Patent Application
20230130549
The present invention relates to a method of producing a synovium-derived mesenchymal stem cell, which includes treating a synovial tissue with an enzyme for a predetermined time without causing the synovial tissue to undergo a disinfection step. The present invention further relates to a production method for a cell preparation for a joint medical treatment using the above method.
In the field of orthopedics, articular cartilage injury and meniscus injury are frequently seen as objects of daily medical practice and are widely recognized as diseases from which a large number of patients suffer. In a case where articular cartilage injury or meniscus injury occurs, arthralgia, a decrease in a mobile region, hydrarthrosis, dyskinesia, or the like occurs. A patient having traumatic articular cartilage injury or meniscus injury is usually treated medically by an orthopaedist. Surgical treatment for cartilage injury or meniscus injury aims at removing debris that causes further deterioration of the joint and restoring the function of the affected joint. However, it is generally known that cartilage and meniscus tissues are difficult to self-regenerate.
On the other hand, due to the recent progress in regenerative medicine technology, cell therapy capable of repairing cartilage or meniscus has become popular. Among the above, the mesenchymal stem cell (MSC) is expected as a cell source for a useful cell therapy. The mesenchymal stem cells can be collected from various body tissues and have been reported to be isolated from the bone marrow tissue (Prockop, D. J., 1997, Science. 276: 71-4), the adipose tissue (Zuk, P. A. et al., 2002, Mol Biol Cell. 13: 4279-95), the muscle tissue (Cao et al., 2003, Nat Cell Biol. 5: 640-6), the synovial tissue (De Bari, C. et al., 2001, Arthritis Rheum. 44: 1928-42), and the periosteal tissue (Fukumoto, T. et al., 2003, Osteoarthritis Cartilage. 11: 55-64). In particular, it has been reported that the synovium-derived mesenchymal stem cell has high proliferation ability and high cartilage forming ability as compared with mesenchymal stem cells derived from various mesenchymal tissues such as bone marrow (Sakaguchi, et al., 2005, Arthritis Rhum. 52: 2521-9). In addition, JP5928961B and JP5656183B disclose methods of medically treating articular cartilage injury and meniscus injury by using synovium-derived mesenchymal stem cells.
Non-Patent Document 1: Prockop, D. J., 1997, Science. 276: 71-4
Non-Patent Document 2: Zuk, P. A. et al., 2002, Mol Biol Cell. 13: 4279-95
Non-Patent Document 3: Cao et al., 2003, Nat Cell Biol. 5: 640-6
Non-Patent Document 4: De Bari, C. et al., 2001, Arthritis Rheum. 44: 1928-42
Non-Patent Document 5: Fukumoto, T. et al., 2003, Osteoarthritis Cartilage. 11: 55-64
Non-Patent Document 6: Sakaguchi, et al., 2005, Arthritis Rhum. 52: 2521-9
Patent Document 1: JP5928961B
Patent Document 2: JP5656183B
JP5928961B and JP5928961B disclose medical treatments using synovium-derived mesenchymal stem cells. On the other hand, in a process of actually producing cells, it was revealed that the production method disclosed above may not achieve a sufficient cell quantity enough to be subjected to an autologous medical treatment.
An object of the present invention is to provide a production method for a synovium-derived mesenchymal stem cell, by which proliferation efficiency is improved so that a sufficient amount of synovium-derived mesenchymal stem cells can be obtained from a synovial tissue. Further, an object of the present invention is to provide a production method for a cell preparation for a joint medical treatment using the production method for a synovium-derived mesenchymal stem cell. A further object of the present invention is to provide synovium-derived mesenchymal stem cell and a cell preparation for a joint medical treatment.
As a result of diligent studies to achieve the above object, the inventors of the present invention have found that the inventors of the present invention succeeded in producing a cell amount that can be subjected to a medical treatment and improving the proliferation ratio by providing a step of subjecting a synovial tissue to an enzyme treatment for a certain period of time or longer without causing it to undergo a disinfection step. From the viewpoint of sterilization and pasteurization, it has been ordinary to use the synovial tissue after causing it to undergo a disinfection step. It was conceived that carrying out the enzyme treatment for a long time without undergoing the disinfection step should be avoided as much as possible since there is an adverse effect such as an increase in impurities (bacteria, endotoxin, and the like) derived from the production step, and as a result, the number of cells that can be produced is expected to be reduced. In fact, in a case where the enzyme treatment time was changed from 1 hour to 1.5 hours after undergoing the disinfection step, the cell quantity was significantly reduced. On the other hand, in a case of deliberately removing the disinfection step, which has not been generally considered, it was found that the cell quantity can be unexpectedly increased, and it was revealed that the proliferation ratio is also significantly increased. The inventors of the present invention found that the effect of significantly increasing the proliferation ratio can be obtained for the first time by making two contrivances, that is, the extension of the enzyme treatment time and the omission of the cell disinfection step. The present invention has been completed based on the above findings.
That is, according to the present invention, the following inventions are provided.
<1> A method of producing a synovium-derived mesenchymal stem cell, which is a production method for a synovium-derived mesenchymal stem cell from a synovial tissue, the method comprising:
treating the synovial tissue with a mixed enzyme including one or more kinds of collagenases and one or more kinds of neutral proteases for 2 hours or more without causing the synovial tissue to undergo a disinfection step.
<2> The method according to <1>, in which the mixed enzyme is Liberase (registered trade name).
<3> The method according to <1> or <2>, in which an enzyme concentration in the enzyme treatment is 0.01 mg/ml to 10 mg/ml.
<4> The method according to any one of <1> to <3>, in which the synovial tissue is derived from a human.
<5> The method according to any one of <1> to <4>, in which the synovial tissue is a synovial tissue derived from a single donor.
<6> The method according to any one of <1> to <5>, in which a subject from which synovium is collected and a subject to which the synovium-derived mesenchymal stem cell is transplanted are the same subject.
<7> The method according to any one of <1> to <6>, in which a mass ratio of the synovial tissue to the enzyme is 1,000:1 to 10:1.
<8> The method according to any one of <1> to <7>, further comprising culturing, for 10 days or more, the synovium-derived mesenchymal stem cell after the enzyme treatment to proliferate the synovium-derived mesenchymal stem cell.
<9> The method according to <8>, in which the culturing for 10 days or more is carried out without culture medium exchange.
<10> The method according to <8> or <9>, in which the culturing for 10 days or more is carried out in a culture medium containing an autologous serum.
<11> The method according to any one of <8> to <10>, in which the synovium -derived mesenchymal stem cell after the enzyme treatment is seeded at a cell number of 100 cells/cm2 or more and 5,000 cells/cm2 or less and cultured for 10 days or more.
<12> The method according to any one of <8> to <11>, in which a proliferation ratio in the culturing for 10 days or more is 3 times or more and 50 times or less.
<13> The method according to any one of <1> to <12>, in which the synovium-derived mesenchymal stem cell is produced without being co-cultured with a cell other than the synovium-derived mesenchymal stem cell.
<14> A production method for a cell preparation for a joint medical treatment, the production method comprising:
<15> The production method for a cell preparation for a joint medical treatment according to <14>, in which the joint medical treatment is a medical treatment for a meniscus injury.
<16> Synovium-derived mesenchymal stem cell produced by the method according to any one of <1> to <13>.
<17> A cell preparation for a joint medical treatment, produced by the method according to <14> or <15>.
<A> Medical treatment method for a joint, comprising:
a step of transplanting synovium-derived mesenchymal stem cell produced by a method according to an aspect of the present invention so that a cartilage injury part or a meniscus injury part is covered with the synovium-derived mesenchymal stem cell; and
According to the present invention, it is possible to improve the proliferation efficiency so that a sufficient amount of synovium-derived mesenchymal stem cells can be obtained from the synovial tissue.
Hereinafter, embodiments for carrying out the present invention will be described in detail.
[Production Method for Synovium-Derived Mesenchymal Stem Cell]A production method for a synovium-derived mesenchymal stem cell according to an embodiment of the present invention is a method of producing a synovium-derived mesenchymal stem cell from a synovial tissue, where the production method includes treating a synovial tissue with a mixed enzyme including one or more kinds of collagenases and one or more kinds of neutral proteases for 2 hours or more without causing the synovial tissue to undergo a disinfection step.
<Synovial Tissue>
The synovial tissue can be collected from the unloaded portion of the joint under anesthesia.
The biological origin of the synovial tissue is not particularly limited, and a synovial tissue derived from any biological material, preferably a mammal, can be used. For example, a synovial tissue derived from a primate (for example, a chimpanzee, a Japanese monkey, or a human) can be used, and a human-derived synovial tissue can be used particularly preferably.
The synovial tissue may be a synovial tissue derived from a single donor or may be a synovial tissue derived from a plurality of donors; however, it is preferably a synovial tissue derived from a single donor.
In a case of producing a synovium-derived mesenchymal stem cell for the intended purpose of administration to a human, it is preferable to use a synovial tissue collected from a donor of which histocompatibility antigen type is identical or similar to that of the recipient. More preferably, a subject from which the synovium is collected and a subject to which the synovium-derived mesenchymal stem cell is transplanted are the same subject. That is, it is preferable to use the synovial tissue collected from the recipient itself (autologous transplantation).
The amount of the synovial tissue to be collected can be determined in consideration of the type of donor or the required amount of synovium-derived mesenchymal stem cells. For example, it is possible to obtain synovium-derived mesenchymal stem cells from the synovial tissue of 0.1 g to 10 g, preferably 0.1 g to 2.0 g, more preferably 0.1 g to 1.5 g, and still more preferably 0.1 g to 1.0 g. The collected synovial tissue is shredded with scissors or the like as necessary, and then subjected to the enzyme treatment described below. In the present invention, the synovial tissue is subjected to an enzyme treatment without causing it to undergo a disinfection step.
<Treatment with Enzyme>
In the present invention, the synovial tissue is treated with an enzyme for 2 hours or more.
As the enzyme, a mixed enzyme including one or more kinds of collagenases and one or more kinds of neutral proteases is used. A particularly preferred enzyme is Liberase (registered trade name). As the Liberase (registered trade name), it is possible to use, for example, Liberase (registered trade name) MNP-S (manufactured by F. Hoffmann-La Roche, Ltd.), which is an enzyme including a collagenase class I, a collagenase class II, and a neutral protease (thermolysin).
The enzymatic reaction can be carried out in an aqueous solution containing an enzyme, and an aqueous solution containing human serum may be used.
The enzyme concentration in the enzyme treatment is preferably 0.01 mg/ml to 10 mg/ml, more preferably 0.1 mg/ml to 10 mg/ml, still more preferably 0.5 mg/ml to 10 mg/ml, ever still more preferably 0.5 mg/ml to 5.0 mg/ml, particularly preferably 0.5 mg/ml to 2.0 mg/ml, and most preferably 0.7 mg/ml to 2.0 mg/ml.
The mass ratio of the synovial tissue to the enzyme is preferably 1,000:1 to 10:1, more preferably 500:1 to 20:1, and still more preferably 200:1 to 40:1.
The enzymatic reaction can be carried out at a temperature of preferably 15° C. to 40° C., more preferably 20° C. to 35° C., and still more preferably 25° C. to 35° C.
The reaction time may be 2 hours or more, more preferably 2.5 hours or more, and still more preferably 3 hours or more. The upper limit of the reaction time is not particularly limited; however, it may be 10 hours or less, 9 hours or less, 8 hours or less, 7 hours or less, 6 hours or less, 5 hours or less, or 4 hours or less.
The enzyme-treated mixture contains synovium-derived mesenchymal stem cells. The enzyme-treated mixture is transferred to a centrifuge tube through a cell strainer and centrifuged, whereby synovium-derived mesenchymal stem cells can be recovered.
<Washing>
In the present invention, the mixture after the enzyme treatment may be washed. The washing can be carried out by resuspending the synovium-derived mesenchymal stem cells recovered with the above-described centrifugation treatment in a culture medium and carrying out centrifugation again (for example, at 400 g for 5 minutes). As the culture medium, a-modified Eagle minimum essential medium (αMEM) can be used, which is not particularly limited. The number of times of washing may be one time or may be a plurality of times.
<Proliferation>
In the present invention, the synovium-derived mesenchymal stem cells may be cultured for 10 days or more to proliferate the synovium-derived mesenchymal stem cells.
As the culture medium that is used in the above-described culture, a culture medium that is used for the general culture of animal cells can be prepared as a basal medium. Examples of the culture medium that is used for general culture of animal cells include αMEM, a Dulbecco's modified Eagle medium (DMEM), a mixed medium of DMEM and F12 (DMEM:F12=1:1), an RPMI medium (a GIBCO (registered trade name) RPMI 1640 medium or the like), and a mixed medium of DMEM/F12 and RPMI (DMEM/F12:RPM=1:1), which are not particularly limited.
The culture medium may be a culture medium containing serum or may be a culture medium not containing serum. In a case of producing a synovium-derived mesenchymal stem cells from the autologous tissue for the intended purpose of administration to a living body, the culture medium may contain a serum of origin of the same species. That is, in a case of producing a synovium-derived mesenchymal stem cells from a human tissue for the intended purpose of administration to a human, a culture medium containing a human serum may be used. In a case where serum is used, the serum may be an autologous serum or may be an allogeneic serum; however, it is preferably an autologous serum. In a case where serum is used, the adding amount of serum in the culture medium is, for example, 20% by volume or less, 10% by volume or less, or 5% by volume or less.
The cell culture conditions are not particularly limited, and general cell culture conditions can be employed. Examples thereof include culture at a temperature of 30° C. to 40° C. and 3% to 7% CO2, which are not particularly limited. As one example, culture at a temperature of 37° C. and 5% CO2 can be mentioned.
In the present invention, it is preferable to carry out the above-described culturing for 10 days or more without culture medium exchange. In addition, in the above-described culturing for 10 days or more, it is preferable that the synovium-derived mesenchymal stem cells are produced without being co-cultured with cells other than the synovium-derived mesenchymal stem cells.
The differentiation of synovium-derived mesenchymal stem cells into cartilage cells progresses as the culture period increases, and thus, it is known that the in situ cartilage forming ability of synovium-derived mesenchymal stem cells decreases when the culture period exceeds a specific length. Therefore, in the present invention, it is preferable to adjust the culture period in order to proliferate the synovium-derived mesenchymal stem cells in an undifferentiated state and in a state having a good in situ cartilage forming ability. In addition, in the present invention, it is necessary to consider the need to prepare a sufficient number of undifferentiated synovial stem cells in order to cover the cartilage injury part and regenerate the affected part. As a result, the culture period is more preferably 5 days or more, 7 days or more, or 10 days or more, more preferably 10 to 14 days, 10 to 21 days, or 10 to 28 days, and still more preferably 10 to 21 days.
It is known that mesenchymal stem cells are differentiated into cartilage cells by culturing them in a cartilage forming culture medium to which transforming growth factor β3 (TGF-β3), dexamethasone, and bone morphogenetic protein 2 (BMP-2) have been added, whereby the cartilage tissue can be prepared in vitro. As a result, in the present invention, the synovium-derived mesenchymal stem cells isolated are preferably cultured in the absence of TGF-β3, dexamethasone, or BMP-2 in order to prevent the synovium-derived mesenchymal stem cells from being differentiated into cartilage cells.
It is also known that in the synovium-derived mesenchymal stem cells, the in situ cartilage forming ability decreases in inverse proportion to the number of passages of the mesenchymal stem cells in vitro. As a result, it is preferable to produce synovium-derived mesenchymal stem cells in the primary culture or first subculture in order to prepare undifferentiated mesenchymal stem cells,
In the present invention, the serum that is used in an autologous medical treatment is of autologous origin, the amount of serum that can be collected from the donor in an autologous medical treatment is limited, and the cell density is required to be equal to or higher than a certain level from the viewpoint of the proliferation of synovium-derived stem cells. For these reasons, it is preferable that the synovium-derived mesenchymal stem cells after the enzyme treatment are seeded at a cell number of 100 cells/cm2 or more and 5,000 cells/cm2 or less, 200 cells/cm2 or more and 5,000 cells/cm2 or less, 500 cells/cm2 or more and 5,000 cells/cm2 or less, 500 cells/cm2 or more and 2,500 cells/cm2 or less, or 500 cells/cm2 or more and 2,000 cells/cm2 or less, and then cultured. In addition, in order to proliferate the synovium-derived mesenchymal stem cells after the enzyme treatment, it is more preferable to culture the cells for 10 days or more.
The proliferation ratio in the above-described culturing for 10 days or more is preferably 3 times or more and 50 times or less, more preferably 4 times or more and 30 times or less, still more preferably 5 times or more and 20 times or less, and particularly preferably 7 times or more and 15 times or less.
The number of cells obtained at the end of the culture is preferably 1.0×107 cells or more, 2.0×107 cells or more, 2.5×107 cells or more, or 3.0×107 cells or more, more preferably 4.0×107 cells or more, still more preferably 5.0×107 cells or more, and particularly preferably 6.0×107 cells or more.
<Synovium-Derived Mesenchymal Stem Cell>
The mesenchymal stem cell is a somatic stem cell derived from a mesodermal tissue (mesenchyme). The mesenchymal stem cells are known to be present in bone marrow, synovium, periosteum, adipose tissue, and muscle tissue, and they are known to have the ability to be differentiated into osteoblasts, cartilage cells, adipose cells, and muscle cells. In relation to the differentiation of mesenchymal stem cells into cartilage cells, it is known that the addition of BMP or TGF-β to the culture solution promotes the differentiation of undifferentiated mesenchymal stem cells into cartilage cells, and the cartilage tissue can be regenerated under in vitro conditions.
The mesenchymal stem cell can be confirmed by detecting a molecule characteristic of the mesenchymal stem cell, for example, an enzyme, a receptor, a low-molecular-weight compound, or the like. Examples of the molecule characteristic of mesenchymal stem cells include, which are not limited to, CD73, CD90, CD105, and CD166, which are cell surface markers (positive markers). In addition, examples of the negative marker that are not expressed in mesenchymal stem cells include, but are not limited to, CD19, CD34, CD45, HLA-DR, CD11b, and CD14. It is noted that CD is an abbreviation for Clusters of diffusion, and HLA-DR is an abbreviation for human leukocyte engine-D-related. These positive markers and negative markers can be used to confirm that a cell is the mesenchymal stem cell. Although an immunological method can be used for the detection of these markers, the detection may be carried out by quantifying the mRNA amount of each molecule.
In the present specification, the synovium-derived mesenchymal stem cell is a stem cell contained in the synovium. The synovium-derived mesenchymal stem cell is a kind of mesenchymal stem cell. The synovium-derived mesenchymal stem cell can be detected, for example, by detecting CD90 positivity, CD45 negativity, or cartilage differentiation potency; however, the detection method is not particularly limited.
According to the present invention, there is provided synovium-derived mesenchymal stem cell produced by the method of the present invention.
The synovium-derived mesenchymal stem cell produced by the method according to the embodiment of the present invention can be used as a cell preparation for a joint medical treatment. Further, the synovium-derived mesenchymal stem cell produced by the method according to the embodiment of the present invention can be also used, for example, for research related to differentiation of mesenchymal stem cells, pharmaceutical screening for various diseases, evaluation of efficacy and safety of pharmaceutical candidate compounds, and the like.
[Production Method for Cell Preparation for Joint Medical Treatment]
The present invention relates to a production method for a cell preparation for a joint medical treatment, which includes;
According to the present invention, there is provided a cell preparation for a joint medical treatment, produced by the above-described production method for a cell preparation for a joint medical treatment.
That is, according to the present invention, it is possible to produce a cell preparation for a joint medical treatment, containing the synovium-derived mesenchymal stem cell obtained by the method according to the embodiment of the present invention as an active ingredient.
Examples of the joint medical treatment include a medical treatment for a disease associated with injury, damage, or inflammation of the joint, and examples of the medical treatment include a medical treatment for a joint disease resulting from degeneration and/or inflammation of the connective tissue such as cartilage, or a non-inflammatory joint disease. Examples of the joint medical treatment include a medical treatment for a disease selected from the group consisting of meniscus injury, traumatic cartilage injury, osteochondritis dissecans, aseptic osteonecrosis, osteoarthritis (knee osteoarthritis or the like), rheumatoid arthritis (chronic rheumatoid arthritis or the like), gout, reactive arthritis, psoriatic arthritis, juvenile arthritis, inflammatory arthritis, and articular cartilage defect, which are not limited to these diseases.
In a case where the synovium-derived mesenchymal stem cell produced by the method according to the embodiment of the present invention is used as a cell preparation for a joint medical treatment, this cell may be made into a pharmaceutical preparation in a form suitable for administration to an individual, by being mixed with a pharmaceutically acceptable carrier according to a conventional method. Examples of the carrier include physiological saline and distilled water for injection, which has been made to be isotonic by adding glucose and other auxiliary agents (for example, D-sorbitol, D-mannitol, sodium chloride, and the like). Further, a buffering agent (for example, a phosphate buffer solution or a sodium acetate buffer solution), a soothing agent (for example, benzalkonium chloride, procaine hydrochloride, or the like), a stabilizer (for example, human serum albumin, polyethylene glycol, or the like), a storage agent, an antioxidant, and the like may be blended.
[Medical Treatment Method for Joint]
The present invention further relates to a medical treatment method for a joint. More specifically, the present invention relates to a medical treatment method for a disease selected from the group consisting of meniscus injury, traumatic cartilage injury, osteochondritis dissecans, aseptic osteonecrosis, osteoarthritis (for example, knee osteoarthritis), rheumatoid arthritis (for example, chronic rheumatoid arthritis), gout, reactive arthritis, psoriatic arthritis, juvenile arthritis, inflammatory arthritis, and articular cartilage defect.
The medical treatment method for a joint according to the embodiment of the present invention includes a step of transplanting the synovium-derived mesenchymal stem cell produced by the method according to the embodiment of the present invention so that a cartilage injury part or a meniscus injury part is covered with the synovium-derived mesenchymal stem cell; and a step of differentiating the synovium-derived mesenchymal stem cell into a cartilage cell to regenerate cartilage tissue in situ at a cartilage injury part or a meniscus injury part.
In a case where the synovium-derived mesenchymal stem cells produced by the method according to the embodiment of the present invention are transplanted into a patient, it is more preferable to apply, per cartilage injury part or meniscus injury part, synovium-derived mesenchymal stem cells of at least 2.0×107 to 1.0×1011 cells, 2.5×107 to 1.0×1011 cells, 3.0×107 to 1.0×1011 cells, 4×107 to 1.0×1011 cells, 2.5×107 to 1.0×1010 cells, 2.5×107 to 1.0×109 cells, 2.5×107 to 1.0×108 cells, or 2.0×107 to 1.0×108 cells, or synovium-derived mesenchymal stem cells of 2.0×107 to 1.0×108 cells, in order to efficiently treat medically the cartilage injury part or the meniscus injury part.
By transplanting the synovium-derived mesenchymal stem cells into the cartilage injury part or the meniscus injury part, the cartilage injury part or the meniscus injury part is covered with the synovium-derived mesenchymal stem cells. The transplantation of the /synovium-derived mesenchymal stem cell can be carried out by open surgery or by arthroscopic surgery. In order to minimize the invasion, it is preferable to arthroscopically transplant the synovium-derived mesenchymal stem cell.
The cartilage injury part or the meniscus injury part may be covered with a suspension of synovium-derived mesenchymal stem cells or may be covered with a cell sheet of synovium-derived mesenchymal stem cells. For example, a gel having bioabsorbability such as gelatin or collagen can be used as a gel-like substance. The synovium-derived mesenchymal stem cell has a high ability to adhere to the cartilage-injury part or the meniscus injury part.
In a case of a medical treatment for cartilage injury, the minimally invasive method according to the embodiment of the present invention is characterized in that the cartilage injury part is covered with synovium-derived mesenchymal stem cells, and it includes the following steps:
In a case of a medical treatment for meniscus injury, the minimally invasive method according to the embodiment of the present invention is characterized in that the meniscus injury part is covered with synovium-derived mesenchymal stem cells, and it includes the following steps:
In order to reliably allow the synovium-derived mesenchymal stem cells to adhere to the surface of the cartilage-injury part or meniscus injury part, the transplanted synovium-derived mesenchymal stem cells are preferably held on the surface of the cartilage injury part or meniscus injury part for at least 10 minutes and preferably 15 minutes. In order to achieve this, the body position is held for at least 10 minutes and preferably 15 minutes in order to achieve that the cartilage injury part or the meniscus injury part faces upward and that the synovium-derived mesenchymal stem cells are held in the cartilage injury part or the meniscus injury part, which faces upward.
In order to further strengthen the adhesion of the synovium-derived mesenchymal stem cells to the cartilage-injury part or the meniscus injury part, the cartilage injury part or the meniscus injury part associated with the synovium-derived mesenchymal stem cells can be covered with the periosteum. The operation is completed after holding the synovium-derived mesenchymal stem cells on the surface of the cartilage injury part or the surface of the meniscus injury part for at least 10 minutes.
In the present invention, the transplanted synovium-derived mesenchymal stem cells are differentiated into cartilage cells at the cartilage-injury part or the meniscus injury part and the cartilage tissue is regenerated in situ at the cartilage-injury part or the meniscus injury part.
During the in situ cartilage formation process of the synovium-derived mesenchymal stem cells, the cartilage tissue is regenerated depending on the local microenvironment (the nutrient supply, the cytokine environment, and the like), and thus no external operation is required. As a result of the in situ cartilage formation of synovium-derived mesenchymal stem cells, the cartilage tissue is regenerated at the cartilage injury part or the meniscus injury part to repair the injury. Then, in a case of cartilage injury, a bone region, a boundary between the cartilage and the bone, a central part of the cartilage, a surface region, and a region adjacent to the original cartilage are formed as the original cartilage tissue, or in a case of the meniscus injury, meniscus cartilage is formed.
The present invention will be further specifically described with reference to Examples; however, the present invention is not limited by Examples.
Production of Synovium-Derived Mesenchymal Stem Cell According to General Production Step (With Tissue Disinfection, Enzyme Treatment Time: 1 Hour and 1 Minute)
Using a human specimen, synovium-derived mesenchymal stem cells were prepared from a synovial tissue according to a general production method. Specifically, an M1 specimen (synovial tissue: 0.62 g) was subjected to disinfection with a 0.1% Isodine solution for 1 minute as a tissue disinfection step. Then, the above-described tissue was shredded with scissors and immersed in 5.0 mL of a Liberase aqueous solution. It is noted that as the Liberase aqueous solution, a solution obtained by dissolving 5.0 mg of Liberase MNP-S (manufactured by F. Hoffmann-La Roche, Ltd.) in 5.0 mL of water for injection containing human autologous serum of a final concentration of 20% was used. The enzymatic reaction was carried out at room temperature of 25° C. for 1 hour and 1 minute. Then, the digested tissue solution was transferred to a 50 mL centrifuge tube through a cell strainer and centrifuged at 400 g for 5 minutes. The supernatant was removed, the obtained cell-concentrated suspension was suspended in a culture medium, and the entire amount thereof was seeded in a flask (1,000 cells/cm2). It is noted that as the culture medium, a culture medium obtained by dissolving, in αMEM, human autologous serum to a final concentration of 10% was used. The culture was carried out in a CO2 incubator (37° C., 5% CO2), and after 2 weeks, the cells were recovered from the flask to produce synovium-derived mesenchymal stem cells. It is noted that a feature of the present cell production is that the culture medium is not exchanged during the culture period. The cell quantity finally obtained in this way was 1.5×107 cells for Ml. In addition, the proliferation ratio calculated as the ratio of the number of cells after culturing for 2 weeks to the number of cells at the time of seeding was 2.0 times. A summary of the results is shown in Table 1.
Production of Synovium-Derived Mesenchymal Stem Cell According to Production Step in Which Enzyme Treatment Time is Extended (With Tissue Disinfection, Enzyme Treatment Time: 1.5 Hours)
Using a human specimen, synovium-derived mesenchymal stem cells were prepared from a synovial tissue under the condition in which the enzyme treatment time was extended by 30 minutes as compared with the general production method. Specifically, an M2 specimen (synovial tissue: 0.85 g) was subjected to disinfection with a 0.1% Isodine solution for 1 minute as a tissue disinfection step. Then, the above-described tissue was shredded with scissors and immersed in 5.0 mL of a Liberase aqueous solution. It is noted that as the Liberase aqueous solution, a solution obtained by dissolving 5.0 mg of Liberase MNP-S (manufactured by F. Hoffmann-La Roche, Ltd.) in 5.0 mL of water for injection containing human autologous serum of a final concentration of 20% was used. The enzymatic reaction was carried out at room temperature of 25° C. for 1.5 hours. Then, the digested tissue solution was transferred to a 50 mL centrifuge tube through a cell strainer and centrifuged at 400 g for 5 minutes. The supernatant was removed, the obtained cell-concentrated suspension was suspended in a culture medium, and the entire amount thereof was seeded in a flask (1,880 cells/cm2). It is noted that as the culture medium, a culture medium obtained by dissolving, in αMEM, human autologous serum to a final concentration of 10% was used. The culture was carried out in a CO2 incubator (37° C., 5% CO2), and after 2 weeks, the cells were recovered from the flask to produce synovium-derived mesenchymal stem cells. It is noted that a feature of the present cell production is that the culture medium is not exchanged during the culture period. The cell quantity finally obtained in this way was 0.8×107 cells as M2. This was less than 1.0×107 cells considered to be necessary for the medical treatment, which was at a level in which a cell amount required for the medical treatment could not be provided. In addition, the proliferation ratio calculated as the ratio of the number of cells after culturing for 2 weeks to the number of cells at the time of seeding was 0.6 times. A summary of the results is shown in Table 1.
Production of Synovium-Derived Mesenchymal Stem Cell According to Production Step in Which Tissue Disinfection Step is Eliminated and Enzyme Treatment Time is Extended (Without Tissue Disinfection, Enzyme Treatment Time: 3 Hours)
Using a human specimen, synovium-derived mesenchymal stem cells were prepared from a synovial tissue under the condition in which the tissue disinfection step was eliminated and the enzyme treatment time was extended by 2 hours, unlike the general production method. Specifically, tissues of an N1 specimen (synovial tissue: 0.42 g), an N2 specimen (synovial tissue: 0.60 g), an N3 specimen (synovial tissue: 0.86 g), and an N4 specimen (synovial tissue: 0.33 g) were each shredded with scissors and immersed in 5.0 mL of a Liberase aqueous solution without causing them to undergo the tissue disinfection step. It is noted that as the Liberase aqueous solution, a solution obtained by dissolving 5.0 mg of Liberase MNP-S (manufactured by F. Hoffmann-La Roche, Ltd.) in 5.0 mL of water for injection containing human autologous serum of a final concentration of 20% was used. The enzymatic reaction was carried out at room temperature of 25° C. for 3 hours. Then, the digested tissue solution was transferred to a 50 mL centrifuge tube through a cell strainer and centrifuged at 400 g for 5 minutes. The supernatant was removed, the collected cell-concentrated suspension was suspended in a culture medium, and the entire amount was seeded in a flask (690 cells/cm2 for N1, 1,059 cells/cm2 for N2, 1,028 cells/cm2 for N3, and 787 cells/cm2 for N4). It is noted that as the culture medium, a culture medium obtained by dissolving, in αMEM, human autologous serum to a final concentration of 10% was used. The culture was carried out in a CO2 incubator (37° C., 5% CO2), and after 2 weeks, the cells were recovered from the flask to produce synovium-derived mesenchymal stem cells. It is noted that a feature of the present cell production is that the culture medium is not exchanged during the culture period. The cell quantities finally obtained in this way were 4.9×107 cells for N1, 7.6×107 cells for N2, 7.0×107 cells for N3, and 6.5×107 cells for N4. This significantly exceeded 1.0×107 cells considered to be necessary for the medical treatment, which was at a level in which a cell amount required for the medical treatment could be sufficiently and stably provided. In addition, the proliferation ratios calculated as the ratio of the number of cells after culturing for 2 weeks to the number of cells at the time of seeding were respectively 9.5 times, 9.6 times, 9.1 times, and 11.0 times, and thus the effect of improving the proliferation ratio was recognized. A summary of the results is shown in Table 1.
The synovium-derived mesenchymal stem cells prepared in Comparative Examples 1 and 2 and Example 1 were subjected to a checking test for the expression of the mesenchymal stem cell markers. As a result, it was confirmed that all of the cells exhibit CD90 positivity, CD45 negativity, and cartilage differentiation potency and thus are synovium -derived mesenchymal stem cells.
<Interpretation of Results>
From the results shown in Table 1, it was revealed that the weight of the synovial tissue is not the dominant parameter with respect to the cell quantity, and two factors, that is, the extension of the enzyme treatment time and the elimination of the disinfection step, are indispensable for proliferation ratio. In addition, as it was conceived that extending the enzyme treatment time should be avoided since it causes injury to the synovial tissue, it was found that in M2 in which the enzyme treatment time was extended by 30 minutes with respect to Ml, the cell quantity is actually reduced significantly, and the proliferation ratio is also decreased. On the other hand, it was conceived that not undergoing the tissue disinfection step should be avoided since the possibility that impurities in the tissue derived from the production step, particularly bacteria, microorganisms, and the like increase during the enzyme treatment time and the culture period increased. However, it was revealed that in a case of deliberately eliminating the tissue disinfection step and significantly extending the enzyme treatment time, a positive effect in terms of the proliferation ratio is obtained unexpectedly. In addition, the cell quantity obtained from the production according to the present invention as a result of achieving the above-described proliferation ratio was significantly exceeded 1.0×107 cells considered to be necessary for the medical treatment, and this significantly exceeded the cell amount (2.0×107 cells) capable of exhibiting the effect even in a case of allogeneic cells. The combination that achieves the present proliferation ratio was conceived to have remarkable value in a method of producing a synovium-derived mesenchymal stem cell assuming autologous cell therapy.
The synovium-derived mesenchymal stem cells produced as N1 to N4 were actually produced from specimens of meniscus injury patients themselves and, after the production, respectively administered to the meniscus injury patients as autologous cell therapy. As a result, favorable symptom relief was observed until 52 weeks after the administration in all the meniscus injury patients to which the synovium-derived mesenchymal stem cells produced as N1 to N4 were respectively administered. An improvement of 22 points or more was confirmed in terms of the Lysholm score (see Table 2 below), which is known as a symptom score, until 52 weeks after the administration compared with that before the treatment, and the reposition was also confirmed in the meniscus checking by magnetic resonance imaging (MRI), which indicated the medical treatment results were favorable.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2020-115374 | Jul 2020 | JP | national |
| 2021-049723 | Mar 2021 | JP | national |
This application is a Continuation of PCT International Application No. PCT/JP2021/025142 filed on Jul. 2, 2021, which claims priority under 35 U.S.C. § 119(a) to Japanese Patent Application No. 2020-115374 filed on Jul. 3, 2020 and Japanese Patent Application No. 2021-049723 filed on Mar. 24, 2021. Each of the above application(s) is hereby expressly incorporated by reference, in its entirety, into the present application.
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/JP2021/025142 | Jul 2021 | US |
| Child | 18145922 | US |
