Patent Application
20090111122
The present invention relates to a method for non-invasively testing non-alcoholic steatohepatitis, and a test kit used for the method.
Chronic liver diseases shift to chronic hepatitis, liver cirrhosis, and finally hepatoma. The major cause thereof is hepatitis C virus or hepatitis B virus infection. In addition, non-alcoholic steatohepatitis (NASH), showing pathological conditions characterized by alcoholic hepatitis-like tissue images, behind which fatty liver lies, without evident drinking history, comes to attract attentions in recent years, and it has also been elucidated that non-alcoholic steatohepatitis progresses to liver cirrhosis and hepatoma.
For the pathology of non-alcoholic steatohepatitis, the two hit theory is estimated, that is, following fatty change of the liver as the first step (first hit), hepatocellular damage (apoptosis) and fibrosis are induced by addition of various stresses as the second step (second hit). Strong correlation of non-alcoholic fatty liver diseases (NAFLDs) including non-alcoholic steatohepatitis with insulin resistance syndromes such as obesity, diabetes and hyperlipidemia is evident, and they are the commonest hepatic diseases in the United States with being supposed that 70% of pycnic types are complicated by fatty liver. Furthermore, since it has been reported that 10% of advanced pycnic types (BMI>30) suffer from non-alcoholic steatohepatitis, it is estimated that 250,000 or more of non-alcoholic steatohepatitis patients exist also in Japan.
At present, hepatitis C virus infection accounts for a little less than about 80% of the causes of onset of hepatoma, and non-alcoholic steatohepatitis accounts for only several percents of the same (Non-patent document 1). However, in contrast to the estimation that onset risk of hepatoma due to hepatitis C virus infection would be decreased in future by screening of blood for transfusion for hepatitis C virus, and development of diagnostic agents for hepatitis C and therapeutic agents for the same such as interferons, hepatoma due to non-alcoholic steatohepatitis is expected to increase also in Japan with increase of insulin resistance syndrome patients due to westernization of the dietary habits.
However, since any specific marker does not exist for non-alcoholic steatohepatitis, it is currently inevitable for diagnosis thereof to use pathological diagnosis based on invasive liver biopsy.
Non-patent document 1: Bugianesi E et al., Gastroenterology, 2002, 123:134-140
An object of the present invention is to develop a method and kit for non-invasive test of non-alcoholic steatohepatitis.
It is considered that hepatocellular damages (apoptosis) induced by various stresses added to fatty liver is involved in non-alcoholic steatohepatitis (Ribeiro P S et al., Am. J. Gastroenterol., 2004 September, 99(9):1708-17).
The inventors of the present invention considered that the stress-dependent hepatocellular damages (apoptosis) arising in non-alcoholic fatty hepatitis could be evaluated on the basis of blood cytochrome c level, as the measurement of apoptosis arising in the living bodies of liver haemophagocytic syndrome (HPS), GVHD, acute lymphatic leukemia and influenzal encephalitis patients disclosed in WO01/35093.
Then, they found that blood cytochrome c levels quantified for non-alcoholic steatohepatitis patients were higher than those for healthy persons, and that the quantified blood cytochrome c values correlated with fat deposition rates in hepatocytes, and accomplished the present invention.
The present invention thus relates to the followings.
[1] A test method for non-alcoholic steatohepatitis, which comprises the step of quantifying cytochrome c in collected blood.
[2] The test method for non-alcoholic steatohepatitis according to [1], which comprises:
(1) the step of quantifying cytochrome c in blood, and
(2) the step of identifying non-alcoholic steatohepatitis when quantified value of cytochrome c is high.
[3] The test method according to [1] or [2], wherein the step of quantifying cytochrome c in blood is a step of quantifying cytochrome c by using an antibody against cytochrome c.
[4] The test method according to [3], wherein the step of quantifying cytochrome c by using an antibody against cytochrome c is a step comprising reacting cytochrome c in blood and the antibody against cytochrome c in an acidic region.
[5] A test kit for non-alcoholic steatohepatitis, which comprises a reagent for quantifying cytochrome c in blood by using an antibody against cytochrome c.
[6] The test kit according to [5], which comprises a buffer solution for reacting cytochrome c in blood and the antibody against cytochrome c in an acidic region.
Hereafter, embodiments of the present invention will be explained in detail.
In this specification, blood means blood, plasma or serum collected from a living body.
As the method for measuring cytochrome c, immunochemical method, electrophoresis, chromatography, and so forth can be contemplated, and an immunochemical method is preferred in view of sensitivity and simplicity.
The immunochemical method referred to herein is a method for quantifying cytochrome c by using an antibody against cytochrome c. The immunochemical method include various methods such as the competitive method in which cytochrome c is labeled, the sandwich method in which the antibody is labeled and the latex bead method in which aggregation of antibody-coated beads is observed, and any immunochemical method may be used for the present invention so long as a method using an antibody against cytochrome c is chosen. The antibody may be a monoclonal antibody or a polyclonal antibody. The labeling method also includes various methods such as labeling with a radioactive isotope, labeling with an electrochemiluminescent compound, labeling with fluorescence, labeling with an enzyme and labeling with biotin, and the present invention is not limited to any one of these examples. The methods for preparing and labeling antibodies are described in, for example, Lecture of Biochemical Experiment Second Series, vol. 5, Methods for Immunobiochemical Research (edited by Japanese Biochemical Society, published by Tokyo Kagaku Dojin), and Lecture of Biochemical Experiment New Edition, vol. 12, Molecular Immunology III (edited by Japanese Biochemical Society, published by Tokyo Kagaku Dojin).
As an example of the immunochemical method for quantifying cytochrome c, the sandwich method will be explained below in the order of the steps thereof.
1) Antibodies against cytochrome c are immobilized on beads or cup. The antibodies to be immobilized may be either polyclonal antibodies or monoclonal antibodies, so long as antibodies providing required sensitivity, preferably sensitivity enabling measurement of 0.5 ng/mL, more preferably 0.1 ng/mL, of cytochrome c are chosen. As the monoclonal antibodies, commercially available antibodies such as Clone: 6H2.B4 (Becton Dickinson) and Clone: 2B5F8 (TECHNE) may be used. The beads may be micro beads, and in such a case, micro beads consisting of magnetic substance are preferred. The immobilization may be attained by either covalent bond or non-covalent bond. In order to block nonspecific bonding sites on the beads or cup, a blocking treatment is usually performed with a protein such as bovine serum albumin (BSA) and casein or a surfactant such as Tween 20.
2) A sample is added to the beads or cup after the sample is diluted with a buffer solution containing a protein such as BSA and casein or a surfactant such as Tween 20, if necessary. Cytochrome c of a known amount is similarly diluted and added.
3) After washing the beads or cap with a buffer solution containing a surfactant such as Tween 20, if possible, labeled anti-cytochrome c antibodies, diluted with a buffer solution containing a protein such as BSA and casein or a surfactant such as Tween 20, if possible, are added to the beads or cup. As the labeled antibodies, either polyclonal antibodies or monoclonal antibodies may be acceptable, so long as antibodies providing required sensitivity, preferably sensitivity enabling measurement of 0.5 ng/mL, more preferably 0.1 ng/mL, of cytochrome c are used. When the antibodies to be immobilized are monoclonal antibodies, monoclonal antibodies of a clone different from that of the monoclonal antibodies to be immobilized are preferably used for the labeled monoclonal antibodies, and commercially available antibodies such as Clone: 6H2.B4 (Becton Dickinson) and Clone: 2B5F8 (TECHNE) may be used.
4) After the beads or cup is washed with a buffer solution containing a surfactant such as Tween 20, if possible, measurement is performed by a method suitable for the label, i.e., radioactivity is measured when labeling is attained with a radioactive isotope, voltage is applied and luminescence is measured when labeling is attained with an electrochemiluminescent compound, or enzymatic activity is measured when labeling is attained with an enzyme. Further, when labeling is attained with biotin, labeled avidin is further added, and measurement is performed by a method suitable for the label.
5) A calibration curve is prepared by using values measured for samples containing cytochrome c in known amounts, and amount of cytochrome c contained in the sample is calculated by using the calibration curve.
By the aforementioned steps, amount of cytochrome c in the sample can be quantified.
In the method of the present invention, it is preferred that the cytochrome c antibody reacts with the sample containing cytochrome c in an acidic range (under acidic condition). The term “acidic range” used in the present specification means a pH range in which influence of interference substances in the blood or in serum, which influence the binding of an antibody and cytochrome c, is attenuated. Although the influence of interference substances can be reduced by lowering pH, the binding between the antibody and cytochrome c is also weakened at the same time. Therefore, pH for the immunochemical measurement according to the present invention may be determined to be a pH that satisfies the following conditions.
1. Measurement sensitivity enabling quantification of 10 ng/mL, preferably 1 ng/mL, of cytochrome c in a buffer solution can be afforded.
2. A recovery rate of 70% or higher, preferably 80% or higher, more preferably 90% or higher, can be afforded in a spiked recovery test in the presence of a body fluid.
Since the effect of pH on binding of an antibody and cytochrome c varies depending on the antibody used, pH used in the immunochemical measurement method can be determined to be a pH optimal for each particular antibody. The pH is preferably 7 or lower, more preferably 3 to 6, still more preferably 3.5 to 5, even more preferably 3.5 to 4.5.
Hereafter, a method for determining pH used for the immunochemical measurement of the present invention will be shown specifically. However, the method for determining pH is not limited to this example.
Cytochrome c is diluted to 1 to 1000 ng/mL in a buffer solution of pH 3 to 7.5 containing appropriate proteins such as BSA, appropriate salts such as NaCl, appropriate surfactants and so forth as required. When the immunochemical measurement method is a sandwich method, the diluted cytochrome c and an immobilized anti-cytochrome c antibody are reacted, after washing, a labeled anti-cytochrome c antibody is added, and the labeling substance is detected based on an activity corresponding to the labeling substance, such as radioactivity in the case of radioactive labeling and enzymatic activity in the case of enzyme labeling.
When a signal obtained from a specimen containing 10 ng/mL, preferably 1 ng/mL, of cytochrome c is sufficiently stronger than that of a specimen not containing cytochrome c but comprising a buffer solution alone, the used pH can be mentioned as a candidate pH of the buffer solution used for the immunochemical measurement method.
When cytochrome c in a body fluid corresponding to a specimen used in the immunochemical measurement method, for example, serum, is measured, a known amount of cytochrome c is added to the serum. The amounts of cytochrome c in serum to which cytochrome c is added and serum to which cytochrome c is not added are measured by the immunochemical method, and the ratio of the measured value to the theoretical value is obtained as a recovery rate.
When the addition amount of cytochrome c is represented by A, the measured value of cytochrome c in serum to which cytochrome c is not added is represented by B, and the measured value of cytochrome c in serum to which cytochrome c is added is represented by C, the recovery rate can be calculated in accordance with either of the following equations:
(1) Measured value (C)/Theoretical value (weighted average of A and B)
(2) Increase in measured value by addition of cytochrome c (C−B)/Addition amount (A)
When the recovery rate is 70% is higher, preferably 80% or higher, more preferably 90% or higher, the pH can be mentioned as a candidate pH of a buffer solution used for the immunochemical measurement method.
Further, in the immunochemical measurement of cytochrome c, a method of using a buffer solution in an acidic range is effective not only for the first reaction in which an immobilized antibody and cytochrome c in a specimen are reacted, but also for the second reaction (the step of reacting cytochrome c and a labeled antibody) when the interference substances cannot be completely removed in the first reaction.
The method of the present invention is not limited to a method of using a buffer solution in an acidic for the first reaction.
The buffer solution used for the reaction of cytochrome c in blood and an antibody against cytochrome c in an acidic range is determined taking 1. influence of pH on measurement sensitivity and 2. influence of pH on added recovery mentioned above into account. Type of the buffer solution is not particularly limited so long as the buffer solution can be prepared to be in an acidic condition, and examples thereof include succinate buffer solution, citrate phosphate buffer solution and so forth.
The present invention also relates to a kit which comprises reagents for quantifying cytochrome c in blood by using an antibody against cytochrome c (cytochrome c measurement reagents), which is used for testing non-alchoholic steatohepatitis. For example, measurement reagents for measuring cytochrome c by a sandwich method as examples of the cytochrome c measurement reagents include, for example, 1) an anti-cytochrome c antibody-coated cup or an anti-cytochrome c antibody coated beads, and 2) a labeled anti-cytochrome c antibody, and preferably further include 3) a standard cytochrome c solution having a known concentration, 4) a diluent, and 5) a washing solution. Further, in the case of using enzyme labeling, the regents may include 6) a substrate for color development, and 7) a solution for terminating the reaction.
The measurement kit of the present invention preferably includes a buffer solution for reacting cytochrome c in blood and an antibody against cytochrome c in an acidic region.
The buffer solution included in the measurement kit of the present invention may be a buffer solution to be used for the reaction as it is or a buffer solution to be diluted before use. Further, it may be a buffer solution adjusted to have a pH in an acidic region suitable for the present invention by adding an acidic or alkaline solution in an appropriate volume, or a buffer solution attached with an instruction describing such pH adjustment.
The method and kit for measurement of cytochrome c disclosed in the present invention can be used for test of non-alcoholic steatohepatitis.
A patient showing a high quantified value of cytochrome c measured by the method and kit for measurement of cytochrome c disclosed in the present invention, usually a patient showing a quantified value exceeding a cutoff value, is identified to be with non-alcoholic steatohepatitis, and the identification can be used as an index for selection of therapies. Although the cutoff value is not particularly limited, so long as non-alcoholic steatohepatitis can be correctly diagnosed, a value deviating by 2SD from average for healthy persons, or 35 ng/mL is usually used.
Cytochrome c level is a favorable index for evaluation of stress-dependent hepatocellular damage, and can serve as a useful clinical test item for quickly and accurately diagnosing non-alcoholic steatohepatitis.
The present invention will be explained more specifically with reference to the following examples. However, the scope of the present invention is not limited by these examples.
Human cytochrome c (TECHNE) in an amount of 110 μg/100 μL and 55 μL of 2 mg/mL ovalbumin dissolved in a 65 mM phosphate buffer solution (pH 7.5) were mixed, to the mixture was added 42 μL of 1 mM glutaraldehyde diluted with a 65 mM phosphate buffer solution (pH 7.5), and the mixture was stirred at room temperature for 2 hours. Then, the mixture was dialyzed against 0.15 M NaCl at 4° C. for 48 hours, an adjuvant was prepared with equal amount of FCA, and 0.1 mL thereof was administered to the peritoneal cavities of BALB/C mice to immunize the mice. The immunization was performed in the same manner 3 times every 2 weeks. Two weeks after the third immunization, 50 μg/100 μL of human cytochrome c dissolved in physiological saline was given to the mice by intravenous injection from the caudal vein. Three days later, the spleens were removed from the mice, and spleen lymphocytes were fused with myeloma cell P3X63 Ag8U.1 according to the polyethylene glycol method in a conventional manner. Screening was performed by using human cytochrome c as an antigen to establish a hybridoma producing a monoclonal antibody against human cytochrome c (clone: 27G9).
The established hybridoma was cultured and proliferated in the S-Clone SF-B medium (Sanko Junyaku Co., Ltd.) and inoculated into the peritoneal cavities of BALB/C mice. After 1 week, ascites was collected. IgG was purified from the collected ascites by using protein A to obtain an anti-cytochrome c antibody (27G9 antibody).
The anti-cytochrome c monoclonal antibody (clone: 2B5F8 (TECHNE)) was dialyzed against a 0.1 M acetate buffer solution (pH 4.2) containing 0.15 M NaCl, and diluted with a 0.1 M acetate buffer solution (pH 4.2) containing 0.15 M NaCl to have an OD 280 nm of 0.56. The diluted antibody in a volume of 1.67 mL was mixed with 3.36 mL of beads (Dynabeads® M-450 Epoxy, Dynal) washed beforehand three times with 3 mL of a 0.1 M acetate buffer solution (pH 4.2) containing 0.15 M NaCl using a magnet, and the mixture was stirred at room temperature for 17 hours. Then, the beads were suspended in 3 mL of a blocking buffer solution (50 mM Tris-HCl, 1% BSA, 0.15 M NaCl, 0.1% NaN3, pH 7.5), and the suspension was stirred at room temperature for 7 hours to block the beads. The blocked beads were washed thrice with 3 mL of 150 mM Tris-HCl, 3% BSA, 0.3% treharose, 0.45 M NaCl, 0.03 vol % Tween 20, 0.3% NaN3, 30 mM EDTA, pH 7.5 and suspended in 12.5 mL of 150 mM Tris-HCl, 0.45 M NaCl, 3% BSA, 0.9% treharose, 0.03 vol % Tween 20, 70 μg/mL mouse IgG, 0.3% NaN3, pH 7.5. This was diluted three times with purified water before use.
The anti-cytochrome c monoclonal antibody prepared in Reference Example 1 (27G9 antibody) was dialyzed against PBS, and the antibody concentration was adjusted to be in the range of 0.5 to 2 mg/mL. To 1 mL of the antibody was added 12.2 μL of a ruthenium complex (ruthenium(II) tris(bipyridyl)-N-hydroxysuccinimide, IGEN Corp. USA) dissolved in dimethyl sulfoxide at a concentration of 10 mg/mL, and the mixture was stirred at room temperature for 30 minutes. Then, to the mixture was added 50 μL of 2 M glycine, and the mixture was stirred at room temperature for 10 minutes. The mixture was applied to a Sephadex G-25 (Amersham Pharmacia Biotec) column (1.5 cm φ×30 cm) equilibrated beforehand with PBS-3 (10 mM potassium phosphate, 0.15 M NaCl, 0.05% NaN3, pH 6) and eluted with PBS-3 to collect 1-mL fractions. The OD of each fraction was measured at 280 nm, and fractions of the first peak were collected to obtain an anti-cytochrome c antibody labeled with a ruthenium complex. The antibody concentration was measured by using Micro BCA Protein Assay Kit (PIERCE).
Standard cytochrome c antigen solutions were prepared by diluting human cytochrome c (TECHNE) with a 0.05 M Tris-HCl buffer solution (pH 7.8) containing 5% BSA, 0.15 M NaCl and 0.1% NaN3 to 3000 ng/mL, 1000 ng/mL, 100 ng/mL, 10 ng/mL and 5 ng/mL.
A solution for diluting samples (0.1 M succinate buffer solution containing 0.15 M NaCl, 15 mM EDTA, 2 volume % Lipidure (registered trademark) BL802 (Nippon Oil & Fats Co., Ltd.), 2 volume % Lipidure (registered trademark) BL405 (Nippon Oil & Fats Co., Ltd.) and 0.1% NaN3, pH 4.0) in a volume of 200 μL was put into a reaction tube for Picolumi® 8220 (Sanko Junyaku Co., Ltd.), and 20 μL of a sample was injected into the tube.
The following measurement was performed by using an electrochemiluminescent enzyme immunoassay apparatus, Picolumi® 8220 (Sanko Junyaku Co., Ltd.).
The anti-cytochrome c antibody-immobilized beads prepared in Reference Example 2 in a volume of 25 μL were added to the reaction tube, allowed to react for 9 minutes, and washed twice with 350 μL of Picolumi® BF washing solution (Sanko Junyaku Co., Ltd.). Then, 200 μL of the ruthenium complex-labeled anti-cytochrome c antibody diluted with the diluent for ruthenium complex-labeled anti-cytochrome c antibody (0.05 M Tris-HCl, 1% BSA, 0.15 M NaCl, 0.3% of trehalose, 0.01 volume % Tween 20, 0.3% NaN3, pH 7.5) prepared in Reference Example 3 to 0.5 to 2 μg/mL were added to the beads, and the reaction was allowed for 9 minutes. The beads were washed twice with 350 μL of Picolumi® BF washing solution, then 300 μL of Picolumi® luminescence electrolytic solution (Sanko Junyaku Co., Ltd.) was added to the beads, and luminescence count value was measured.
The results were plotted with human cytochrome c standard antigen concentrations as abscissa against the luminescence count values of human cytochrome c standard antigen as ordinate to prepare a standard curve, and the amounts of cytochrome c contained in the samples were calculated from the luminescence count values on the basis of the standard curve.
Cytochrome c amounts in serum of healthy persons and non-alcoholic steatohepatitis patients were quantified by using an established ELISA system for cytochrome c.
As a result, as shown in
It was demonstrated that test of non-alcoholic steatohepatitis based on quantified values of serum cytochrome c was possible.
Fat deposition rates in hepatocytes collected from non-alcoholic steatohepatitis patients by biopsy and quantified values of serum cytochrome c in the patients were compared.
The fat deposition rates in the hepatocytes of the patients were calculated from areas of fat deposition in liver tissues collected by biopsy and stained with HE staining (hematoxylin and eosin staining) and AZAN staining. Further, serum cytochrome c levels in the patients were quantified by the method described above. As a result, as shown
It was demonstrated that, by measuring blood cytochrome c, fat deposition in hepatocytes and stress accompanying it can be non-invasively evaluated without biopsy of the liver, and thus blood cytochrome c could serve as a favorable index of non-alcoholic steatohepatitis.
According to the present invention, it became possible to non-invasively diagnose non-alcoholic steatohepatitis by quantifying blood cytochrome c.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2006-105516 | Apr 2006 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP07/57779 | 4/6/2007 | WO | 00 | 11/24/2008 |
