Patent Application
20180259512
The present invention relates to a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, a composition comprising the cell, use of the composition for the diagnosis of thyroid disease, and a method for diagnosing thyroid disease using the composition, etc.
A thyroid stimulating hormone (TSH) produced by the pituitary gland binds to a thyroid stimulating hormone receptor (TSHR) present in the thyroid gland to promote the secretion of a thyroid hormone. Since the thyroid hormone is a hormone that enhances systemic metabolism, abnormal increase or abnormal decrease in the action of this hormone variously affects the mind and body, causing thyroid disease. For example, regarding Graves' disease, a thyroid stimulating antibody (TSAb) is produced in the body, and this antibody, instead of TSH, overstimulates TSHR so that the functions of the thyroid gland are increased and symptoms such as enlargement of the thyroid gland, exophthalmos and tachycardia appear. On the other hand, among hypothyroidisms, there are some diseases in which a thyroid stimulation blocking antibody (TSBAb) is produced so that the functions of the thyroid gland are decreased and symptoms such as a weight gain, depression, and general fatigue appear.
So far, the assay of these autoantibodies (TSAb and TSBAb) contained in blood has been used for the diagnosis of Graves' disease and hypothyroidism.
The representative examples of a method for measuring the autoantibodies have been reported as follows:
a radioreceptor assay method (TBII method) using a radioisotope-labeled TSH or a monoclonal antibody against TSHR, in which said radioisotope-labeled TSH or said monoclonal antibody against TSHR competitively inhibits the binding of the autoantibody in a patient's serum to TSHR so that an amount of the bound autoantibody can be measured; and
a bioassay method (TSAb method) for measuring an amount of TSAb, in which porcine thyroid gland cells or the like are treated with an antibody that binds to TSHR and the amount of TSAb is determined by measuring an increase in the concentration of cAMP in the thyroid gland cells using radioisotope-labeled cAMP (Non Patent Literatures 1 and 2).
Non Patent Literature 1: Methods in Enzymology, 74, 405-420 (1981)
Non Patent Literature 2: J Clin Endocrinol Metab. 1986 May; 62 (5): 855-62
An object of the present invention is to provide a composition for measurement of TSAb and/or TSBAb and a composition for diagnosis of thyroid disease, etc., which can be manipulated more conveniently than conventional methods without a use of a radioisotope that requires special techniques or equipment. Moreover, a further object of the present invention is to provide a method for diagnosing thyroid disease using the composition, etc.
The present inventor used a calcium sensitive protein to measure the amount of calcium ion entry into a cell stimulated by cAMP which is formed by the binding of a thyroid stimulating antibody (TSAb) to a thyroid stimulating hormone receptor (TSHR). As a result, the present inventor has successfully measured the amount of TSAb without using a radioisotope. Furthermore, the present inventor has also successfully measured the amount of a thyroid stimulation blocking antibody (TSBAb) using similar principles, and consequently completed the present invention.
Specifically, the present invention relates to a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, and a composition and a kit comprising the cell.
Moreover, the present invention relates to a composition and a kit for measuring the amount of a thyroid stimulating antibody and/or the amount of a thyroid stimulation blocking antibody in a biological sample, a composition and a kit for diagnosing thyroid disease, a composition and a kit for determining a human having a high risk of developing thyroid disease, or a composition and a kit for determining therapeutic effect on human under treatment of thyroid disease, comprising a cell expressing TSHR, a cAMP dependent calcium channel and a calcium sensitive protein.
Furthermore, the present invention relates to a method for diagnosing thyroid disease, a method for determining a human having a high risk of developing thyroid disease, or a method for determining the effectiveness of treatment of thyroid disease, comprising the following steps (1), (2), and (3) or (1′), (2), and (3):
(1) preparing a mixture containing a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, a luminescent substrate for the calcium sensitive protein, a Ca2+-free medium or a Ca2+/Mg2+-free medium, TSH and a sample derived from the blood of a test subject; or
(1′) preparing a mixture containing a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, a luminescent substrate for the calcium sensitive protein, a Ca2+-free medium or a Ca2+/Mg2+-free medium and a sample derived from the blood of a test subject;
(2) adding a Ca2+-containing solution to the mixture prepared in (1) or (1′); and
(3) measuring the luminescence of the calcium sensitive protein emitted from the cell.
Furthermore, the present invention also relates to a method for diagnosing hypothyroidism, a method for determining a human having a high risk of developing hypothyroidism, or a method for determining the effectiveness of treatment of hypothyroidism, comprising the following steps (1) to (3):
(1) preparing a mixture containing a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, a luminescent substrate for the calcium sensitive protein, a Ca2+-containing medium, TSH and a sample derived from the blood of a test subject;
(2) adding a forskolin-containing solution to the mixture prepared in (1); and
(3) measuring the luminescence of the calcium sensitive protein emitted from the cell.
The present invention eliminates the need of complicated procedures accompanied with use of radioisotopes. Thus, the measurement of the amount of a thyroid stimulating antibody (TSAb) and the amount of a thyroid stimulation blocking antibody (TSBAb) contained in a biological sample and the diagnosis of thyroid disease can be achieved by simple and safe procedures.
The present invention provides a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, and a composition comprising the cell.
The thyroid stimulating hormone receptor (TSHR) can be any receptor to which a thyroid stimulating hormone (TSH) binds, and includes receptors that activate adenylate cyclase to increase cAMP. The origin of TSHR is not particularly limited as long as it is a mammal. The origin can be, for example, a human, a mouse, bovine, a rat or a pig. Moreover, TSHR may have one or several amino acids modified (added, substituted, deleted, etc.) appropriately in the amino acid sequence, or TSHR may be a protein that consists of an amino acid sequence having 70% or more, 80% or more, 85% or more, 90% or more, 95% or more, 98% or more, or 99% or more homology to the amino acid sequence of natural TSHR; binds to TSH; and has the function of increasing cAMP through activation of adenylate cyclase.
TSHR can be a protein having the amino acid sequence represented by SEQ ID NO: 1. Furthermore, TSHR can be a protein that consists of an amino acid sequence having 70% or more, 80% or more, 85% or more, 90% or more, 95% or more, 98% or more, or 99% or more homology to the amino acid sequence represented by SEQ ID NO: 1; binds to TSH; and has the function of increasing cAMP through activation of adenylate cyclase.
Alternatively, TSHR can be a chimeric protein of TSHR with a receptor analogous to TSHR, for example, a corpus luteum hormone receptor, a follicle stimulating hormone receptor or a human chorionic gonadotropin receptor. These chimeric proteins may be prepared by substituting a portion other than amino acid residues 8-89 or 8-165 in TSHR with an appropriate portion of the corpus luteum hormone receptor, the follicle stimulating hormone receptor or the human chorionic gonadotropin receptor. For example, for preparing the TSHR-corpus luteum hormone receptor chimeric protein, amino acid residues 90-165 in TSHR may be substituted with the segment Mc2 of an LH-CG receptor, and amino acid residues 261-370 in the TSHR may further be substituted with the segment Mc4 of the LH-CG receptor.
As used herein, TSH is not particularly limited as long as it is derived from a mammal. TSH can be derived from, for example, a human, a mouse, bovine, a rat, or a pig. TSH may have one or several amino acids modified (added, substituted, deleted, etc.) appropriately in the amino acid sequence, or may be a protein that consists of an amino acid sequence having 70% or more, 80% or more, 85% or more, 90% or more, 95% or more, 98% or more, or 99% or more homology to the amino acid sequence of natural TSH; binds to TSHR; and has the function of increasing cAMP through activation of adenylate cyclase.
The cAMP dependent calcium channel is a channel that changes the amount of calcium ion entry into a cell in response to change in the concentration of cAMP, and includes channels that increase the amount of calcium ion entry into a cell in response to increase in the concentration of cAMP. Examples of the cAMP dependent calcium channel include a CNG (cyclic nucleotide gated ion channel) calcium channel. Optionally, the cAMP dependent calcium channel may have one or several amino acids modified (added, substituted, deleted, etc.) in the amino acid sequence and may be modified (including substituted, added, and deleted) such that it exhibits, for example, higher sensitivity to cAMP than cGMP. The CNG calcium channel can be a protein that consists of an amino acid sequence having 70% or more, 80% or more, 85% or more, 90% or more, 95% or more, 98% or more, or 99% or more homology to the amino acid sequence of the natural CNG calcium channel and increases the amount of calcium ion entry into a cell in response to increase in the concentration of cAMP. Examples of the modification include the substitution of the 460th cysteine in a mouse CNG calcium channel with tryptophan, the substitution of the 583rd glutamic acid in a mouse CNG calcium channel with methionine, the substitution of the 537th threonine in a bovine CNG calcium channel with serine, methionine, valine, or alanine, and combinations thereof. These substitutions exemplified above are not limited to the animal species in which the substitutions are found respectively, and are also applicable to amino acid substitution at corresponding sites in other animal species. For example, threonine in a mouse CNG calcium channel corresponding to the 537th threonine in the bovine CNG calcium channel can be substituted with serine, methionine, valine, or alanine. Such substitution can be performed at one or more position(s). For example, the substitution of the 460th cysteine in the mouse CNG calcium channel with tryptophan is performed, and the substitution of the 583rd glutamic acid with methionine can also be performed.
The CNG calcium channel can consist of an α-subunit and/or a β-subunit. It may be of any constitution, for example, consisting of at least one subunit selected from the group consisting of an α2 subunit, an α3 subunit, an α4 subunit, and a β1b subunit. Furthermore, the subunit may be modified as described above.
The origin of the CNG calcium channel is not particularly limited as long as it is a mammal. The origin can be, for example, a human, a mouse, bovine, a rat or a pig. The CNG calcium channel can be a protein having the amino acid sequence represented by SEQ ID NO: 2. Furthermore, the CNG calcium channel can be a protein that consists of an amino acid sequence having 70% or more, 80% or more, 85% or more, 90% or more, 95% or more, 98% or more, or 99% or more homology to the amino acid sequence represented by SEQ ID NO: 2 and increases the amount of calcium ion entry into a cell in response to increase in the concentration of cAMP.
The calcium sensitive protein includes proteins whose structure is changed in response to calcium, and includes proteins that emit luminescence in response to calcium and proteins that function as a so-called calcium sensor.
Examples of the calcium sensitive protein include aequorin, cameleon (Invitrogen Corp.), Case12 (Evrogen), clytin, obelin, mitrocomin, mineopsin, berovin, a protein comprising two GFPs differing in color, bound to calcium sensitive calmodulin and a partial sequence of myosin light chain kinase binding thereto, a calcium sensitive protein comprising calmodulin bound to between the 144th and 146th residues in the amino acid sequence of GFP, and a protein of probe No. G3-85 or A1-2 described in Japanese Patent Laid-Open No. 2002-153279, and apoproteins thereof, if any, (e.g., apoaequorin).
The amino acid sequence of the calcium sensitive protein may be modified (added, substituted, deleted, etc.) appropriately according to the purpose or may be modified to increase the amount of luminescence and/or to improve an SN ratio. The modification includes the addition, substitution, and deletion of one or several amino acids in the amino acid sequence. The calcium sensitive protein includes proteins that consist of an amino acid sequence having 70% or more, 80% or more, 85% or more, 90% or more, 95% or more, 98% or more, or 99% or more homology to the amino acid sequence of the natural calcium sensitive protein and emit luminescence in response to calcium. For example, the calcium sensitive protein may be modified such that its gene is optimized for human codon usage and it has a mitochondrial targeting signal.
The calcium sensitive protein can be a protein having the amino acid sequence represented by SEQ ID NO: 3. Furthermore, the calcium sensitive protein can be a protein that consists of an amino acid sequence having 70% or more, 80% or more, 85% or more, 90% or more, 95% or more, 98% or more, or 99% or more homology to the amino acid sequence represented by SEQ ID NO: 3 and emits luminescence in response to calcium.
The cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention transiently or stably expresses each of the thyroid stimulating hormone receptor (TSHR), the cAMP dependent calcium channel and the calcium sensitive protein. The cell is not particularly limited and can be a cell line such as a CHO cell, a HEK293 cell, or a 3T3 cell. For example, the cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention can be a CHO cell stably expressing each protein, wherein TSHR has the amino acid sequence represented by SEQ ID NO: 1, the cAMP dependent calcium channel is a modified CNG calcium channel having the amino acid sequence represented by SEQ ID NO: 2 and the calcium sensitive protein is modified apoaequorin having the amino acid sequence represented by SEQ ID NO: 3. Furthermore, the cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention can be, for example, a CHO cell stably expressing TSHR, the cAMP dependent calcium channel and the calcium sensitive protein, each of which is a protein that consists of an amino acid sequence having 70% or more, 80% or more, 85% or more, 90% or more, 95% or more, 98% or more, or 99% or more homology to the amino acid sequence of any one of SEQ ID NOs: 1-3 and maintains the functions of the thyroid stimulating hormone receptor (TSHR), the cAMP dependent calcium channel or the calcium sensitive protein.
Moreover, a cell naturally expressing one or more protein(s) selected from the group consisting of the thyroid stimulating hormone receptor (TSHR), the cAMP dependent calcium channel and the calcium sensitive protein may be used. In this case, the cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention can also be prepared by forcing the cell to transiently or stably express the protein(s) that are not expressed in the cell. Examples of such cell include a thyroid gland-derived cell endogenously expressing the TSHR (e.g., FRTL-5 or Nthy-ori 3-1) that is forced to transiently or stably express each of the cAMP dependent calcium channel and the calcium sensitive protein and an olfactory tissue-derived cell endogenously expressing the CNG calcium channel that is forced to transiently or stably express each of the TSHR and the calcium sensitive protein.
The cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention can be cryopreserved. The cryopreservation can be performed at an appropriate temperature, for example, −20° C. or −80° C., in a cell cryopreservation solution. The cell cryopreservation solution is not limited and includes CELLBANKER® (Nippon Zenyaku Kogyo Co., Ltd.), BAMBANKER® (Lymphotec Inc.), Cellvation® (CELOX LABORATORIES, Inc.), CryoStor® (BIOLIFE SOLUTIONS Ltd.), etc. Cells can be cryopreserved in a large number of the same lot so that a cell-derived measurement error among compositions or kits is drastically reduced. As a result, the reproducibility of measurement results can be improved. Moreover, the cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention maintains sensitivity sufficient for detecting a thyroid stimulating antibody (TSAb) and a thyroid stimulation blocking antibody (TSBAb) present in human blood, even after being cryopreserved and thawed using a warm bath or the like. Moreover, after thawing, the cell is merely transferred into an appropriate container and cultured for approximately 2 hours, and the state of the cell is not deteriorated by a reagent added for detecting TSAb and TSBAb, or by human blood-derived components.
A composition comprising the cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention (e.g., an aqueous solution comprising the cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention) can be used for assaying the amount of a thyroid stimulating antibody and/or the amount of a thyroid stimulation blocking antibody, for diagnosing thyroid disease, for determining a human having a high risk of developing thyroid disease, and/or for determining therapeutic effect on a human under treatment of thyroid disease.
As used herein, the thyroid disease includes hyperthyroidism and hypothyroidism. The hyperthyroidism includes Graves' disease, and the hypothyroidism includes Hashimoto's disease. As used herein, the Hashimoto's disease includes hypothyroidism that is TSBAb-positive in blood, atrophic thyroiditis free from goiter, atrophic thyroiditis caused by TSBAb and myxedema.
The cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein is as described above.
The thyroid stimulating antibody (TSAb) is an antibody capable of acting as a TSHR agonist and can be found in the blood of a Graves' disease patient.
The thyroid stimulation blocking antibody (TSBAb) is an antibody capable of binding to TSHR and acting as a TSHR antagonist and includes, for example, antibodies that competitively inhibit the binding of TSH to TSHR. The thyroid stimulation blocking antibody (TSBAb) can be found in the blood of a hypothyroidism patient, for example, in the blood of a Hashimoto's disease patient.
The thyroid stimulating antibody (TSAb) or the thyroid stimulation blocking antibody (TSBAb) present in a biological sample can be measured by use of the following mechanism of action:
TSAb increases cAMP through the action on TSHR of the cell according to the present invention. As a result, the CNG calcium channel is activated so that calcium entry into the cell is increased. Thus, the calcium sensitive protein emits luminescence. This means that the presence of TSAb in the sample is represented by the luminescence of the calcium sensitive protein as an output.
Upon addition together with TSH, TSBAb competitively inhibits the binding of the TSH to TSHR. As a result, the action of TSH is inhibited to prevent increase in the concentration of cAMP and thereby also prevent CNG calcium channel-mediated increase in calcium entry. Thus, the luminescence of the calcium sensitive protein is reduced. This means that the presence of TSBAb in the sample is represented by the suppression of luminescence of the calcium sensitive protein as an output.
Upon addition together with TSH, TSBAb competitively inhibits the binding of the TSH to TSHR. As a result, the action of TSH is inhibited to prevent increase in the concentration of cAMP. In this case, if TSBAb is absent, the concentration of cAMP is increased by the action of TSH to activate the CNG calcium channel. However, after the given time, the CNG calcium channel is desensitized and thus, does not respond to newly added forskolin (or agent increasing the concentration of cAMP). Accordingly, if TSBAb is absent in the sample, calcium entry into the cell does not occur. This means that the absence of TSBAb is represented by the suppression of luminescence of the calcium sensitive protein as an output. On the other hand, if TSBAb is present in the sample, the CNG calcium channel is not desensitized. Thus, the luminescence of the calcium sensitive protein is not reduced.
In one embodiment of the present invention, use of the composition according to the present invention based on the mechanism of action described above can detect a thyroid stimulating antibody and/or a thyroid stimulation blocking antibody in a biological sample; can compare the concentrations of a thyroid stimulating antibody and/or a thyroid stimulation blocking antibody between two biological samples; or can measure the relative amounts of a thyroid stimulating antibody and/or a thyroid stimulation blocking antibody in two biological samples. Furthermore, use of the composition according to the present invention can also measure the concentrations of a thyroid stimulating antibody and/or a thyroid stimulation blocking antibody in a biological sample.
As used herein, the biological sample includes organism-derived samples such as blood and a sample prepared from blood and includes, for example, human blood, a sample prepared from human blood, canine blood, a sample prepared from canine blood, feline blood, and a sample prepared from feline blood.
Using the composition according to the present invention, one can measure a thyroid stimulating antibody and/or a thyroid stimulation blocking antibody in human blood. Thus, a test subject can be diagnosed as having thyroid disease or not.
When the mechanism of action described above in (1) is used, Graves' disease can be diagnosed using the composition according to the present invention. For example, Graves' disease can be diagnosed by measuring the amount of luminescence of the calcium sensitive protein emitted from the cell treated with a blood sample of a test subject and the amount of luminescence of the calcium sensitive protein emitted from the cell treated with the same amount of a blood sample (standard) of a normal individual as that of the blood sample of the test subject. In this case, when the amount of luminescence emitted from the cell treated with the blood sample of the test subject is higher than that emitted from the cell treated with the blood sample (standard) of the normal individual, the serum concentration of a thyroid stimulating antibody (TSAb) of the test subject can be determined to be higher than that of the normal individual. Thus, the test subject can be diagnosed as Graves' disease.
Moreover, the respective amounts of luminescence (integrated values) emitted from the cells treated with blood samples of a large population of normal individuals, for example, 50 to 100 normal individuals, are measured in advance, and a mean thereof and standard deviation (SD) may be calculated. When the amount of luminescence emitted from the cell treated with a blood sample of a test subject is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the amounts of luminescence (integrated values) emitted from the cells treated with the blood samples of the normal individual population, the serum concentration of a thyroid stimulating antibody of the test subject can be determined to be higher than that of the normal individuals. Thus, the test subject can be diagnosed as Graves' disease.
In the present specification and claims, a value obtained from the “sample derived from the blood of a normal individual” can be, for example, a measured value of a blood sample (standard) of a normal individual or a value obtained in advance from measured values of a normal individual population, unless otherwise specified.
Alternatively, the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a test subject/the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a normal individual×100(%) may be calculated (hereinafter, this calculated value is defined as a calculated value A). The respective amounts of luminescence (integrated values) emitted from the cells treated with respective blood samples of a large population of normal individuals and a large population of untreated Graves' disease patients (e.g., 50 to 100 individuals per population) are measured in advance, and a cutoff value may be set such that a true positive rate of Graves' disease and/or a true negative rate (i.e., being a normal individual) are, for example, 80% or more, 90% or more, 92% or more, 94% or more, 96% or more, or 98% or more, respectively. When the calculated value A is higher than the cutoff value, the test subject can be diagnosed as Graves' disease. The cutoff value can be set appropriately depending on the properties of a target population, such as age and sex and can be set to, for example, 120%, 130%, 140%, 150%, 160%, 170%, 180%, 190%, or 200%.
Furthermore, an antibody (TSAb) standard (e.g., NIBSC 90/672 or 65/122) is also used, and its concentration may be serially diluted to prepare a calibration curve. With reference to the calibration curve, the actual serum concentration of an antibody (TSAb) is calculated from the measured amount of luminescence of the calcium sensitive protein emitted from the cell treated with a blood sample of a test subject. This concentration can be compared with the previously measured serum concentration of an antibody (TSAb) in each of a large population of normal individuals and a large population of untreated Graves' disease patients (e.g., 50 to 100 individuals per population), or known data reported in a document or the like to diagnose the test subject as being Graves' disease or not. For example, when the concentration is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the serum concentrations of (TSAb) of the normal individual population, the test subject can be diagnosed as Graves' disease.
For the measurement of the amount of luminescence, it is preferred to measure the integrated value for the given time. For example, the integrated value can be measured for 5 seconds, 10 seconds, 15 seconds, 20 seconds, 30 seconds, 40 seconds, 50 seconds, or 1 minute.
Moreover, when the mechanism of action described above in (2)(a) is utilized, hypothyroidism (including Hashimoto's disease) can be diagnosed using the composition according to the present invention. For example, hypothyroidism can be diagnosed by measuring the amount of TSH-induced luminescence of the calcium sensitive protein in the cell treated with a blood sample of a test subject and the amount of TSH-induced luminescence of the calcium sensitive protein in the cell treated with the same amount of a blood sample (standard) of a normal individual as that of the blood sample of the test subject. In this case, when the amount of luminescence emitted from the cell treated with the blood sample of the test subject is lower than that emitted from the cell treated with the blood sample (standard) of the normal individual, the serum concentration of a thyroid stimulation blocking antibody (TSBAb) of the test subject can be determined to be higher than that of the normal individual. Thus, the test subject can be diagnosed as hypothyroidism.
Moreover, the respective amounts of TSH-induced luminescence (integrated values) of the calcium sensitive proteins in the cells treated with blood samples of a large population of normal individuals, for example, 50 to 100 normal individuals, are measured in advance, and a mean thereof and standard deviation (SD) may be calculated. When the amount of TSH-induced luminescence from the cell treated with a blood sample of a test subject is lower than the mean−nSD (e.g., n=1, 2, 3, 4, or 5) of the amounts of TSH-induced luminescence (integrated values) from the cells treated with the blood samples of the normal individual population, the serum concentration of a thyroid stimulation blocking antibody (TSBAb) in the test subject can be determined to be higher than that in the normal individuals. Thus, the test subject can be diagnosed as hypothyroidism.
Alternatively, the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a test subject/the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a normal individual×100(%) may be calculated (hereinafter, this calculated value is defined as a calculated value B). The respective amounts of luminescence (integrated values) attributed to respective blood samples of a large population of normal individuals and a large population of untreated hypothyroidism patients (e.g., 50 to 100 individuals per population) are measured in advance, and a cutoff value is set such that a true positive rate of hypothyroidism and/or a true negative rate (i.e., being a normal individual) are, for example, 80% or more, 90% or more, 92% or more, 94% or more, 96% or more, or 98% or more, respectively. When the calculated value B is lower than the cutoff value, the test subject can also be diagnosed as hypothyroidism. The cutoff value can be set appropriately depending on the properties of a target population, such as age and sex and can be set to, for example, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90%.
Furthermore, an antibody (TSBAb) standard having a known concentration is also used, and its concentration may be serially diluted to prepare a calibration curve. With reference to the calibration curve, the actual serum concentration of an antibody (TSBAb) is calculated from the measured amount of TSH-induced luminescence of the calcium sensitive protein in the cell treated with a blood sample of a test subject. This concentration can be compared with the previously measured serum concentration of an antibody (TSBAb) in each of a large population of normal individuals and a large population of untreated hypothyroidism patients (e.g., 50 to 100 individuals per population), or known data reported in a document or the like to diagnose the test subject as hypothyroidism or not. For example, when the concentration is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the serum concentrations of (TSBAb) of the normal individual population, the test subject can be diagnosed as hypothyroidism.
For the measurement of the amount of luminescence, it is preferred to measure the integrated value for the given time. For example, the integrated value can be measured for 5 seconds, 10 seconds, 15 seconds, 20 seconds, 30 seconds, 40 seconds, 50 seconds, or 1 minute.
Moreover, when the mechanism of action described above in (2)(b) is utilized, hypothyroidism (including Hashimoto's disease) can be diagnosed using the composition according to the present invention. For example, hypothyroidism can be diagnosed by measuring the amount of forskolin-induced luminescence of the calcium sensitive protein in the cell treated with a blood sample of a test subject and the amount of forskolin-induced luminescence of the calcium sensitive protein in the cell treated with the same amount of a blood sample (standard) of a normal individual as that of the blood sample of the test subject. In this case, when the amount of luminescence emitted from the cell treated with the blood sample of the test subject is higher than that emitted from the cell treated with the blood sample (standard) of the normal individual, the serum concentration of a thyroid stimulation blocking antibody (TSBAb) of the test subject can be determined to be higher than that of the normal individual. Thus, the test subject can be diagnosed as hypothyroidism.
Moreover, the respective amounts of forskolin-induced luminescence (integrated values) of the calcium sensitive proteins in the cells treated with blood samples of a large population of normal individuals, for example, 50 to 100 normal individuals, are measured in advance, and a mean thereof and standard deviation (SD) may be calculated. When the amount of forskolin-induced luminescence from the cell treated with a blood sample of a test subject is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the amounts of forskolin-induced luminescence (integrated values) from the cells treated with the blood samples of the normal individual population, the serum concentration of a thyroid stimulation blocking antibody (TSBAb) of the test subject can be determined to be higher than that of the normal individuals. Thus, the test subject can also be diagnosed as hypothyroidism.
Alternatively, the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a test subject/the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a normal individual×100(%) may be calculated (hereinafter, this calculated value is defined as a calculated value C). The respective amounts of luminescence (integrated values) attributed to respective blood samples of a large population of normal individuals and a large population of untreated hypothyroidism patients (e.g., 50 to 100 individuals per population) are measured in advance, and a cutoff value is set such that a true positive rate of hypothyroidism and/or a true negative rate (i.e., being a normal individual) are, for example, 80% or more, 90% or more, 92% or more, 94% or more, 96% or more, or 98% or more, respectively. When the calculated value C is higher than the cutoff value, the test subject can also be diagnosed as hypothyroidism. The cutoff value can be set appropriately depending on the properties of a target population, such as age and sex and can be set to, for example, 150%, 200%, 300%, 400%, 500%, 600%, 700%, 800%, or 900%.
Furthermore, an antibody (TSBAb) standard having a known concentration is also used, and its concentration may be serially diluted to prepare a calibration curve. The actual serum concentration of an antibody (TSBAb) is calculated from the measured forskolin-induced luminescence of the calcium sensitive protein in the cell treated with a blood sample of a test subject. This concentration can be compared with the previously measured serum concentration of an antibody (TSBAb) in each of a large population of normal individuals and a large population of untreated hypothyroidism patients (e.g., 50 to 100 individuals per population), or known data reported in a document or the like to diagnose the test subject as hypothyroidism or not. For example, when the concentration is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the serum concentrations of (TSBAb) of the normal individual population, the test subject can be diagnosed as hypothyroidism.
For the measurement of the amount of luminescence, it is preferred to measure the integrated value for the given time. For example, the integrated value can be measured for 5 seconds, 10 seconds, 15 seconds, 20 seconds, 30 seconds, 40 seconds, 50 seconds, or 1 minute.
Moreover, a human having a high risk of developing thyroid disease, for example, a human having a high risk of developing Graves' disease or hypothyroidism, can be determined using the composition according to the present invention.
For example, when the serum concentration of a thyroid stimulating antibody measured using the composition according to the present invention in medical examination is lower than the numeric value of a Graves' disease patient and higher than the numeric value of a normal individual, this person can be determined as a human having a high risk of developing Graves' disease. When the serum concentration of a thyroid stimulation blocking antibody is lower than the numeric value of hypothyroidism and higher than the numeric value of a normal individual, this person can be determined as a human having a high risk of developing hypothyroidism. Moreover, when the serum concentration of a thyroid stimulating antibody measured using the composition according to the present invention in medical examination is gradually increased over time, this person can be determined as a human having a high risk of developing Graves' disease. When the serum concentration of a thyroid stimulation blocking antibody is gradually increased over time, this person can be determined as a human having a high risk of developing hypothyroidism.
Furthermore, the effectiveness of treatment for a human under treatment of thyroid disease, for example, a human with Graves' disease or hypothyroidism under treatment thereof, can also be determined using the composition according to the present invention.
For example, the concentration of a thyroid stimulating antibody or a thyroid stimulation blocking antibody of blood samples collected from the same individual both before and after treatment, and time-dependent change in the concentration can be measured using the composition according to the present invention to determine the presence or absence of effectiveness of the treatment. When the serum concentration of the thyroid stimulating antibody measured using the composition according to the present invention is lower after treatment than before treatment, the treatment of Graves' disease can be determined as being effective. When the serum concentration of the thyroid stimulation blocking antibody measured using the composition according to the present invention is lower before treatment than after treatment, the treatment of hypothyroidism can be determined as being effective.
The present invention provides a kit that comprises a composition comprising the cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention and can further comprise at least one selected from the group consisting of a medium for cell culture, a detection solution, a luminescent substrate for the calcium sensitive protein or an aqueous solution thereof, an antibody separation solution, a plate for cell culture or a test tube, TSH or an aqueous solution thereof, an anti-TSH antibody and a normal human IgG control serum. For example, each substance constituting the kit and the composition are individually packaged, and these packages can be placed together in one container such as a box to prepare a kit.
The cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein according to the present invention can be prepared appropriately and is prepared, for example, at a concentration of 3×104 cells/ml to 3×106 cells/ml. The cell according to the present invention may be prepared, for example, by suspending it at a concentration of 3×106 cells/ml in an aqueous solution. When a 96-well plate is used as a plate for cell culture, the cell can be plated at a concentration of, for example, 3×103 cells to 3×105 cells per well of the 96-well plate.
The medium for cell culture is not limited as long as it can maintain the cell according to the present invention. The medium for cell culture can be Ca2+-free or Ca2+/Mg2+-free.
The detection solution can contain CaCl2, trypan blue, a cation that is capable of causing aequorin luminescence and can be substituted for calcium (e.g., a cadmium ion or a strontium ion), a magnesium ion, a zinc ion, a sulfuric acid ion and/or a carbonic acid ion. The concentrations of CaCl2 and trypan blue can be adjusted appropriately by those skilled in the art. For example, the concentration of CaCl2 is 9 to 18 mM, and the concentration of trypan blue is 0.001 to 0.010%. The detection solution is, for example, an aqueous solution containing 9 mM CaCl2 and 0.002% trypan blue. The final concentration of CaCl2 when the amount of luminescence of the calcium sensitive protein is measured can be set to 3 to 6 mM. Further, the detection solution can contain a cation that can be substituted for calcium, a magnesium ion, a zinc ion, a sulfuric acid ion and/or a carbonic acid ion, for example, by dissolving the cation that can be substituted for calcium, the magnesium ion, the zinc ion, the sulfuric acid ion and/or the carbonic acid ion in the detection solution.
The luminescent substrate for the calcium sensitive protein includes coelenterazine or a coelenterazine derivative that serves as a luminescent substrate for aequorin. The coelenterazine derivative includes ViviRen®, (Promega Corp.). The concentration of ViviRen can be set appropriately and is, for example, 0.6 to 30 mM. The aqueous solution of the luminescent substrate for the calcium sensitive protein is, for example, an aqueous solution of 4 mM ViviRen (Promega Corp.). The final concentration of ViviRen when the amount of luminescence of the calcium sensitive protein is measured can be set to 0.24 to 12 μM.
The antibody separation solution is not limited as long as a thyroid stimulating antibody and a thyroid stimulation blocking antibody can be collected from a blood sample. The antibody separation solution can contain 10 to 30% PEG6000. The antibody separation solution can be, for example, an aqueous solution containing 30% PEG6000.
Examples of the plate for cell culture include those allowing measurement of the amount of luminescence using a luminometer, for example, a 96-well plate allowing cell culture.
The test tube is not particularly limited and can be selected appropriately by those skilled in the art. For example, a test tube suitable for an apparatus for measuring luminescence emitted from the calcium sensitive protein can be used.
TSH is not limited as long as it can be used as a TSHR agonist. TSH may be used as a positive control. TSH can be, but not limited to, bovine TSH. TSH can be prepared appropriately by those skilled in the art and may be adjusted to 0.01 to 100 mU/ml. For example, bovine TSH is prepared as 1 mU/ml aqueous solution. The final concentration of bovine TSH when the amount of luminescence of the calcium sensitive protein is measured can be set to 0.6 μU/ml to 6 mU/ml. The final concentration of bovine TSH when the amount of luminescence of the calcium sensitive protein is measured is, for example, 100 μU/ml. Moreover, TSAb may be used instead of or in addition to TSH. TSAb can be a monoclonal antibody or a polyclonal antibody.
The normal human IgG control serum may be used as a negative control and can be prepared appropriately by those skilled in the art.
The anti-TSH antibody may be a polyclonal antibody or may be a monoclonal antibody. The anti-TSH antibody can be an antibody derived from an appropriate mammal and includes a mouse anti-TSH antibody, a rat anti-TSH antibody, a rabbit anti-TSH antibody and a goat anti-TSH antibody. The anti-TSH antibody may be modified appropriately by those skilled in the art. Moreover, TSH that serves as an antigen is also appropriately selected. TSH that serves as an antigen includes human TSH, mouse TSH, rat TSH, rabbit TSH, feline TSH and canine TSH. Examples of the anti-TSH antibody used in the kit of the present invention include a goat anti-human TSH polyclonal antibody. The concentration of the anti-TSH antibody can be set appropriately by those skilled in the art. For example, the concentration of an anti-TSH antibody solution packaged in the kit may be set to 0.01 μg/ml to 100 μg/ml. The final concentration of the anti-TSH monoclonal antibody when the amount of luminescence of the calcium sensitive protein is measured can be, for example, 0.05 to 5.48 μg/ml.
Among hypothyroidism patients, there is a patient whose amount of TSH in blood is a high value. In this case, the calcium sensitive protein in the cell emits luminescence due to the TSH. Thus, this patient may be diagnosed as Graves' disease though he or she is a hypothyroidism patient. However, a blood sample derived from the hypothyroidism patient having a high amount of TSH is added together with the anti-TSH antibody to the cell according to the present invention to neutralize the TSH derived from the patient. Thus, the incorrect diagnosis of the patient as Graves' disease can be avoided. Moreover, the amount of luminescence emitted from the calcium sensitive protein can be compared between the case where the anti-TSH antibody is added together with the patient-derived blood sample to the cell of the present invention and the case where the patient-derived blood sample is added to the cell of the present invention without the addition of the anti-TSH antibody, and thereby information about the amount of TSH of the blood of the patient can be obtained. A physician can more correctly diagnose thyroid disease by combining the information with clinical symptoms of the patient.
Moreover, the kit of the present invention further contains the serum of a thyroid disease patient, for example, the sera of a Graves' disease patient and/or a hypothyroidism patient. Such a serum can be used as a control or a standard for concentration calculation in the diagnosis of thyroid disease, in the assessment of a risk of developing the disease, or in the assessment of the effectiveness of treatment of the disease.
Furthermore, the kit of the present invention may contain a substance activating adenylate cyclase, for example, forskolin. The presence or absence of a thyroid stimulation blocking antibody in a sample derived from the blood of a test subject can be determined by adding the sample together with TSH to the cell, culturing the cell for the given time, and then adding forskolin thereto. Moreover, the concentration of a thyroid stimulation blocking antibody of the sample can also be measured. As a result, hypothyroidism (e.g., Hashimoto's disease) can be diagnosed, a human having a risk of developing hypothyroidism (e.g., Hashimoto's disease) can be determined, or therapeutic effect on a patient that has undergone the treatment of hypothyroidism (e.g., Hashimoto's disease) can be determined.
The composition or the kit according to the present invention is also useful for diagnostic aid that helps a physician to diagnose Graves' disease and/or hypothyroidism in view of clinical symptoms of the patient and/or other examination results. For example, the measurement of the amount of a thyroid stimulating antibody (TSAb) in a blood sample of a patient exhibiting hyperthyroidism using the composition or the kit according to the present invention can be useful for the differential diagnosis between Graves' disease and destructive hyperthyroidism (e.g., painless thyroiditis or subacute thyroiditis).
The present invention also provides a method for diagnosing Graves' disease, comprising the following steps (A) to (C):
(A) preparing a mixture containing a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, a luminescent substrate for the calcium sensitive protein, a Ca2+-free medium and a sample derived from the blood of a test subject;
(B) adding a Ca2+-containing solution to the mixture prepared in (A); and
(C) measuring the luminescence of the calcium sensitive protein emitted from the cell.
The Ca2+-free medium used in the step (A) of the method can be selected appropriately by those skilled in the art and can be a Ca2+/Mg2+-free medium.
The Ca2+-containing solution used in the step (B) of the method can be selected appropriately by those skilled in the art and can be, for example, a CaCl2 solution. The Ca2+-containing solution may further contain a cation that can be substituted for calcium (e.g., a cadmium ion or a strontium ion), a magnesium ion, a zinc ion, a sulfuric acid ion and/or a carbonic acid ion.
The mixture prepared in the step (A) of the method may further contain an anti-TSH antibody. The containing anti-TSH antibody in the mixture prepared in the step (A) of the method can avoid a hypothyroidism patient whose amount of TSH in blood is a high value from being incorrectly diagnosed as Graves' disease.
The order of addition of the substances described in the step (A) of the method can be set appropriately by those skilled in the art.
The present invention provides, for example, a method for diagnosing Graves' disease, comprising the following steps:
(1) culturing a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, in a Ca2+-free medium supplemented with a luminescent substrate for the calcium sensitive protein;
(2) adding a sample derived from the blood of a test subject to the cultured cell, which is further cultured; and
(3) adding a CaCl2 solution to the cultured cell, and measuring the luminescence of the calcium sensitive protein emitted from the cell.
In the method, the cell may be cryopreserved. In this case, the cell can be thawed by mild operation such as a warm bath. The thawed cell may be cultured in a Ca2+/Mg2+-free medium supplemented with a luminescent substrate for the calcium sensitive protein. The luminescent substrate for the calcium sensitive protein includes coelenterazine and ViviRen®.
The Ca2+-free medium is not limited as long as the cell can be maintained. For example, 130 mM NaCl, 5 mM KCl, 20 mM HEPES, 1 mM MgCl2, 4.8 mM NaHCO3, 5% PEG6000, pH 7.4 are used. Moreover, the Ca2+-free medium can be a Ca2+/Mg2+-free medium. The cell can be seeded at an appropriate concentration into an appropriate container and is seeded, for example, at a concentration of 3 to 30×104 cells/ml and 90 μl/well into a 96-well plate compatible with a luminometer. The incubation time in the step (1) can be any time as long as it is equal to or longer than 2 hours. The incubation time can be set to 2-8 hours and is, for example, 3 hours. In general, for recovering from damage caused by subculture and increasing the amount of luminescence of the calcium sensitive protein such as aequorin, cells are usually cultured for approximately 12-24 hours after seeding the cells. In the present invention, it has been confirmed that even if the cells are cultured for approximately 2 hours, cell death caused by additives is not induced and the calcium sensitive protein exhibits strong luminescence. It has been confirmed that even approximately 2 hours after the cell seeding, strong luminescence from the calcium sensitive protein can be detected, for example, by employing aequorin as the calcium sensitive protein, optimizing its DNA sequence for human codon, and introducing a mitochondrial targeting signal, and further employing ViviRen® as the luminescent substrate for the calcium sensitive protein.
The blood-derived sample added in the step (2) is prepared by adding an aqueous PEG solution to the blood of a test subject or the like and collecting a precipitated fraction. For example, 30% PEG6000 is used as the aqueous PEG solution. Moreover, in some cases, a sample derived from the blood of a Graves' disease patient as a positive control and/or a blood sample derived from a normal individual as a negative control can also be used and each added to the cell in the step (2), respectively. The incubation time in the step (2) is not limited and can be set to 30-60 minutes, for example, 30 minutes. As a result, cAMP is accumulated in the cell. Thus, more stable, strong luminescence than that in the absence of culture after sample addition can be measured immediately after addition of the CaCl2 solution.
As long as the incubation times in the steps (2) and (3) are within approximately 4 hours in total, it is not required to perform sterile culture because of the short time.
In the step (2), an anti-TSH antibody may be further added to the cultured cell. The anti-TSH antibody may be a polyclonal antibody or may be a monoclonal antibody. The anti-TSH antibody can be an antibody derived from an appropriate mammal and includes a mouse anti-TSH antibody, a rat anti-TSH antibody, a rabbit anti-TSH antibody and a goat anti-TSH antibody. The anti-TSH antibody may be modified appropriately by those skilled in the art. Moreover, TSH that serves as an antigen is also appropriately selected. TSH that serves as an antigen includes human TSH, mouse TSH, rat TSH, rabbit TSH, feline TSH and canine TSH. Examples of the anti-TSH antibody used in the method of the present invention include a goat anti-human TSH polyclonal antibody.
The CaCl2-containing solution used in the step (3) may further contain a cation that can be substituted for calcium (e.g., a cadmium ion or a strontium ion), a magnesium ion, a zinc ion, a sulfuric acid ion and/or a carbonic acid ion. The concentrations of Ca2+, the cation that can be substituted for calcium, the magnesium ion, the zinc ion, the sulfuric acid ion and the carbonic acid ion that may be contained in the CaCl2 solution can be set appropriately by those skilled in the art such that the cell can be maintained and the calcium sensitive protein such as aequorin appropriately emits luminescence.
In the step (3), the luminescence is emitted by the calcium sensitive protein such as aequorin immediately after addition of the CaCl2 solution and can be measured by a method which is well known by those skilled in the art. For example, a luminometer capable of automatically and continuously performing stirring and measurement (PerkinElmer Inc., ARVO-Sx) is used, and the amount of luminescence can be measured by integrating luminescence values for 15-30 seconds after stirring. The apparatus that can be used in the measurement of the amount of luminescence can be selected appropriately by those skilled in the art.
As a result of carrying out the method, when the amount of luminescence of the calcium sensitive protein (e.g., aequorin) emitted from the cell treated with the sample derived from the blood of a test subject is higher than that emitted from the cell treated with a sample derived from the blood of a normal individual, the test subject can be diagnosed as Graves' disease. Moreover, the serum concentration of an antibody can be determined and compared with a standard antibody concentration of a Graves' disease patient and/or a normal individual to diagnose the test subject as Graves' disease or not.
For example, the amount of luminescence emitted from the cell treated with a blood sample of a test subject and the amount of luminescence emitted from the cell treated with the same amount of a blood sample (standard) of a normal individual as that of the blood sample of the test subject are measured. When the amount of luminescence emitted from the cell treated with the blood sample of the test subject is higher than that emitted from the cell treated with the blood sample (standard) of a normal individual, the serum concentration of a thyroid stimulating antibody (TSAb) of the test subject can be determined to be higher than that of the normal individual. Thus, the test subject can be diagnosed as Graves' disease.
Moreover, the respective amounts of luminescence (integrated values) from the cells treated with blood samples of a large population of normal individuals, for example, 50 to 100 normal individuals, are measured in advance, and a mean thereof and standard deviation (SD) may be calculated. When the amount of luminescence emitted from the cell treated with a blood sample of a test subject is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the amounts of luminescence (integrated values) emitted from the cells treated with the blood samples of the normal individual population, the serum concentration of a thyroid stimulating antibody of the test subject can be determined to be higher than that of the normal individuals. Thus, the test subject can be diagnosed as Graves' disease.
Furthermore, the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a test subject/the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a normal individual×100(%) may be calculated (this calculated value is defined as a calculated value D). The respective amounts of luminescence (integrated values) emitted from the cells treated with respective blood samples of a large population of normal individuals and a large population of untreated Graves' disease patients (e.g., 50 to 100 individuals per population) are measured in advance, and a cutoff value is set such that a true positive rate of Graves' disease and/or a true negative rate (i.e., being a normal individual) are each, for example, 80% or more, 90% or more, 92% or more, 94% or more, 96% or more, or 98% or more. When the calculated value D is higher than the cutoff value, the test subject can also be diagnosed as Graves' disease. The cutoff value can be set appropriately depending on the properties of a target population, such as age and sex and can be set to, for example, 120%, 130%, 140%, 150%, 160%, 170%, 180%, 190%, or 200%.
Furthermore, an antibody (TSAb) standard (e.g., NIBSC 90/672 or 65/122) is also used, and its concentration may be serially diluted to prepare a calibration curve. With reference to the calibration curve, the actual serum concentration of an antibody (TSAb) is calculated from the measured amount of luminescence of the calcium sensitive protein in the cell treated with a blood sample of a test subject. This concentration can be compared with the previously measured serum concentration of an antibody (TSAb) of each of a large population of normal individuals and a large population of untreated Graves' disease patients (e.g., 50 to 100 individuals per population), or known data reported in a document or the like to diagnose the test subject as Graves' disease or not. For example, when the concentration is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the serum concentrations of (TSAb) of the normal individual population, the test subject can also be diagnosed as Graves' disease.
Moreover, as a result of carrying out the method, when the amount of luminescence of the calcium sensitive protein (e.g., aequorin) emitted from the cell treated with the sample derived from the blood of a test subject is higher than that emitted from the cell treated with a sample derived from the blood of a normal individual and is lower than that emitted from the cell treated with a sample derived from the blood of a Graves' disease patient, the test subject can be determined as a human having a high risk of developing Graves' disease. Alternatively, the serum concentration of an antibody can be determined and compared with a standard antibody concentration of a Graves' disease patient and/or a normal individual to diagnose the test subject as a human having a high risk of developing Graves' disease or not.
Furthermore, in the step (2), samples taken before and after the treatment of the same Graves' disease patient are added as the sample derived from the blood of a test subject. The amount of luminescence of the calcium sensitive protein (e.g., aequorin) emitted from the cell can be compared between the samples to determine the effectiveness of the treatment. As a result of the test, when the amount of luminescence of the calcium sensitive protein such as aequorin is lower in the sample taken after the treatment than in the sample taken before the treatment, the treatment can be determined as being effective.
The present invention also provides a method for diagnosing hypothyroidism, comprising the following steps (A) to (C):
(A) preparing a mixture containing a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, a luminescent substrate for the calcium sensitive protein, a Ca2+-free medium, TSH or a stimulating TSAb monoclonal antibody and a sample derived from the blood of a test subject;
(B) adding a Ca2+-containing solution to the mixture prepared in (A); and
(C) quantifying the luminescence of the calcium sensitive protein emitted from the cell.
The Ca2+-free medium used in the step (A) of the method can be selected appropriately by those skilled in the art and can be a Ca2+/Mg2+-free medium.
The Ca2+-containing solution used in the step (B) of the method can be selected appropriately by those skilled in the art and can be, for example, a CaCl2 solution. Moreover, the Ca2+-containing solution may further contain a cation that can be substituted for calcium (e.g., a cadmium ion or a strontium ion), a magnesium ion, a zinc ion, a sulfuric acid ion, and/or a carbonic acid ion.
The order of addition of the substances described in the step (A) of the method can be set appropriately by those skilled in the art.
The present invention provides, for example, a method for diagnosing hypothyroidism (e.g., Hashimoto's disease), comprising the following steps:
(1) culturing a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, in a Ca2+-free medium supplemented with a luminescent substrate for the calcium sensitive protein;
(2) adding a sample derived from the blood of a test subject together with TSH to the cultured cell, which is further cultured; and
(3) adding a CaCl2 solution to the cultured cell, and measuring the luminescence of the calcium sensitive protein emitted from the cell.
The steps (1)-(3) can be carried out appropriately by those skilled in the art with reference to the method for diagnosing Graves' disease described above.
In some cases, in the step (2), a sample derived from the blood of a normal individual as a negative control and/or a sample derived from the blood of a hypothyroidism patient as a positive control can be used, and each of them can be added to the cell, respectively. Moreover, the incubation time in the step (2) is not limited and can be set to 30-120 minutes, for example, 30 minutes. Furthermore, in the step (2), TSH can be bovine TSH. In some cases, TSAb can be added instead of or in addition to TSH. TSAb can be a monoclonal antibody.
As a result of carrying out the method, when the amount of luminescence of the calcium sensitive protein (e.g., aequorin) emitted from the cell treated with the sample derived from the blood of a test subject is lower than that emitted from the cell treated with a sample derived from the blood of a normal individual, the test subject can be diagnosed as hypothyroidism. Moreover, the serum concentration of an antibody can be determined and compared with a standard antibody concentration of a hypothyroidism patient and/or a normal individual to diagnose the test subject as hypothyroidism or not.
For example, the amount of luminescence emitted from the cell treated with a blood sample of a test subject and the amount of luminescence emitted from the cell treated with the same amount of a blood sample (standard) of a normal individual as that of the blood sample of the test subject are measured. When the amount of luminescence emitted from the cell treated with the blood sample of a test subject is lower than that emitted from the cell treated with the blood sample (standard) of a normal individual, the serum concentration of a thyroid stimulation blocking antibody (TSBAb) of the test subject can be determined to be higher than that of the normal individual. Thus, the test subject can be diagnosed as hypothyroidism.
Moreover, the respective amounts of TSH-induced luminescence (integrated values) of the calcium sensitive proteins in the cells treated with blood samples of a population of a large number of normal individuals, for example, 50 to 100 normal individuals, are measured in advance, and a mean thereof and standard deviation (SD) may be calculated. When the amount of TSH-induced luminescence from the cell treated with a blood sample of a test subject is lower than the mean−nSD (e.g., n=1, 2, 3, 4, or 5) of the amounts of TSH-induced luminescence (integrated values) from the cells treated with the blood samples of the normal individual population, the serum concentration of a thyroid stimulation blocking antibody (TSBAb) of the test subject can be determined to be higher than that of the normal individuals. Thus, the test subject can also be diagnosed as hypothyroidism.
Furthermore, the amount of luminescence (integrated value) in the cell treated with a blood sample of a test subject/the amount of luminescence (integrated value) from the cell treated with a blood sample of a normal individual×100(%) may be calculated (hereinafter, this calculated value is defined as a calculated value E). The respective amounts of luminescence (integrated values) attributed to respective blood samples of a large population of normal individuals and a large population of untreated hypothyroidism patients (e.g., 50 to 100 individuals per population) are measured in advance, and a cutoff value is set such that a true positive rate of hypothyroidism and/or a true negative rate (i.e., being a normal individual) are each, for example, 80% or more, 90% or more, 92% or more, 94% or more, 96% or more, or 98% or more. When the calculated value E is lower than the cutoff value, the test subject can also be diagnosed as hypothyroidism. The cutoff value can be set appropriately depending on the properties of a target population, such as age and sex and can be set to, for example, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90%.
Furthermore, an antibody (TSBAb) standard having a known concentration is also used, and its concentration may be serially diluted to prepare a calibration curve. With reference to the calibration curve, the actual serum concentration of an antibody (TSBAb) is calculated from the measured amount of luminescence emitted from the cell treated with a blood sample of a test subject. This concentration can be compared with the previously measured serum concentration of an antibody (TSBAb) of each of a large population of normal individuals and a large population of untreated hypothyroidism patients (e.g., 50 to 100 individuals per population), or known data reported in a document or the like to diagnose the test subject as hypothyroidism or not. For example, when the concentration is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the serum concentrations of (TSBAb) in the normal individual population, the test subject can also be diagnosed as hypothyroidism.
Moreover, as a result of carrying out the method, when the amount of luminescence of the calcium sensitive protein (e.g., aequorin) emitted from the cell treated with the sample derived from the blood of a test subject is lower than that emitted from the cell treated with a sample derived from the blood of a normal individual and is higher than that emitted from the cell treated with a sample derived from the blood of a hypothyroidism patient, the test subject can be determined as a human having a high risk of developing hypothyroidism. Alternatively, the serum concentration of an antibody can be determined and compared with a standard antibody concentration in a hypothyroidism patient and/or a normal individual to determine the test subject as a human having a high risk of developing hypothyroidism or not.
Furthermore, in the step (2), samples taken before and after the treatment of the same hypothyroidism patient are added as the sample derived from the blood of a test subject. The amount of luminescence of the calcium sensitive protein (e.g., aequorin) emitted from the cell can be compared between the samples to determine the effectiveness of the treatment. As a result of the test, when the amount of luminescence of the calcium sensitive protein such as aequorin is higher in sample taken after the treatment than in the sample taken before the treatment, the treatment can be determined as being effective.
The present invention further provides a method for diagnosing hypothyroidism, comprising the following steps (A) to (C):
(A) preparing a mixture containing a cell according to any of claims 1 to 10, a luminescent substrate for the calcium sensitive protein, a Ca2+-containing medium, TSH or a stimulating TSAb monoclonal antibody and a sample derived from the blood of a test subject;
(B) adding forskolin to the mixture prepared in (A); and
(C) quantifying the luminescence of the calcium sensitive protein emitted from the cell.
The Ca2+-containing medium used in the step (A) of the method can be selected appropriately by those skilled in the art and can be, for example, a medium containing CaCl2. Moreover, the Ca2+-containing medium may further contain a cation that can be substituted for calcium (e.g., a cadmium ion or a strontium ion), a magnesium ion, a zinc ion, a sulfuric acid ion, and/or a carbonic acid ion. The concentrations of Ca2+, the cation that can be substituted for calcium, the magnesium ion, the zinc ion, the sulfuric acid ion and the carbonic acid ion that may be contained in the Ca2+-containing medium can be set appropriately by those skilled in the art such that the cell can be maintained and the calcium sensitive protein such as aequorin appropriately emits luminescence.
The order of addition of substances described in the step (A) of the method can be set appropriately by those skilled in the art.
The present invention provides, for example, a method for diagnosing hypothyroidism (e.g., Hashimoto's disease), comprising the following steps:
(1) culturing a cell expressing a thyroid stimulating hormone receptor (TSHR), a cAMP dependent calcium channel and a calcium sensitive protein, in a Ca2+-containing medium treated with a luminescent substrate for the calcium sensitive protein;
(2) adding a sample derived from the blood of a test subject together with TSH to the cultured cell, which is further cultured; and
(3) adding forskolin to the cultured cell, and measuring the luminescence of the calcium sensitive protein emitted from the cell.
The steps (1)-(3) can be carried out appropriately by those skilled in the art with reference to the method for diagnosing Graves' disease described above.
In some cases, in the step (2), a sample derived from the blood of a normal individual as a negative control and/or a sample derived from the blood of a hypothyroidism patient as a positive control can be used and each of them can be added to the cell, respectively. Moreover, the incubation time in the step (2) is not limited and can be set to 10-120 minutes, for example, 10 minutes. Furthermore, in the step (2), TSH can be bovine TSH. In some cases, TSAb can be added instead of or in addition to TSH. TSAb can be a monoclonal antibody.
In the step (3), the concentration of forskolin can be set appropriately by those skilled in the art.
As a result of carrying out the method, when the amount of luminescence of the calcium sensitive protein (e.g., aequorin) emitted from the cell treated with the sample derived from the blood of a test subject is higher than that emitted from the cell treated with a sample derived from the blood of a normal individual, the test subject can be diagnosed as hypothyroidism. Moreover, the serum concentration of an antibody can be determined and compared with a standard antibody concentration in a hypothyroidism patient and/or a normal individual to diagnose the test subject as hypothyroidism or not.
For example, the amount of luminescence emitted from the cell treated with a blood sample of a test subject and the amount of luminescence emitted from the cell treated with the same amount of a blood sample (standard) of a normal individual as that of the blood sample of the test subject are measured. When the amount of luminescence emitted from the cell treated with the blood sample of a test subject is higher than that emitted from the cell treated with the blood sample (standard) of a normal individual, the serum concentration of a thyroid stimulation blocking antibody (TSBAb) of the test subject can be determined to be higher than that of the normal individual. Thus, the test subject can be diagnosed as hypothyroidism.
Moreover, the respective amounts of luminescence (integrated values) from the cells treated with blood samples of a population of a large number of normal individuals, for example, 50 to 100 normal individuals, are measured in advance, and a mean thereof and standard deviation (SD) may be calculated. When the amount of luminescence emitted from the cell treated with a blood sample of a test subject is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the amounts of luminescence (integrated values) emitted from the cells treated with the blood samples of the normal individual population, the serum concentration of a thyroid stimulation blocking antibody (TSBAb) of the test subject can be determined to be higher than that of the normal individuals. Thus, the test subject can also be diagnosed as hypothyroidism.
Furthermore, the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a test subject/the amount of luminescence (integrated value) emitted from the cell treated with a blood sample of a normal individual×100(%) may be calculated (hereinafter, this calculated value is defined as a calculated value F). The respective amounts of luminescence (integrated values) attributed to respective blood samples of a large population of normal individuals and a large population of untreated hypothyroidism patients (e.g., 50 to 100 individuals per population) are measured in advance, and a cutoff value is set such that a true positive rate of hypothyroidism and/or a true negative rate (i.e., being a normal individual) are each, for example, 80% or more, 90% or more, 92% or more, 94% or more, 96% or more, or 98% or more. When the calculated value F is higher than the cutoff value, the test subject can also be diagnosed as hypothyroidism. The cutoff value can be set appropriately depending on the properties of a target population, such as age and sex and can be set to, for example, 150%, 200%, 300%, 400%, 500%, 600%, 700%, 800%, or 900%.
Furthermore, an antibody (TSBAb) standard having a known concentration is also used, and its concentration may be serially diluted to prepare a calibration curve. With reference to the calibration curve, the actual serum concentration of an antibody (TSBAb) is calculated from the measured amount of luminescence emitted from the cell treated with a blood sample of a test subject. This concentration can be compared with the previously measured serum concentration of an antibody (TSBAb) of each of a large population of normal individuals and a large population of untreated hypothyroidism patients (e.g., 50 to 100 individuals per population), or known data reported in a document or the like to diagnose the test subject as hypothyroidism or not. For example, when the concentration is higher than the mean+nSD (e.g., n=1, 2, 3, 4, or 5) of the serum concentrations of (TSBAb) of the normal individual population, the test subject can also be diagnosed as hypothyroidism.
Moreover, as a result of carrying out the method, when the amount of luminescence of the calcium sensitive protein (e.g., aequorin) emitted from the cell treated with the sample derived from the blood of a test subject is higher than that emitted from the cell treated with a sample derived from the blood of a normal individual and is lower than that emitted from the cell treated with a sample derived from the blood of a hypothyroidism patient, the test subject can be determined as a human having a high risk of developing hypothyroidism. Alternatively, the serum concentration of an antibody can be determined and compared with a standard antibody concentration of a hypothyroidism patient and/or a normal individual to determine the test subject as a human having a high risk of developing hypothyroidism or not.
Furthermore, in the step (2), samples taken before and after the treatment of the same hypothyroidism patient are added as the sample derived from the blood of a test subject. The amount of luminescence of the calcium sensitive protein (e.g., aequorin) emitted from the cell can be compared between the samples to determine the effectiveness of the treatment. As a result of the test, when the amount of luminescence of the calcium sensitive protein such as aequorin is lower in the sample taken after treatment than in the sample taken before the treatment, the treatment can be determined as being effective.
Hereinafter, the present invention will be further described with reference to Examples. However, the present invention is not limited to them.
The cDNA sequence of a human thyroid stimulating hormone receptor (Genbank No. NM_000369) (SEQ ID NO: 5) was amplified by the PCR method from a human thyroid gland-derived cDNA library and cloned into pUC18. The hTSHR cDNA cloned in pUC18 was cleaved with BamHI and recloned into a pZeoSV2 vector (Invitrogen Corp.) to prepare pZeoSV2 hTSHR.
The cDNA sequence of a cyclic nucleotide dependent calcium channel (Genbank No. BC048775) (SEQ ID NO: 4) was amplified by the PCR method from a mouse olfactory epithelial cell-derived cDNA library and cloned into a 1994-bp expression vector (pCMVSPORT, Invitrogen Corp.) to prepare pmCNGα2 (
CHO cells were seeded at a cell concentration of 1.0×105 cells/ml into a 10-cm2 Petri dish. On the next day, the cells were transfected with 1 μg of pZeoSV2 hTSHR, 2 μg of pmCNGα2MW, and 2 μg of pcDNA mt sAEQ per Petri dish using FuGENE6 ™ (Roche Applied Science). On the next day, the cells were dissociated from the Petri dish by the addition of 400 μL of a Versene solution (EDTA) to the Petri dish and suspended in a DMEM/F12 medium containing 10 mL of 5% cFCS. The obtained suspension was centrifuged at 1000 rpm for 5 minutes. Then, the pellet was dissolved at a concentration of 2-5×106 cells/mL in 1 mL of CELLBANKER and stored at −80° C.
2. Concentration Dependent Curve and Lowest Detection Sensitivity of Bovine TSH (bTSH) Obtained Using Frozen Cell
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer (130 mM NaCl, 5 mM KCl, 20 mM HEPES, 1 mM MgCl2, 4.8 mM NaHCO3, 5% PEG6000, pH 7.4). After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen (Promega Corp.) was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate. After culture at 37° C. for 3 hours in a CO2 atmosphere, bTSH serially diluted with PBS was added thereto (n=6) at a concentration of 10 μL/well, and the cells were cultured for 30 minutes. Then, 3 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer (PerkinElmer Inc., ARVO-Sx; hereinafter, the same model was used in Examples). A bTSH concentration dependent curve is shown in
As shown in
As shown in
Moreover, since aequorin performs luminescent reaction, the high signal to blank ratio (S/N ratio), (i.e., a 100 μU/mL of bTSH, S/N ratio of approximately 45 times (9000000/200000)), obtained by the method of the present invention was far superior to that of the YAMASA kit (100 μU/mL of bTSH, SN=7).
A human Graves' disease patient-derived TSAb standard: MRC Research standard B 1966 Long-acting Thyroid Stimulator (NIBSC: National Institute for Biological Standards and Control, code 65/122) was diluted with a normal individual serum to prepare H (1.88 mU LAST/ml), M (1.25 mU LAST/ml), and L (0.94 mU LAST/ml) control samples. 150 μL of 30% PEG6000 was added to 50 μL of each prepared control serum, and the mixtures were stirred and then left standing at 4° C. for 5 minutes. After centrifugation at 3000 rpm at 4° C. for 20 minutes, the obtained precipitates were separately dissolved in 400 μL of a sample buffer to prepare sample solutions. 1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer. After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen was added thereto. The mixture was seeded at a concentration of 80 μL/well into a 96-well plate. After culture at 37° C. for 3 hours in a CO2 atmosphere, the prepared samples were separately added thereto (n=2) at a concentration of 20 μL/well, and the cells were cultured for 30 minutes. Then, 9 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer. Comparison was made in the case where each six of the L, M, and H samples were simultaneously purified and assayed (within-run reproducibility), the case where the L, M, and H samples were independently purified and assayed at different 10 days (between-run reproducibility), and the case where the L, M, and H samples of different production lots were purified and assayed on the same day (lot-to-lot reproducibility). In addition to the assay samples, H (576 TSAb %), M (342 TSAb %), and L (197 TSAb %) separately scored using the YAMASA kit were added to the plate, and a calibration curve was drawn. A value determined from the obtained regression line was defined as a sample concentration (TSAb % based on the YAMASA kit) (YAMASA TSAb %=Value of sample/Value of normal individual serum×100(%)).
The method of the present invention was confirmed to produce high reproducibility because the assay system had high sensitivity and a high S/N ratio. Moreover, 5-6% CV demonstrated that the method of the present invention had high lot-to-lot reproducibility. The assay system with little difference between different lots could be constructed using the CHO cells and the optimized transfection conditions.
The CV value of the reproducibility of the existing TSAb kit available from YAMASA CORP. has been reported to be 10-15%, demonstrating high reproducibility of the method of the present invention.
Moreover, since the existing kit is produced by freezing porcine tissue-derived thyroid gland cells, its problem is that lot-to-lot variation is large due to individual difference among pigs from which the tissue is derived (lot-to-lot CV: 10-19%). By contrast, the method of the present invention was confirmed to have high reproducibility even among different lots.
4. Study on Incubation Time after Addition of Substrate (ViviRen) for Aequorin Luminescence
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer. After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen was added thereto. After the addition, 30 minutes, or 1, 2, 3, 4, 5, 6, 7, or 8 hours, the mixture was seeded at a concentration of 90 μL/well into a 96-well plate. bTSH serially diluted with PBS was added thereto at a concentration of 10 μL/well, and the cells were cultured for 30 minutes. Then, 9 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
It was demonstrated that the amount of luminescence reached a plateau at 2 hours after ViviRen addition (see
10 mL of CHO cells having a concentration of 1×105 cells/mL was seeded into a 10-cm2 Petri dish and cultured for 1 day. Then, 3 ug of pcDNA mt sAEQ, 1 ug of pmCNGα2MW, and 0 to 1 ug of pZeoSV2 TSHR plasmid were mixed and further mixed with 600 μL of DMEM/F12 and 18 μL of FuGENE6 (Roche Applied Science), and transfection was performed. After further overnight culture, the medium was removed, and the cells were washed with 10 mL of PBS. Then, 800 μL of Versene was added thereto, and the cells were cultured at 37° C. for 5 minutes and then suspended in 10 mL of DMEM/F12 cFCS. After centrifugation at 1000 rpm for 5 minutes, the precipitate was dissolved in 10 mL of DMEM/F12 cFCS, and 6.5 μL of 4 mM ViviRen was added thereto. After culture at 37° C. for 3 hours, the medium was replaced by PBS, and the culture solution was seeded at a concentration of 90 μL/well to a 96-well plate. 30 minutes after addition of a concentration series of bTSH, 3 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
It was demonstrated that the receptor plasmid in an amount of 1 ug/plate in transfection was required for obtaining the optimum amount of luminescence (see
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer. After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate. A cell series whose cell concentration was adjusted to concentrations 3×103 cells/mL to 3×105 cells/mL was prepared. 7.5 μL of 4 mM ViviRen was added thereto, and the mixture was seeded at a concentration of 90 μL/well into a 96-well plate. After culture at 37° C. for 3 hours in a CO2 atmosphere, bTSH serially diluted with PBS was added thereto at a concentration of 10 μL/well, and the cells were cultured for 30 minutes. Then, 9 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
As shown in
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer. After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate. After culture at 37° C. for 3 hours in a CO2 atmosphere, bTSH serially diluted with PBS was added thereto at a concentration of 10 μL/well, and the cells were cultured for 30 minutes. Then, a CaCl2 detection solution (final concentrations: 0 to 30 mM) was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
It was demonstrated that the optimum CaCl2 concentrations were 3 to 6 mM at which a low value at background (0) and the high amount of luminescence in the sample were obtained (see
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer. After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen was added thereto. The mixture was seeded at a concentration of 80 μL/well into a 96-well plate. The cells were cultured at 37° C. for 3 hours in a CO2 atmosphere. IgG fractions of a positive control serum series (adhering to Roche NIBSC 90/672; 40 IU/mL, 13 IU/mL, 8 IU/mL, and 4 IU/mL) purified and diluted with 30% PEG6000 were separately diluted 1/2, 1/4, 1/8, 1/16, or 1/32-fold with a sample buffer, and each solution was added thereto at a concentration of 20 μL/well. After culture for 30 minutes, 9 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
As shown in
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer. After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate. After culture at 37° C. for 3 hours in a CO2 atmosphere, a hypothyroidism patient-derived thyroid stimulation blocking antibody (TSBAb) fraction and a normal individual serum-derived IgG fraction purified with 30% PEG6000 were separately added thereto at a concentration of 10 μL/well. At the same time, bTSH (final concentrations: 100 μU to 2.5 μU/mL) was further added thereto at a concentration of 10 μL/well. After culture for 30 minutes, 9 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
It was demonstrated that 90% or more luminescence was inhibited in the hypothyroidism patient-derived antibody fraction in the presence of 2.5 to 10 μU/mL bTSH (see
When the blocking antibody is detected, reduction in signal in the presence of bTSH is generally observed. Conventional methods are known to have the disadvantage that the S/N ratio is as low as 5 to 10-fold and a measurement range becomes narrow due to the low S/N ratio. By contrast, the method of the present invention has a wide measurement range such that the S/N ratio in the presence or absence of bTSH is 50-fold. Thus, the blocking antibody can be detected with high sensitivity.
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer. After centrifugation at 1000 rpm for 5 minutes, 10 mL of a DMEM/F12 cFCS medium containing calcium was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate. After culture at 37° C. for 3 hours in a CO2 atmosphere, a hypothyroidism patient-derived thyroid stimulation blocking antibody (TSBAb) fraction and a normal individual serum-derived IgG fraction purified with 30% PEG6000 were separately added thereto at a concentration of 10 μL/well. At the same time, bTSH (final concentrations: 100 μU to 2.5 μU/mL) was further added at a concentration of 10 μL/well. After culture for 30 minutes, 10−4 M forskolin solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
In
Under this condition, calcium is present in a medium at the time of bTSH addition to cells; thus luminescent reaction occurs immediately after bTSH addition in the absence of the blocking antibody as seen in normal individual sera. By contrast, in the presence of the blocking antibody (TSBAb), TSBAb inhibits the action of bTSH, so that luminescent reaction does not occur. In this state, upon subsequent addition of forskolin, which activates adenylate cyclase, cAMP is formed to cause luminescence without the mediation of a TSH receptor. However, in the absence of TSBAb, the cells are already desensitized by luminescent reaction that has occurred once via adenylate cyclase activated by bTSH. Thus, luminescence does not occur even by the further addition of forskolin as the second stimulus. By contrast, in the presence of TSBAb, the blocking antibody prevents bTSH from activating adenylate cyclase. Thus, upon subsequent addition of forskolin, cAMP is formed to cause luminescent reaction.
Conventional methods for detecting a blocking antibody are indicated by % inhibition with respect to a normal individual. However, the problem of indication using % inhibition is a lack of quantitative reliability in a high concentration range of 90% or more.
The method of the present invention using cell desensitization action and forskolin can be indicated by increase in the amount of luminescence with respect to a normal individual. Thus, the upper limit is not defined, and the presence or absence of the blocking antibody can be detected with linearity even in a high concentration range.
11. Sensitivity Comparison with Existing Kit Using Stimulating Antibody Standard
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer. After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate. MRC Research standard B 1966 (NIBSC 65/122) was diluted with a normal individual serum to prepare a concentration series. 150 μL of 30% PEG6000 was added to 50 μL of each control sample in the prepared series, and the mixtures were stirred and then left standing at 4° C. for 5 minutes. After centrifugation at 3000 rpm at 4° C. for 20 minutes, the obtained precipitates were separately dissolved in 50 μL of a sample buffer to prepare sample solutions. After culture at 37° C. for 3 hours in a CO2 atmosphere, the sample solutions were separately added thereto at a concentration of 10 μL/well, and the cells were cultured for 30 minutes. 9 mM CaCl2 detection solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
Values separately measured using the existing YAMASA kit using the porcine thyroid gland are also shown. The existing YAMASA kit resulted in 200 TSAb % at 0.94 mU LAST/mL and failed to detect concentrations below the sensitivity threshold. By contrast, the method of the present invention was confirmed to be able to detect the stimulating antibody with 2018 TSAb % at 0.94 mU LAST/mL and with 242 TSAb % even at 0.06 mU LAST/mL and to be able to detect the stimulating antibody with great sensitivity which is about 16 times higher than that of the existing kit (see
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer (130 mM NaCl, 5 mM KCl, 20 mM HEPES, 1 mM MgCl2, 4.8 mM NaHCO3, 5% PEG6000, pH 7.4). After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen (Promega Corp.) was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate. After culture at 37° C. for 3 hours in a CO2 atmosphere, H (high value), M (median value), and L (low value) samples purified with 30% PEG6000 were separately added thereto (n=6) at a concentration of 10 μL/well. After culture for 30 minutes, 9 mM CaCl2 solution was added thereto at a concentration of 50 μL/well and stirred for 3 seconds. Then, the amount of luminescence was measured over times for 13 seconds using a luminometer. As a result, as shown in
(1) Method for Detecting Thyroid Stimulation Blocking Antibody (TSBAb) Using Competitive Inhibition Against bTSH
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer (130 mM NaCl, 5 mM KCl, 20 mM HEPES, 1 mM MgCl2, 4.8 mM NaHCO3, 5% PEG6000, pH 7.4). After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen (Promega Corp.) was added thereto. After culture at 37° C. for 3 hours in a CO2 atmosphere, 90 μL of the cell solution was mixed with 10 μL of each sample in a dilution series of a hypothyroidism patient-derived blocking antibody purified with 30% PEG6000, and cultured for 30 minutes. Then, 9 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
As shown in
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer (3 mM CaCl2, 130 mM NaCl, 5 mM KCl, 20 mM HEPES, 1 mM MgCl2, 4.8 mM NaHCO3, 5% PEG6000, pH 7.4). After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen (Promega Corp.) was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate. Each sample in a dilution series of a hypothyroidism patient-derived blocking antibody purified with 30% PEG6000 was added thereto at a concentration of 10 μL/well, and further, a bTSH solution (final concentration: 100 μL/mL) was added thereto at a concentration of 10 μL/well. After culture at 37° C. for 30 minutes in a CO2 atmosphere, 10−4 M forskolin solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
As shown in
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer (130 mM NaCl, 5 mM KCl, 20 mM HEPES, 1 mM MgCl2, 4.8 mM NaHCO3, 5% PEG6000, pH 7.4). After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen (Promega Corp.) was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate. High value (H), median value (M), low value (L), and normal individual (N) serum samples purified with 30% PEG6000 were separately added thereto at a concentration of 10 μL/well. After culture for 30 minutes to 1.5 hours, 9 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
As shown in
(2) Study on Duration of Action in Method for Detecting Thyroid Stimulation Blocking Antibody (TSBAb) Using Competitive Inhibition Against bTSH
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a sample buffer (130 mM NaCl, 5 mM KCl, 20 mM HEPES, 1 mM MgCl2, 4.8 mM NaHCO3, 5% PEG6000, pH 7.4). After centrifugation at 1000 rpm for 5 minutes, 10 mL of a sample buffer was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen (Promega Corp.) was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate, and the cells were cultured for 3 hours. A hypothyroidism patient-derived serum sample and a normal individual serum sample purified with 30% PEG6000 were separately added thereto at a concentration of 10 μL/well, and further, a bTSH solution (final concentration: 10 μU/mL) was added thereto at a concentration of 10 μL/well. After culture for 10 minutes to 2 hours, 9 mM CaCl2 solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
As shown in
1 ml (3×106 cells/ml) of the frozen cells prepared in 1 was thawed in a warm bath and suspended in 10 mL of a CO2 independent medium (Cat No. 18045, Invitrogen Corp.). After centrifugation at 1000 rpm for 5 minutes, 10 mL of a CO2 independent medium was added to the obtained precipitate, and 7.5 μL of 4 mM ViviRen (Promega Corp.) was added thereto. The mixture was seeded at a concentration of 90 μL/well into a 96-well plate, and the cells were cultured for 3 hours. A hypothyroidism patient-derived serum sample and a normal individual serum sample purified with 30% PEG6000 were separately added thereto at a concentration of 10 μL/well, and further, a bTSH solution (final concentration: 100 μU/mL) was added thereto at a concentration of 10 μL/well. After culture for 10 minutes to 2 hours, 10-4 M forskolin solution was added thereto at a concentration of 50 μL/well, and the amount of luminescence was measured using a luminometer.
As shown in
The frozen cells prepared in 1 and a diagnostic kit for Graves' disease provided by the present invention containing a medium for cell culture, a cell washing solution, ViviRen, a calcium solution, a goat anti-hTSH antibody, a control serum and a 96-well plate described below were used to study serum TSAb activity in various thyroid disease patient groups. Specifically, the sera of 198 untreated Graves' disease patients, 18 hypothyroidism patients, 48 normal individuals, 2 Plummer's disease cases, 6 postpartum thyroiditis cases, 22 painless thyroiditis cases and 22 subacute thyroiditis cases, all of which were clinically and definitely diagnosed, were used (see Table 2). 150 μL of 30% PEG6000 was added to 50 μL of the serum of each patient, and the mixtures were stirred and then left standing at 4° C. for 5 minutes. After centrifugation at 3000 rpm at 4° C. for 20 minutes, the obtained precipitates were separately dissolved in 400 μL of a medium for cell culture (5% PEG6000, CO2 independent medium (calcium chloride, D-calcium pantothenate, L-glutamine, phenol red-free, Invitrogen Corp.)) to prepare sample solutions. The sample solutions were separately added (n=2) at a concentration of 10 μL/well to a 96-well plate. 1 ml (3×106 cells/ml) of the frozen cells was thawed in a warm bath and suspended in 10 mL of a cell washing solution (CO2 independent medium). After centrifugation at 1000 rpm for 5 minutes, 12 mL of a medium for cell culture was added to the obtained precipitate to prepare a cell solution. 7.5 μL of 4 mM ViviRen was added to the cell solution, and the mixture was seeded at a concentration of 90 μL/well into a 96-well plate. After culture for 4 hours, 3 mM calcium solution was added thereto at a concentration of 100 μL/well, and the amount of luminescence was measured using a luminometer. Among hypothyroidism patients, there is a patient having a high hTSH value in serum. Thus, for neutralizing the action of hTSH, 1.2 μL of a goat anti-hTSH polyclonal antibody (Meridian Life Science, Inc.) was added to the medium for cell culture, and assay was performed under this condition. A measured value in each patient was calculated based on a one-point calibration curve obtained by defining, as 1800, the measured value of a control serum containing NIBSC 65/122 diluted (1.874 mU LAST/mL) with a normal individual serum. Moreover, the sera of the same patients as above were assayed using the existing kit (TSAb kit, YAMASA CORP.) according to the instruction included in the kit.
A TSAb cutoff value was set from the serum TSAb values of normal individuals. The frequency distribution of serum TSAb values of 48 normal individuals is shown in
The TSAb value of each thyroid disease is shown in
The present invention can provide a method and a kit for determining a TSH receptor antibody, which are easy to manipulate and are safe. Thus, thyroid disease can be diagnosed.
The present application is based on and claims priority of Japanese patent application No. 2009-155183, the entire contents of which are hereby incorporated by reference.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2009-155183 | Jun 2009 | JP | national |
This is a continuation of application Ser. No. 13/381,402, which is the National Stage of PCT/JP2010/060731 filed Jun. 24, 2010, and claims the benefit of JP 2009-155183, filed Jun. 30, 2009, all of which are incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13381402 | Feb 2012 | US |
| Child | 15954434 | US |
