodents. Mice in particular are nonhuman animals that meet these requirements at a high level.
Nonhuman animals carrying a gene encoding the aforementioned soluble protein can be obtained by producing transgenic animals into which a gene encoding the soluble protein has been introduced as an exogenous gene. For example, transgenic mice can be produced according to known methods (Proc. Natl. Acad. Sci. USA 77: 7380-7384 (1980)). Specifically, subject genes are introduced into mammalian totipotent cells, and then the cells are brought up into individuals. A subject transgenic mouse can be obtained from the individuals thus obtained by screening for individuals in which the introduced gene has been integrated into both somatic cells and germ cells. Fertilized eggs, early embryos, and cultured cells with multipotency such as ES cells, and such, can be used as the totipotent cells for introducing a gene. More specifically, they can be produced by the method in the Examples described below.
The nonhuman animals carrying a gene encoding a soluble protein of the present invention may be offspring of the above-mentioned transgenic animals. Once transgenic animals are established, transmission to the offspring of the characteristics (in the present invention, the characteristic of immunotolerance) caused by the introduced gene is usually easy. However, since the previously developed transgenic animals into which baculovirus gp64 has been introduced had developed the problem of male infertility, it was difficult to efficiently reflect the characteristic of immunotolerance in their offspring. On the other hand, in the present invention, by producing transgenic animals using genes encoding soluble forms of the membrane proteins, the expression of unfavorable characteristics found in the transgenic animals into which genes encoding full-length membrane proteins have been introduced was avoided. As one example, the use of a gene encoding a soluble form of the baculovirus gp64 protein in the production of transgenic animals has made it simple to transmit characteristics to the offspring by maintaining male fertility and efficient reproduction. Since transgenic animals carrying soluble gp64 can reproduce efficiently, and their offspring also carry the characteristic of immunotolerance, they become useful as animals to be immunized for antibody production and such, as described below. Therefore, by making nonhuman animals carry a gene encoding a soluble protein rather than a full-length membrane protein, immunized animals in which immunotolerance has been induced against that membrane protein can be more widely and easily used.
Nonhuman animals carrying a gene encoding a soluble form of a membrane protein of the present invention can be produced based on gene deficient animals in which the target antigenic protein is deleted (so-called knockout animals). Nonhuman animals carrying a gene encoding the soluble form of the membrane protein may also be produced by crossing background antigen-expressing transgenic animals with such target antigenic protein knockout animals. This enables the characteristics of background antigen expression and target antigenic protein deletion to be conferred to the nonhuman animals. In such animals carrying both characteristics, immunotolerance against background antigens is induced, while the target antigen is more readily recognized as a foreign substance since the animals do not innately carry the target antigen; therefore, the desired antibodies can be obtained efficiently.
In the nonhuman animals of the present invention, in which immunotolerance against background antigens is induced, suppression of antibody production against all background antigens that may be comprised in an immunogen is not necessarily important. Production of antibodies that recognize background antigens is tolerated if it is within a range that does not interfere with production and collection of antibodies against the target antigen. Therefore, for example, even animals to be immunized in which immunotolerance has been induced against only the major background antigens may be utilized as favorable immunized animals of the present invention.
The present invention relates to methods for producing antibodies by utilizing nonhuman animals that carry genes encoding the abovementioned soluble forms of membrane proteins.
These methods comprise the step of immunizing nonhuman animals carrying a gene encoding the abovementioned soluble form of a membrane protein with an immunogen comprising, other than a target antigen, this membrane protein as a background antigen, and the step of obtaining antibodies against the previously-described target antigen or genes encoding these antibodies.
The immunogens of the present invention comprise, other than a target antigen, at least a membrane protein as a background antigen. Generally, a target antigen comprises substances derived from biological materials. Biological materials are complex mixtures comprising various components. Thus, target antigens are usually prepared using various mixtures as starting materials. Therefore, it is difficult to obtain highly-purified target antigens. In other words, it involves a lot of time and effort to isolate a large quantity of a highly pure target antigen. The present invention provides methods that enable efficient acquisition of antibodies against target antigens using such immunogens which have, other than a target antigen, membrane proteins contaminating as background antigens.
More specifically, examples of the immunogens of the present invention comprise cells, cell culture solutions, cell lysates, viruses, and crude antigens, in which membrane proteins may be contaminating as background antigens. When using cells or viruses, a gene encoding a desired antigen can be introduced into the cells or viruses by gene recombination techniques, and those that artificially express the desired antigen can be used. Whole cells or viruses as well as portions thereof can be used as the immunogens. Furthermore, just cell membrane or viral envelope portions may be used as the immunogens. When such whole cells or viruses, or portions thereof, such as their cell membrane or viral envelope, are used as the immunogen, membrane proteins comprised in the cell membrane or viral envelope contaminate as background antigens.
One preferable immunogen of the present invention is a viral particle or portion thereof. Viruses are comprised of relatively simple components, including nucleic acids, and limited proteins, saccharides, and such. Consequently, the types of background antigens that may interfere with target antigen acquisition are also limited. Background antigens from viral particles or portions thereof that interfere with the acquisition of target antigen comprise membrane proteins on the surface of the particles. When administered to the animals to be immunized, the particle surfaces are highly antigenic, and can readily induce antibody production. Therefore, the methods for producing antibodies based on the present invention can be carried out more favorably if, even from among these few background antigens, immunotolerance in the animals to be immunized is induced against background antigens that are membrane proteins on the particle surface and the like.
In the present invention, baculovirus is one among the preferred among the viruses that can be used as immunogens. Baculoviruses are insect viruses that comprise a structure whereby a double-stranded DNA genome is covered with a capsid protein. Expression systems using Nucleopolyhedrovirus (NPV), a type of baculovirus, are useful as systems for expressing exogenous genes. NPV comprises strong promoter activity. Therefore, any protein can be produced in large quantities by inserting an exogenous gene into the NPV genome. Specifically, strong expression of any exogenous gene is induced by recombinantly substituting the gene coding for the protein called polyhedron with the exogenous gene.
The foreign genes that are expressed in the aforementioned baculovirus expression systems are not particularly limited, and any gene may be used; however, since baculoviruses can be utilized as systems suitable for expressing membrane proteins, an example of a suitable gene is a gene encoding a membrane protein. In the baculovirus expression systems, a subject membrane protein can be expressed along with a baculovirus envelope protein in a form that retains its structure. Another advantage of the baculovirus expression systems is that the expression products can be easily recovered as budding viral particles.
As methods for expressing membrane proteins which are the target antigens using baculoviruses, for example, the method using budding baculoviruses described in WO 98/46777 and Loisel et al. (Loisel, T. P. et al., Nature Biotech. 15: 1300-1304 (1997)) can be used. More specifically, a recombinant vector for insect cells comprising a gene encoding an exogenous protein is constructed, and introduced, along with baculoviral DNA, into insect cells such as Sf9. The exogenous membrane protein encoded by the recombinant vector is expressed on mature viral particles (virions), which are released by infected cells to the outside of cells prior to infected cell death. Recombinant viruses that express the exogenous protein can thus be obtained.
In the present invention, a budding virus is a virus that is released from infected cells by budding. Generally, viruses covered with an envelope can bud from cells infected with these viruses, and are released continuously, even when the cells have not been destroyed. On the other hand, adenoviruses that are not covered by an envelope, and herpes viruses that are covered by a nuclear envelope, are released from the cells all at once, upon cell destruction. Budding viruses are particularly preferable in the present invention. In addition, those skilled in the art can suitably select hosts to be infected with a recombinant virus, depending on the type of virus used, so long as viral replication is possible in the host. For example, insect cells such as Sf9 cells can be used when using baculoviruses. Generally, protein expression systems using baculoviruses and insect cells are considered to be useful systems because modifications that occur at the same time as translation or post-translationally, such as fatty acid acetylation or glycosylation, are carried out in the same way as with mammalian cells and because the expression level of heterologous proteins in such systems is greater than that in mammalian cell systems (Luckow V. A. and Summers M. D., Virol. 167: 56 (1988)).
The viruses expressing exogenous proteins, which are the target antigens, can be obtained by, for example, culturing a host that has been infected with a recombinant virus comprising a gene that encodes an exogenous protein. Alternatively, using methods such as the above-mentioned methods of WO 98/46777 and Loisel et al (Loisel, T. P. et al., Nature Biotech. 15: 1300-1304 (1997)), a recombinant vector encoding an exogenous protein can be introduced into an insect cell along with a baculovirus, and exogenous proteins can be expressed on the envelope of the baculovirus released outside of the cell. In addition, using methods like that of Strehlow et al. (D. Strehlow et al., Proc. Natl. Acad. Sci. USA. 97: 4209-4214 (2000)), packaging cells such as PA317 can be infected with recombinant Moloney murine leukemia viruses, which are constructed using vectors derived from Moloney viruses into which exogenous protein-encoding genes have been introduced, and the exogenous proteins can be expressed on the envelope of viruses released outside of the cells. These are examples of viruses for expressing exogenous proteins and the viruses of the present invention that express exogenous proteins, useful as immunogens, are not limited to those that are constructed using the above methods.
Recombinant viruses constructed as described above can be purified using known methods, as necessary. For example, known methods for purifying viruses comprise augmented density gradient centrifugation (Albrechtsen et al., J. Virological Methods 28: 245-256 (1990); Hewish et al., J. Virological Methods 7: 223-228 (1983)), size exclusion chromatography (Hjorth and Mereno-Lopez, J. Virological Methods 5: 151-158 (1982); Crooks et al., J. Chrom. 502: 59-68 (1990); Mento S. J. (Viagene, Inc.) 1994 Williamsburg Bioprocessing Conference), affinity chromatography using monoclonal antibodies, sulphated fucose-containing polysaccharides and the like (Najayou et al., J. Virological Methods 32: 67-77 (1991); Diaco et al., J. Gen. Virol. 67: 345-351 (1986); Fowler, J. Virological Methods 11: 59-74 (1986); Japanese Patent Saikohyo Publication No. (JP-A) 97/032010 (unexamined Japanese national phase publication corresponding to a Japanese international publication)), and DEAE ion exchange chromatography (Haruna et al., Virology 13: 264-267 (1961)). Thus, purification can be carried out using the above methods or combinations thereof.
Animals to be immunized are immunized using immunogens prepared as described above. The immunized animals used in the present invention are nonhuman animals in which immunotolerance against a background antigen membrane protein comprised in an immunogen has been induced. Induction of immunotolerance against a background antigen membrane protein can be carried out as described above, by making animals to be immunized carry a gene encoding a soluble form of this membrane protein.
When a baculovirus expression system, which was shown above as an expression system suitable for membrane protein preparation, is used for immunogen preparation, preferably, nonhuman animals made to carry a gene encoding a soluble gp64 and induced to have immunotolerance against gp64 are used as the immunized animals. Herein, nonhuman animals carrying a gene encoding the full-length gp64 may be used as the immunized animals, however, the use of soluble gp64 transgenic animals and such is preferred since they can be widely used, and can be produced efficiently since both males and females are fertile. Therefore, for example, in a preferred embodiment of the present invention, nonhuman animals carrying a gene encoding a soluble gp64 are used as immunized animals, and a budding baculovirus made to express a membrane protein as the target antigen is used as the immunogen to carry out the immunizations.
By using the antibody-production methods of the present invention, the inhibitory effect on the acquisition of antibodies against a target antigen due to contamination of membrane proteins as background antigens can be suppressed. Consequently, the use of this invention enables sufficient application of the advantages of a baculovirus expression system as an exogenous protein expression system, even in the preparation of immunogens.
Well-known methods can be used for the methods of immunizing to obtain antibodies. Animals can be immunized with an immunogen using known methods. General methods comprise injecting a sensitizing antigen into a mammal by subcutaneous or intraperitoneal injection. Specifically, an immunogen is diluted with an appropriate volume of Phosphate-Buffered Saline (PBS), physiological saline, or such and as desired, the suspension is mixed with an appropriate volume of a conventional adjuvant. This is emulsified and administered to the mammals. For example, Freund's complete adjuvant can be used as an adjuvant. In addition, after this, an immunogen that has been mixed with an appropriate volume of Freund's incomplete adjuvant is preferably administered several times every four to 21 days. In this way immunization occurs, and the increased level of a desired antibody in the serum can be confirmed using conventional methods.
An increase in the level of a desired antibody in the serum is confirmed, blood is collected from the immunized mammals, and the serum is separated. As polyclonal antibodies, serum comprising polyclonal antibodies can be used. Where necessary, fractions comprising polyclonal antibodies can be isolated from this serum, and this fraction can also be used.
Methods for producing monoclonal antibodies can be combined with the antibody production methods of the present invention. After confirming the increase in the level of the intended antibody in the serum of a mammal that was sensitized by the above-described antigen, the antibody-producing cells are extracted from the mammal and cloned to obtain monoclonal antibodies. Spleen cells and such can be used as antibody-producing cells. Antibody-producing cells can be cloned by cell fusion methods. Mammalian myeloma cells and such can be used as parent cells to be fused with the above-mentioned antibody-producing cells. Even more preferably, myeloma cells that comprise unique auxotrophy or drug resistance can be examples of useful selective markers for fusion cells (hybridoma cells). By basically following the methods known in the art, fusion cells can be obtained from the antibody-producing cells and the myeloma cells described above. Methods for producing monoclonal antibodies by using the cell fusion techniques have been established, for example, by Milstein et al. (Galfre, G. and Milstein, C., Methods Enzymol. (1981) 73, 3-46).
The hybridoma cells produced by cell fusion techniques are selected by culturing in a selective medium. A selective medium is chosen in accordance with the characteristic features and such of the myeloma cells used for the cell fusion. HAT medium (a medium comprising hypoxanthine, aminopterine, and thymidine), for example, can be used as a selective medium. The hybridoma cells are cultured in the HAT medium for a time sufficient to kill all cells other than the intended hybridoma cells (e.g. all non-fused cells). Generally, hybridoma cells can be selected by continuing culture for several days to several weeks. Then, a standard limiting dilution method is carried out to screen and clone the hybridoma cells that produce the subject antibodies.
Subsequently, the hybridoma cells thus obtained can be intraperitoneally transplanted into mice to obtain ascites fluid comprising the monoclonal antibodies. Monoclonal antibodies can also be purified from the ascites fluid. For example, monoclonal antibodies can be purified by ammonium sulfate precipitation methods, protein A or protein G columns, DEAE ion exchange chromatography, or affinity columns coupled with a target antigen.
Monoclonal antibodies obtained in this way can also be made into recombinant antibodies produced using gene recombination technologies (for example, see Borrebaeck, C. A. K. and Larrick, J. W., Therapeutic Monoclonal Antibodies, UK, Macmillan Publishers Ltd., 1990). Recombinant antibodies are produced by cloning the DNAs that encode them from antibody-producing cells, such as hybridomas and antibody-producing sensitized lymphocytes, then incorporating these DNAs into a suitable vector, and introducing this vector into a host.
Furthermore, antibody fragments and modified antibodies can be obtained by combining antibody alteration and modification techniques with the antibody production method of the present invention. For example, an antibody fragment can be an Fab, F(ab′)2, Fv, or a single chain Fv (scFv) where the Fvs of an H chain and L chain are linked by a suitable linker (Huston, J. S. el al., Proc. Natl. Acad. Sci. U.S.A., (1988) 85, 5879-5883). Antibodies bound to various molecules such as polyethylene glycols (PEG), can also be used as the modified antibodies. Such modified antibodies can be obtained by chemically modifying the obtained antibodies. These methods have already been established in the art.
The methods for producing antibodies of the present invention can be combined with modification techniques used for human antibodies. Human antibodies of interest can be obtained by using transgenic animals carrying the complete repertoire of human antibody genes as a basis (see International Patent Application Publication Nos. WO 93/12227, WO 92/03918, WO 94/02602, WO 94/25585, WO 96/34096, and WO 96/33735), introducing a gene encoding a soluble form of a background antigen, making them carry the ability to produce human antibodies and the immunotolerance against the background antigen, and immunizing them with a desired antigen.
The antibodies obtained by the methods of the present invention can be chimeric antibodies comprising non-human antibody-derived variable regions, derived from the immunized animals, and human antibody-derived constant regions. In addition, they can also be humanized antibodies comprising complementarity determining regions (CDRs) of non-human antibodies derived from the immunized animals and the framework regions (FRs) and constant regions derived from human antibodies. These modified antibodies can be produced using known methods. Specifically, for example, a chimeric antibody is an antibody comprising the antibody heavy chain and light chain variable regions of an immunized animal, and the antibody heavy chain and light chain constant regions of a human. A chimeric antibody can be obtained by (1) ligating a DNA encoding a variable region of an immunized animal-derived antibody to a DNA encoding a constant region of a human antibody; (2) incorporating this into an expression vector; and (3) introducing the vector into a host for production of the antibody.
A humanized antibody, which is also called a reshaped human antibody, is a modified antibody. A humanized antibody is constructed by transplanting a complementarity determining region (CDR) of an antibody derived from an immunized animal, into the CDR of a human antibody. Conventional genetic recombination techniques for the preparation of such antibodies are known.
Specifically, a DNA sequence designed to ligate a mouse antibody CDR with a human antibody framework region (FR) is synthesized by PCR, using several oligonucleotides constructed to comprise overlapping portions at their ends. A humanized antibody can be obtained by (1) ligating the resulting DNA to a DNA which encodes a human antibody constant region; (2) incorporating this into an expression vector; and (3) introducing the vector into a host to produce the antibody (see, European Patent Application Publication No. EP 239,400, and International Patent Application Publication No. WO 96/02576). Those human antibody FRs that are ligated via the CDR, such that the CDR forms a favorable antigen-binding site, are selected. As necessary, amino acids in the framework region of an antibody variable region may be substituted such that the CDR of a reshaped human antibody forms an appropriate antigen-binding site (Sato, K. et al., Cancer Res. (1993) 53, 851-856).
Furthermore, genes coding for the antibodies can be obtained from the antibody-producing cells of an immunized animal. Methods used to obtain genes that code for antibodies are not limited. For example, genes coding for antibodies can be obtained by amplification using the PCR method, by using as templates those genes that code for variable regions or CDRs. Primers for the amplification of genes that code for antibodies are known in the art. Subject antibodies can be produced by expressing genes thus obtained in an appropriate expression system. Alternatively, the genes obtained by the present invention can be utilized to produce various modified antibodies (chimeric antibodies comprising human antibody-derived constant regions and humanized antibodies in which the CDRs of an immunized animal-derived antibody is transplanted to the CDRs of a human antibody).
The present invention provides systems for antibody production that comprise nonhuman animals carrying a gene encoding a soluble form of a membrane protein.
When an immunogen is prepared using a viral expression vector, in certain cases, membrane proteins derived from that virus or from host cells into which the viral expression vector has been introduced may contaminate as background antigens. These background antigen membrane proteins are not products of the exogenous target antigen gene, and in most cases, they are derived from the expression system, such as from the vector or host. Therefore, the background antigen membrane proteins that may contaminate are identified for every expression system. Then, a gene encoding a soluble form of this membrane protein is introduced into nonhuman animals by transgenic techniques, and whether immunotolerance against the membrane protein has been induced is confirmed in the obtained transgenic animals. Whether or not immunotolerance has been induced in the nonhuman animals can be confirmed as indicated in the Examples, by confirming the production of antibodies against the background antigen membrane protein in the serum.
Because the background antigen membrane protein is expressed in its soluble form, the expression of unfavorable phenotypes, such as the loss of fertility in males observed with the baculovirus gp64, is avoided in these nonhuman animals in which the induction of immunotolerance against the background antigen has been confirmed; such animals may thus be provided as widely useful animals to be immunized. Therefore, systems that can support efficient antibody production can be constructed by combining the animals to be immunized that carry a gene encoding a soluble form of a membrane protein of the present invention with an expression system that produces this membrane protein as a background antigen.
For example, by combining a baculovirus expression system described in detail above with nonhuman animals carrying a gene encoding a soluble gp64, the advantages of a baculovirus expression system can be reflected in antibody production. More specifically, in a baculovirus expression system, desired proteins, particularly membrane proteins, can be expressed as target antigens along with gp64 while maintaining their three-dimensional structure, and the expression products can be easily collected as budding viruses. These budding viruses are used as the immunogens and immunization is performed on the nonhuman animals carrying a gene encoding a soluble gp64 as the immunized animals. Since immunotolerance against gp64 is induced in these nonhuman animals carrying a gene encoding a soluble gp64, even if a large amount of gp64 is expressed on the budding virus serving as the immunogen, antibody production against this gp64 is suppressed and antibodies against the membrane protein serving as the target antigen can be produced. Therefore, even when gp64 is present on a baculovirus as a background antigen, by using nonhuman animals carrying a gene encoding a soluble gp64, antibody production against the target antigen can be favorably induced. As a result, the antibodies obtainable by the present system will be extremely pure antibodies against the target antigen.
All prior art references cited herein are incorporated by reference into this description.
The transmembrane region (nucleotides 1465 to 1539) was deleted from the gp64 gene (SEQ ID NO: 1; full length: 1539 bp) to prepare by PCR a gene fragment comprising only the extracellular region (soluble gp64; 1464 bp; SEQ ID NO: 3).
More specifically, a 5′ primer in which the 5′-terminal sequence of gp64, the restriction enzyme EcoRI recognition sequence, and a KOZAK sequence are linked (64F1: 5′-GAATTCCACCATGGTAAGCGCTATTGTT-3′; SEQ ID NO: 5); a 3′ primer in which the EcoRI recognition sequence is 5′-end linked to the sequence immediately before the transmembrane region of gp64 (s64R1: 5′-GAATTCTCATTATACATGACCAAACATGAACGA-3′; SEQ ID NO: 6) (FIG. 1-a and FIG. 1-b); and the pCAG-gp64 vector serving as a template DNA were used, and a polymerase chain reaction (PCR) was performed under the following conditions: the composition of the PCR reaction solution was 5 μL of 10× ExTaq buffer (TaKaRa), 4 μL of dNTP mixture comprised in the ExTaq kit, 1 μL of 64F1 primer (10 μmole/L), 1 μL of s64R1 primer (10 μmole/L), 1 μL of pCAG-gp64 (500 pg/μL), 0.5 μL of ExTaq (5 units/μL, TaKaRa), and 37.5 μL of H2O. The reaction was carried out by heating at 94° C. for five minutes, and then performing 25 cycles of 94° C. for 15 seconds, 57° C. for 30 seconds, and 72° C. for 30 seconds. The mixture was then treated at 72° C. for seven minutes, and stored at 4° C. The amplified band was subcloned into pGEM-Teasy (Promega) and E. coli (DH5α, TOYOBO) were transformed with this. Colony PCR was performed using the T7 primer (5′-TAATACGACTCACTATA-3′, SEQ ID NO: 7) and SP6 primer (5′-CATACGATTTAGGTGACACTATAG-3′, SEQ ID NO: 8), the nucleotide sequences of clones found to carry the insert were analyzed with an ABI Prism 377 DNA sequencer using the BigDye Cycle Sequence kit (Applied Biosystems) and the T7 primer or the SP6 primer, and a clone carrying the desired gene was confirmed. The fragment comprising gp64 was cut out from this clone by EcoRI restriction enzyme treatment, inserted into pCAGGS vector treated with the restriction enzyme EcoRI, and E. coli (DH5α) were transformed with this. The direction of insertion of the gp64 fragment was determined from the size of the band (approximately 2.1 kb) obtained by XhoI and XbaI restriction enzyme treatment and the pCAG-sgp64 vector was produced (
A DNA injection fragment for use in Tgm production was prepared by treating the pCAG-sgp64 vector with the restriction enzymes SalI and PstI, then cutting out the fragment comprising the sgp64 gene (approximately 3.7 kb), collecting the fragment using a Gel Extraction Kit (QIAGEN), and then diluting this fragment to 3 ng/PL using PBS. Mouse pronuclear stage embryos into which the DNA fragment was to be inserted were collected as follows: BALB/cA female mice (Japan Clea) were subjected to superovulation treatment (5 IU of eCG (Serotropin, Teikoku Zoki) was administered intraperitoneally, and 48 hours later, 5 IU of hCG (Puberogen, Sankyo) was administered intraperitoneally), and then mated with male mice of the same strain (Japan Clea). The next morning, the oviducts of female mice found to have a vaginal plug were perfused to collect the pronuclear stage embryos. The DNA fragment was injected into pronuclear stage embryos using a micromanipulator (“Modern Techniques in Gene Targeting” (Yodosha), 190-207, 2000). The following day, embryos that had developed to the two-cell stage were transplanted into the left and right oviducts of one-day pseudopregnant recipient females at ten or so embryos per oviduct (20 or so embryos per individual). Recipient females that did not deliver litters by the expected delivery date were subjected to caesarian section and the pups were nursed by foster parents.
Based on the above methods, the DNA fragment was injected into 497 BALB/cA pronuclear stage mice embryos, and of these the 430 that developed into two-cell stage embryos were transplanted into the oviducts of pseudopregnant recipient females. As a result, 66 pups were obtained. Gene introduction into the obtained pups was confirmed as described below.
The mouse tails were collected and treated at 55° C. overnight with Lysis buffer (50 mM Tris-HCl pH 8.0, 0.1 M NaCl, 20 mM EDTA, 1% SDS, Proteinase K 1 mg/mL; TaKaRa). Genomic DNA was then extracted using an automatic nucleic acid isolation system (KURABO, NA-1000P), and the introduced gene was confirmed by Southern blotting and PCR. Confirmation of the introduced gene by Southern blotting was performed by treating the extracted genomic DNA (15 μg) with the restriction enzyme EcoRI, electrophoresing in an agarose gel, and transferring onto a nylon membrane (Hybond N+; Amersham) by the alkaline blotting method. An approximately 1.5 kb restriction enzyme EcoRI-treated fragment of the pCAG-sgp64 vector comprising sgp64 was used as a probe. This was labeled with 32p and Southern blotting was performed by hybridizing it with the blotted genomic DNA. Hybridization was carried out overnight at 45° C. using 5× SSPE, 50% formamide, 5× Denhardt, and 0.5% SDS as the hybridization solution. The nylon membranes were washed in 2× SSC containing 0.1% SDS at 65° C. for 30 minutes, and then in 1× SSC containing 0.1% SDS at 65° C. for 30 minutes. Thereafter, signals were detected using BAS2000 (FUJIX).
Confirmation of the introduced gene by PCR was carried out using the above-mentioned 64F1 as the sense primer, and the above-mentioned s64R1 as the antisense primer, under the following conditions: the composition of the PCR reaction solution was 1 μL of genomic DNA (100 ng/μL), 5 μL of 10× ExTaq buffer (TaKaRa), 4 μL of dNTP mixture comprised in the ExTaq kit, 1 μL of 64F1 primer (10 μmole/L), 1 μL of s64R1 primer (10 μmole/L), 0.5 μL of ExTaq (5 units/μL, TaKaRa), and 37.5 μL of H2O. The reaction was carried out by heating at 94° C. for five minutes, and then performing 35 cycles of 94° C. for 15 seconds, 57° C. for 30 seconds, and 72° C. for 30 seconds; subsequently, the mixture was treated at 72° C. for seven minutes, and then stored at 4° C. The amplified product was subjected to electrophoresis, and the presence or absence of a band of approximately 1.5 kb was verified.
This method confirmed that three of the 66 pups were Tgm carrying the sgp64 gene (hereinafter, Tgm obtained by inserting the DNA fragment will be referred to as “founder mice”) (Table 1). One of the three founder mice was male, and the other two were female.
When eight weeks old, the obtained founder mice were mated with BALB/cA mice. Specifically, of the three founder mice, 26 pups were obtained by mating the male founder mouse (line number 41) with five females, and of these pups, 12 were Tgm (F1 mice). Nine of the 16 pups obtained from the first female founder mouse (line number 36) were Tgm (F1 mice, including males and females), and four of these were males (Table 2). Eight of the 15 pups obtained from the other female founder mouse (line number 51) were Tgm (F1 mice, including males and females), and one of these was a male (Table 2).
The fertility of the male Tgm (F1 mice) obtained in Example 2 was examined. Fertility was confirmed by mating eight-week-old male sgp64Tgm (F1 mice) with BALB/cA mice, and confirming the presence and number of pups.
Male Tgm (F1 mice) obtained from each of the three founder lines (one animal from each line) were mated with two females to give nine pups (five females, four males), nine pups (two females, seven males), and ten pups (six females, four males) respectively, and of these, nine pups (five females, four males), eight pups (two females, six males), and five pups (four females, one male) were Tgm (Table 3). The male Tgm in all three lines were confirmed to have normal fertility.
To confirm induction of tolerance to gp64, sgp64Tgm were immunized with a budding baculovirus (pepT1-AcMNPV (pepT1-BV)), as set out below.
Immunization was carried out by producing an emulsion according to standard methods using Freund's complete adjuvant (Difco) and incomplete adjuvant (Difco), and administering it subcutaneously. The first immunizing dose was 1 mg/animal, and the second immunizing dose was 0.5 mg/animal. The second immunization was carried out 14 days after the first. After 17 days from the first immunization, blood was sampled from the orbit, and serum was collected. As controls, non-transgenic mice were immunized similarly, and their sera were collected.
The following Western blot analysis was carried out to confirm tolerance to gp64 in the Tgm:
pepT1-BV used as the antigen was subjected to SDS-PAGE at 1 μg/lane using a 12% gel and under reducing conditions. After electrophoresis, electroblotting onto a PVDF membrane was carried out. The serum collected above was diluted to 1/1000, and reacted with this membrane, which was then washed three times for five minutes at room temperature using PBS-T (PBS containing 0.05% Tween20). After washing, biotin-anti-mouse IgG(y) (Zymed) diluted to 1/1000, and streptavidin-alkaline phosphatase (Zymed) were reacted with the membrane. Alkaline Phosphatase Staining Kit (Nakalai) was used for staining.
In the case of non-transgenic mice (non-Tgm), staining with anti-mouse IgG resulted in strong staining for all three mice (
The present invention provided new transgenic animals that overcome the problem of male infertility, which existed in conventional transgenic animals into which the gene for the baculovirus membrane protein gp64 had been introduced. The above-mentioned problem was solved by expressing a soluble gp64 (that is, expressing gp64 outside the cell membrane), which was prepared by methods such as deleting a sequence encoding the transmembrane region from the gene encoding the gp64 membrane protein. Therefore, the emergence of unfavorable phenotypes, such as the unfavorable characteristic of male infertility in transgenic animals into which a gene encoding a full-length membrane protein has been introduced, can be avoided in transgenic animals into which a gene encoding a soluble form of the membrane protein has been introduced, as in the present invention.
As described above, just as for transgenic animals into which genes encoding a full-length membrane protein had been introduced, transgenic animals into which genes encoding a soluble protein had been introduced have been confirmed to have induced immunotolerance to the membrane protein. Therefore, when the immunogens have contaminating membrane proteins as background antigens, it is advantageous to use, as animals to be immunized, the transgenic animals which carry genes encoding soluble proteins that lack a transmembrane region, and such, of these membrane proteins as exogenous genes. That is, since immunotolerance against background antigen membrane proteins is induced, antibodies specific to the desired antigen are produced advantageously, and since unfavorable phenotypes of transgenic animals into which the full-length membrane protein has been introduced can be avoided in these immunized animals, they will be utilized even more readily as systems for antibody production.
The antibodies produced using the animals of the present invention are not contaminated or very slightly contaminated by antibodies against background antigens, and they are therefore provided as highly pure antibodies.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2004-107669 | Mar 2004 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2005/006298 | 3/31/2005 | WO | 00 | 6/26/2007 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2005/094572 | 10/13/2005 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 5500346 | Bright et al. | Mar 1996 | A |
| 5849525 | Hediger | Dec 1998 | A |
| 6270978 | Bright et al. | Aug 2001 | B1 |
| 6713278 | Bouvier et al. | Mar 2004 | B1 |
| 20050004227 | Saitoh | Jan 2005 | A1 |
| 20050222391 | Kodama et al. | Oct 2005 | A1 |
| 20050281825 | Kodama et al. | Dec 2005 | A1 |
| 20060084119 | Saitoh et al. | Apr 2006 | A1 |
| 20060210569 | Kodama et al. | Sep 2006 | A1 |
| Number | Date | Country |
|---|---|---|
| 9676557 | Jun 1997 | AU |
| 1142473 | Oct 2001 | EP |
| 1 514 928 | Mar 2005 | EP |
| 1 731 032 | Dec 2006 | EP |
| 6-261761 | Sep 1994 | JP |
| 8-134100 | May 1996 | JP |
| 11-000172 | Jan 1999 | JP |
| 2001-197846 | Jul 2001 | JP |
| 2001-139496 | May 2005 | JP |
| 1999-0071666 | Sep 1999 | KR |
| WO 9719919 | Jun 1997 | WO |
| WO 9846777 | Oct 1998 | WO |
| WO 0028016 | May 2000 | WO |
| WO 03033024 | Apr 2003 | WO |
| WO 03047621 | Jun 2003 | WO |
| WO 03083116 | Oct 2003 | WO |
| WO 03104453 | Dec 2003 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20080040820 A1 | Feb 2008 | US |
