Patent Application
20210148932
The present invention relates to a method for measuring serum amyloid A (hereafter, referred to as “SAA”) of various animals and a reagent for measurement thereof.
SAA is a precursor protein of amyloid A protein that is deposited in tissue upon amyloidosis, which is a serum protein with a molecular weight of approximately 12,000 (Non-Patent Document 1). The serum concentration of SAA is known to increase in inflammatory diseases other than amyloidosis, and SAA is thus recognized as a sensitive inflammation marker (Non-Patent Document 2).
Also, SAA is known to serve as an important inflammation marker in animal species other than humans (Non-Patent Documents 3 to 7).
For example, Patent Document 1 discloses an apparent correlation between the SAA protein level in a milk sample obtained from the breast of a lactating mammal (e.g., bovine) and the inflammatory response level of the breast tissue (i.e., mastitis). Patent Document 2 discloses that infectious diseases can be distinguished from noninfectious causes of diseases based on the SAA concentration in a blood sample obtained from a mammal (e.g., horse) showing abnormal symptoms or actions.
For example, Patent Document 3 discloses a monoclonal antibody that specifically binds to human SAA, and Patent Document 4 discloses a monoclonal antibody that specifically binds to equine SAA. In the past, however, no reagents capable of measuring SAA derived from various animal species including humans involving the use of monoclonal antibodies were known.
Under the above circumstances, it is an object of the present invention to provide a reagent that can measure SAA derived from various animal species.
The present inventors have conducted concentrated studies in order to attain the above objects. As a result, they found an animal species cross-reactive monoclonal antibody that recognizes SAA derived from various animal species from among anti-human SAA monoclonal antibodies. This has led to the completion of the present invention.
Specifically, the present invention includes the following.
(1) A method for immunologically measuring SAA comprising a step of measuring SAA using a reagent for measuring SAA obtained from a plurality of animal species comprising an animal species cross-reactive anti-SAA monoclonal antibody or a fragment thereof.
(2) The method according to (1), wherein the animal species cross-reactive anti-SAA monoclonal antibody or a fragment thereof binds to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 or a region in the vicinity of a corresponding amino acid residue in other mature SAA protein.
(3) The method according to (2), wherein the epitope is amino acid residues in the 80th to the 90th positions from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 or corresponding amino acid residues in other mature SAA protein.
(4) The method according to any one of (1) to (3), wherein the plurality of animal species are a plurality of animal species selected from the group consisting of a human, a bovine, a dog, a cat, a rabbit, a horse, a monkey, a pig, a sheep, a donkey, and a mouse.
(5) The method according to any one of (1) to (4), wherein the method for immunological measurement is the latex turbidimetric immunoassay.
(6) A reagent for measuring SAA obtained from a plurality of animal species comprising an animal species cross-reactive anti-SAA monoclonal antibody or a fragment thereof.
(7) The measurement reagent according to (6), wherein the animal species cross-reactive anti-SAA monoclonal antibody or a fragment thereof binds to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 or a region in the vicinity of a corresponding amino acid residue in other mature SAA protein.
(8) The measurement reagent according to (7), wherein the epitope is amino acid residues in the 80th to the 90th positions from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 or corresponding amino acid residues in other mature SAA protein.
(9) The measurement reagent according to any one of (6) to (8), wherein the plurality of animal species are a plurality of animal species selected from the group consisting of a human, a bovine, a dog, a cat, a rabbit, a horse, a monkey, a pig, a sheep, a donkey, and a mouse.
(10) An animal species cross-reactive anti-SAA monoclonal antibody or a fragment thereof binding to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 or a region in the vicinity of a corresponding amino acid residue in other mature SAA protein.
(11) The antibody or a fragment thereof according to (10), wherein the epitope is amino acid residues in the 80th to the 90th positions from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 or corresponding amino acid residues in other mature SAA protein.
(12) The antibody or a fragment thereof according to (10) or (11), wherein the animal species are a plurality of animal species selected from the group consisting of a human, a bovine, a dog, a cat, a rabbit, a horse, a monkey, a pig, a sheep, a donkey, and a mouse.
(13) A reagent for measuring SAA obtained from an animal comprising the antibody or a fragment thereof according to any one of (10) to (12).
This description includes part or all of the content as disclosed in the description and/or drawings of Japanese Patent Application No. 2017-124578, which is a priority document of the present application.
With the use of the reagent for measuring SAA according to the present invention, SAA, which is an inflammation marker for various animal species, can be easily detected or measured.
Hereafter, the present invention is described in detail.
The reagent for measuring SAA obtained from a plurality of (i.e., 2 or more) animal species according to the present invention (hereafter, referred to as “the reagent for measuring SAA according to the present invention”) comprises an animal species cross-reactive anti-SAA monoclonal antibody or a fragment thereof. The animal species cross-reactive anti-SAA monoclonal antibody or a fragment thereof used in the present invention (hereafter, referred to as “the monoclonal antibody or a fragment thereof according to the present invention”) is a monoclonal antibody capable of recognizing SAA derived from various animal species and binding to such protein or a fragment thereof. With the use of the method for measuring SAA and a reagent for measuring SAA thereof according to the present invention, SAA as an inflammation marker in various animal species can be immunologically measured.
Examples of SAA that the monoclonal antibody or a fragment thereof according to the present invention can recognize include SAA derived from animal species, such as a human, a bovine, a dog, a cat, a rabbit, a horse, a monkey, a pig, a sheep, a donkey, and a mouse.
The monoclonal antibody or a fragment thereof according to the present invention preferably binds to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 (e.g., amino acid residues in the 76th to the 94th positions from the N terminus, in particular, amino acid residues in the 80th to the 90th positions from the N terminus) or a region in the vicinity of a corresponding amino acid residue in other mature SAA protein. The monoclonal antibody or a fragment thereof according to the present invention that binds to such epitope exhibits high binding property to SAA obtained from a plurality of animal species. A region of amino acid residues in other mature SAA protein (e.g., a mature SAA protein derived from an animal species other than a human) corresponding to a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 to which the monoclonal antibody or a fragment thereof according to the present invention binds as an epitope can be determined via, for example, alignment comparison between the amino acid sequence of the mature human SAA1 protein and the amino acid sequence of other mature SAA protein in accordance with a conventionally known method.
The monoclonal antibody according to the present invention may be of any immunoglobulin (Ig) class (e.g., IgA, IgG, IgE, IgD, IgM, or IgY) and any subclass (e.g., IgG1, IgG2, IgG3, IgG4, IgA1, or IgA2). The immunoglobulin light chain may be a κ chain or λ chain.
Examples of the monoclonal antibody fragment according to the present invention include Fab, Fab′, F(ab′)2, Fv, Fd, and Fabc. Methods for preparing such fragments are known in the art. For example, such fragments can be obtained by digestion of antibody molecules with a protease such as papain or pepsin or via a known genetic engineering technique.
The monoclonal antibody according to the present invention can be obtained by preparing hybridomas from antibody-producing cells obtained from non-human mammals immunized with antigens (human SAA) (e.g., spleen cells or lymphatic cells) and myeloma cells via fusion, proliferating the obtained hybridomas in a selection medium containing hypoxanthine, aminopterin, and thymidine (“HAT medium”), cloning cells producing monoclonal antibodies exhibiting specific affinity to the antigens used for immunization (human SAA) or fragment peptide antigens thereof (e.g., a peptide antigen comprising a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1), obtaining anti-human SAA monoclonal antibody-producing cell lines, proliferating the anti-human monoclonal antibody-producing cells in the mouse abdominal cavity, and purifying the antibody from the resulting ascites fluid. Examples of nonhuman mammals include rodents such as mice and rats. Myeloma cells derived from the same animal as the immunized animals are preferably used, and examples thereof include mouse myeloma cells and rat myeloma cells. Antibody-producing cells can be fused to myeloma cells with the use of polyethylene glycol (PEG) or via electrical fusion.
The prepared monoclonal antibody can be purified by a method known in the art, such as chromatography using a protein A or a protein G column, ion exchange chromatography, hydrophobic chromatography, salting out with ammonium sulfate, gel filtration, or affinity chromatography, in adequate combination.
The present invention also relates to a method for immunologically measuring SAA comprising a step of measuring SAA using the reagent for measuring SAA according to the present invention. Specifically, SAA in a biological sample derived from various animal species is brought into contact with the monoclonal antibody or a fragment thereof according to the present invention in the reagent for measuring SAA according to the present invention to cause an antigen-antibody reaction, and SAA in the sample is detected or measured based on the formed immune complex.
A biological sample that comprises or may comprise SAA is sufficient, and examples thereof include whole blood, serum, plasma, urine, puncture fluid, sweat, saliva, lymph, and spinal fluid samples.
Examples of methods for immunological measurement include: single radial immunodiffusion comprising observing the expression of a precipitate line formed by an immune complex resulting from binding of the monoclonal antibody or a fragment thereof according to the present invention to SAA in the biological sample on an agar plate; enzyme immunoassay (EIA) or radioimmunoassay involving the use of the monoclonal antibody or a fragment thereof according to the present invention labeled with an enzyme or radioactive isotope; and use of an insoluble carrier comprising the monoclonal antibody or a fragment thereof according to the present invention immobilized thereon. Examples of insoluble carriers include particles such as latex particles (such as polyethylene or polystyrene particles), alumina particles, silica particles, gold colloid particles, and magnetic particles. Among such insoluble carriers, latex particles are preferable, and polystyrene latex particles are particularly preferable.
Insoluble carrier particles are preferably of 50 to 500 nm in diameter, and more preferably of 75 to 350 nm in diameter.
An antibody or a fragment thereof can be immobilized on an insoluble carrier in accordance with a conventional technique. Specifically, an antibody or a fragment thereof is mixed with an insoluble carrier, and an antibody or a fragment thereof is allowed to physically adsorb to the insoluble carrier surface. Thus, an antibody or a fragment thereof can be immobilized on the insoluble carrier.
When an insoluble carrier comprising an amino or carboxyl group introduced on its surface is used, an antibody or a fragment thereof can be immobilized on the insoluble carrier surface via a chemical bond involving the use of a glutaraldehyde or carbodiimide reagent.
Examples of methods involving the use of insoluble carriers include: a latex turbidimetric immunoassay involving the use of latex particles comprising the monoclonal antibody or a fragment thereof according to the present invention immobilized thereon; gold colloid-based agglutination colorimetry involving the use of gold colloid particles comprising the monoclonal antibody or a fragment thereof according to the present invention immobilized on gold colloids; and immunochromatographic assays involving the use of the monoclonal antibody or a fragment thereof according to the present invention labeled with metal colloids and a capture antibody that captures an immune complex of the monoclonal antibody or a fragment thereof according to the present invention and SAA on a membrane such as nitrocellulose membrane. According to the latex turbidimetric immunoassay, specifically, latex particles comprising the monoclonal antibody or a fragment thereof according to the present invention immobilized on the latex are allowed to react with SAA in a biological sample, and SAA is measured based on agglutination of latex particles as a result of formation of the immune complex and changes in turbidity caused by latex agglutination. According to immunochromatographic assays, a biological sample is supplied onto a membrane such as nitrocellulose membrane, SAA in the biological sample reacts with the monoclonal antibody or a fragment thereof according to the present invention in a label-reagent-retaining region that retains the monoclonal antibody or a fragment thereof according to the present invention labeled with metal colloids or the like to form an immune complex, the immune complex migrates on the membrane by the capillary action, the immune complex is captured by a capture antibody immobilized in a given position on the membrane, and SAA is detected based on the color developed as a result of the capturing.
As described above, the reagent for measuring SAA according to the present invention is used for a method for immunologically measuring SAA. When the method for immunological measurement involves the use of an insoluble carrier, for example, the reagent for measuring SAA according to the present invention can contain an insoluble carrier comprising the monoclonal antibody or a fragment thereof according to the present invention immobilized thereon, such as a latex solution containing latex particles. When immunochromatographic assays are performed, the reagent for measuring SAA according to the present invention can be used for an immunochromatographic device composed of an insoluble carrier comprising the monoclonal antibody or a fragment thereof according to the present invention immobilized thereon, such as gold colloids, and a membrane such as nitrocellulose membrane comprising the monoclonal antibody or a fragment thereof according to the present invention immobilized thereon (e.g., a membrane such as nitrocellulose membrane supported on a carrier comprising a sample supply region, a label-reagent-retaining region that retains the monoclonal antibody or a fragment thereof according to the present invention labeled with metal colloids or the like, and a detection region comprising a capture antibody immobilized on a given position).
In addition to the monoclonal antibody or a fragment thereof according to the present invention, the reagent for measuring SAA according to the present invention can comprise a buffer that imparts a pH level necessary for immunological reaction, a reaction enhancer that accelerates immunological reaction, a reaction stabilizer or blocker that suppresses non-specific reaction, a preservative that improves storage stability of a reagent, such as sodium azide, and the like.
Examples of buffers include the following.
Good's buffers:
Among such buffers, Good's buffers, such as HEPES and PIPES, adjust a pH level to an advantageous level for the immunological reaction. In addition, the influence thereof imposed on proteins is small. Thus, such buffers are particularly preferable. A pH level necessary for the immunological reaction is 5 to 11, and it is preferably 6 to 9.
As a reaction enhancer, for example, polyethylene glycol and dextran sulfate are known. In addition, BSA (bovine serum albumin), animal serum, IgG, IgG fragments (Fab and Fc), albumin, milk protein, amino acid, polyamino acid, choline, a polysaccharide such as sucrose, gelatin, degraded gelatin, casein, a polyhydric alcohol such as glycerin, and the like are known to effectively stabilize the reaction or inhibit the non-specific reaction in the immunological reaction in the form of reaction stabilizers or blockers.
The reagent for measuring SAA according to the present invention comprising various components described above can be supplied in a liquid or dry state. In order to realize distribution of the reagent in a liquid state, the reagent may further be supplemented with, for example, various surfactants, saccharides, or inactive proteins, so as to improve protein stability. Such stabilizers are also effective as stabilizers or excipients when drying the reagent.
Hereafter, the present invention is described in greater detail with reference to the Examples, although the technical scope of the present invention is not limited to these Examples.
In the Comparative Examples and the Examples below, epitopes of the mature human SAA1 protein (the amino acid sequence as shown in SEQ ID NO: 1) to which monoclonal antibodies bind are as described below:
Clone 17: a region in the vicinity of the amino acid residue in the 30th position from the N terminus;
Clone 14: a region in the vicinity of the amino acid residue in the 15th position from the N terminus;
Clones 15 and 18: a region in the vicinity of the amino acid residue in the 90th position from the N terminus; and
Clones 21 and 25: unknown, although an epitope for Clone 21 is deduced to be the same as that for Clone 15 etc. based on reactivity with bovine SAA.
Whether or not bovine SAA could be measured using a latex reagent comprising the anti-human SAA polyclonal antibody immobilized on polystyrene latex particles was examined.
The anti-human SAA polyclonal antibody was immobilized on polystyrene latex particles of 130 nm in diameter.
The anti-human SAA polyclonal antibody was immobilized on the polystyrene latex particles in accordance with a conventional technique. Specifically, the anti-human SAA polyclonal antibody was mixed with polystyrene latex, so as to allow the anti-human SAA polyclonal antibody to physically adsorb on the polystyrene latex surface. Thus, the anti-human SAA polyclonal antibody was immobilized on the polystyrene latex particles.
Bovine plasma specimens sampled with time before and after surgery were measured by using the above latex reagent with the Hitachi 7170S automatic analyzer (Hitachi High-Technologies). Specifically, 2.0 μl of the plasma specimen was mixed with 100 μl of the first reagent (50 mM HEPES buffer, pH 7.4), the mixture was incubated at 37° C. for 5 minutes, 100 μl of the second reagent (a polyclonal antibody-immobilized latex solution containing 10 mM HEPES buffer, pH 7.4) was added thereto, the reaction was allowed to proceed at 37° C., and changes in the absorbance were measured at the dual wavelength of 800/570 nm (sub wavelength/main wavelength) for approximately 5 minutes after the second reagent was added.
The SAA concentration in the plasma specimens was calculated from the calibration curve obtained by measuring the sample with known SAA concentration.
The SAA concentration in the bovine plasma specimens sampled with time before and after surgery was 0.62 to 1.72 mg/l, which was below the measurement range of the SAA reagent prepared with the polyclonal antibody (5 to 500 mg/l) (
The SAA reagent prepared with the use of the anti-human SAA polyclonal antibody exhibited low reactivity with bovine SAA, and, accordingly, bovine SAA could not be measured. While bovine SAA could be measured via EIA involving the use of the polyclonal antibody as described in Example 1, it could not be measured via the latex turbidimetric immunoassay.
The monoclonal antibody reacting with bovine SAA was screened.
The bovine plasma specimens sampled before and after surgery were immobilized on a microplate (antigen immobilization), the anti-human SAA polyclonal antibodies and the anti-human SAA monoclonal antibodies (Clones 14, 15, 17, 18, 21, and 25 shown in Table 1 of Patent Document 3) were allowed to react therewith, and reactivity was then examined via EIA in which the POD-labeled anti-rabbit IgG antibody or the POD-labeled anti-rat IgG antibody was allowed to react.
Concerning reactivity with the bovine plasma specimens at 2 days after surgery, the reactivity of Clone 18 was the highest, followed by Clone 21, Clone 15, and the polyclonal antibody in descending order, and no difference was observed in reactivity of other clones before and after surgery (
It was confirmed that the anti-human SAA polyclonal antibody reacted with the bovine plasma while the reaction level was low and the monoclonal antibodies (Clone 17 and Clone 25) did not react with the bovine plasma specimens at the acute stage. Among the monoclonal antibodies used for screening, 3 monoclonal antibody clones (Clone 18, Clone 21, and Clone 15) that would react with the bovine plasma specimens at the acute stage were identified.
The latex reagents for measuring animal SAA were examined.
Latex reagents were prepared with the use of the anti-human SAA monoclonal antibody (Clone 15) and polystyrene latex particles of 130 nm in diameter or of 220 nm and 80 nm in diameter, and the dilution series of serum specimens with known SAA concentration and bovine, dog, and cat serum specimens were measured. As a comparative example, the measurement with commercially available LZ test “Eiken” SAA (Eiken Chemical Corporation) was also carried out.
The anti-human SAA monoclonal antibody was immobilized on the polystyrene latex particles in accordance with a known method. Specifically, the anti-human SAA monoclonal antibody was mixed with polystyrene latex, so as to allow the anti-human SAA monoclonal antibody to physically adsorb on the polystyrene latex surface. Thus, the anti-human SAA monoclonal antibody was immobilized on the polystyrene latex particles.
The dilution series of serum specimens with known SAA concentration (human SAA) and bovine, dog, and cat serum specimens were measured with the use of the Hitachi 7170S automatic analyzer (Hitachi High-Technologies). Specifically, 2.0 μl of the serum specimen was mixed with 100 μl of the first reagent (50 mM HEPES buffer, pH 7.4), the mixture was incubated at 37° C. for 5 minutes, 100 μl of the second reagent (a monoclonal antibody-immobilized latex solution containing 10 mM HEPES buffer, pH 7.4) was added thereto, the reaction was allowed to proceed at 37° C., and changes in the absorbance were measured at the dual wavelength of 800/570 nm (sub wavelength/main wavelength) for approximately 5 minutes after the second reagent was added.
The SAA concentration in the bovine, dog, and cat serum specimens were calculated from the calibration curve obtained by measuring the sample with known SAA concentration.
3-1. Reagent Preparation with Monoclonal Antibody
The monoclonal antibody (Clone 15) was immobilized on two types of latex particles (i.e., particles of 220 nm in diameter and particles of 80 nm in diameter), and a latex reagent (SAA-M) comprising these two 2 types of latex particles at 2:1 was prepared.
With the use of the monoclonal antibody (Clone 15) binding to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1, SAA latex reagents reacting with SAA obtained from a bovine, a dog, and a cat can be prepared.
Whether or not SAA of various animal species could be measured with the use of the monoclonal antibody (Clone 15) binding to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 was examined.
SAA in various animal species was measured using the latex reagent immobilizing the monoclonal antibody (Clone 15) (animal SAA reagent).
As a comparative example, measurement was carried out in the same manner with the use of the LZ test “Eiken” SAA (LZ-SAA) described in Example 2. An animal species (rabbit) that would not react with the LZ test “Eiken” SAA (LZ-SAA) was subjected to measurement of CRP that would be elevated in case of inflammatory diseases as with SAA for reference.
The animal SAA reagent was prepared in the same manner as in Example 2 except for the use of polystyrene latex particles of 215 nm in diameter.
SAA in various animal specimens was measured with the use of the Hitachi 7170S automatic analyzer (Hitachi High-Technologies). Specifically, 3.0 μl each of various specimens was mixed with 100 μl of the first reagent (50 mM HEPES buffer, pH 7.4), the mixture was incubated at 37° C. for 5 minutes, 100 μl of the second reagent (a monoclonal antibody-immobilized latex solution containing 10 mM HEPES buffer, pH 7.4) was added thereto, the reaction was allowed to proceed at 37° C., and changes in the absorbance were measured at wavelength of 600 nm for approximately 5 minutes after the second reagent was added.
The SAA concentration in various animal specimens was calculated from the calibration curve obtained by measuring the sample with known SAA concentration.
While SAA could not be measured in the comparative example (the LZ test “Eiken” SAA) (below the measurement sensitivity), SAA in specimens obtained from various animals (i.e., a bovine, a horse, a monkey, a donkey, a sheep, a pig, a mouse, and a rabbit) could be measured with the use of the animal SAA reagent (the monoclonal antibody (Clone 15) binding to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1; corresponding to “the reagent for measuring SAA according to the present invention”).
With the use of the animal SAA reagent (the monoclonal antibody (Clone 15)), SAA in various animal species can be measured.
The monoclonal antibodies obtained from Clone 18 and Clone 21 binding to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 were examined as to whether or not SAA in various animal specimens could be measured as with the case of the monoclonal antibody of Clone 15.
Various animal serum samples obtained from a human, a cat, a dog, a horse, a bovine, a monkey, a capybara, and a mouse were immobilized on a microplate (antigen immobilization), the anti-SAA monoclonal antibodies obtained from Clone 15, Clone 18, and Clone 21 were allowed to react therewith, and reactivity was then examined via EIA in which the POD-labeled anti-rat IgG antibody was allowed to react.
The results of measurement are shown in
With the use of “the monoclonal antibody of Clone 18 that binds to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 according to the present invention” and “the monoclonal antibody of Clone 21 that binds to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 according to the present invention,” SAA in various animal specimens could be measured as with the use of “the monoclonal antibody of Clone 15 that binds to SAA by recognizing, as an epitope, a region in the vicinity of an amino acid residue in the 90th position from the N terminus of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 according to the present invention.” As shown in the chart shown in
It was suggested that the monoclonal antibody of Clone 18 and the monoclonal antibody of Clone 21 exhibit equivalent properties as the monoclonal antibody of Clone 15.
The amino acid sequences of the mature human SAA1 protein consisting of the amino acid sequence as shown in SEQ ID NO: 1 to which the monoclonal antibodies obtained from Clone 15, Clone 18, and Clone 21 would bind as epitopes were examined.
As shown in Table 1 and
Subsequently, the anti-SAA monoclonal antibodies obtained from Clone 15, Clone 18, and Clone 21 were allowed to react with the peptides on the arrays, and the biotin-labeled goat anti-rat IgG antibody was then allowed to react therewith. Thereafter, fluorescence-labeled streptavidin was allowed to react with the arrays, and reactivity of anti-SAA monoclonal antibodies to the peptides was examined.
Positive controls shown in Table 1 and
Biotin-BSA: biotin-labeled BSA was immobilized on glass slides instead of a peptide derived from a mature human SAA1 protein; and
Rat IgG (Raybiotech): biotin-labeled goat anti-rat IgG antibody was immobilized on glass slides instead of a peptide derived from a mature human SAA1 protein.
The results are shown in
As shown in
The anti-SAA monoclonal antibodies obtained from Clone 15, Clone 18, and Clone 21 sufficiently bound to Peptides #7 to #11. Accordingly, it was suggested that such antibodies bind to the mature human SAA1 protein by recognizing, as an epitope, the amino acid sequence common among Peptides #7 to #11 (QAANEWGRSGK: SEQ ID NO: 14) (
All publications, patents, and patent applications cited herein are incorporated herein by reference in their entirety.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2017-124578 | Jun 2017 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2018/024114 | 6/26/2018 | WO | 00 |
