JPH0821834A - Screening method for alimentary canal disease and kit thereof - Google Patents

Abstract

PURPOSE:To detect an alimentary canal disease with high accuracy by measuring only the lactoferrin having the molecular weight of the normal size in feces. CONSTITUTION:The lactoferrin of pH2, lactoferrin after reacting on pepsin, or lactoferrin of the normal size is not digested so well, and the tendency is remarkable when it reacts on pepsin which is the digesting enzyme of a stomach in particular, and there is a large possibility that the lactoferrin incompletely digested in the stomach appears in feces. It is considered that higher accuracy is attained when only the lactoferrin having the molecular weight of about 80000 in feces is measured for detecting the disease of a small intestine or a large intestine. Enzyme immunoassay is used for the measuring method. When a monoclonal antibody not reacting on the lactoferrin in the feces exposed to about pH2 or the lactoferrin after reacting on pepsin and reacting on the lactoferrin having the normal molecular weight is selected for use, an alimentary canal disease can be detected more surely.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for detecting gastrointestinal tract diseases with high accuracy and an antibody therefor, and more particularly to a method for detecting gastrointestinal tract diseases using a monoclonal anti-human lactoferrin antibody.

[0002]

2. Description of the Related Art The applicant has already applied for a screening method for colorectal cancer and its kit (Japanese Patent Application No.
No. 194089), a method for reliably detecting colorectal cancer or colorectal polyps using lactoferrin or myeloperoxidase in feces as a measurement target is proposed. In this invention, the lactoferrin concentration in feces is measured by the ELISA method using a polyclonal anti-human lactoferrin antibody.

[0003]

[Problems to be Solved by the Invention and Items to be Solved] However, when the lactoferrin concentration of each of the fecal samples classified by the molecular weight by the gel filtration method was measured, the results shown in FIG. 1 were obtained. The issue is how to evaluate. That is, according to FIG. 1, in addition to lactoferrin having a molecular weight of less than 80,000, the presence of lactoferrin having a molecular weight of about half thereof is remarkably observed in the fecal samples of patients with various digestive tract diseases. Therefore, the present inventor diligently studied what the meaning of the presence of lactoferrin having a molecular weight of about half is as follows.

First, the filtration pattern of lactoferrin extracted from leukocytes was examined using the same gel filtration method as described above. The result is as shown in FIG.
It is confirmed that the presence of lactoferrin having a molecular weight of about half is not recognized in neutrophil-derived lactoferrin as much as in FIG. Therefore, it is necessary to study the relationship between the gel filtration patterns of FIG. 2 and FIG. Therefore, next, what kind of change was observed in fecal lactoferrin when its pH was changed was examined. That is, a stool liquid of a healthy person containing no lactoferrin was prepared, purified lactoferrin was added thereto to change the pH to 6, 4 and 2, and each was examined by a gel filtration method. The results are shown in FIG. 3, and it was revealed that the presence of lactoferrin having a molecular weight of about half becomes more prominent as the acidity increases.

[0005] In order to examine how lactoferrin is digested by pepsin, which is a gastric digestive enzyme, the stool fluid of healthy humans was prepared, and purified lactoferrin was added thereto to act on pepsin. The thing was examined by the gel filtration method. The result is shown in Figure 4.
It was confirmed that only those having a molecular weight of half were remarkably observed. From the results of FIGS. 3 and 4 described above, it was revealed that the presence of lactoferrin having a half molecular weight was remarkably observed in the case where the acidity was about pH 2 and pepsin acted. Since there is no place where pepsin acts or the acidity increases in the small intestine or later, the results of FIGS. 3 and 4 show that lactoferrin in saliva is digested halfway in the stomach and is excreted in feces. It is speculated that it may have appeared.

Therefore, the concentration of lactoferrin in saliva was measured. OraSure (Epitope, Inc. Beaverton,
1.75 times diluted saliva with TBS
Dilute 10 times with (0.1mol, pH8.0) and finally 17.5
Lactoferrin was measured by the ELISA method using a double-diluted saliva as a sample. According to the result, healthy person 2
Lactoferrin concentration in saliva of 0 (7 men, 13 women) was 6.5 ± 3.3 μg / ml (mean ± SD), maximum 1
0.8 and a minimum of 2.4 μg / ml. Since the amount of saliva secreted is 1000 to 1500 ml per day, about 10 mg of lactoferrin per day is supplied to the digestive tract from the above-mentioned concentration of lactoferrin in saliva. on the other hand,
As shown in Japanese Patent Application No. 5-194089, the normal upper limit of the lactoferrin concentration in the feces of healthy subjects is 2.4 μg.
/ G stool (= 0.5mg / 200g stool)
When the results of FIG. 1 are examined based on this value, it is more strongly conjectured that the lactoferrin having a small molecular weight may be one in which the lactoferrin in saliva could not be digested in the stomach.

[0007] FIG. 5 is a graph showing the results of investigating to what extent various proteins are digested by pepsin which is a gastric digestive enzyme. That is, each protein was dissolved in 0.01 N-HCl at a rate of 2500 ng / ml, and pepsin (S
(igma) is added at a final concentration of 0.01 mg / ml and the results are shown at 25 ° C. As is clear from FIG.
Transferrin, albumin, and hemoglobin
It is confirmed that lactoferrin is difficult to be digested, although it is digested by pepsin in 10 minutes. FIG. 6 is a graph showing the results of examining the extent to which various proteins are digested by trypsin, which is a small intestinal digestive enzyme.
That is, 2500 ng / m of each protein was added to 0.1M-TBS.
Dissolve at a ratio of 1 and add trypsin (Sigma) to a final concentration of 1 m.
The results obtained by adding g / ml and operating at 37 ° C are shown.
As shown in FIG. 6, it is confirmed that hemoglobin and albumin are digested, but lactoferrin and transferrin are hardly digested.

FIG. 7 shows lactoferrin adjusted to pH 2 and
It is the result of investigating the digested state when trypsin was reacted with lactoferrin after reacting with pepsin and lactoferrin of normal size. In each case, it was confirmed that there was not much digestion, and this tendency was confirmed to be particularly remarkable for lactoferrin after the reaction with pepsin. FIG. 5 described above
~ According to the results of Fig. 7, it is considered possible that lactoferrin digested halfway in the stomach appears in the feces. Therefore, to detect small and large bowel disease,
It is considered that the accuracy is improved when only the lactoferrin in feces having a molecular weight of about 80,000 is measured. This invention has been made based on the above consideration, and reliably detects gastrointestinal tract diseases by measuring only lactoferrin having a normal-sized molecular weight, and
It is intended to provide an anti-human lactoferrin antibody that effectively functions in an immunological assay method such as an enzyme immunoassay.

[0009]

In order to achieve the above-mentioned object, in the present invention, it was decided to screen gastrointestinal tract diseases using only lactoferrin having a normal-sized molecular weight in feces as a measurement target. Although a specific measuring method is not particularly limited, it is preferable to use an immunological measuring method such as an enzyme immunoassay or a latex agglutination reaction method. in this case,
Of the monoclonal antibodies, those that do not react with lactoferrin in feces exposed to about pH 2 or lactoferrin after reacting with pepsin, but react with lactoferrin of normal molecular weight are selected and used for digestion The tube disease can be detected more reliably. In addition, lactoferrin in feces exposed to about pH 2 or a monoclonal anti-human lactoferrin antibody that does not react with lactoferrin after reacting with pepsin, an enzyme-labeled anti-human lactoferrin antibody, and a reagent for measuring the enzyme A screening kit is composed of the above. The enzyme-labeled anti-human lactoferrin antibody corresponds to a monoclonal anti-human lactoferrin antibody or a polyclonal anti-human lactoferrin antibody.

The present invention having the above structure will be described in more detail below. When a splenic lymphocyte of a mouse immunized with human lactoferrin and a myeloma cell of a mouse are fused to produce a monoclonal anti-human lactoferrin antibody-producing hybridoma, the hybridoma shows various characteristics as shown in FIG. Produces cloned anti-human lactoferrin antibody. Therefore, among the produced monoclonal anti-human lactoferrin antibodies, those that do not react with lactoferrin in feces exposed to about pH 2 or lactoferrin after reacting with pepsin, but react with normal-sized lactoferrin are selected. Then, this was designated as the monoclonal antibody according to the present invention (hereinafter referred to as the monoclonal antibody M28). In addition, FIG. 9 shows the polyclonal antibody (DAKO) and the monoclonal antibody M2 according to the present invention.
8 is a diagram showing what kind of characteristic difference 8 and another homemade monoclonal antibody (M267) show in the same sample (feces involved in digestive tract disease).

FIG. 10 shows the reaction characteristics of the polyclonal antibody (DAKO) and the monoclonal antibody M28 to lactoferrin extracted from leukocytes, both of which are shown. It was confirmed that neutrophil-derived lactoferrin reacts similarly.
FIG. 11 shows that the liquid of feces of a healthy person is prepared, and purified lactoferrin is added thereto to change the pH to 8, 6, 4, 2.
The results of investigating the reactivity of the monoclonal antibody M28 against each by gel filtration method are shown in the figure. It is confirmed that the polyclonal antibody (DAKO) also reacts with lactoferrin at pH 2, but the monoclonal antibody M28 shows a different reaction from the polyclonal antibody as the acidity increases.

FIG. 12 shows the monoclonal antibody M28 to half-size lactoferrin after being reacted with pepsin.
And the difference in the reactivity of the polyclonal antibody (DAKO). FIG. 13 illustrates the difference in reactivity between the monoclonal antibody M28 and the polyclonal antibody (DAKO) with respect to fecal samples of patients with colorectal cancer (a), neoplastic colitis (b), and gastric ulcer (c). Monoclonal antibody M
It is confirmed that with 28, only the presence of normal size lactoferrin is detected. FIG. 14 is a graph showing the results of measuring the lactoferrin concentration of 231 healthy subjects using a polyclonal antibody (DAKO) and a monoclonal antibody M28. Cutoff value is 1 when using polyclonal antibody (DAKO)
14 ng / ml, whereas monoclonal antibody M
When 28 is used, the cutoff value is 45n, which is less than half.
Since it is g / ml, it is considered that the detection accuracy is improved by using the monoclonal antibody M28.

[0013]

[Examples] FIGS. 15 to 18 show lactoferrin concentration measurement results (μg / g stool) when a polyclonal antibody (DAKO) and a monoclonal antibody M28 were used for various gastrointestinal diseases, respectively. It was done. As shown in the figure, a clear correlation is observed in the measurement results, and it is confirmed that the detection accuracy is improved by using the monoclonal antibody M28. The monoclonal antibody M
The cutoff value when using 28 is about 1 μg / g stool, and the cutoff value when using the polyclonal antibody (DAKO) is about 2.4 μg / g stool. 15 to 18
The concentration of lactoferrin in Japanese Patent Application No. 5-19
The same ELISA method as that of No. 4089 is used.
Hereinafter, the measurement of lactoferrin using the monoclonal antibody M28 will be described.

Each of microplates (SUMILON, Japan)
Well, 100 μl of 0.1 M Tris buffer containing 5 μg / ml of anti-human lactoferrin antibody (monoclonal antibody M28)
Each of them is dispensed and left overnight at 4 ° C. to physically adsorb and solidify on the surface. Separately, an alkaline phosphatase (Beehringer-Mannheim, FRG) is enzymatically labeled with an anti-human lactoferrin antibody by the periodate method to prepare. 100 for each well
Contains μl of 1% BSA (Beehringer-Mannheim, FRG)
Dispense Tris buffer (0.1mol / l pH8.0), then
Add 50 μl of stool sample, mix, and incubate at 37 ° C. for 1 hour. It is then washed 3 times with deionized water containing 0.05% Tween20. After that, 100 μl of alkaline phosphatase-labeled anti-human lactoferrin antibody solution (Tris buffer containing 1% BSA) was added to each well and mixed,
React at 37 ° C. for 1 hour and wash 3 times as before.

Further, 100 μl of a substrate buffer for the Kind-King method
Is added to each well and reacted at 37 ° C. for 30 minutes. Here, the substrate buffer is Disodium Phenyl-phosphate (WAKO Junya
ku Japan) 0.215g and 4-aminoantipyrine (WAKO Junyaku
Made in Japan) 0.09g, carbonate buffer (0.05mol / l pH 10.1)
5) It was dissolved in 100 ml. Next, 100 μl of coloring solution is added to each well to develop the color. Here, the coloring liquid is 20
2.6 ml boric acid (WAKO Junyaku Jap) in 0 ml deionized water
0.38 g of Potassium ferricyani
It is a solution of de (made by WAKO Junyaku Japan). Finally, the color of each well is measured by a colorimeter (Sank
o Junyaku Japan) and colorimetrically compare with 510 / 680nm wavelength light, and calculate the lactoferrin concentration in feces from the calibration curve. When mice are injected with human lactoferrin, they make antibodies. Therefore, lymphocytes taken from the mouse spleen are fused with mouse myeloma cells to form hybridomas. Then, this hybridoma produces a large amount of the desired monoclonal antibody. on the other hand,
The polyclonal antibody is a purified antibody produced by injecting human lactoferrin into rabbits.

[0016]

Industrial Applicability As described above, the screening method according to the present invention uses the immunological assay method in which only lactoferrin having a normal-sized molecular weight in feces is used as the assay target. As shown, colon cancer, colon polyps, Crohn's disease, neoplastic colitis, etc. can be detected more reliably.

[Brief description of drawings]

FIG. 1 is a diagram showing the reactivity of a polyclonal anti-human lactoferrin antibody to the gel filtration fraction of fecal lactoferrin in cases of colorectal cancer, neoplastic colitis, and gastric ulcer.

FIG. 2 illustrates a gel filtration pattern of neutrophil-derived lactoferrin.

FIG. 3 shows changes in stool lactoferrin from pH 2 to pH 6.

FIG. 4 shows changes in lactoferrin upon digestion with pepsin.

FIG. 5 shows the state of digestion of various proteins with pepsin.

FIG. 6 shows the digestion state of various proteins with trypsin.

FIG. 7 shows digestion of lactoferrin with trypsin.

FIG. 8 shows the reactivity of the monoclonal antibody with the gel fraction of lactoferrin in feces.

FIG. 9 shows the reactivity of a polyclonal antibody and a monoclonal antibody against lactoferrin in feces.

FIG. 10 shows the reactivity of neutrophil-derived lactoferrin with an anti-human lactoferrin antibody.

FIG. 11 shows the reactivity of lactoferrin in pH-adjusted feces juice with an anti-human lactoferrin antibody.

FIG. 12 shows the reactivity of anti-human lactoferrin antibody against pepsin-digested lactoferrin.

FIG. 13 shows the reactivity of anti-human lactoferrin antibody against the fecal lactoferrin gel filtration fraction in cases of colon cancer, neoplastic colitis and gastric ulcer.

FIG. 14 shows the results of determining the cutoff value of the lactoferrin concentration from a healthy subject group using the monoclonal antibody M28 and the polyclonal antibody.

FIG. 15 shows the lactoferrin concentration of colorectal cancer patients obtained using the monoclonal antibody M28 and the polyclonal antibody.

FIG. 16 shows the lactoferrin concentration of colon polyp patients, using the monoclonal antibody M28 and the polyclonal antibody.

FIG. 17 shows the lactoferrin concentration in patients with Crohn's disease, using the monoclonal antibody M28 and the polyclonal antibody.

FIG. 18 shows the lactoferrin concentration of a patient with neoplastic colitis determined using the monoclonal antibody M28 and the polyclonal antibody.

Claims (5)

[Claims] 1. A method for screening a gastrointestinal tract disease, which comprises measuring only lactoferrin having a normal molecular weight in feces as a measurement target. 2. The method for screening a digestive tract disease according to claim 1, wherein an immunological measurement method such as an enzyme immunoassay or a latex agglutination method is used. 3. A monoclonal anti-human lactoferrin antibody that does not react with lactoferrin in feces exposed to about pH 2 or lactoferrin after reacting with pepsin is used. The method for screening a digestive tract disease according to the description. 4. A monoclonal anti-human lactoferrin antibody that does not react with lactoferrin in feces exposed to about pH 2 or lactoferrin after reacting with pepsin, an enzyme-labeled anti-human lactoferrin antibody, and the enzyme assay A screening kit comprising at least a reagent for measuring gastrointestinal tract diseases by measuring the lactoferrin concentration in feces by an immunological assay method. 5. A monoclonal anti-human lactoferrin antibody used for the purpose of detecting gastrointestinal tract diseases using an immunological assay method after reacting with lactoferrin or pepsin in feces exposed to about pH 2. Anti-human lactoferrin antibody that does not react with lactoferrin.