Pluripotent stem cell manufacturing system

Abstract

To manufacture pluripotent stem cells efficiently according to the conditions of samples.SOLUTION: According to one embodiment, a pluripotent stem cell manufacturing system includes an acquiring unit and an estimating unit. The acquiring unit acquires storage information on the storage of a sample from a donor, and surviving cell number information on the number of surviving cells contained in the sample. The estimating unit estimates tissue stem cell number information on the number of tissue stem cells contained in the sample, based on the storage information and the surviving cell number information.SELECTED DRAWING: Figure 2

Description

[Technical Field]

[0001] The embodiments disclosed in this specification and drawings relate to a pluripotent stem cell production system. [Background technology]

[0002] With the advancement of regenerative medicine, various pluripotent stem cell production systems have been proposed. There is a need to produce pluripotent stem cells from autologous blood, but low cost and high throughput production is required. There is also a need to efficiently produce pluripotent stem cells according to the condition of the blood used. The production process should be simpler, but at the same time, production failure is unacceptable, so a production system that satisfies both needs is required. [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Special Publication No. 2018-526992 [Patent Document 2] Japanese Patent Application Publication No. 2019-124594 [Patent Document 3] Special Publication No. 2014-217353 Summary of the Invention [Problem to be solved by the invention]

[0004] One of the problems to be solved by the embodiments disclosed in this specification and the drawings is to efficiently produce pluripotent stem cells according to the state of a sample. However, the problems to be solved by the embodiments disclosed in this specification and the drawings are not limited to the above problem. Problems corresponding to the effects of each configuration shown in the embodiments described below can also be positioned as other problems. [Means for solving the problem]

[0005] The pluripotent stem cell production system according to the present embodiment includes an acquisition unit and an estimation unit. The acquisition unit acquires storage information related to the storage of a donor's sample and viable cell count information related to the number of viable cells contained in the sample. The estimation unit estimates tissue stem cell count information related to the number of tissue stem cells contained in the sample based on the storage information and the viable cell count information. [Brief explanation of the drawings]

[0006] [Figure 1] FIG. 1 is a diagram showing an example of the configuration of a pluripotent stem cell production system according to this embodiment. [Figure 2] FIG. 2 is a diagram showing an example of the configuration of the tissue stem cell number estimation device of FIG. [Figure 3] FIG. 3 is a diagram showing an example of the configuration of the pluripotent stem cell production apparatus of FIG. [Figure 4] FIG. 4 is a diagram showing an example of a manufacturing process of induced pluripotent stem cells using the pluripotent stem cell manufacturing system of FIG. [Figure 5] FIG. 5 is a diagram schematically illustrating input and output of the trained model used in step S3 of FIG. [Figure 6] FIG. 6 is a diagram showing an example of a manufacturing process table used in step S4 of FIG. [Figure 7] FIG. 7 is a diagram showing an example of a display screen showing the hematopoietic stem cell count information and the manufacturing process displayed in step S5 of FIG. [Figure 8] FIG. 8 is a diagram showing an example of another display screen showing the hematopoietic stem cell count information and the manufacturing process displayed in step S5 of FIG. [Figure 9] FIG. 9 is a diagram showing a schematic diagram of the manufacturing process of induced pluripotent stem cells at level "1" (expansion culture omitted). [Figure 10] FIG. 10 is a diagram showing a schematic diagram of the process for producing induced pluripotent stem cells at level "2" (short-term culture). [Figure 11] FIG. 11 is a diagram showing a schematic diagram of the process for producing induced pluripotent stem cells at level "3" (normal culture). [Figure 12]FIG. 12 is a diagram showing another example of the display screen displayed in step S5 of FIG. [Figure 13] FIG. 13 is a diagram illustrating a learning process for a trained model and a manufacturing process table. DETAILED DESCRIPTION OF THE INVENTION

[0007] Hereinafter, an embodiment of a pluripotent stem cell production system will be described in detail with reference to the drawings.

[0008] The pluripotent stem cell production system according to this embodiment is a mechanical system that produces pluripotent stem cells derived from a sample donor from tissue stem cells contained in the sample. The pluripotent stem cells according to this embodiment are pluripotent cells such as embryonic stem cells (ES cells: Embryonic Stem Cells), somatic cell-derived embryonic stem cells (ntES cells: Nuclear Transfer Embryonic Stem Cells), and induced pluripotent stem cells (iPS cells: Induced Pluripotent Stem Cells). In addition, induced pluripotent stem cells are also called induced pluripotent stem cells. Tissue stem cells are multipotent cells such as hematopoietic stem cells, neural stem cells, liver stem cells, kidney stem cells, and skin stem cells. The sample may be any tissue related to the donor, such as blood, bone marrow, or skin. The donor may be human or animal.

[0009] 1 is a diagram showing an example of the configuration of a pluripotent stem cell production system 1 according to this embodiment. The pluripotent stem cell production system 1 includes a tissue stem cell number estimation device 10, a cell measurement device 20, and a pluripotent stem cell production device 30.

[0010] The tissue stem cell number estimation device 10 is a computer that estimates information regarding the number of tissue stem cells contained in a donor's sample (hereinafter referred to as tissue stem cell number information). The cell measuring device 20 is a mechanical device that measures cells contained in a donor's sample using various principles. The pluripotent stem cell production device 30 is a mechanical system that produces pluripotent stem cells derived from the donor's sample from the donor's sample. The pluripotent stem cell production device 30 produces pluripotent stem cells according to a production process that corresponds to the tissue stem cell number information estimated by the tissue stem cell number estimation device 10.

[0011] Figure 2 is a diagram showing an example of the configuration of the tissue stem cell number estimation device 10 of Figure 1. As shown in Figure 2, the tissue stem cell number estimation device 10 has a processing circuit 11, a storage device 13, a display device 15, an input device 17, and a communication device 19. The processing circuit 11, the storage device 13, the display device 15, the input device 17, and the communication device 19 are communicatively connected to one another via a bus.

[0012] The processing circuit 11 has a processor. The processor executes a program related to this embodiment to realize at least one function among an acquisition function 111, an estimation function 112, a determination function 113, a learning function 114, and a display control function 115. The program is stored in a computer-readable recording medium such as the storage device 13 or a portable recording medium.

[0013] By implementing the acquisition function 111, the processing circuit 11 acquires various pieces of information. For example, the processing circuit 11 acquires information regarding the storage of the donor's sample (hereinafter referred to as storage information). The processing circuit 11 also acquires information regarding the number of viable cells contained in the donor's sample (hereinafter referred to as viable cell count information). The sample is stored in advance at a storage facility. The sample is provided to the pluripotent stem cell production system 1 from the storage facility. The storage information is information regarding the storage of the sample at the storage facility. The viable cell count information is information regarding the number of viable cells contained in the sample after storage at the storage facility has ended and before processing by the pluripotent stem cell production apparatus 30 begins. The sample contains not only tissue stem cells used in the production of pluripotent stem cells but also various other cells that may be removed as unnecessary matter. Viable cells are cells that remain alive in the sample and include not only tissue stem cells but also various other cells. The viable cell count information is a factor that affects the success or failure of pluripotent stem cell production and is an example of information for evaluating the state of a blood sample or viable cells.

[0014] By implementing the estimation function 112, the processing circuit 11 estimates information regarding the number of tissue stem cells contained in the sample (hereinafter referred to as tissue stem cell count information) based on the storage information and viable cell count information acquired by the acquisition function 111. The tissue stem cell count information is a factor that affects the success or failure of pluripotent stem cell production, and is an example of information for evaluating the state of a blood sample or viable cells. As an example, the processing circuit 11 estimates the tissue stem cell count information by applying the storage information and viable cell count information to a trained model.

[0015] By implementing the determination function 113, the processing circuitry 11 determines a manufacturing process for producing pluripotent stem cells from tissue stem cells based on the tissue stem cell count information estimated by the estimation function 112. As an example, the processing circuitry 11 determines the manufacturing process based on a table (hereinafter referred to as the manufacturing process table) that associates the level of tissue stem cell count information with the manufacturing process.

[0016] By implementing the learning function 114, the processing circuit 11 trains the learned model used in the estimation function 112 and the manufacturing process table used in the decision function 113.

[0017] By implementing the display control function 115, the processing circuitry 11 displays various information via the display device 15. For example, the processing circuitry 11 displays information on the number of tissue stem cells estimated by the estimation function 112 and the manufacturing process determined by the determination function 113.

[0018] The storage device 13 is a storage device such as a RAM, a ROM, a hard disk drive (HDD), a solid state drive (SSD), or a semiconductor storage device that stores various information. For example, the storage device stores various programs, etc. As hardware, the storage device 13 may be a drive device that reads and writes various information from and to a portable recording medium such as a CD-ROM drive, a DVD drive, or a flash memory.

[0019] The display device 15 displays various information. For example, a CRT display, a liquid crystal display, an organic EL display, an LED display, a plasma display, or any other display known in the art can be used as appropriate for the display device 15. The display device 15 may also be a projector.

[0020] The input device 17 is an interface for inputting various commands from an operator. A keyboard, a mouse, various switches, etc. can be used as the input device 17. The input device 17 supplies output signals corresponding to the various commands to the processing circuit 11 via the bus.

[0021] The communication device 19 communicates data with the cell measuring device 20, the pluripotent stem cell production device 30, etc. via wired or wireless connections (not shown). For example, the communication device 19 receives viable cell count information from the cell measuring device 20. The communication device 19 also transmits information about the production process determined by the determination function 113 to the pluripotent stem cell production device 30.

[0022] Figure 3 is a diagram showing an example of the configuration of the pluripotent stem cell production apparatus 30 of Figure 1. As shown in Figure 3, the pluripotent stem cell production apparatus 30 has a control circuit 31, an unnecessary substance removal unit 32, an expansion culture unit 33, a tissue stem cell extraction unit 34, a factor introduction unit 35, a pluripotent stem cell culture unit 36, a storage unit 37, a first switching unit 38, and a second switching unit 39.

[0023] The control circuit 31 includes a processor such as a CPU or a GPU. The control circuit 31 controls the waste removal unit 32, expansion culture unit 33, tissue stem cell extraction unit 34, factor introduction unit 35, pluripotent stem cell culture unit 36, storage unit 37, first switch unit 38, and second switch unit 39 to produce donor-derived pluripotent stem cells from tissue stem cells contained in a blood sample according to a production process based on the tissue stem cell number information estimated by the tissue stem cell number estimation device 10.

[0024] The waste removal unit 32 is a mechanical device that removes waste from the donor's sample. For example, a centrifuge or a filter device may be used as the waste removal unit 32. By removing the waste, tissue stem cells are extracted. The waste removal unit 32 is connected to the expansion culture unit 33 via the flow path R1, the first switching unit 38, and the flow path R2. A liquid containing tissue stem cells is supplied to the expansion culture unit 33 via the flow path R1, the first switching unit 38, and the flow path R2.

[0025] The expansion culture unit 33 is a mechanical device that expands and cultures tissue stem cells. For example, the expansion culture unit 33 has a culture vessel and a dispensing mechanism. The dispensing mechanism is connected to flow path R2. The dispensing mechanism aspirates a liquid containing tissue stem cells and dispenses it into the culture vessel. Various reagents, such as media, are also added to the culture vessel by the dispensing mechanism. The culture time in the expansion culture unit 33 can be adjusted as desired. The expansion culture unit 33 is connected to the tissue stem cell extraction unit 34 via flow path R3. The liquid containing the expanded tissue stem cells is supplied to the tissue stem cell extraction unit 34 via flow path R3. Note that, in the expansion culture unit 33, trace amounts of waste matter are also supplied along with the tissue stem cells, and therefore, the waste matter proliferates along with the tissue stem cells during expansion culture.

[0026] The tissue stem cell extraction unit 34 extracts tissue stem cells from the liquid containing tissue stem cells supplied from the expansion culture unit 33. For example, a flow cytometer device is used as the tissue stem cell extraction unit 34. The flow cytometer device is connected to flow path R3. The flow cytometer device aligns the cells contained in the liquid supplied from the expansion culture unit 33 and optically detects, counts, and selects the cells. This results in the extraction of tissue stem cells. The tissue stem cell extraction unit 34 is connected to the factor introduction unit 35 via flow path R4, a second switching unit 39, and flow path R5.

[0027] The factor introduction unit 35 introduces an induction factor into the tissue stem cells extracted by the tissue stem cell extraction unit 34 to establish pluripotent stem cells. For example, the factor introduction unit 35 has a channel through which a liquid containing tissue stem cells flows and a pump that supplies the induction factor to the channel. The induction factor, also known as a Yamanaka factor, initializes tissue stem cells. Specifically, it is an Oct family gene, a Klf family gene, a Myc family gene, or their respective gene products. For example, Oct3 / 4 is used as an Oct family gene, Klf4 is used as an Klf family gene, and c-Myc or L-Myc is used as an Myc family gene. The induction factor may also be a Sox family gene or its gene product. Sox2 is used as an example of a Sox family gene. When the induction factor is introduced into the tissue stem cells, the tissue stem cells are initialized and pluripotent stem cells are established. The factor introduction unit 35 is connected to the pluripotent stem cell culture unit 36 ​​via channel R6. A liquid containing pluripotent stem cells is supplied to the pluripotent stem cell culture unit 36 ​​via channel R6.

[0028] The pluripotent stem cell culture unit 36 ​​cultures the pluripotent stem cells supplied from the factor introduction unit 35. Specifically, the pluripotent stem cell culture unit 36 ​​has a culture vessel and a dispensing mechanism. The dispensing mechanism dispenses a liquid containing pluripotent stem cells into the culture vessel. The dispensing mechanism adds various reagents, such as medium, to the culture vessel as appropriate. After a predetermined culture period has passed, multiple cell clumps consisting of pluripotent stem cells are produced in the culture vessel. The pluripotent stem cell culture unit 36 ​​is connected to the storage unit 37 via flow channel R7. The cell clumps are supplied to the storage unit 37 via flow channel R7.

[0029] The storage unit 37 stores the pluripotent stem cells supplied from the pluripotent stem cell culture unit 36. Specifically, the storage unit 37 freezes a plurality of cell clumps made of pluripotent stem cells in a cell cryopreservation solution and seals them in a container of your choice.

[0030] As shown in Figure 3, the waste removal unit 32 is selectively connected to the expansion culture unit 33 and the factor introduction unit 35 via a first switching unit 38. Specifically, the waste removal unit 32 and the first switching unit 38 are connected via flow path R1, and the first switching unit 38 and the expansion culture unit 33 are connected via flow path R2. A second switching unit 39 is provided between the tissue stem cell extraction unit 34 and the factor introduction unit 35, and the tissue stem cell extraction unit 34 and the second switching unit 39 are connected via flow path R4 and flow path R5, respectively. The first switching unit 38 and the second switching unit 39 are connected via flow path R8.

[0031] The first switching unit 38 is configured by a three-way valve or the like that can individually open and close an outlet hole on the flow path R2 side (hereinafter referred to as the first outlet hole) and an outlet hole on the flow path R8 side (hereinafter referred to as the second outlet hole). The first switching unit 38 individually opens and closes the first outlet hole and the second outlet hole in accordance with a switching signal from the control circuit 31.

[0032] The second switching unit 39 is configured by a three-way valve or the like that can individually open and close an inlet on the flow path R4 side (hereinafter referred to as a first inlet) and an inlet on the flow path R8 side (hereinafter referred to as a second inlet). The second switching unit 39 individually opens and closes the first inlet and the second inlet in accordance with a switching signal from the control circuit 31.

[0033] Next, an example of the operation of the pluripotent stem cell production system 1 having the above configuration will be described. In the following description, it is assumed that the donor is a fetus, the sample is a blood sample, the tissue stem cells are hematopoietic stem cells, and the pluripotent stem cells are induced pluripotent stem cells (iPS cells). The type of blood sample is not particularly limited, and peripheral blood or umbilical cord blood can be used. Peripheral blood mononuclear cells (PBMCs) fractionated from any blood of the donor may also be used. However, in the following description, the blood sample is assumed to be umbilical cord blood as an example.

[0034] Umbilical cord blood is fetal blood contained in the umbilical cord that connects the fetus and mother. Umbilical cord blood contains a high proportion of undifferentiated cell fractions, CD34+CD33- and CD34+CD38- cells, among CD34+ cells. It also contains a large number of more undifferentiated hematopoietic stem cells, making it a suitable source for generating induced pluripotent stem cells. Adult peripheral blood contains almost no hematopoietic stem cells. Umbilical cord blood banks for hematopoietic stem cell transplantation have been established, and approximately 10,000 samples, each 40–150 ml, are frozen and stored in Japan. These samples are intended for transplantation, and quality assurance guidelines are established for proper storage. Strict testing is conducted at the start of storage. However, depending on factors such as storage period and conditions at each blood bank, the viability of CD34+ cells after thawing ranges from 34% to 99%, and there have been reports of variability in the quality of umbilical cord blood samples.

[0035] Attempts are being made to produce iPS cells from autologous blood using myiPS cells. The various types of blood mentioned above are being considered for use as autologous blood. A robust production method that can accommodate the various conditions of various blood samples is required for myiPS cells. To improve throughput while maintaining low costs, the production process must be simpler. However, because production failure is unacceptable, a production system that satisfies both needs is desired.

[0036] FIG. 4 is a diagram showing an example of a manufacturing process for induced pluripotent stem cells using the pluripotent stem cell manufacturing system of FIG. 1. As shown in FIG. 4, the cell measuring device 20 counts the number of viable cells contained in a donor's blood sample (input blood) (step S1). The blood sample is stored frozen in a cord blood storage facility, such as a cord blood bank. The blood sample is thawed before being used to manufacture pluripotent stem cells. Some cells die during the freezing, storage, and thawing of the blood sample. After the blood sample is thawed, the cell measuring device 20 counts the number of viable cells contained in the thawed blood sample. The volume of the blood sample to be measured may be standardized to an arbitrary volume, such as 10 ml. However, this is not intended to be limiting.

[0037] A cell counter is used as the cell measuring device 20. In this case, the cell measuring device 20 photographs the blood sample using an optical imaging device to generate an optical image, and processes the optical image to measure the number of viable cells or the ratio of said numbers. Alternatively, the cell measuring device 20 optically detects the blood sample to generate an optical spectrum, and analyzes the optical spectrum to measure the number of viable cells or the ratio of said numbers. The ratio of the number of viable cells is defined as the number of viable cells relative to the total number of cells contained in the blood sample. Numerical information regarding the number or ratio of viable cells is an example of viable cell count information. The viable cell count information is information for evaluating the current state of the blood sample. The viable cell count information is acquired by the processing circuit 11 using the acquisition function 111 of the processing circuit 11.

[0038] When step S1 is performed, the processing circuit 11, by implementing the acquisition function 111, reads the blood sample storage information from the blood sample container (step S2). The storage information is information related to the storage of the blood sample and is information that can be used to estimate the current state of the blood sample. A blood data sheet is attached to the blood sample container. A code such as a one-dimensional or two-dimensional code is printed or attached to the blood data sheet, linking the storage information, such as the storage conditions at the blood sample storage facility. For example, in blood storage facilities such as umbilical cord blood banks, the blood cell count, CD34-positive cell count, CD34-positive cell count or rate, storage years, and storage period at the start of storage for each blood sample are recorded as storage conditions. By reading the code printed or attached to the blood sample container with a code reader, the processing circuit 11 acquires the storage information linked to the code. Note that letters, numbers, etc. representing the storage information may be printed on the blood data sheet. In this case, too, the processing circuit 11 reads the letters, numbers, etc. printed on the blood data sheet using an optical character reader or the like, and obtains the storage information represented by the letters, numbers, etc.

[0039] The donor's identification information may be acquired as the stored information. The donor's identification information may be any information that affects the quality of the blood sample, such as the donor's name, age, weight, race, etc. A code representing the donor's identification information may also be printed on the blood data sheet. Furthermore, letters, numbers, etc. representing the donor's identification information may be printed. By reading this information, the processing circuit 11 can acquire the donor's identification information as stored information.

[0040] The blood sample according to the present embodiment is not limited to a blood sample frozen and stored in a storage facility such as a cord blood bank. For example, a blood sample collected from a donor and stored or transported in an unfrozen state may be used. The storage information includes the date and time of blood collection and the donor's identification information.

[0041] After step S2 is performed, the processing circuitry 11 estimates hematopoietic stem cell count information related to the number of hematopoietic stem cells by implementing the estimation function 112 (step S3). The hematopoietic stem cell count information is an example of tissue stem cell count information. In step S3, the processing circuitry 11 estimates the hematopoietic stem cell count information using the trained model.

[0042] FIG. 5 is a diagram schematically illustrating the input and output of the trained model used in step S3. As shown in FIG. 5, the trained model is a machine learning model whose parameters have been trained to input the viable cell count information acquired in step S1 and the storage information acquired in step S2 and output hematopoietic stem cell count information. Examples of the machine learning model that can be used include a neural network and a support vector machine. The output hematopoietic stem cell count information is, for example, numerical information regarding the number or ratio of hematopoietic stem cells. This number or ratio of hematopoietic stem cells is the number or ratio of hematopoietic stem cells estimated to be contained in the viable cells at the time of measurement of the input viable cell count information. More specifically, it is the number or ratio of hematopoietic stem cells contained in the blood sample before expansion culture by expansion culture unit 33. The trained model is generated in advance by learning function 114 and stored in storage device 13.

[0043] Note that specific examples of input and output of the trained model are not limited to those described above. For example, the input viable cell count information may be optical image information or optical spectrum information about the blood sample generated by the cell measuring device 20 in step S1. The optical image information and optical spectrum information indicate the current state of the blood sample and are expected to have a certain correlation with the hematopoietic stem cell count information contained in the blood sample.

[0044] After step S3 is performed, processing circuitry 11, by implementing decision function 113, determines a manufacturing process for induced pluripotent stem cells based on the hematopoietic stem cell count information estimated in step S3 (step S4). In step S4, processing circuitry 11 determines a manufacturing process corresponding to the hematopoietic stem cell count information estimated in step S3 based on a correspondence relationship between multiple levels of the hematopoietic stem cell count information and multiple manufacturing processes corresponding to the multiple levels. This correspondence relationship is realized, for example, by an LUT (Look Up Table). Hereinafter, this LUT will be referred to as a manufacturing process table. The manufacturing process table is generated in advance by learning function 114 and stored in storage device 13.

[0045] FIG. 6 shows an example of a manufacturing process table used in step S4. As shown in FIG. 6, the manufacturing process table associates levels with manufacturing processes. The levels are divided into multiple stages according to the numerical value of the number or ratio of hematopoietic stem cells. Each level is defined by a range of the number or ratio of hematopoietic stem cells. The range of the number or ratio of hematopoietic stem cells corresponding to each level is predetermined, for example, by the learning function 114. Note that an operator can also set any value via the input device 17. The manufacturing process refers to a manufacturing process of induced pluripotent stem cells using the pluripotent stem cell manufacturing apparatus 30 that is suitable for the corresponding level. Specifically, "suitable for the corresponding level" refers to a manufacturing process that produces a sufficient amount of induced pluripotent stem cells while minimizing the time and cost required for the production of the induced pluripotent stem cells. In other words, the correspondence between the level and the manufacturing process is determined so as to achieve a balance between the quality of the induced pluripotent stem cells and the time and cost required for production.

[0046] Level "1" is a level classified as a level in which the number or ratio of pluripotent stem cells is sufficient. In the manufacturing process of level "1," expansion culture using the expansion culture section 33 is omitted. This is because if the number or ratio of hematopoietic stem cells contained in the blood sample is sufficient, a sufficient amount of induced pluripotent stem cells can be produced without expansion culture. Instead of performing expansion culture, the time required for expansion culture and the costs of various reagents can be reduced.

[0047] Level "2" is a level classified as a level where the number or ratio of pluripotent stem cells is somewhat small. In the manufacturing process for level "2," expansion culture is performed for only a short period of time using the expansion culture section 33. If the number or ratio of hematopoietic stem cells contained in the blood sample is somewhat small, expansion culture can be performed for a short period of time to obtain a sufficient amount of induced pluripotent stem cells while reducing the time required for expansion culture and reagent costs compared to normal. The expansion culture time can be set to any time as long as it is shorter than the normal expansion culture time.

[0048] Level "3" is a level classified as a low number or ratio of pluripotent stem cells. In the manufacturing process for level "3," expansion culture is carried out for a normal period of time using the expansion culture section 33. If the number or ratio of hematopoietic stem cells contained in the blood sample is low, expansion culture must be carried out for a normal period of time to obtain a sufficient amount of induced pluripotent stem cells. The normal expansion culture time is about one week, but this can be set to any time depending on the blood sample, culture environment, etc.

[0049] Level "0" is a level classified as unsuitable for producing induced pluripotent stem cells because the number or ratio of pluripotent stem cells is significantly low. In a production process at level "0," production of induced pluripotent stem cells using the pluripotent stem cell production device 30 is halted. This is because expansion culture does not increase the number of hematopoietic stem cells, making it impossible to produce induced pluripotent stem cells. By halting production, it is possible to reduce the time required for the induced pluripotent stem cell production process and the costs of various reagents.

[0050] In step S4, the processing circuit 11 identifies the level to which the hematopoietic stem cell count information estimated in step S3 belongs from among the multiple levels defined in the manufacturing process table, and searches the manufacturing process table using that level as a search key to determine the manufacturing process associated with that level.

[0051] In step S3, the processing circuitry 11 estimates the number or ratio of hematopoietic stem cells, which is hematopoietic stem cell count information, and in step S4, determines a level to which the number or ratio of hematopoietic stem cells belongs and determines a manufacturing process corresponding to the level. The level is information corresponding to the number or ratio of hematopoietic stem cells and is an example of hematopoietic stem cell count information. That is, in step S3, the processing circuitry 11 may estimate the level by applying a trained model to the viable cell count information and storage information. In this case, the trained model can be generated by inputting the viable cell count information and storage information and training parameters to output a level corresponding to the viable cell count information.

[0052] Furthermore, the manufacturing process in the manufacturing process table is defined by whether or not expansion culture is performed and / or the culture time of expansion culture, but is not limited to this. For example, the manufacturing process may be defined by the manufacturing stage to be performed within the manufacturing process. For example, if expansion culture is omitted from the manufacturing process, the manufacturing process may be defined as follows: removal of unnecessary substances → introduction of induction factors → pluripotent stem cell culture → storage.

[0053] After step S4 is performed, processing circuitry 11 displays the hematopoietic stem cell count information estimated in step S3 and the manufacturing process determined in step S4 (step S5) by implementing display control function 115. In step S5, processing circuitry 11 displays the hematopoietic stem cell count information and the manufacturing process in a predetermined layout on display device 15.

[0054] FIG. 7 is a diagram showing an example of a display screen 50 displaying hematopoietic stem cell count information and manufacturing steps displayed in step S5. The display screen 50 is displayed on the display device 15. As shown in FIG. 7, the display screen 50 displays an ID, which is identification information for the donor or blood sample. The display screen 50 also displays display fields 51, 52, and 53. The hematopoietic stem cell count information estimated in step S3 is displayed in display field 51. The level of the hematopoietic stem cell count information estimated in step S3 may also be displayed in display field 51. The manufacturing steps determined in step S4 are displayed in display field 52. The predicted manufacturing time for the manufacturing steps determined in step S4 is displayed in display field 53. The predicted manufacturing time is calculated or determined by the processing circuit 11 according to the manufacturing steps determined in step S4. For example, a standard processing time is set for each manufacturing step of induced pluripotent stem cells, and the predicted manufacturing time can be calculated by summing the standard processing times for the manufacturing steps to be performed. Alternatively, the predicted manufacturing time may be associated with each level in the manufacturing step table.

[0055] For example, as shown in Figure 7, if a manufacturing process of level "1" is determined in step S4, display field 51 displays "Estimated number of hematopoietic stem cells: XXX" and "Sufficient amount (level 1)," display field 52 displays "Omit expansion culture," and display field 53 displays "Estimated manufacturing time: △△ hours □□ minutes." By displaying display screen 50, the operator can confirm the hematopoietic stem cell count information and the manufacturing process in advance. The operator can also confirm the estimated manufacturing time in advance.

[0056] FIG. 8 shows an example of another display screen 60 showing hematopoietic stem cell count information and the manufacturing process. Display screen 60 is displayed on display device 15. Display screen 60 is the display screen when a decision is made in step S4 to discontinue production at level "0." In this case, display field 51 displays "Estimated number of hematopoietic stem cells: . . . " and "Inadequate amount (level 0)." Display field 52 displays "Production will be discontinued" and "Please increase the amount of blood sample or use another blood sample." Display field 53 displays "Estimated production time: Error." By displaying display screen 60, the operator can confirm that the number of hematopoietic stem cells is inadequate and that production will be discontinued. In this case, the operator can request a resend of a blood sample from the same donor to a cord blood storage facility or other facility. Alternatively, the operator can start over from step S1 using a blood sample from another donor.

[0057] If level "1," "2," or "3" is determined in step S4, information regarding the manufacturing process determined in step S4 is transmitted from the tissue stem cell number estimation device 10 to the pluripotent stem cell manufacturing device 30 via the communication device 19.

[0058] After step S5 is performed, the control circuit 31 of the pluripotent stem cell production apparatus 30 produces induced pluripotent stem cells derived from the donor's blood sample according to the production process determined in step S4 (step S6). In step S6, the control circuit 31 controls the waste removal unit 32, expansion culture unit 33, tissue stem cell extraction unit 34, factor introduction unit 35, pluripotent stem cell culture unit 36, storage unit 37, first switch unit 38, and second switch unit 39 to produce induced pluripotent stem cells according to the production process determined in step S4.

[0059] FIG. 9 is a schematic diagram illustrating the process for producing induced pluripotent stem cells in level "1" (expansion culture omitted). As shown in FIG. 9, in level "1," the inlet and second outlet of the first switching unit 38 are open and the first outlet is closed, while the second inlet and outlet of the second switching unit 39 are open and the first inlet is closed. This closes flow paths R2, R3, and R4 leading from the waste removal unit 32 to the factor introduction unit 35 via the expansion culture unit 33 and tissue stem cell extraction unit 34, and opens flow path R8 leading directly from the waste removal unit 32 to the factor introduction unit 35. In this case, a blood sample is first introduced into the waste removal unit 32, which removes waste from the blood sample. It is assumed that the blood sample after removal contains a sufficient amount of hematopoietic stem cells. The hematopoietic stem cells are then supplied directly to the factor introduction unit 35 via flow paths R1, R8, and R5, where induction factors are introduced into the hematopoietic stem cells. The introduction of an induction factor initializes hematopoietic stem cells, establishing induced pluripotent stem cells. The induced pluripotent stem cells are supplied to pluripotent stem cell culture unit 36 ​​via flow channel R6 and cultured in pluripotent stem cell culture unit 36. Because there is a sufficient amount of hematopoietic stem cells, it is estimated that a sufficient amount of induced pluripotent stem cells will be produced. The induced pluripotent stem cells are then supplied to storage unit 37 via flow channel R7, sealed in a container, and stored.

[0060] If it is estimated that the blood sample contains a sufficient amount of hematopoietic stem cells, expansion culture can be omitted, as shown in Figure 9. This allows obtaining a sufficient amount of induced pluripotent stem cells while reducing the time required for expansion culture and the costs of various reagents.

[0061] FIG. 10 is a schematic diagram illustrating the process for producing induced pluripotent stem cells at level "2" (short-term culture). As shown in FIG. 10, in level "2," the inlet and first outlet of the first switching unit 38 are open, while the second outlet is closed. The first inlet and outlet of the second switching unit 39 are open, while the second inlet is closed. This opens channels R2, R3, and R4 leading from the waste removal unit 32 to the factor introduction unit 35 via the expansion culture unit 33 and tissue stem cell extraction unit 34, while channel R8 leading directly from the waste removal unit 32 to the factor introduction unit 35 is closed. It is estimated that the blood sample from which waste materials have been removed by the waste removal unit 32 contains a relatively small number of hematopoietic stem cells. The hematopoietic stem cells are then expanded for a short period of time in the expansion culture unit 33, and the expanded hematopoietic stem cells are extracted by the tissue stem cell extraction unit 34. The extracted hematopoietic stem cells are supplied to the factor introduction unit 35. Thereafter, induced pluripotent stem cells are established in the factor introduction section 35, the induced pluripotent stem cells are cultured in the pluripotent stem cell culture section 36, and the induced pluripotent stem cells are sealed in a container and stored in the storage section 37.

[0062] If it is estimated that the blood sample contains a relatively small number of hematopoietic stem cells, expansion culture is carried out for a short period of time, as shown in Figure 10. This allows for obtaining a sufficient number of induced pluripotent stem cells even when the number of hematopoietic stem cells is relatively small, while also reducing the time required for expansion culture and the costs of various reagents.

[0063] FIG. 11 is a schematic diagram illustrating the process for producing induced pluripotent stem cells at level "3" (normal time culture). As shown in FIG. 11, in level "3," as in level "2," the inlet and first outlet of first switching unit 38 are open and the second outlet is closed, while the first inlet and outlet of second switching unit 39 are open and the second inlet is closed. This opens channels R2, R3, and R4, and closes channel R8. It is estimated that the blood sample after waste removal unit 32 contains a small amount of hematopoietic stem cells. The hematopoietic stem cells are then expanded for a standard time in expansion culture unit 33, and the expanded hematopoietic stem cells are extracted by tissue stem cell extraction unit 34. The extracted hematopoietic stem cells are supplied to factor introduction unit 35. Thereafter, induced pluripotent stem cells are established in the factor introduction section 35, the induced pluripotent stem cells are cultured in the pluripotent stem cell culture section 36, and the induced pluripotent stem cells are sealed in a container and stored in the storage section 37.

[0064] If the blood sample is estimated to contain a small number of hematopoietic stem cells, expansion culture is performed for a standard period of time, as shown in Figure 11. This allows for the production of a sufficient number of induced pluripotent stem cells despite the small number of hematopoietic stem cells.

[0065] When step S6 is performed, the process of producing induced pluripotent stem cells using the pluripotent stem cell production system according to this embodiment is completed.

[0066] The manufacturing process for induced pluripotent stem cells shown in Figure 4 is not limited to this example, and various modifications are possible. For example, the order of steps S1 and S2 may be reversed. As another example, step S5 may not be performed. Furthermore, it is not necessary to display both the hematopoietic stem cell count information and the manufacturing process in step S5; only either the hematopoietic stem cell count information or the manufacturing process may be displayed.

[0067] As another example, the levels of hematopoietic stem cell count information are not limited to the above four levels. For example, level "0" does not need to be provided. At a minimum, two levels may be provided: a first level indicating that the number of hematopoietic stem cells is inappropriate, and a second level indicating that the number of hematopoietic stem cells is appropriate. The first level may be associated with a manufacturing process in which expansion culture is performed for a given period of time, and the second level may be associated with a manufacturing process in which expansion culture is omitted.

[0068] Levels "2" and "3" may be further divided into multiple stages depending on the culture time. For example, level "2" may be divided into multiple sub-levels corresponding to culture times shorter than the standard time. Level "3" may be divided into multiple sub-levels corresponding to culture times longer than the standard time. By subdividing the levels in this way, a more appropriate culture time can be ensured depending on the condition of the blood sample, and ultimately, it becomes possible to more precisely adjust the quality of the induced pluripotent stem cells and the production time and production costs.

[0069] As another example, in the above manufacturing process, the manufacturing process determined in step S4 is automatically executed according to the control of the control circuit 31, but this is not limited to this and may be executed only when approval is obtained from the operator.

[0070] 12 is a diagram showing another example of the display screen 70 displayed in step S5. In addition to the display fields 51 to 53, the display screen 70 displays an adopt button 54 and a reject button 55. The adopt button 54 is a GUI (Graphical User Interface) button for notifying the processing circuitry 11 that the manufacturing process determined in step S4, i.e., the manufacturing process displayed in the display field 52, is to be adopted. The reject button 55 is a GUI button for notifying the processing circuitry 11 that the manufacturing process determined in step S4, i.e., the manufacturing process displayed in the display field 52, is not to be adopted.

[0071] If the accept button 54 is pressed via the input device 17, the processing circuit 11 notifies the pluripotent stem cell production apparatus 30 of the production process determined in step S4. As a result, induced pluripotent stem cells are produced according to this production process. If the reject button 55 is pressed via the input device 17, the processing circuit 11 rejects the production process determined in step S4 and notifies the pluripotent stem cell production apparatus 30 of a preset standard production process. For example, a production process that performs expansion culture for a standard time may be set as the standard production process. As a result, induced pluripotent stem cells are produced according to the standard production process. By requesting approval from the operator, it is possible to produce induced pluripotent stem cells according to the process desired by the operator.

[0072] Next, we will explain how to generate a trained model and a manufacturing process table.

[0073] FIG. 13 is a diagram schematically illustrating the learning process of the trained model and manufacturing process table. As shown in FIG. 13, in the learning process, viable cell count information, storage information, hematopoietic stem cell count information, and production result information are collected. A combination of viable cell count information, storage information, and hematopoietic stem cell count information is called a learning sample because it is used to train the trained model. The learning sample is collected during the process of manufacturing induced pluripotent stem cells from a blood sample through expansion culture. The viable cell count information and storage information are used as input data in the learning sample. The hematopoietic stem cell count information is used as teaching data or output data in the learning sample. The hematopoietic stem cell count information and production result information are used to create the manufacturing process table.

[0074] As shown in FIG. 13 , the processing circuit 11, by implementing the acquisition function 111, acquires storage information for the blood sample from a blood data sheet or the like attached to the blood sample container. The cell measuring device 20 measures the blood sample before removal of unwanted matter by the unwanted matter removal unit 32, and obtains viable cell count information regarding the number of viable cells contained in the blood sample. The viable cell count information is acquired by the tissue stem cell count estimation device 10 by the acquisition function 111 of the processing circuit 11. Then, unwanted matter contained in the blood sample is removed by the unwanted matter removal unit 32. Next, the cell measuring device 20 measures the blood sample after the unwanted matter has been removed, and obtains the viable cell count information regarding the number of viable cells contained in the blood sample as hematopoietic stem cell count information regarding the number of hematopoietic stem cells contained in the viable cells.

[0075] Subsequently, the following steps are performed: expansion culture for a normal culture time in the expansion culture unit 33; extraction of hematopoietic stem cells in the tissue stem cell extraction unit 34; introduction of an induction factor in the factor introduction unit 35; culture of the induced pluripotent stem cells in the pluripotent stem cell culture unit 36; and storage of the induced pluripotent stem cells in the storage unit 37. The induced pluripotent stem cells stored in the storage unit 37 are measured to obtain a production result. The production result is evaluated as successful or unsuccessful based on the number of induced pluripotent stem cells. For example, the number of induced pluripotent stem cells stored in the storage unit 37 is measured by the cell measurement device 20, and the number is compared with a threshold. If the number is greater than the threshold, the production is determined to be successful; if the number is less than the threshold, the production is determined to be unsuccessful. Information regarding the determination result is acquired by the tissue stem cell number estimation device 10 via the acquisition function 111 of the processing circuit 11. In this manner, information on the viable cell count, storage information, hematopoietic stem cell count, and production result information for various blood samples are collected.

[0076] Once the viable cell count information, storage information, hematopoietic stem cell count information, and production result information are collected, the machine learning model and manufacturing process table are trained. First, the training of the machine learning model will be described. By implementing the learning function 114, the processing circuitry 11 trains the machine learning model based on multiple training samples to generate a trained model that inputs viable cell count information and storage information and outputs hematopoietic stem cell count information. Various combinations of viable cell count information and hematopoietic stem cell count information are possible. For example, a trained model that inputs viable cell count and storage information and outputs hematopoietic stem cell count may be generated. Alternatively, a trained model that inputs viable cell rate and storage information and outputs hematopoietic stem cell rate may be generated. Alternatively, a trained model that inputs image information and / or optical spectrum information of viable cells and storage information and outputs hematopoietic stem cell count or hematopoietic stem cell rate may be generated.

[0077] The hematopoietic stem cell count information may be information about the number of hematopoietic stem cells after expansion culture. In this case, for example, after expansion culture in the expansion culture unit 33, the number of hematopoietic stem cells after expansion culture is measured using the cell measuring device 20, a flow cytometer, or the like. The processing circuit 11 calculates the number of hematopoietic stem cells before expansion culture by multiplying the number of hematopoietic stem cells after expansion culture by a coefficient. The coefficient may be empirically determined depending on the expansion culture time, culture conditions, etc. The number of hematopoietic stem cells before expansion culture calculated in this manner can be used as training data for the learning sample.

[0078] Next, learning of the manufacturing process table will be described. Processing circuitry 11 determines the number of classifications (level number) for the hematopoietic stem cell count levels, the range of hematopoietic stem cell count (level range) defining each level, and the manufacturing process corresponding to each level, in accordance with instructions from the operator via input device 17. At this time, the number of levels and level range may be determined by analyzing viable cell count information, hematopoietic stem cell count information, and production results. For example, processing circuitry 11 may sequentially update or correct the provisionally determined number of levels and level range using sequentially obtained hematopoietic stem cell count information and production results as feedback. Statistical calculations, machine learning, etc. may be used as the above analysis method.

[0079] As described above, the hematopoietic stem cell count information may be a level related to the hematopoietic stem cell count. In this case, the processing circuit 11 determines a level corresponding to the hematopoietic stem cell count before expansion culture and uses the determined level as training data for the learning sample.

[0080] (Variation 1) The trained model according to Modification 1 may output a manufacturing process. Since there is a one-to-one correspondence between the level and the manufacturing process, the trained model can also output a manufacturing process. The trained model according to Modification 1 may be trained to input viable cell count information and storage information and output a manufacturing process. The manufacturing process as the teaching data for the training sample may be determined by the processing circuit 11, for example, based on the number of hematopoietic stem cells measured from a blood sample after removal of unnecessary substances. Specifically, a level is determined based on the number of hematopoietic stem cells, and a manufacturing process corresponding to that level is determined.

[0081] (Variation 2) In the pluripotent stem cell production apparatus 30 according to the above embodiment, the control circuit 31 automatically controls the waste removal unit 32, expansion culture unit 33, tissue stem cell extraction unit 34, factor introduction unit 35, pluripotent stem cell culture unit 36, and storage unit 37. The waste removal unit 32, expansion culture unit 33, tissue stem cell extraction unit 34, factor introduction unit 35, pluripotent stem cell culture unit 36, and storage unit 37 according to Modification 2 may be manually operated. In Modification 2, for example, the production process does not need to be determined in step S4 of FIG. 4 . In this case, in step S5, the processing circuit 11 displays the tissue stem cell count information estimated in step S3. The operator simply confirms the displayed tissue stem cell count information and then produces pluripotent stem cells according to the production process corresponding to the tissue stem cell count information.

[0082] Specifically, if tissue stem cell count information corresponding to level 1 is displayed in step S5, the operator removes unnecessary substances using the unnecessary substance removal unit 32, then operates the factor introduction unit 35 to introduce an induction factor into the hematopoietic stem cells, and operates the pluripotent stem cell culture unit 36 ​​to culture the pluripotent stem cells. If tissue stem cell count information corresponding to level 2 is displayed in step S5, the operator removes unnecessary substances using the unnecessary substance removal unit 32, then operates the expansion culture unit 33 to expand the hematopoietic stem cells for a short period of time. After expansion, the operator extracts hematopoietic stem cells using the tissue stem cell extraction unit 34, operates the factor introduction unit 35 to introduce an induction factor into the hematopoietic stem cells, and operates the pluripotent stem cell culture unit 36 ​​to culture the pluripotent stem cells. If tissue stem cell count information corresponding to level 3 is displayed in step S5, the operator removes unnecessary substances using the unnecessary substance removal unit 32, then operates the expansion culture unit 33 to expand the hematopoietic stem cells for a standard period of time. After expansion, the operator extracts hematopoietic stem cells using the tissue stem cell extraction unit 34, operates the factor introduction unit 35 to introduce an induction factor into the hematopoietic stem cells, and operates the pluripotent stem cell culture unit 36 ​​to culture the pluripotent stem cells.

[0083] In addition, in Modification 2, the manufacturing process may also be determined in step S4. In this case, the manufacturing process determined in step S4 is displayed by processing circuitry 11 in step S5. The operator simply produces pluripotent stem cells in accordance with the displayed manufacturing process.

[0084] (Variation 3) 1 to 3 are merely examples, and the present embodiment is not limited thereto. For example, all or part of the tissue stem cell count estimation device 10 may be incorporated into the pluripotent stem cell production device 30. As an example of partial incorporation, for example, the determination function 113 of the processing circuit 11 may be incorporated into the pluripotent stem cell production device 30. Furthermore, the cell measuring device 20 may be incorporated into the tissue stem cell count estimation device 10 or the pluripotent stem cell production device 30.

[0085] (Summary) As in some of the above-described embodiments, the pluripotent stem cell production system 1 includes a tissue stem cell number estimation device 10. The tissue stem cell number estimation device 10 acquires storage information regarding the storage of a donor's sample and viable cell count information regarding the number of viable cells contained in the sample. Based on the storage information and the viable cell count information, the tissue stem cell number estimation device 10 estimates the tissue stem cell count information regarding the number of tissue stem cells contained in the sample.

[0086] According to the above configuration, it is possible to obtain information on the number of tissue stem cells contained in a sample according to the current state of the sample. Therefore, the operator can use the information on the number of tissue stem cells to estimate an appropriate production process that balances the quantity of pluripotent stem cells and production costs, thereby producing pluripotent stem cells according to this well-balanced production process. Furthermore, according to this embodiment, the production process for pluripotent stem cells can be automatically determined from the information on the number of tissue stem cells, making it easier to produce pluripotent stem cells according to this well-balanced production process. Furthermore, according to this embodiment, it is also possible to automate the production of pluripotent stem cells, making it easier and more stable to produce pluripotent stem cells according to this well-balanced production process.

[0087] According to at least one of the embodiments described above, pluripotent stem cells can be produced efficiently depending on the state of the sample.

[0088] The term "processor" used in the above description refers to a circuit such as a CPU, a GPU, an application specific integrated circuit (ASIC), a programmable logic device (e.g., a simple programmable logic device (SPLD), a complex programmable logic device (CPLD), and a field programmable gate array (FPGA)). A processor realizes its functions by reading and executing a program stored in a memory circuit. Note that instead of storing a program in a memory circuit, a program may be directly embedded in the processor circuit. In this case, the processor realizes its functions by reading and executing the program embedded in the circuit. Furthermore, instead of executing a program, a function corresponding to the program may be realized by combining logic circuits. Note that each processor in this embodiment is not limited to being configured as a single circuit, but may be configured as a single processor by combining multiple independent circuits to realize its function. Furthermore, multiple components in FIGS. 1, 2, and 3 may be integrated into a single processor to realize its function.

[0089] Although several embodiments have been described, these embodiments are presented as examples and are not intended to limit the scope of the invention. These embodiments can be implemented in various other forms, and various omissions, substitutions, modifications, and combinations of embodiments can be made without departing from the spirit of the invention. These embodiments and their modifications are included within the scope and spirit of the invention, as well as within the scope of the invention and its equivalents as defined in the claims. [Explanation of symbols]

[0090] 1. Pluripotent stem cell production system 10 Tissue stem cell number estimation device 11 Processing circuit 13 Storage device 15 Display equipment 17 Input Devices 19. Communications equipment 20 Cell measurement device 30 Pluripotent stem cell production equipment 31 Control circuit 32 Unwanted material removal section 33 Expansion Culture Section 34 Tissue stem cell extraction section 35 Factor introduction part 36 Pluripotent Stem Cell Culture Department 37 Storage Department 38 First switching section 39 Second switching section 111 Acquisition Function 112 Estimation Function 113 Decision Function 114 Learning Function 115 Display control function

Claims

1. an acquiring unit that acquires storage information regarding storage of a donor's blood and viable cell count information regarding the number of viable cells contained in the blood, the storage information including identification information of the donor, the CD34-positive cell count at the time storage of the blood began, the CD34-positive cell rate, the number of years of storage, and / or the storage period; an estimation unit that estimates hematopoietic stem cell count information regarding the number of hematopoietic stem cells contained in the blood based on the storage information and the viable cell count information; a determination unit that determines the level of the number of hematopoietic stem cells contained in the blood from the hematopoietic stem cell count information, and determines a manufacturing process corresponding to the hematopoietic stem cell count information for manufacturing pluripotent stem cells from the hematopoietic stem cells based on the determined level and a correspondence relationship between a plurality of predetermined levels and a plurality of manufacturing processes; a production unit that has at least a factor introduction unit that introduces an induction factor for initializing the hematopoietic stem cells into the hematopoietic stem cells and a pluripotent stem cell culture unit that cultures pluripotent stem cells established by introducing the induction factor into the hematopoietic stem cells, and that produces donor-derived pluripotent stem cells from the hematopoietic stem cells according to the production process; Equipped with the estimation unit estimates the hematopoietic stem cell number information by applying the storage information and the viable cell number information to a trained model; The trained model is a machine learning model trained to input storage information and viable cell count information and output hematopoietic stem cell count information. Pluripotent stem cell manufacturing system.

2. 2. The pluripotent stem cell manufacturing system of claim 1, wherein the decision unit adopts, as the manufacturing process, a manufacturing process that does not perform expansion culture of the hematopoietic stem cells when the hematopoietic stem cell count information is at a first level, and adopts a manufacturing process that performs expansion culture when the hematopoietic stem cell count information is not at the first level.

3. 2. The pluripotent stem cell production system according to claim 1, wherein the decision unit adopts, as the production process, a production process that does not perform expansion culture of the hematopoietic stem cells when the hematopoietic stem cell count information is at a first level, a production process that performs the expansion culture for a first time when the hematopoietic stem cell count information is at a second level lower than the first level, and a production process that performs the expansion culture for a second time longer than the first time when the hematopoietic stem cell count information is at a third level lower than the second level.

4. The pluripotent stem cell production system according to claim 1 , wherein the decision unit decides to discontinue production of pluripotent stem cells when the hematopoietic stem cell count information is at a fourth level that is unsuitable for producing pluripotent stem cells.

5. The pluripotent stem cell production system according to claim 1 , wherein the blood is umbilical cord blood that has been stored in an umbilical cord blood storage facility.

6. The pluripotent stem cell manufacturing system of claim 1, wherein the viable cell count information includes numerical information on the number of viable cells contained in the blood, numerical information on the ratio of the number of viable cells, image information on the blood, and / or optical spectrum information on the blood.

7. The pluripotent stem cell production system according to claim 1 , wherein the estimation unit estimates the hematopoietic stem cell count information regarding the number of hematopoietic stem cells presumed to be contained in the blood before expansion culture.

8. The pluripotent stem cell production system according to claim 1 , further comprising a display unit that displays the information on the number of hematopoietic stem cells.

9. The pluripotent stem cell production system according to claim 1 , further comprising a display unit that displays the production process.

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