Method for producing CD3 positive cells

Abstract

To provide a method for producing a CD3 positive cell in which CD3 being a T-cell marker is expressed on a cell membrane, or an extended culture method and a kit for extended culture, in order to make it possible to stably supply a differentiated T-cell.SOLUTION: A method for producing a CD3 positive cell includes: (I) a process of culturing a CD3 positive cell in the presence of CD3 / TCR composite agonist, fibronectin or a modified product thereof; and CD30 agonist, and (II) a process of culturing the CD3 positive cell cultured in the process (I) in the absence of CD3 / TCR composite agonist and fibronectin or a modified product thereof and in the presence of CD30 agonist, and the process (I) and process (II) are repeated in this order.SELECTED DRAWING: None

Description

[Technical field]

[0001] The present invention relates to a method for producing or expanding CD3-positive cells (or CD3-positive CD197-positive cells), which comprises a step of culturing CD3-positive cells in the presence of a CD3 / TCR complex agonist, fibronectin or a variant thereof, and a CD30 agonist, and a kit for expanding CD3-positive cells.The present invention also relates to a method for maintaining CD3-positive cells as CD3-positive CD197-positive cells, which comprises a step of stimulating a CD30 signal in CD3-positive cells, and a kit for maintaining CD3-positive cells as CD3-positive CD197-positive cells.

[0002] BACKGROUND OF THEINVENTION Immunotherapy, which has been shown to have a strong survival benefit even for cancers for which conventional treatments are ineffective, is becoming a major player in cancer treatment. CART therapy, which involves the transfer of autologous T cells transfected with anti-CD19 chimeric antigen receptor (CAR) genes, has shown high complete remission rates for B-cell malignancies, and two CART therapies for B-cell acute lymphoblastic leukemia and diffuse large B-cell lymphoma were approved by the FDA in 2017. In addition, many clinical trials are underway for TCR-T cell therapies, which involve the transfection of T cell receptor (TCR) genes that recognize cancer cell antigens. These gene-modified T cell therapies using the patient's own (autologous) T cells have shown very good clinical outcomes, but the cumbersome process, which involves the transportation and gene modification of T cells and cell culture, and takes more than several weeks, makes it difficult to control costs and control quality, and also leads to loss of treatment opportunities for patients with rapidly progressing cancers, so there is a strong demand for the development of off-the-shelf allogeneic T cell therapies. As a method for expanding and culturing T cells collected from a patient, a method for producing CD8-positive Tc1 lymphocytes or CD8-positive Tc2 lymphocytes by contacting a T cell population with an anti-CD3 agonist antibody and an anti-CD30 agonist antibody (Patent Document 1) and a method for expanding and culturing tumor-specific T cells by acquiring a T cell population from a cancer patient and contacting the T cell population with an anti-CD3 agonist antibody, an anti-CD28 antibody, and a VEGF inhibitor (Patent Document 2) have been reported. However, T cells derived from healthy individuals or patients have limited proliferation ability, and the number of genetically modified T cells that can be produced from T cells that can be collected in one apheresis is limited. In addition, it has been reported that when T cells are expanded and cultured by stimulation of TCR, the expression of CCR7 (CD197), a cell surface marker of naive cells and memory T cells, increases transiently, but then disappears within a few days (Non-Patent Document 1). It has also been reported that memory T cells ("T cell persistence") are important for in vivo antitumor activity, and that a high in vivo antitumor effect was observed by increasing the number of administered CART cells, which are memory T cells (Non-Patent Document 2). Therefore, cell populations obtained by expanding and culturing T cells with low CD197 expression were not suitable for cancer treatment.

[0003] On the other hand, T cells differentiated from pluripotent stem cells such as iPS cells and ES cells (differentiated T cells) are made from pluripotent stem cells that can theoretically proliferate infinitely, so it is theoretically possible to produce unlimited amounts of genetically modified T cells. However, the method of expanding iPS cells while maintaining their pluripotency is expensive and technically difficult, so there are limitations to the method of mass-producing iPS cells and obtaining differentiated T cells, especially CD197-positive T cells, from them. As a result, there has been a demand for an alternative approach to mass-obtaining T cells, especially CD197-positive T cells. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] International Publication No. 2003 / 038062 [Patent Document 2] US Publication No. 2014 / 0255368 [Non-patent literature]

[0005] [Non-Patent Document 1] Sallusto et al., Eur. J. Immunol. vol. 29, 2037-2045, 1999 [Non-Patent Document 2] Kaartinen et al., Cytotherapy vol. 19, 689-702, 2017 Summary of the Invention [Problem to be solved by the invention]

[0006] An object of the present invention is to provide a method for producing or expanding CD3-positive cells in which CD3, a T cell marker, is expressed on the cell membrane, and a kit for expansion, in order to enable a stable supply of differentiated T cells, particularly CD197-positive T cells. Another object of the present invention is to provide a method for maintaining CD197-positive T cells and a kit for maintaining CD197-positive T cells. [Means for solving the problem]

[0007] As a result of intensive research conducted by the present inventors to achieve the above object, it was found that CD8 positive T cells (iPS cell-derived CD8 positive T cells) obtained from iPS cells into which a TCR gene has been introduced can be efficiently proliferated when the CD8 positive T cells are cultured using a medium containing an anti-CD30 agonist antibody on a culture vessel on which an anti-CD3 agonist antibody and RetroNectin (registered trademark) are immobilized. Furthermore, it was confirmed that the proliferation efficiency and antigen-specific cytotoxic activity of the T cells are not affected even if the iPS cell-derived CD8 positive T cells are repeatedly proliferated by the culture method. In addition, it was found that when the iPS cell-derived CD8 positive T cells are cultured using an anti-CD30 agonist antibody, the expression rate of CD197 is higher than when the anti-CD30 agonist antibody is not used, and the proliferated T cells exist as central memory T cells. In addition, similar to iPS cell-derived CD8-positive T cells, human peripheral blood-derived CD8-positive T cells and iPS cell-derived CD8-positive T cells into which anti-CD19-CAR gene has been introduced (iPS cell-derived anti-CD19-CART cells) could also be efficiently proliferated by adding anti-CD30 agonist antibody to the medium when cultured on a culture vessel with anti-CD3 agonist antibody / Retronectin (registered trademark) solid-phased. Furthermore, when the human peripheral blood-derived CD8-positive T cells or the iPS cell-derived anti-CD19-CART cells were cultured using anti-CD30 agonist antibody, the expression of CD197 was maintained for a long period of time compared to when anti-CD30 agonist antibody was not used, and it was found that the human peripheral blood-derived CD8-positive T cells could survive for a long period of time in vivo. Based on the above findings, the present invention was completed.

[0008] That is, the present invention provides the following. [1] A method for producing CD3 positive cells, comprising the step (I) of culturing CD3 positive cells in the presence of a CD3 / TCR complex agonist, fibronectin or a modified form thereof, and a CD30 agonist. [2] The method according to [1], further comprising the step (II) of culturing the CD3-positive cells cultured in step (I) in the absence of a CD3 / TCR complex agonist and fibronectin or a variant thereof, and in the presence of a CD30 agonist. [3] The method according to [1] or [2], wherein the CD3 positive cells are derived from pluripotent stem cells. [4] The method according to [3], wherein the pluripotent stem cells are iPS cells. [5] The method according to any one of [1] to [4], wherein the CD3-positive cells are chimeric antigen receptor-expressing CD3-positive cells. [6] The method according to any one of [1] to [5], wherein the CD3 positive cells are CD3 positive CD8 positive cells. [7] The method according to [6], wherein the CD3+CD8+ cells are CD3+CD8+CD4+ cells. [8] The method according to any one of [1] to [7], wherein the CD3 positive cells are γTCR positive and / or δTCR positive cells. [9] The method according to any one of [1] to [8], wherein the CD3 / TCR complex agonist is a CD3 agonist and / or a TCR agonist.

[10] The method according to [9], wherein the CD3 agonist is an anti-CD3 agonist antibody or a binding fragment thereof.

[11] The method according to

[10] , wherein the anti-CD3 agonist antibody or binding fragment thereof is an anti-CD3 agonist antibody or binding fragment thereof produced from a UCHT1 clone.

[12] The method according to [9], wherein the TCR agonist is at least one selected from the group consisting of an anti-TCR antibody or a binding fragment thereof, an HLA / peptide complex or a multimer thereof, and an HLA / superantigen complex or a multimer thereof.

[13] The method according to

[10] or

[11] , wherein the anti-CD3 agonist antibody or its binding fragment is immobilized on a culture vessel.

[14] The method according to

[13] , wherein the immobilization of the anti-CD3 agonist antibody or a binding fragment thereof is carried out by contacting 1 ng / ml to 50,000 ng / ml of the anti-CD3 agonist antibody or a binding fragment thereof with a culture vessel.

[15] The method according to any one of [1] to

[14] , wherein the fibronectin or a modified form thereof is Retronectin (registered trademark).

[16] The method according to

[15] , wherein the RetroNectin (registered trademark) is immobilized on a culture vessel.

[17] The method according to

[16] , wherein the immobilization of RetroNectin (registered trademark) is carried out by contacting 1 to 150 μg / mL of the RetroNectin (registered trademark) with a culture vessel.

[18] The method according to any one of [1] to

[17] , wherein the CD30 agonist is at least one selected from the group consisting of an anti-CD30 agonist antibody or a binding fragment thereof, and a CD30 ligand or a binding fragment thereof.

[19] The method according to

[18] , wherein the anti-CD30 agonist antibody or a binding fragment thereof is contained in a culture medium.

[20] The method according to

[19] , wherein the concentration of the anti-CD30 agonist antibody or its binding fragment in the medium is 1 ng / ml to 1000 ng / ml.

[21] The method according to any one of [1] to

[20] , wherein the medium contains at least one selected from IL-7, IL-15, IL-18 and IL-21.

[22] The method according to

[21] , wherein the culture medium contains IL-7, IL-15, IL-18 and IL-21.

[23] The method according to

[21] or

[22] , wherein the culture medium further contains TL1A and / or IL-12.

[24] The method according to any one of [1] to

[23] , wherein the produced CD3-positive cells are further CD197-positive.

[25] CD3 positive cells obtained by the method described in any one of [1] to

[24] .

[26] A method for expanding CD3-positive cells, comprising the step of culturing CD3-positive cells in the presence of a CD3 / TCR complex agonist, fibronectin or a variant thereof, and a CD30 agonist.

[27] A kit for expanding CD3 positive cells, including: (1) CD3 / TCR complex agonists, and Fibronectin or its modified form A culture vessel having the immobilized (2) Medium containing a CD30 agonist.

[28] A method for maintaining CD3-positive cells as CD3-positiveCD197-positive cells, comprising the step of stimulating a CD30 signal in CD3-positive cells.

[29] The method according to

[28] , wherein the CD3 positive cells are CD3 positive CD8 positive cells.

[30] The method according to

[29] , wherein the CD3+CD8+ cells are CD3+CD8+CD4+ cells.

[31] The method according to any one of

[28] to

[30] , wherein the medium used in the stimulating step contains at least one selected from IL-7, IL-15, IL-18 and IL-21.

[32] The method according to

[31] , wherein the medium used in the stimulating step contains IL-7, IL-15, IL-18 and IL-21.

[33] The method according to

[31] or

[32] , wherein the medium used in the stimulating step further contains TL1A and / or IL-12.

[34] A kit containing a CD30 agonist to maintain CD3+CD197+ cells.

[35] A chimeric antigen receptor comprising an antigen-binding domain, a transmembrane domain, and an intracellular signaling domain, wherein the intracellular signaling domain comprises the intracellular signaling domain of CD30 or a variant thereof.

[36] A nucleic acid comprising a polynucleotide encoding the chimeric antigen receptor described in

[35] .

[37] A chimeric antigen receptor expression vector comprising the nucleic acid described in

[36] .

[38] A chimeric antigen receptor-expressing cell comprising the chimeric antigen receptor expression vector described in

[37] .

[39] The cell described in

[38] , wherein the chimeric antigen receptor-expressing cell is a CD3-positive cell.

[40] A pharmaceutical comprising the cell according to

[38] or

[39] .

[41] The pharmaceutical described in

[40] for use in the prevention or treatment of a tumor expressing an antigen recognized by the chimeric antigen receptor described in

[35] .

[42] A method for killing cells expressing an antigen recognized by the chimeric antigen receptor described in

[35] , comprising the cells described in

[38] or

[39] .

[43] A cell described in

[38] or

[39] for use in the prevention or treatment of a tumor expressing an antigen recognized by the chimeric antigen receptor described in

[35] .

[44] Use of the cell described in

[38] or

[39] for producing a preventive or therapeutic agent for a tumor expressing an antigen recognized by the chimeric antigen receptor described in

[35] .

[45] A method for preventing or treating a tumor expressing an antigen recognized by the chimeric antigen receptor described in

[35] , comprising administering a cell described in

[38] or

[39] . Effect of the Invention

[0009] By culturing CD3 positive cells in the presence of a CD3 / TCR complex agonist, fibronectin or its modified form, and a CD30 agonist, T cells can be efficiently produced or expanded. Furthermore, the CD3 positive cells produced or expanded by the above-mentioned culture are CD197 positive cells, so that when used in gene-modified T cell therapy, long-term efficacy can be expected. Furthermore, by stimulating the CD30 signal of CD3 positive cells, the cells can be maintained as CD197 positive cells for a long period of time. [Brief description of the drawings]

[0010] [Figure 1]FIG. 1 shows concentrations suitable for immobilization of anti-CD3 agonistic antibody and RetroNectin (registered trademark), determined by ELISA. [Diagram 2] FIG. 1 shows the number of iPSC-derived T cells (measured by ATP amount) 12 days after stimulation with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark). [Diagram 3] 1 shows the proliferation curves of iPSC-derived T cells stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) or anti-CD3 / CD28 beads, where the vertical axis indicates the cell number and the horizontal axis indicates the number of days since the start of the stimulation. [Figure 4] FIG. 1 shows the proliferation curves of iPSC-derived T cells stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) at each stimulation cycle. [Diagram 5] FIG. 1 shows the antigen-specific cytotoxic activity of iPSC-derived T cells proliferated by stimulation with solid-phase anti-CD3 agonist antibody / RetroNectin (registered trademark). [Figure 6] 1 shows the enhancement of proliferation of iPSC-derived T cells stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) by the addition of anti-CD30 agonist antibody. The vertical axis indicates the number of cells, and the horizontal axis indicates the number of days since the start of the above stimulation. [Figure 7] This figure shows the proliferation curves of iPSC-derived T cells when the proliferation test of iPSC-derived T cells was completed after the first stimulation with solid-phased anti-CD3 agonist antibody / RetroNectin (registered trademark), or solid-phased anti-CD3 agonist antibody / RetroNectin (registered trademark) and anti-CD30 agonist antibody, and then stimulated again (second stimulation) in the same manner. The vertical axis shows the cell number, and the horizontal axis shows the number of days since the start of the second stimulation. [Figure 8] FIG. 1 shows the expression of CD197 and CD45RA on the membrane surface of iPSC-derived T cells on day 7 after stimulation with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark), or immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) and anti-CD30 agonist antibody. [Figure 9] FIG. 1 shows the antigen-specific cytotoxic activity of iPSC-derived T cells proliferated by stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark) and anti-CD30 agonist antibody. [Figure 10] 1 shows the proliferation curves of human peripheral blood-derived CD8-positive T cells stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark), or with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) and anti-CD30 agonist antibody. The vertical axis shows the cell count, and the horizontal axis shows the number of days since the start of the stimulation. [Figure 11] FIG. 1 shows the expression of CD197 on the membrane surface of human peripheral blood-derived CD8-positive T cells after stimulation with various ILs and anti-CD3 / CD28 beads containing anti-CD30 antibody. [Figure 12] FIG. 1 shows the numbers of surviving human CD8-positive T cells in the blood, spleen, and bone marrow of mice 4 weeks after human peripheral blood-derived CD8-positive T cells were intravenously transplanted into irradiated immunodeficient mice after stimulation with various ILs and anti-CD3 / CD28 beads containing anti-CD30 antibody. [Figure 13] This figure shows the growth curves of iPS cell-derived T cells (iPS-T) and iPS cell-derived anti-CD19-CART cells (iPS-CART anti-CD19) stimulated with solid-phase anti-CD3 agonist antibody / RetroNectin (registered trademark) and anti-CD30 agonist antibody. The vertical axis shows the cell number, and the horizontal axis shows the number of days since the start of the above stimulation. [Figure 14] 1 shows the growth curves of iPS cell-derived anti-CD19-CART cells stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark), or with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) and anti-CD30 agonist antibody. The vertical axis shows the cell number, and the horizontal axis shows the number of days since the start of the stimulation. [Figure 15]FIG. 1 shows the expression of CD197 on the membrane surface of iPS cell-derived anti-CD19-CART cells stimulated with immobilized anti-CD3 agonist antibody / Retronectin (registered trademark), or with immobilized anti-CD3 agonist antibody / Retronectin (registered trademark) and anti-CD30 agonist antibody. [Figure 16] FIG. 13 shows the cytotoxic activity of iPS cell-derived anti-CD19-CART cells stimulated with immobilized anti-CD3 agonistic antibody / RetroNectin (registered trademark) against CD19-expressing Raji cells by the addition of an anti-CD30 agonistic antibody. [Figure 17] FIG. 1 shows the cytotoxic activity of iPS cell-derived anti-CD19-CART cells (iCD19-CD30-CART) containing a CD30-derived intracellular domain against CD19-expressing Raji cells. [Figure 18] 1 shows the cell proliferation of γδ T cells (iγδ T cells) differentiated from non-T cell-derived iPS cells stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) by the addition of an anti-CD30 agonist antibody. The vertical axis shows the cell proliferation fold, and the horizontal axis shows the number of days since the start of the above stimulation. [Figure 19] 1 shows the cell proliferation of anti-CD19-CAR γδ T cells (iCAR γδ T cells) stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) by the addition of anti-CD30 agonist antibody. The vertical axis shows the cell number, and the horizontal axis shows the number of days since the start of the above stimulation. [Figure 20] FIG. 1 shows the antigen-specific cytotoxic activity of iCD19CAR / IL-15γδT cells expanded by stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark). [Figure 21] This figure shows the effect of iCD19CAR / IL-15γδT cells expanded by stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark) on extending the survival time of mice bearing human CD19-expressing tumors. [Figure 22]FIG. 13 shows the anti-tumor effect of iCD19CAR / IL-15αβ T cells expanded by stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark). [Diagram 23] FIG. 1 shows concentrations suitable for immobilization of anti-CD3 agonist antibody (UCHT1) and RetroNectin (registered trademark), determined by ELISA. [Figure 24] FIG. 1 shows the proliferation rate of iPSC-derived T cells on day 13 after stimulation with solid-phase anti-CD3 agonistic antibody (UCHT1) / RetroNectin (registered trademark) and anti-CD30 agonistic antibody.

[0011] Detailed Description of the Invention As used herein, "gene expression" includes both the synthesis of mRNA from a specific nucleotide sequence of the gene (also referred to as transcription or mRNA expression) and the synthesis of a protein based on the information in the mRNA (also referred to as translation or protein expression); unless otherwise specified, "gene expression" or simply "expression" refers to protein expression.

[0012] As used herein, "positive" means that the protein or mRNA is expressed in a detectable amount by a method known in the art. Protein detection can be performed using immunological assays using antibodies, such as ELISA, immunostaining, Western blotting, and flow cytometry. In addition, a reporter protein can be expressed together with the protein, and the target protein can be detected by detecting the reporter protein. The presence of a protein can be detected by detecting the function of the protein (for example, if the protein is a transcription factor, a gene whose expression is controlled by the protein can be detected, and if the protein is an enzyme, a substrate or product catalyzed by the protein can be detected). mRNA detection can be performed using, for example, nucleic acid amplification methods and / or nucleic acid detection methods such as RT-PCR, microarrays, biochips, and RNAseq.

[0013] As used herein, "negative" means that the expression level of the protein or mRNA is below the lower limit of detection by all or any of the above known techniques. The lower limit of detection of the expression of the protein or mRNA may vary depending on the technique.

[0014] As used herein, "culture" refers to maintaining, propagating (growing) and / or differentiating cells in an in vitro environment. "Culturing" means maintaining, propagating (growing) and / or differentiating cells outside a tissue or body, for example, in a cell culture dish or flask.

[0015] As used herein, "expansion culture" refers to culturing for the purpose of proliferating a desired cell population and increasing the number of cells. The increase in cell number may be achieved by the increase in cell number due to cell proliferation exceeding the decrease in cell number due to cell death, and does not require proliferation of all cells in the cell population. The increase in cell number may be 1.1-fold, 1.2-fold, 1.5-fold, 2-fold, 3-fold, 4-fold, 5-fold, 6-fold, 7-fold, 8-fold, 9-fold, 10-fold, 15-fold, 20-fold, 30-fold, 40-fold, 50-fold, 100-fold, 300-fold, 500-fold, 1,000-fold, 3,000-fold, 5,000-fold, 10,000-fold, 100,000-fold, 1,000,000-fold, or more than 1.

[0016] As used herein, the term "stimulation" refers to the binding of a substance to various receptors and the like to activate downstream signal pathways.

[0017] As used herein, "enrich" refers to increasing the amount of a particular component in a composition, such as a composition of cells, and "enriched," when used to describe a composition of cells, e.g., a cell population, refers to a cell population in which the amount of a particular component is increased compared to the proportion of such component in the cell population prior to enrichment. For example, a composition, such as a cell population, can be enriched for a target cell type, and thus the proportion of the target cell type is increased compared to the proportion of target cells present in the cell population prior to enrichment. A cell population can also be enriched for a target cell type by cell selection and sorting methods known in the art. A cell population can also be enriched by certain sorting or selection processes described herein. In certain embodiments of the invention, a method of enriching a target cell population results in a cell population that is at least 20%, 30%, 40%, 50%, 60%, 70%, 80%, 85%, 90%, 95%, 97%, 98% or 99% enriched for the target cell population.

[0018] As used herein, a "cell population" refers to two or more cells of the same or different types. A "cell population" also refers to a mass of cells of the same or different types.

[0019] The present invention provides a method for producing or expanding CD3-positive cells (hereinafter referred to as the production method or expansion method of the present invention), which comprises a step of culturing CD3-positive cells in the presence of a CD3 / TCR complex agonist, fibronectin or a modified form thereof, and a CD30 agonist. CD3 / TCR complex agonists and CD30 agonists can stimulate the CD3 / TCR complex and CD30, respectively.

[0020] In the production method or expansion culture method of the present invention, the CD3 positive cells to be cultured are not particularly limited as long as they express CD3 on the cell membrane. The CD3 positive cells are preferably CD3 positive CD8 positive cells (CD3 positive CD8 positive CD4 positive cells or CD3 positive CD8 positive CD4 negative cells), more preferably CD3 positive CD8 positive CD4 negative cells. Another preferred example of the CD3 positive cells is CD3 positive CD4 positive cells (CD3 positive CD4 positive CD8 positive cells or CD3 positive CD4 positive CD8 negative cells). Furthermore, in the production method or expansion culture method of the present invention, the CD3 positive cells to be cultured may be CD30 positive before culture, or may be differentiated to CD30 positive during culture. Therefore, when the CD3 positive cells are CD30 positive before culture, the CD3 positive cells are preferably CD3 positive CD8 positive CD30 positive cells (CD3 positive CD8 positive CD4 positive CD30 positive cells or CD3 positive CD8 positive CD4 negative CD30 positive cells), more preferably CD3 positive CD8 positive CD4 negative CD30 positive cells. Another preferred example of the CD3 positive cells is CD3 positive CD4 positive CD30 positive cells (CD3 positive CD4 positive CD8 positive CD30 positive cells or CD3 positive CD4 positive CD8 negative CD30 positive cells).

[0021] In the production method or expansion culture method of the present invention, the CD3 positive cells obtained as a result of production or expansion culture are not particularly limited as long as they express CD3 on the cell membrane, and include the same cells as the CD3 positive cells cultured in the production method or expansion culture method of the present invention. Furthermore, the CD3 positive cells produced or expanded are preferably further CD197 positive. When the CD3 positive cells produced or expanded are further CD197 positive, the cells are specifically CD3 positive CD8 positive CD197 positive cells (CD3 positive CD8 positive CD4 positive CD197 positive cells or CD3 positive CD8 positive CD4 negative CD197 positive cells), more preferably CD3 positive CD8 positive CD4 negative CD197 positive cells. Alternatively, the cells are CD3 positive CD4 positive CD30 positive CD197 positive cells (CD3 positive CD4 positive CD8 positive CD30 positive CD197 positive cells or CD3 positive CD4 positive CD8 negative CD30 positive CD197 positive cells). Among CD3-positive cells, CD197-positive cells are classified into stem cell memory T cells or central memory T cells depending on the presence or absence of CD45RA expression. These T cells have a high self-proliferative capacity and can supply effector T cells, making them suitable for anti-tumor immunity. The produced or expanded CD3 positive cells are preferably further CD197 positive CD45RA negative. When the produced or expanded CD3 positive cells are further CD197 positive CD45RA negative, the cells are specifically CD3 positive CD8 positive CD197 positive CD45RA negative cells (CD3 positive CD8 positive CD4 positive CD197 positive CD45RA negative cells or CD3 positive CD8 positive CD4 negative CD197 positive CD45RA negative cells), more preferably CD3 positive CD8 positive CD4 negative CD197 positive CD45RA negative cells. Alternatively, the cells are CD3 positive CD4 positive CD30 positive CD197 positive CD45RA negative cells (CD3 positive CD4 positive CD8 positive CD30 positive CD197 positive CD45RA negative cells or CD3 positive CD4 positive CD8 negative CD30 positive CD197 positive CD45RA negative cells). Among CD3 positive cells, CD197 positive CD45RA negative cells are also called central memory T cells.

[0022] CD3 is a molecule that is expressed during the maturation process of T cells and forms a larger complex (CD3 / TCR complex) with the T cell receptor (TCR), and is also known as a T cell marker. It is a complex of four types of polypeptides: gamma, delta, epsilon, and zeta chains. TCR, which forms a complex with CD3, is a molecule that transmits signals into T cells, and includes dimers consisting of two of the alpha chain (TCRα), beta chain (TCRβ), gamma chain (TCRγ), and delta chain (TCRδ), and includes a heterodimer consisting of TCRα and TCRβ (αβTCR), a heterodimer consisting of TCRγ and TCRδ (γδTCR), and a homodimer consisting of the same TCR chain. In vivo, CD8, like CD3, is expressed during the maturation process of T cells, and is expressed together with CD4 in the early stages of maturation, but only CD4 expression is lost with differentiation into cytotoxic T cells. CD8 functions as a co-receptor of the CD3 / TCR complex and recognizes MHC class I / antigen peptides. It is a homodimer of an α-chain polypeptide or a heterodimer of two types of polypeptides, α and β chains. In vivo, CD4 is expressed together with CD8 at the early stage of T cell maturation, but the expression of CD8 alone is lost as T cells differentiate into helper T cells. Like CD8, CD4 also functions as a co-receptor of the CD3 / TCR complex, but unlike CD8, it is a molecule that recognizes MHC class II / antigen peptides. CD30 is known to be expressed on activated lymphocytes (T cells and B cells). It has six cytidine-rich pseudo-repeat motifs as an extracellular domain and a TNF receptor-associated factor (TRAF) binding sequence that stimulates NFκB signaling as an intracellular domain. CD197 and CD45RA are used as marker molecules to distinguish naive T cells or stem cell memory T cells (CD197 positive, CD45RA positive), central memory T cells (CD197 positive, CD45RA negative), effector memory T cells (CD197 negative, CD45RA negative), and effector T cells (CD197 negative, CD45RA positive).

[0023] In the production method or expansion culture method of the present invention, the CD3-positive cells to be cultured may be cells collected from a mammal or cells obtained by differentiating pluripotent stem cells, but are preferably cells obtained by differentiating pluripotent stem cells.

[0024] When the CD3-positive cells are cells collected from a mammal, the cells can be isolated and collected, for example, by collecting peripheral blood mononuclear cells (PBMCs) from the mammal by apheresis, and then using an anti-CD3 antibody column, density gradient centrifugation, etc. Mammals from which CD3-positive cells are collected include humans and non-human animals (e.g., dogs, cats, mice, rats, hamsters, guinea pigs, rabbits, pigs, cows, goats, horses, sheep, monkeys, etc.), with humans being preferred.

[0025] When CD3-positive cells are cells obtained by differentiating pluripotent stem cells, examples of the pluripotent stem cells include embryonic stem cells (ES cells), induced pluripotent stem cells (iPS cells), embryonic tumor cells (EC cells), and embryonic germ stem cells (EG cells), with ES cells or iPS cells (more preferably human iPS cells) being preferred.

[0026] When the pluripotent stem cells are ES cells, they can be prepared by a method known per se. Methods for producing ES cells include, for example, a method for culturing the inner cell mass of mammalian blastocyst stage embryos (see, for example, Manipulating the Mouse Embryo: A Laboratory Manual, Second Edition, Cold Spring Harbor Laboratory Press (1994)), a method for culturing early embryos produced by somatic cell nuclear transfer (Wilmut et al., Nature, 385, 810 (1997); Cibelli et al., Science, 280, 1256 (1998); Akira Iritani et al., Proteins, Nucleic Acids, and Enzymes, 44, 892 (1999); Baguisi et al., Nature Biotechnology, 17, 456 (1999); Wakayama et al., Nature, 394, 369 (1998); Wakayama et al., Nature Genetics, 22, 127 (1999); Wakayama et al., Proc. Natl. Acad. Sci. USA, 96, 127 (1999)). 14984(1999); RideoutIII et al., Nature Genetics, 24,109(2000)), but are not limited thereto. ES cells can be obtained from a given institution, and can also be purchased commercially. For example, human ES cell lines H1, H7, H9, H13, and H14 are available from WiCell Research Institute in the United States, HES1 to 6 are available from ES Cell International in Australia, SA002, SA181, and SA611 are available from Cellartis AB in Sweden, HUES1 to 17 are available from the HUES Cell Facility in the United States, KhES-1 to KhES-5 are available from the Institute for Frontier Medical Sciences, Kyoto University, and SEES1 to SEES7 are available from the National Center for Child Health and Development. When ES cells are produced by somatic cell nuclear transfer, the type of somatic cells and the source from which the somatic cells are collected are the same as those for producing iPS cells described below.

[0027] When the pluripotent stem cells are iPS cells, the iPS cells can be generated by introducing a nuclear reprogramming substance into a somatic cell. The somatic cells that can be used as a starting material for generating iPS cells may be any cells other than germ cells derived from a mammal (e.g., mouse or human). For example, these include keratinizing epithelial cells (e.g., keratinizing epidermal cells), mucosal epithelial cells (e.g., epithelial cells of the tongue surface), exocrine gland epithelial cells (e.g., mammary gland cells), hormone-secreting cells (e.g., adrenal medullary cells), metabolic / storage cells (e.g., hepatocytes), luminal epithelial cells that form the interface (e.g., type I alveolar cells), luminal epithelial cells of the inner chain duct (e.g., vascular endothelial cells), ciliated cells with transport function (e.g., airway epithelial cells), cells that secrete extracellular matrix (e.g., fibroblasts), contractile cells (e.g., smooth muscle cells), cells of the blood and immune system (e.g., T lymphocytes), cells related to the senses (e.g., rod cells), neurons of the autonomic nervous system (e.g., cholinergic neurons), supporting cells of sensory organs and peripheral neurons (e.g., companion cells), neurons and glial cells of the central nervous system (e.g., astrocytes), pigment cells (e.g., retinal pigment epithelial cells), and their precursor cells (tissue precursor cells). There is no particular limit to the degree of differentiation of cells, and both undifferentiated precursor cells (including somatic stem cells) and terminally differentiated mature cells can be used as the source of somatic cells in the present invention. Examples of undifferentiated precursor cells include tissue stem cells (somatic stem cells) such as adipose-derived stromal (stem) cells, neural stem cells, hematopoietic stem cells, mesenchymal stem cells, and dental pulp stem cells.

[0028] As nuclear reprogramming substances to be introduced into somatic cells to generate iPS cells, various combinations of reprogramming genes have been reported so far (e.g., WO 2007 / 069666, Nature Biotechnology, 26, 101-106 (2008), Cell, 126, 663-676 (2006), Cell, 131, 861-872 (2007), Nat. Cell Biol., 11, 197-203 (2009), Nature, 451, 141-146 (2008), Science, 318, 1917-1920 (2007), Stem Cells, 26, 1998-2005 (2008), Cell Research (2008) 600-603, Nature 454: 646-650). (2008), Cell Stem Cell, 2: 525-528(2008), WO2008 / 118820, Nat. Cell Biol., 11, 197-203 (2009), Nat. Cell Biol., 11, 197-203 (2009), Science, 324: 797-801 (2009). In addition, the proteins encoded by the above-mentioned reprogramming genes can be introduced into somatic cells as nuclear reprogramming substances (Cell Stem Cell, 4: 381-384(2009), Cell Stem Cell, doi:10.1016 / j.stem.2009.05.005 (2009)). In particular, when considering using the resulting iPS cells for therapeutic purposes, a combination of the three factors Oct3 / 4, Sox2 and Klf4 is preferable.

[0029] iPS cell colonies can be selected using drug resistance and reporter activity as indicators (Cell, 126, 663-676 (2006); Nature, 448, 313-317 (2007)) or by visual observation of morphology (Cell, 131, 861-872 (2007)). The identity of the cells can be confirmed by the expression of various ES cell-specific genes and teratoma formation as indicators.

[0030] Currently, there are various types of iPSCs, including iPSCs established by Yamanaka et al. by introducing four factors, Oct3 / 4, Sox2, Klf4, and c-Myc, into mouse fibroblasts (Takahashi K, Yamanaka S., Cell, (2006) 126: 663-676); iPSCs derived from human cells established by introducing the same four factors into human fibroblasts (Takahashi K, Yamanaka S., et al. Cell, (2007) 131: 861-872.); Nanog-iPSCs established by selecting using the expression of Nanog as an indicator after introducing the above four factors (Okita, K., Ichisaka, T., and Yamanaka, S. (2007). Nature 448, 313-317.); and iPSCs created by a method that does not include c-Myc (Nakagawa M, Yamanaka S., et al. Nature Biotechnology, (2008) 26, 101-106), and iPSCs established by introducing six factors using a virus-free method (Okita K et al. Nat. Methods 2011 May;8(5):409-12, Okita K et al. Stem Cells. 31(3):458-66.) can also be used. In addition, iPSCs created by Thomson et al. and established by introducing four factors, OCT3 / 4, SOX2, NANOG, and LIN28 (Yu J., Thomson JA. et al., Science (2007) 318: 1917-1920.), iPSCs created by Daley et al. (Park IH, Daley GQ. et al., Nature (2007) 451: 141-146), and iPSCs created by Sakurada et al. (JP Patent Publication No. 2008-307007) can also be used. In addition, all published papers (e.g., Shi Y., Ding S., et al., Cell Stem Cell, (2008) Vol3, Issue 5,568-574; Kim JB., Scholer HR., et al., Nature, (2008) 454, 646-650; Huangfu D., Melton, DA., et al., Nature Biotechnology, (2008) 26, No 7, Any of the iPSCs known in the art, described in the above publications (e.g., JP 2008-307007 A, JP 2008-283972 A, US2008-2336610, US2009-047263, WO2007-069666, WO2008-118220, WO2008-124133, WO2008-151058, WO2009-006930, WO2009-006997, WO2009-007852), can be used. As the artificial pluripotent stem cell line, various iPSC lines established by NIH, RIKEN, Kyoto University, etc. can be used. For example, human iPSC lines include RIKEN's HiPS-RIKEN-1A line, HiPS-RIKEN-2A line, HiPS-RIKEN-12A line, Nips-B2 line, etc., and Kyoto University's 253G1 line, 253G4 line, 1201C1 line, 1205D1 line, 1210B2 line, 1383D2 line, 1383D6 line, 201B7 line, 409B2 line, 454E2 line, 606A1 line, 610B1 line, 648A1 line, 1231A31 line, FfI-01s04 line, etc., with the 1231A3 line being preferred.

[0031] When CD3-positive cells are cells obtained by differentiating pluripotent stem cells, the TCR expressed in the CD3-positive cells includes dimers consisting of two of TCRα, TCRβ, TCRγ, and TCRδ, and includes heterodimers consisting of TCRα and TCRβ (αβTCR), heterodimers consisting of TCRγ and TCRδ (γδTCR), and homodimers consisting of the same TCR chain. These TCRs may be endogenous dimers or exogenous dimers, but are preferably dimers containing exogenous TCRα and exogenous TCRβ. As used herein, an "exogenous TCR" refers to a heterodimer consisting of an exogenous TCRα and an exogenous TCRβ, a heterodimer consisting of an exogenous TCRγ and an exogenous TCRδ, and / or a homodimer consisting of the same exogenous TCR chain. When the TCR is a dimer containing endogenous TCRα and endogenous TCRβ, the pluripotent stem cell may be a pluripotent stem cell produced from a cell containing a nucleic acid containing a base sequence encoding endogenous TCRα and a nucleic acid containing a base sequence encoding endogenous TCRβ. Such cells include, for example, T cells (CD8 positive CD4 negative cells, CD8 negative CD4 positive cells, CD4 positive CD8 positive cells, etc.). When the TCR is a dimer containing exogenous TCRα and exogenous TCRβ, the pluripotent stem cell may be a cell containing a nucleic acid containing a base sequence encoding exogenous TCRα and a nucleic acid containing a base sequence encoding exogenous TCRβ. As used herein, an "exogenous TCR nucleic acid" refers to a nucleic acid comprising a base sequence encoding exogenous TCR alpha, a nucleic acid comprising a base sequence encoding exogenous TCR beta, a nucleic acid comprising a base sequence encoding exogenous TCR gamma, and / or a nucleic acid comprising a base sequence encoding exogenous TCR delta.

[0032] The method for introducing exogenous TCR nucleic acid (e.g., a nucleic acid comprising a base sequence encoding exogenous TCRα and a nucleic acid comprising a base sequence encoding exogenous TCRβ) into pluripotent stem cells is not particularly limited, but for example, the following method can be used.

[0033] When the exogenous TCR nucleic acid is in the form of DNA, for example, vectors such as viruses, plasmids, and artificial chromosomes can be introduced into pluripotent stem cells by techniques such as lipofection, liposomes, and microinjection. Examples of viral vectors include retroviral vectors, lentiviral vectors, adenoviral vectors, adeno-associated viral vectors, and Sendai viral vectors. Examples of artificial chromosome vectors include human artificial chromosomes (HAC), yeast artificial chromosomes (YAC), and bacterial artificial chromosomes (BAC, PAC). Plasmids for mammalian cells can be used. The vector can contain control sequences such as promoters, enhancers, ribosome binding sequences, terminators, and polyadenylation sites so that the exogenous TCR can be expressed, and can further contain, as necessary, selection marker sequences such as drug resistance genes (e.g., kanamycin resistance genes, ampicillin resistance genes, and puromycin resistance genes), thymidine kinase genes, and diphtheria toxin genes, and reporter gene sequences such as fluorescent proteins, β-glucuronidase (GUS), and FLAG. Examples of promoters include SV40 promoter, LTR promoter, CMV (cytomegalovirus) promoter, RSV (Rous sarcoma virus) promoter, MoMuLV (Moloney mouse leukemia virus) LTR, HSV-TK (herpes simplex virus thymidine kinase) promoter, EF-α promoter, CAG promoter, and drug-responsive promoter. An example of a drug-responsive promoter is the TRE promoter (CMV minimal promoter having a Tet responsive sequence with seven consecutive tetO sequences) that expresses a gene in the presence of a corresponding drug. When using the TRE promoter, it is preferable to use a mode in which a fusion protein with reverse tetR (rtetR) and VP16AD is simultaneously expressed in the same cell to induce gene expression in the presence of a corresponding drug (e.g., tetracycline or doxycycline is exemplified).More preferably, it is a vector having both the TRE promoter and a mode for expressing the fusion gene of rtetR and VP16AD in the same vector.

[0034] In the present invention, a polycistronic expression scheme may be used to simultaneously express exogenous TCRα and exogenous TCRβ. For polycistronic expression, the gene-encoding sequences may be linked by an IRES or a foot and mouth disease virus (FMDV) 2A coding region.

[0035] In another embodiment, the above vector may have a transposon sequence before and after the expression cassette (a gene expression unit including a promoter, a gene sequence, and a terminator) in order to excise the sequence encoding an exogenous TCR incorporated into the chromosome as necessary. An example of the transposon sequence is, but is not limited to, piggyBac. In another embodiment, the vector may have a loxP sequence or an FRT sequence before and after the expression cassette in order to remove the expression cassette.

[0036] When the exogenous TCR nucleic acid is in the form of RNA, it may be introduced into the pluripotent stem cells by techniques such as electroporation, lipofection, and microinjection.

[0037] In the production method or expansion method of the present invention, the CD3-positive cells to be cultured may also be cells expressing a chimeric antigen receptor.

[0038] In the present invention, the term "chimeric antigen receptor (CAR)" refers to a fusion protein comprising an antigen-binding domain, a transmembrane domain, and an intracellular signaling domain. The antigen-binding domain of the CAR comprises a single-chain antibody (scFv) in which the light chain (VL) and heavy chain (VH) of the variable region of an antibody are linked in series via a linker (e.g., GS linker). After recognizing an antigen with the scFv region, CD3-positive cells expressing the CAR transmit the recognition signal into the cell through the intracellular signaling domain. By introducing the CAR into the CD3-positive cells, it is possible to confer specificity for the target antigen. In addition, since the CAR can directly recognize antigen molecules independent of HLA class I or class II, it is possible to cause a strong immune response even against cells with reduced expression of HLA class I or class II genes.

[0039] The antigen targeted by the CAR includes, but is not limited to, a tumor antigen. The tumor antigen may be a tumor-specific antigen (TSA) or a tumor-associated antigen (TAA). Specific examples of such tumor antigens include one or more antigens selected from the group consisting of differentiation antigens such as MART-1 / MelanA (MART-I), gp100 (Pmel 17), tyrosinase, TRP-1, and TRP-2; tumor-specific multilineage antigens such as WT1, Glypican-3, MAGE-1, MAGE-3, BAGE, GAGE-1, GAGE-2, and p15; fetal antigens such as CEA; overexpressed tumor genes or mutated tumor suppressor genes such as p53, Ras, and HER-2 / neu; unique tumor antigens resulting from chromosomal translocations such as BCR-ABL, E2A-PRL, H4-RET, IGH-IGK, and MYL-RAR; and viral antigens such as the Epstein-Barr virus antigen EBVA and the human papillomavirus (HPV) antigens E6 and E7. Other tumor antigens include CD19, CD20, EGP2, erB2,3,4, GD2, GD3, Mesothelin, PSMA, 8H9, Lewis-Y, MUC1, TSP-1 80, MAGE-4, MAGE-5, MAGE-6, RAGE, NY-ESO, p185erbB2, p180erbB-3, c-met, nm-23H1, PSA, TAG-72, CA 19-9, CA 72-4, CAM 17.1, NuMa, K-ras, β-catenin, CDK4, Mum-1, p 15, p 16, 43-9F, 5T4, 791Tgp72, α-fetoprotein, β-HCG, BCA225, BTAA, CA 125, CA 15-3 / CA 27.29 / BCAA, CA 195, CA 242, CA-50, CAM43, CD68 / P1, CO-029, FGF-5, G250, Ga733 / EpCAM, HTgp-175, M344, MA-50, MG7-Ag, MOV18, NB / 70K, NY-CO-1, RCAS1, SDCCAG16, TA-90 / Mac-2 binding protein / cyclophilin C-related protein, TAAL6, TAG72, TLP and TPS.

[0040] Examples of the transmembrane domain of CAR include transmembrane domains derived from proteins selected from the group consisting of TCR α chain, β chain or ζ chain, CD28, CD3ε chain, CD45, CD4, CD5, CD8, CD9, CD16, CD22, CD33, CD37, CD64, CD80, CD86, CD134, 4-1BB (CD137) and CD154, among which the transmembrane domain derived from CD8 is preferred. In addition, for example, a transmembrane domain derived from a molecule from which the first intracellular signaling domain linked to the antigen binding domain is derived is also preferably used. For example, when the molecule from which the first intracellular signaling domain linked to the antigen binding domain is derived is CD28, the transmembrane domain may also be derived from CD28. Alternatively, an artificially designed transmembrane domain may be used.

[0041] Examples of the intracellular signaling domain of CAR include, but are not limited to, intracellular domains derived from one or more proteins selected from the group consisting of FcRγ chain, FcRβ chain, CD3γ chain, CD3δ chain, CD3ε chain, CD3ζ chain, CD5, CD22, CD79a, CD79b, and CD66d. Among these, the intracellular domain derived from the CD3ζ chain is preferred. When tyrosine phosphorylation of ITAM contained in the intracellular domain of the CD3ζ chain is induced, intracellular Ca 2+A series of responses such as an increase in T cell concentration and cytokine secretion are shown, and finally cell division occurs, and CD3 positive cells show cytotoxic activity as CTLs. The intracellular signaling domain may further include an intracellular domain of a costimulatory molecule, and examples of such costimulatory molecules include, but are not limited to, intracellular domains of one or more proteins selected from the group consisting of CD27, CD28, 4-1BB (CD137), OX40, CD30, CD40, PD-1, ICOS, lymphocyte function-associated antigen-1 (LFA-1), CD2, CD7, LIGHT, NKG2C, B7-H3, and CD83. Among these, intracellular domains derived from CD28, 4-1BB (CD137), and CD30 are preferred. CD28 can be bound to promote T cell proliferation by increasing IL-2 production. 4-1BB can also promote differentiation into memory cells by suppressing apoptosis caused in the final stage of T cell activation. CD30 can further enhance the proliferation of CD3 positive cells with CD3 antibodies and maintain them as CD197 positive cells for a long period of time. By selecting the type and number of costimulatory molecules, the strength and duration of CAR activity can be controlled (e.g., Mol Ther. 2009;17:1453-1464.). When the intracellular signaling domain contains one or more intracellular domains, the order of the domains is not limited.

[0042] A spacer may be incorporated between the antigen-binding domain and the transmembrane domain of CAR, or between the intracellular signaling domain and the transmembrane domain of CAR, and the spacer may be a peptide usually consisting of 300 amino acids or less, preferably 10 to 100 amino acids, and most preferably 25 to 50 amino acids. Specific examples of the spacer include, but are not limited to, a hinge region derived from IgG1, and a peptide containing the CH2CH3 region of immunoglobulin and a part of CD3.

[0043] Specific examples of CARs include, but are not limited to, first-generation CARs in which an scFv and a CD3 ζ chain are linked via a spacer; second-generation CARs in which a transmembrane domain and an intracellular domain derived from CD28 are incorporated between the scFv and CD3 ζ chain of the first-generation CAR to enhance the activation ability of T cells; and third-generation CARs in which an intracellular domain of a costimulatory molecule other than CD28 (4-1BB or OX40) is incorporated between the intracellular domain of CD28 and the CD3 ζ chain of the second-generation CAR.

[0044] In the production method or expansion method of the present invention, the CD3-positive cells to be cultured may further be cells that co-express a CAR and a fusion protein of IL-15 and IL-15Rα (IL-15 / IL-15Rα). The CAR expressed together with IL-15 / IL-15Rα may be the same as the above-mentioned CAR.

[0045] In the present invention, "IL-15 / IL-15Rα" means a fusion protein containing IL-15 and IL-15Rα. In the IL-15 signal transduction system, IL-15Rα expressed on antigen-presenting cells usually binds to IL-15, and presents IL-15 to the IL-15 receptor consisting of Rβ and γc on CD8-positive CD4-negative cells (trans-presentation), thereby maintaining the cytotoxic activity of CD8-positive CD4-negative cells. Therefore, when a CD3-positive cell expressing IL-15 / IL-15Rα is CD8-positive CD4-negative, the CD3-positive cell can transmit the IL-15 signal into its own cell via the IL-15 receptor. Alternatively, a CD3-positive cell expressing IL-15 / IL-15Rα can transmit the IL-15 signal into another CD8-positive CD4-negative cell via the IL-15 receptor. As described above, IL-15 / IL-15Rα can maintain the cytotoxic activity of CD8-positive CD4-negative cells, and therefore a continuous cytotoxic effect can be expected against cells targeted by CAR.

[0046] IL-15 / IL-15Rα may be a transmembrane protein or a secretory protein. It is known that the IL-15-binding domain, which is 1-65 amino acids from the N-terminus of the mature IL-15Rα protein, is the region responsible for binding to IL-15 (Wei X. et al., J. Immunol., 167:277-282, 2001). Therefore, the transmembrane protein may be a protein that has an IL-15-binding domain and the transmembrane domain of IL-15Rα. On the other hand, the secretory protein may be a protein that has an IL-15-binding domain and lacks the transmembrane domain of IL-15Rα.

[0047] IL-15 / IL-15Rα may incorporate a spacer between IL-15 and IL-15Rα, and the spacer may be a peptide usually consisting of 300 amino acids or less, preferably 10 to 100 amino acids, and most preferably 20 to 50 amino acids. Specific examples of the spacer include, but are not limited to, a GS linker.

[0048] IL-15 / IL-15Rα is not particularly limited as long as it is a peptide in which IL-15 and IL-15Rα are linked via a spacer, and specifically includes a peptide consisting of SEQ ID NO: 8. Alternatively, IL-15 / IL-15R is not particularly limited as long as it is capable of binding to an IL-15 receptor and transmitting an IL-15 signal into cells, and specifically includes a peptide comprising an amino acid sequence having about 90% or more, preferably about 95% or more, more preferably about 97% or more, particularly preferably about 98% or more, and most preferably about 99% or more homology with the amino acid sequence shown in SEQ ID NO: 8. Here, "homology" refers to the ratio (%) of identical amino acids and similar amino acid residues to the total overlapping amino acid residues in the optimal alignment (preferably, the algorithm can take into account the introduction of gaps into one or both of the sequences for optimal alignment) when two amino acid sequences are aligned using a mathematical algorithm known in the art. "Similar amino acids" refer to amino acids that are similar in physicochemical properties, and examples of such amino acids include aromatic amino acids (Phe, Trp, Tyr), aliphatic amino acids (Ala, Leu, Ile, Val), polar amino acids (Gln, Asn), basic amino acids (Lys, Arg, His), acidic amino acids (Glu, Asp), amino acids with hydroxyl groups (Ser, Thr), and amino acids with small side chains (Gly, Ala, Ser, Thr, Met) that are classified into the same group. It is predicted that substitution with such similar amino acids will not cause a change in the phenotype of the protein (i.e., it is a conservative amino acid substitution). Specific examples of conservative amino acid substitutions are well known in the art and are described in various documents (see, for example, Bowie et al., Science, 247:1306-1310 (1990)). The amino acid sequence homology in this specification can be calculated using the homology calculation algorithm NCBI BLAST (National Center for Biotechnology Information Basic Local Alignment Search Tool) under the following conditions (expectation value = 10; gaps allowed; matrix = BLOSUM62; filtering = OFF).

[0049] When expressing a chimeric antigen receptor and / or IL-15 / IL-15Rα in CD3-positive cells cultured in the production method or expansion method of the present invention, the method for introducing a CAR nucleic acid and / or an IL-15 / IL-15Rα nucleic acid into cells (e.g., pluripotent stem cells) is not particularly limited, and for example, the same method as the method for introducing a TCR nucleic acid can be used.

[0050] In the production method or expansion culture method of the present invention, when the cultured CD3-positive cells are cells obtained by differentiating pluripotent stem cells, the pluripotent stem cells can be differentiated into CD3-positive cells according to a method known per se. Specific methods for differentiating pluripotent stem cells into CD3-positive cells are described, for example, in International Publication No. 2016 / 076415 and International Publication No. 2017 / 221975. Specific methods for differentiating pluripotent stem cells into CD3-positive cells can include, for example, (1) a step of differentiating pluripotent stem cells into hematopoietic progenitor cells, and (2) a step of differentiating the hematopoietic progenitor cells into CD3-positive cells.

[0051] (1) Differentiating pluripotent stem cells into hematopoietic progenitor cells In step (1), hematopoietic progenitor cells (HPCs) refer to CD34-positive cells, preferably CD34-positive and CD43-positive cells. In this step (1), hematopoietic progenitor cells and hematopoietic stem cells are not distinguished from each other, and unless otherwise specified, they refer to the same cell.

[0052] The method for differentiating pluripotent stem cells into hematopoietic progenitor cells is not particularly limited as long as it is capable of differentiating into hematopoietic progenitor cells. For example, there may be mentioned a method of culturing pluripotent stem cells in an induction medium for hematopoietic progenitor cells, as described in WO 2013 / 075222, WO 2016 / 076415, Liu S. et al., Cytotherapy, 17 (2015); 344-358, and the like.

[0053] In step (1), the induction medium for hematopoietic progenitor cells is not particularly limited, and a medium used for culturing animal cells can be prepared as the basal medium. Examples of the basal medium include Dulbecco's medium (e.g., IMDM), Eagle's medium (e.g., DMEM, EMEM, BME, MEM, αMEM), Ham's medium (e.g., F10 medium, F12 medium), RPMI medium (e.g., RPMI-1640 medium, RPMI-1630 medium), MCDB medium (e.g., MCDB104, 107, 131, 151, 153 medium), Fisher's medium, 199 medium, medium for primate ES cells (culture medium for primate ES / iPS cells, ReproCell), medium for mouse ES cells (TX-WES culture medium, ThromboX), serum-free medium (mTeSR, Stemcell Examples of the basal medium include, but are not limited to, ReproFF, StemSpan (registered trademark) SFEM, StemSpan (registered trademark) H3000, Stemline II, ESF-B medium, ESF-C medium, CSTI-7 medium, Neurobasal medium (Life Technologies), StemPro-34 medium, StemFit (registered trademark) (e.g., StemFit AK03N, StemFit AK02N), etc. Furthermore, these media can be used by mixing, etc., as necessary, and examples thereof include DMEM / F12 medium, etc. The basal medium may contain serum or may be used without serum. The basal medium may be appropriately supplemented with 10-20% serum (fetal bovine serum (FBS), human serum, horse serum) or serum substitutes (KSR, etc.), insulin, various vitamins, L-glutamine, various amino acids such as non-essential amino acids, 2-mercaptoethanol, various cytokines (interleukins (IL-2, IL-7, IL-15, etc.), stem cell factor (SCF (Stem cell factor)), activin, etc.), various hormones, various growth factors (leukemia inhibitory factor (LIF), basic fibroblast growth factor (bFGF), TGF-β, etc.), various extracellular matrices, various cell adhesion molecules, antibiotics such as penicillin / streptomycin and puromycin, pH indicators such as phenol red, and the like.Furthermore, if necessary, the basal medium may contain, for example, vitamin C (e.g., ascorbic acid), albumin, insulin, transferrin, selenium compounds (e.g., sodium selenite), fatty acids, trace elements, 2-mercaptoethanol, thioglycerol (e.g., α-monothioglycerol (MTG)), lipids, L-alanyl-L-glutamine (e.g., Glutamax (registered trademark)), growth factors, low molecular weight compounds, antibiotics, antioxidants, pyruvic acid, buffers, inorganic salts, and the like.

[0054] In step (1), vitamin C means L-ascorbic acid and its derivatives, and L-ascorbic acid derivatives mean those which become vitamin C by enzymatic reaction in vivo. Examples of the ascorbic acid derivatives used in step (1) include vitamin C phosphate, ascorbic acid glucoside, ascorbyl ethyl, vitamin C ester, ascorbyl tetrahexyldecanoate, ascorbyl stearate, and ascorbyl-2-phosphate-6 palmitate. Vitamin C phosphate (e.g., ascorbic acid 2-phosphate) is preferred, and examples thereof include L-ascorbyl phosphate salts such as sodium L-ascorbate phosphate or magnesium L-ascorbate phosphate.

[0055] When vitamin C is used, it is preferable to add (supplement) vitamin C every 4 days, every 3 days, every 2 days, or every day, and more preferable to add every day. In one embodiment, the vitamin C is added in an amount equivalent to 5 ng / ml to 500 ng / ml in the culture solution (e.g., an amount equivalent to 5 ng / ml, 10 ng / ml, 25 ng / ml, 50 ng / ml, 100 ng / ml, 200 ng / ml, 300 ng / ml, 400 ng / ml, or 500 ng / ml). In another embodiment, the vitamin C is added in an amount equivalent to 5 μg / ml to 500 μg / ml in the culture medium (e.g., an amount equivalent to 5 μg / ml, 10 μg / ml, 25 μg / ml, 50 μg / ml, 100 μg / ml, 200 μg / ml, 300 μg / ml, 400 μg / ml, or 500 μg / ml).

[0056] The medium used in step (1) may further contain at least one cytokine selected from the group consisting of BMP4 (bone morphogenetic protein 4), VEGF (vascular endothelial growth factor), SCF (stem cell factor), TPO (thrombopoietin), FLT-3L (Flt3 Ligand), and bFGF (basic fibroblast growth factor). More preferred is a culture supplemented with BMP4, VEGF, and bFGF, and even more preferred is a culture supplemented with BMP4, VEGF, SCF, and bFGF.

[0057] When cytokines are used, their concentrations in the culture medium can be, for example, 5 ng / ml to 500 ng / ml for BMP4, 5 ng / ml to 500 ng / ml for VEGF, 5 ng / ml to 500 ng / ml for SCF, 3 ng / ml to 300 ng / ml for TPO, 1 ng / ml to 100 ng / ml for FLT-3L, and 5 ng / ml to 500 ng / ml for bFGF.

[0058] The medium may be supplemented with a TGFβ inhibitor. The TGFβ inhibitor is a small molecule inhibitor that interferes with the signal transduction of the TGFβ family, and includes, for example, SB431542, SB202190 (RK Lindemann et al., Mol. Cancer 2:20(2003)), SB505124 (GlaxoSmithKline), NPC30345, SD093, SD908, SD208 (Scios), LY2109761, LY364947, LY580276 (Lilly Research Laboratories), etc. For example, when the TGFβ inhibitor is SB431542, the concentration in the medium is preferably 0.5 μM to 100 μM.

[0059] Pluripotent stem cells may be cultured in an adhesive or floating manner. In the case of adhesive culture, the culture may be performed using a culture vessel coated with an extracellular matrix component, or may be co-cultured with feeder cells. The feeder cells are not particularly limited, but examples thereof include fibroblasts (mouse embryonic fibroblasts (MEF), mouse fibroblasts (STO), etc.). It is preferable that the feeder cells are inactivated by a method known per se, for example, irradiation with radiation (such as gamma rays) or treatment with an anticancer drug (such as mitomycin C). Examples of the extracellular matrix components include fibrous proteins such as matrigel (Niwa A, et al. PLoS One.6(7):e22261, 2011), gelatin, collagen, and elastin, glycosaminoglycans and proteoglycans such as hyaluronic acid and chondroitin sulfate, and cell adhesive proteins such as fibronectin, vitronectin, and laminin.

[0060] Suspension culture is a method of culturing cells in a non-adherent state to a culture vessel, and can be performed using, but is not limited to, a culture vessel that has not been artificially treated (e.g., coated with extracellular matrix, etc.) to improve adhesion to cells, or a culture vessel that has been artificially treated to suppress adhesion (e.g., coated with polyhydroxyethyl methacrylate (poly-HEMA) or nonionic surface-active polyol (Pluronic F-127, etc.)). In suspension culture, it is preferable to form embryoid bodies (EBs) and then culture them.

[0061] Hematopoietic progenitor cells can also be prepared from net-like structures (also called ES-sac or iPS-sac) obtained by culturing pluripotent stem cells. Here, the term "net-like structure" refers to a three-dimensional sac-like structure (with an internal space) derived from pluripotent stem cells, which is formed from an endothelial cell population and contains hematopoietic progenitor cells.

[0062] The culture temperature condition in step (1) is not particularly limited, but is, for example, about 37°C to 42°C, preferably about 37°C to 39°C. In addition, a person skilled in the art can appropriately determine the culture period while monitoring the number of hematopoietic progenitor cells. As long as hematopoietic progenitor cells are obtained, the number of days is not particularly limited, but is, for example, at least 6 days or more, 7 days or more, 8 days or more, 9 days or more, 10 days or more, 11 days or more, 12 days or more, 13 days or more, 14 days or more, preferably 14 days. A long culture period is usually not a problem in the production of hematopoietic progenitor cells, but is, for example, preferably 35 days or less, more preferably 21 days or less. In addition, the culture may be performed under hypoxic conditions, and in the present specification, hypoxic conditions are exemplified by oxygen concentrations of 15%, 10%, 9%, 8%, 7%, 6%, 5% or less.

[0063] (2) Differentiating hematopoietic progenitor cells into CD3-positive cells The method for differentiating hematopoietic progenitor cells into CD3-positive cells is not particularly limited as long as it allows differentiation of hematopoietic progenitor cells into CD3-positive cells. Examples of the method include a method of culturing hematopoietic progenitor cells under culture conditions similar to those for inducing T cells from hematopoietic progenitor cells, as described in WO 2016 / 076415 or WO 2017 / 221975.

[0064] In step (2), the medium for inducing differentiation into CD3 positive cells is not particularly limited, and a medium used for culturing animal cells can be prepared as the basal medium. Examples of the basal medium include the same as those used in step (1) above. The medium may contain serum or may be used serum-free. If necessary, the basal medium may contain, for example, vitamin C (e.g., ascorbic acid), albumin, insulin, transferrin, selenium compounds (e.g., sodium selenite), fatty acids, trace elements, 2-mercaptoethanol, thioglycerol (e.g., α-monothioglycerol (MTG)), lipids, amino acids, L-glutamine, L-alanyl-L-glutamine (e.g., Glutamax (registered trademark)), non-essential amino acids, vitamins, growth factors, low molecular weight compounds, antibiotics (e.g., penicillin, streptomycin), antioxidants, pyruvic acid, buffers, inorganic salts, cytokines, and the like.

[0065] When vitamin C is used in step (2), the vitamin C may be the same as those described in step (1) and may be added in the same manner. In one embodiment, the concentration of vitamin C in the medium or culture solution is preferably 5 μg / ml to 200 μg / ml. In another embodiment, the vitamin C is added in an amount equivalent to 5 μg / ml to 500 μg / ml in the culture solution (e.g., an amount equivalent to 5 μg / ml, 10 μg / ml, 25 μg / ml, 50 μg / ml, 100 μg / ml, 200 μg / ml, 300 μg / ml, 400 μg / ml, or 500 μg / ml).

[0066] In step (2), it is preferable to use a p38 inhibitor and / or SDF-1 (stromal cell-derived factor 1). As used herein, the term "p38 inhibitor" refers to a substance that inhibits the function of p38 protein (p38 MAP kinase), and examples thereof include, but are not limited to, chemical inhibitors of p38, dominant-negative mutants of p38, or nucleic acids encoding the same.

[0067] Examples of chemical inhibitors of p38 in step (2) include, but are not limited to, SB203580 (4-(4-fluorophenyl)-2-(4-methylsulfonylphenyl)-5-(4-pyridyl)-1H-imidazole) and derivatives thereof, SB202190 (4-(4-fluorophenyl)-2-(4-hydroxyphenyl)-5-(4-pyridyl)-1H-imidazole) and derivatives thereof, SB239063 (trans-4-[4-(4-fluorophenyl)-5-(2-methoxy-4-pyrimidinyl)-1H-imidazol-1-yl]cyclohexanol) and derivatives thereof, SB220025 and derivatives thereof, PD169316, RPR200765A, AMG-548, BIRB-796, SClO-469, SCIO-323, VX-702, and FR167653. These compounds are commercially available, for example, SB203580, SB202190, SB239063, SB220025 and PD169316 from Calbiochem, and SCIO-469 and SCIO-323 from Scios, etc. As chemical inhibitors of p38, SB203580 (4-(4-fluorophenyl)-2-(4-methylsulfonylphenyl)-5-(4-pyridyl)-1H-imidazole) and derivatives thereof are preferred.

[0068] Examples of the dominant negative mutant of p38 in step (2) include p38T180A, in which threonine at position 180 located in the DNA binding region of p38 is point mutated to alanine, and p38Y182F, in which tyrosine at position 182 of human and mouse p38 is point mutated to phenylalanine. The p38 inhibitor is contained in the medium in a range of, for example, about 1 μM to about 50 μM. When SB203580 is used as the p38 inhibitor, it can be contained in the medium in a range of 1 μM to 50 μM, 5 μM to 30 μM, or 10 μM to 20 μM.

[0069] The SDF-1 in step (2) may be not only SDF-1α or its mature form, but also isoforms such as SDF-1β, SDF-1γ, SDF-1δ, SDF-1ε, or SDF-1φ, or their mature forms, or may be a mixture of these in any ratio. Preferably, SDF-1α is used. SDF-1 is also called CXCL-12 or PBSF.

[0070] In step (2), SDF-1 may have one or several amino acids substituted, deleted, added, and / or inserted in its amino acid sequence, so long as it has chemokine activity (SDF-1 with such amino acid substitution, deletion, addition, and / or insertion is also called "SDF-1 mutant"). Similarly, sugar chains may be substituted, deleted, and / or added in SDF-1 or SDF-1 mutant. Examples of the SDF-1 mutant include those that retain at least four cysteine ​​residues (Cys30, Cys32, Cys55, and Cys71 in the case of human SDF-1α) and have 90% or more identity to the amino acid sequence of the natural form, but are not limited to these amino acid mutations. SDF-1 may be from a mammal, such as a human, or a non-human mammal, such as a monkey, sheep, cow, horse, pig, dog, cat, rabbit, rat, or mouse. For example, the protein registered under GenBank accession number NP_954637 can be used as human SDF-1α, and the protein registered under GenBank accession number NP_000600 can be used as SDF-1β.

[0071] SDF-1 may be commercially available, may be purified from nature, or may be produced by peptide synthesis or genetic engineering. SDF-1 is contained in the medium, for example, in the range of about 10 ng / ml to about 100 ng / ml. Alternatively, SDF-1 substitutes having SDF-1-like activity may be used instead of SDF-1. Examples of such SDF-1 substitutes include CXCR4 agonists, and low molecular weight compounds having CXCR4 agonist activity may be added to the medium instead of SDF-1.

[0072] The medium used in step (2) may further contain at least one, preferably all, of cytokines selected from the group consisting of SCF, TPO (thrombopoietin), FLT-3L, and IL-7. The concentrations of these cytokines are, for example, 10 ng / ml to 100 ng / ml for SCF, 10 ng / ml to 200 ng / ml for TPO, 1 ng / ml to 100 ng / ml for IL-7, and 1 ng / ml to 100 ng / ml for FLT-3L.

[0073] In step (2), the hematopoietic progenitor cells may be cultured in an adherent or floating state. In the case of adherent culture, the culture vessel may be coated and used, or the hematopoietic progenitor cells may be co-cultured with feeder cells or the like. An example of the feeder cells to be co-cultured is bone marrow stromal cell line OP9 cells (available from Riken BioResource Center). The OP9 cells are preferably OP9-DL4 cells or OP9-DL1 cells that constitutively express DLL4 or DLL1 (e.g., Holmes R1 and Zuniga-Pflucker JC. Cold Spring Harb Protoc. 2009(2)). In the case of using OP9 cells as feeder cells in step (2), the step may be performed by appropriately adding separately prepared DLL4 or DLL1, or a fusion protein of DLL4 or DLL1 with Fc or the like, to the medium. In the case of using feeder cells, it is preferable to appropriately replace the feeder cells and perform the culture. The replacement of the feeder cells may be performed by transferring the target cells being cultured onto the feeder cells that have been seeded in advance. The replacement can be performed every 5 days, 4 days, 3 days, or 2 days. When embryoid bodies are cultured in suspension to obtain hematopoietic progenitor cells, it is preferable to dissociate them into single cells and then perform adhesion culture. Co-culture with feeder cells is possible, but it is preferable to perform culture without using feeder cells. In the case of adherent culture, examples of coating agents for coating a culture vessel include Matrigel (Niwa A, et al. PLos One, 6(7):e22261, 2011), collagen, gelatin, laminin, heparan sulfate proteoglycan, retronectin, DLL4 or DLL1, or fusion proteins of DLL4 or DLL1 with an Fc region of an antibody (hereinafter sometimes referred to as Fc) (e.g., DLL4 / Fc chimera), entactin, and / or combinations thereof, with a combination of retronectin and a fusion protein of DLL4 with Fc or the like being preferred.

[0074] In step (2), the culture temperature conditions are not particularly limited, but for example, about 37°C to about 42°C, preferably about 37 to about 39°C. In addition, those skilled in the art can appropriately determine the culture period while monitoring the number of CD3-positive cells, etc. As long as CD3-positive cells are obtained, the number of days is not particularly limited, but for example, at least 10 days or more, 12 days or more, 14 days or more, 16 days or more, 18 days or more, 20 days or more, 22 days or more, 23 days or more, preferably 21 days. In addition, 90 days or less is preferable, and 42 days or less is more preferable.

[0075] The cells obtained by the above steps include CD3 positive cells, and a specific method for differentiating pluripotent stem cells into CD3 positive cells may further include the following step (3).

[0076] (3) Obtaining CD3+CD8+CD4-cells (or CD3+CD8+CD4-CD30+cells) or enriching CD3+cells Methods for obtaining CD3 positive CD8 positive CD4 negative cells (or CD3 positive CD8 positive CD4 negative CD30 positive cells) include, for example, methods described in International Publication No. 2016 / 076415 and International Publication No. 2017 / 221975. CD3 positive cells may also be enriched using similar methods.

[0077] In step (3), the medium used for obtaining CD3+CD8+CD4-negative cells (or CD3+CD8+CD4-negative CD30+ cells) or enriching CD3+ cells is not particularly limited, and a medium used for culturing animal cells can be prepared as the basal medium. Examples of the basal medium include the same medium as that used in step (1) above. The medium may contain serum or may be serum-free. If necessary, the basal medium may contain, for example, vitamin C (e.g., ascorbic acid), albumin, insulin, transferrin, selenium compounds (e.g., sodium selenite), fatty acids, trace elements, 2-mercaptoethanol, thioglycerol (e.g., α-monothioglycerol (MTG)), lipids, amino acids, L-glutamine, L-alanyl-L-glutamine (e.g., Glutamax (registered trademark)), non-essential amino acids, vitamins, growth factors, low molecular weight compounds, antibiotics (e.g., penicillin, streptomycin), antioxidants, pyruvic acid, buffers, inorganic salts, cytokines, hormones, and the like.

[0078] When vitamin C is used in step (3), the vitamin C may be the same as those described in step (1) and may be added in the same manner. In one embodiment, the concentration of vitamin C in the medium or culture solution is preferably 5 μg / ml to 200 μg / ml. In another embodiment, the vitamin C is added in an amount equivalent to 5 μg / ml to 500 μg / ml in the culture solution (e.g., an amount equivalent to 5 μg / ml, 10 μg / ml, 25 μg / ml, 50 μg / ml, 100 μg / ml, 200 μg / ml, 300 μg / ml, 400 μg / ml, or 500 μg / ml).

[0079] When a hormone is used in step (3), the hormone may be an adrenal cortical hormone. The adrenal cortical hormone is a glucocorticoid or a derivative thereof, and examples thereof include cortisone acetate, hydrocortisone, fludrocortisone acetate, prednisolone, triamcinolone, methylprednisolone, dexamethasone, betamethasone, and beclomethasone propionate. Dexamethasone is preferable. When the adrenal cortical hormone is dexamethasone, its concentration in the medium is 1 nM to 100 nM.

[0080] In step (3), the medium contains a CD3 / TCR complex agonist. The CD3 / TCR complex agonist is not particularly limited as long as it is a molecule capable of transmitting a signal from the CD3 / TCR complex into the CD3-positive cell by specifically binding to at least a part of the CD3 / TCR complex. Examples of the CD3 / TCR complex agonist include a CD3 agonist and / or a TCR agonist. Examples of the CD3 agonist include an anti-CD3 agonist antibody or a binding fragment thereof, and examples of the TCR agonist include at least one selected from the group consisting of an anti-TCR antibody or a binding fragment thereof, an MHC / antigen peptide complex or a multimer thereof, and an MHC / superantigen complex or a multimer thereof. When an anti-CD3 agonist antibody is used, the anti-CD3 agonist antibody includes both a polyclonal antibody and a monoclonal antibody, but is preferably a monoclonal antibody. The antibody may belong to any of the immunoglobulin classes, IgG, IgA, IgM, IgD, or IgE, but is preferably an IgG. Examples of the anti-CD3 agonist antibody include an antibody (OKT3) produced from an OKT3 clone and an antibody (UCHT1) produced from a UCHT1 clone, and preferably UCHT1. When the anti-CD3 agonist antibody is OKT3, OKT3 contains RYTMH (SEQ ID NO: 9), YINPSRGYTNYNQKFKD (SEQ ID NO: 10), and YYDDHYCLDY (SEQ ID NO: 11) as the complementarity determining regions 1 to 3 of the heavy chain variable region, and contains SASSSVSYMN (SEQ ID NO: 12), DTSKLAS (SEQ ID NO: 13), and QQWSSNPFT (SEQ ID NO: 14) as the complementarity determining regions 1 to 3 of the light chain variable region. Furthermore, OKT3 preferably contains a heavy chain variable region containing the amino acid sequence represented by SEQ ID NO: 21 and a light chain variable region containing the amino acid sequence represented by SEQ ID NO: 22.When the anti-CD3 agonist antibody is UCHT1, UCHT1 contains GYSFTGYTMN (SEQ ID NO: 15), LINPYKGVST (SEQ ID NO: 16), and SGYYGDSDWYFDV (SEQ ID NO: 17) as the complementarity determining regions 1 to 3 of the heavy chain variable region, and RASQDIRNYLN (SEQ ID NO: 18), YTSRLHS (SEQ ID NO: 19), and QQGNTLPWT (SEQ ID NO: 20) as the complementarity determining regions 1 to 3 of the light chain variable region. Furthermore, UCHT1 preferably contains a heavy chain variable region containing the amino acid sequence represented by SEQ ID NO: 23 and a light chain variable region containing the amino acid sequence represented by SEQ ID NO: 24. The concentration of the anti-CD3 agonist antibody in the medium is, for example, 10 ng / ml to 1000 ng / ml, preferably 50 ng / ml to 800 ng / ml, and more preferably 250 ng / ml to 600 ng / ml.

[0081] When a cytokine is used in step (3), examples of the cytokine include IL-2, IL-7, etc. When the cytokine is IL-2, its concentration in the medium is 10 U / ml to 1000 U / ml, and when the cytokine is IL-7, its concentration in the medium is 1 ng / ml to 1000 ng / ml.

[0082] In step (3), the culture temperature conditions are not particularly limited, but for example, about 37°C to about 42°C, preferably about 37°C to about 39°C. Furthermore, those skilled in the art can appropriately determine the culture period while monitoring the number of CD3-positive cells, etc. As long as CD3-positive cells are obtained, the number of days is not particularly limited, but for example, at least 1 day or more, 2 days or more, 3 days or more, 4 days or more, 5 days or more, preferably 6 days. Furthermore, 28 days or less is preferable, and 14 days or less is more preferable.

[0083] As described above, CD3 + cells cultured in the production method or expansion method of the present invention can be obtained by differentiating pluripotent stem cells.

[0084] The production method or expansion method of the present invention comprises the step of culturing CD3 positive cells in the presence of a CD3 / TCR complex agonist, fibronectin or a modified form thereof, and a CD30 agonist (hereinafter referred to as step (I) of the present invention).

[0085] In step (I) of the present invention, the CD3 / TCR complex agonist may be the same as the CD3 / TCR complex agonist used in the above step (3).

[0086] When the CD3 / TCR complex agonist used in step (I) of the present invention (or step (3) above) is an anti-CD3 agonist antibody or an anti-TCR antibody, the polyclonal antibody can be produced, for example, by the following method. For example, in the case of a polyclonal antibody against CD3, a mixture of CD3 or a partial peptide containing an epitope thereof (e.g., γ, δ, ε, ζ or η chain) and complete or incomplete Freund's adjuvant (FCA or FIA) is used as a sensitizing antigen, and in the case of a polyclonal antibody against TCR, a mixture of TCR or a partial peptide containing an epitope thereof (e.g., α, β, γ or δ chain) and complete or incomplete Freund's adjuvant (FCA or FIA) is used as a sensitizing antigen to immunize a mammal such as a rabbit, mouse, rat, goat, guinea pig or hamster (booster immunization is performed once to several times about every 1 to 4 weeks from the first immunization), and the antibody titer of the serum partially collected from the blood about 3 to 10 days after each booster immunization is measured using a conventionally known antigen-antibody reaction to confirm the increase. Furthermore, about 3 to 10 days after the final immunization, whole blood is collected and antiserum is purified. Polyclonal antibodies can also be purified as a single immunoglobulin class using conventional separation techniques such as salting out (e.g., ammonium sulfate fractionation), centrifugation, dialysis, column chromatography, and the like.

[0087] In addition, when the anti-CD3 agonist antibody or anti-TCR antibody used in step (I) of the present invention (or the above step (3)) is a monoclonal antibody, the monoclonal antibody can be obtained from a hybridoma (fused cell) that is usually produced by cell fusion. That is, as in the case of the above polyclonal antibody, antibody-producing cells are isolated from a mammal immunized with CD3 or TCR or a partial peptide containing an epitope thereof, and the antibody-producing cells are fused with myeloma cells to form hybridomas, and the hybridomas are cloned and a clone that produces an antibody that shows specific affinity to CD3 or TCR as a marker antigen is selected. In addition, antibody-producing cells generated by acting CD3 on previously isolated spleen cells or lymphocytes in a culture medium can also be used. In this case, human-derived antibody-producing cells can also be prepared.

[0088] A hybridoma secreting a monoclonal antibody can be prepared according to the method of Kohler and Milstein (Nature, Vol. 256, pp. 495-497, 1975) and its modifications. That is, a monoclonal antibody is prepared by culturing a hybridoma obtained by fusing antibody-producing cells, such as spleen cells, thymus cells, lymph node cells, peripheral lymphocytes, myeloma cells or tonsil cells, preferably spleen cells, obtained from an animal immunized as described above, with myeloma cells (myeloma) of a mammal, preferably the same species, such as mouse, rat, guinea pig, hamster, rabbit or human, more preferably mouse, rat or human. The culture can be performed in vitro or in vivo, such as in the peritoneal cavity of a mammal, such as mouse, rat, guinea pig, hamster or rabbit, preferably mouse or rat, more preferably mouse, and the antibody can be obtained from the culture supernatant or ascites of the mammal, respectively.

[0089] Examples of myeloma cells used in cell fusion include mouse-derived myeloma cells (e.g., P3-NSI-1-Ag4-1, P3-X63-Ag8-U1, P3-X63-Ag8-653, SP2 / 0-Ag14, and BW5147), rat-derived myeloma cells (e.g., 210RCY3-Ag1.2.3), and human-derived myeloma cells (e.g., U-266AR1, GML500-6TG-A1-2, UC729-6, CEM-AGR, D1R11, and CEM-T15).

[0090] Hybridoma clones that produce monoclonal antibodies can be screened by culturing the hybridomas, for example, in a microtiter plate, and measuring the reactivity of the culture supernatant in wells in which growth is observed against CD3 by radioimmunoassay, enzyme immunoassay, fluorescent immunoassay, or the like.

[0091] Monoclonal antibodies can be isolated and purified by subjecting the antibody-containing culture supernatant or ascites fluid produced by the methods described above to ion exchange chromatography or affinity column chromatography using an anti-immunoglobulin column or protein G column, etc.

[0092] The monoclonal antibody used in step (I) of the present invention (or the above step (3)) is not limited to the above-mentioned production method and may be obtained by any method. Furthermore, while monoclonal antibodies usually have sugar chains with different structures depending on the type of mammalian animal used for immunization, the monoclonal antibody of the present invention is not limited by the structural differences in the sugar chains and includes monoclonal antibodies derived from any mammalian animal.

[0093] Furthermore, the anti-CD3 agonist antibody or anti-TCR antibody includes natural antibodies such as the above-mentioned polyclonal antibodies and monoclonal antibodies (mAbs), chimeric antibodies (humanized antibodies) that can be produced using gene recombination techniques, and single-chain antibodies, as well as binding fragments of these antibodies. The binding fragment of an antibody means a partial region of the above-mentioned antibody that has specific binding activity, and specifically includes Fab, Fab', F(ab')2, scAb, scFv, or scFv-Fc.

[0094] In addition, those skilled in the art can prepare fusion antibodies of anti-CD3 agonist antibodies or anti-TCR antibodies or their binding fragments with other peptides or proteins, or prepare modified antibodies by binding a modifying agent. The other peptides or proteins used for fusion are not particularly limited as long as they do not reduce the binding activity of the antibody, and examples of such peptides or proteins include human serum albumin, various tag peptides, artificial helix motif peptides, maltose-binding protein, glutathione S-transferase, various toxins, and other peptides or proteins that can promote multimerization. The modifying agents used for modification are not particularly limited as long as they do not reduce the binding activity of the antibody, and examples of such modifying agents include polyethylene glycol, sugar chains, phospholipids, liposomes, and low molecular weight compounds.

[0095] In addition, commercially available reagents can be used as the anti-CD3 agonist antibody. The commercially available anti-CD3 agonist antibody is not particularly limited, and for example, an antibody produced from an OKT3 clone (OKT3) (anti-human CD3 functional grade purified (Clone: ​​OKT3) (eBioscience)) and an antibody produced from a UCHT1 clone (UCHT1) (CD3 antibody (Clone: ​​UCHT1) (GeneTex)) can be used, and preferably UCHT1 can be used.

[0096] Furthermore, when the CD3 / TCR complex agonist used in step (I) of the present invention (or the above-described step (3)) is an MHC / antigen peptide complex, the MHC / antigen peptide complex is not particularly limited as long as it is a molecule that is specifically recognized by the CD3 / TCR complex of a CD3-positive cell and can transmit a signal into the CD3-positive cell.

[0097] The MHC constituting the MHC / antigen peptide complex may be MHC class I or MHC class II, but is preferably MHC class I.

[0098] In step (I) of the present invention (or the above step (3)), the MHC class I is not particularly limited as long as it is a molecule that forms a complex with an antigen peptide, is recognized by the CD3 / TCR complex and CD8, and transmits a signal into a CD3-positive cell. Examples of MHC class I include dimers consisting of an α chain (HLA-A, HLA-B, HLA-C, HLA-E, HLA-F, or HLA-G in the case of humans, and H-2K, H-2D, or H-2L in the case of mice) and β2 microglobulin, preferably dimers consisting of HLA-A, HLA-B, HLA-C, HLA-E, HLA-F, or HLA-G, and β2 microglobulin, and more preferably dimers consisting of HLA-A, HLA-B, or HLA-C, and β2 microglobulin. In the production method or expansion culture method of the present invention, specific examples of MHC class I include, but are not limited to, HLA-A*02:01, HLA-A*24:02, or HLA-A*01:01. In addition, the antigen peptide is not particularly limited as long as it is a peptide presented by MHC class I. Examples of antigen peptides presented by MHC class I include peptides derived from proteins derived from HER-2 / neu, MART-1, NY-ESO-1, Gp-100, MUC-1, p53, prostate specific antigen (PSA), hTERT, WT1, survivin, CEA, MAGE-3, or a group of viruses strongly associated with the development of malignant tumors, and preferably WT1-derived peptides. In addition, specific examples of WT1-derived peptides include RMFPNAPYL (SEQ ID NO: 1), SLGEQQYSV (SEQ ID NO: 2), or CMTWNQMNL (SEQ ID NO: 3) (its modified peptide CYTWNQMNL (SEQ ID NO: 4)).

[0099] In step (I) of the present invention (or step (3)), the MHC class II is not particularly limited as long as it is a molecule that forms a complex with an antigen peptide, is recognized by the CD3 / TCR complex and CD4, and transmits a signal into a CD3-positive cell. Examples of the MHC class II include HLA-DR, HLA-DQ, and HLA-DP in humans, and H-2A or H-2B in mice, each of which is a dimer consisting of an α chain and a β chain (for example, HLA-DR is an α chain, HLA-DRA, and a β chain, HLA-DRB1), and preferably HLA-DR, HLA-DQ, or HLA-DP. In addition, the antigen peptide is not particularly limited as long as it is a peptide presented by the MHC class II. Examples of the antigen peptide presented by the MHC class II include peptides derived from proteins derived from WT1, PSA, MAGE-3, CEA, survivin, tyrosinase, or a virus group that is strongly associated with the development of malignant tumors, and preferably, WT1-derived peptides.

[0100] The MHC and / or antigen peptide (hereinafter referred to as MHC, etc.) may be a protein that has been chemically synthesized or biochemically synthesized in a cell-free translation system, or may be a recombinant protein produced from a transformant into which a nucleic acid having a base sequence encoding the MHC, etc. has been introduced.

[0101] When MHC and the like are produced according to a known peptide synthesis method, either a solid-phase synthesis method or a liquid-phase synthesis method may be used. The desired protein can be produced by condensing an amino acid derivative in which a protecting group has been added to the carboxyl group and the functional group of the side chain with an amino acid derivative in which the amino group and the functional group of the side chain are protected, and then removing the protecting groups. Here, the condensation and removal of the protecting group are carried out according to a method known per se, for example, the methods described in (1) to (5) below. (1) M. Bodanszky and M.A. Ondetti, Peptide Synthesis, Interscience Publishers, New York (1966) (2) Schroeder and Luebke, The Peptide, Academic Press, New York (1965) (3) Nobuo Izumiya et al., Fundamentals and Experiments of Peptide Synthesis, Maruzen Co., Ltd. (1975) (4) Haruaki Yajima and Shumpei Sakakibara, Biochemistry Experiment Course 1, Chemistry of Proteins IV 205 (1977) (5) Haruaki Yajima, editor, Pharmaceutical Development, Vol. 14, Peptide Synthesis, Hirokawa Shoten

[0102] The MHC etc. thus obtained can be purified and isolated by known purification methods, such as solvent extraction, distillation, column chromatography, liquid chromatography, recrystallization, and combinations thereof. When the MHC etc. obtained by the above-mentioned method is in a free form, the free form can be converted into an appropriate salt by a known method or a method similar thereto. Conversely, when the MHC etc. is obtained as a salt, the salt can be converted into the free form or another salt by a known method or a method similar thereto.

[0103] Furthermore, MHC etc. can also be produced by culturing a transformant containing a nucleic acid encoding it, and isolating and purifying MHC etc. from the resulting culture. The nucleic acid encoding MHC etc. may be DNA or RNA, or may be a DNA / RNA chimera. DNA is preferred. The nucleic acid may be double-stranded or single-stranded. If double-stranded, it may be double-stranded DNA, double-stranded RNA, or a DNA:RNA hybrid. If single-stranded, it may be a sense strand (i.e., coding strand) or an antisense strand (i.e., non-coding strand).

[0104] Examples of DNA encoding MHC and the like include genomic DNA, cDNA derived from cells of warm-blooded animals (e.g., humans, cows, monkeys, horses, pigs, sheep, goats, dogs, cats, guinea pigs, rats, mice, rabbits, hamsters, birds, etc.), and synthetic DNA. cDNA encoding MHC and the like can be used to encode any cell of the above animals [e.g., hepatocytes, spleen cells, nerve cells, glial cells, pancreatic β cells, bone marrow cells, mesangial cells, Langerhans cells, epidermal cells, epithelial cells, goblet cells, endothelial cells, smooth muscle cells, fibroblasts, fibrocytes, muscle cells, adipocytes, immune cells (e.g., macrophages, T cells, B cells, natural killer cells, mast cells, neutrophils, basophils, eosinophils, monocytes), megakaryocytes, synovial cells, chondrocytes, osteocytes, osteoblasts, osteoclasts, mammary gland cells, hepatocytes or stromal cells, or precursor cells or stem cells of these cells, as well as any other cell of the above animals [e.g., hepatocytes, spleen cells, nerve cells, glial cells, pancreatic β cells, bone marrow cells, mesangial cells, Langerhans cells, epidermal cells, epithelial cells, goblet cells, endothelial cells, smooth muscle cells, fibroblasts, fibrocytes, muscle cells, adipocytes, immune cells (e.g., macrophages, T cells, B cells, natural killer cells, mast cells, neutrophils, basophils, eosinophils, monocytes), megakaryocytes, synovial cells, chondrocytes, osteocytes, osteoblasts, osteoclasts, mammary gland cells, hepatocytes or stromal cells, or precursor cells or or cancer cells, etc.) or any tissue in which such cells are present [for example, the brain, various parts of the brain (e.g., olfactory bulb, amygdala, basal sphere, hippocampus, thalamus, hypothalamus, cerebral cortex, medulla oblongata, cerebellum), spinal cord, pituitary gland, stomach, pancreas, kidney, liver, gonads, thyroid gland, gallbladder, bone marrow, adrenal gland, skin, lung, digestive tract (e.g., large intestine, small intestine), blood vessels, heart, thymus, spleen, submandibular gland, peripheral blood, prostate, testis, ovary, placenta, uterus, bone, joint, adipose tissue (e.g., brown adipose tissue, white adipose tissue), skeletal muscle, etc.] can be used as a template to directly amplify the target gene by polymerase chain reaction (hereinafter abbreviated as "PCR") and reverse transcriptase-PCR (hereinafter abbreviated as "RT-PCR"). Alternatively, cDNAs encoding MHC etc. can be cloned from a cDNA library prepared by inserting the above-mentioned total RNA or mRNA fragment into an appropriate vector by colony or plaque hybridization, PCR, etc. The vector used for the library may be any of bacteriophage, plasmid, cosmid, phagemid, etc.

[0105] DNA encoding MHC etc. can be amplified by PCR using a synthetic DNA primer having a part of the base sequence encoding the MHC etc., or cloned by hybridizing the DNA incorporated into an appropriate expression vector with a labeled DNA fragment or synthetic DNA encoding a part or the entire region of MHC etc. Hybridization can be performed according to a method known per se or a method equivalent thereto, for example, the method described in Molecular Cloning, 2nd Edition (J. Sambrook et al., Cold Spring Harbor Lab. Press, 1989). When using a commercially available library, hybridization can be performed according to the method described in the attached instruction manual. Hybridization can be preferably performed under stringent conditions.

[0106] Highly stringent conditions include, for example, a hybridization reaction in 6×SSC (sodium chloride / sodium citrate) at 45° C., followed by one or more washes in 0.2×SSC / 0.1% SDS at 65° C. Those skilled in the art can easily adjust the stringency to a desired level by appropriately changing the salt concentration of the hybridization solution, the temperature of the hybridization reaction, the probe concentration, the length of the probe, the number of mismatches, the hybridization reaction time, the salt concentration of the washing solution, the washing temperature, etc. When a commercially available library is used, hybridization can be performed according to the method described in the instruction manual attached to the library.

[0107] An expression vector containing DNA encoding MHC or the like can be produced, for example, by excising a desired DNA fragment from DNA encoding MHC or the like and ligating the DNA fragment downstream of a promoter in an appropriate expression vector.

[0108] Examples of expression vectors that can be used include plasmids derived from E. coli (e.g., pBR322, pBR325, pUC12, pUC13); animal cell expression plasmids (e.g., pA1-11, pXT1, pRc / CMV, pRc / RSV, pcDNAI / Neo); and animal virus vectors such as retrovirus, vaccinia virus, and adenovirus.

[0109] The promoter may be any promoter suitable for the host used to express the gene.

[0110] For example, when the host is an animal cell, the SRα promoter, SV40 promoter, LTR promoter, CMV (cytomegalovirus) promoter, RSV (Rous sarcoma virus) promoter, MoMuLV (Moloney murine leukemia virus) LTR, HSV-TK (herpes simplex virus thymidine kinase) promoter, etc. are used. Among them, the CMV promoter, SRα promoter, etc. are preferred.

[0111] When the host is a bacterium of the genus Escherichia, the trp promoter, lac promoter, recA promoter, λPL promoter, lpp promoter, T7 promoter, and the like are preferred.

[0112] In addition to the above, expression vectors that contain enhancers, splicing signals, polyA addition signals, selection markers, SV40 replication origins (hereinafter sometimes abbreviated as SV40 ori), etc., can be used. Examples of selection markers include the dihydrofolate reductase gene (hereinafter sometimes abbreviated as dhfr, methotrexate (MTX) resistance), ampicillin resistance gene (hereinafter sometimes abbreviated as amp r ), neomycin resistance gene (hereafter referred to as neo r In particular, when using dhfr gene-deficient Chinese hamster cells and the dhfr gene as a selection marker, the target gene can be selected by a thymidine-free medium.

[0113] Furthermore, if necessary, a base sequence (signal codon) encoding a signal sequence suitable for the host may be added to the 5'-end of the DNA encoding the MHC etc. (or replace the native signal codon). For example, when the host is an Escherichia bacterium, the PhoA signal sequence, the OmpA signal sequence, etc. are used; when the host is an animal cell, the insulin signal sequence, the α-interferon signal sequence, the antibody molecule signal sequence, etc. are used.

[0114] MHC etc. can be produced by transforming a host with an expression vector containing DNA encoding the above-mentioned MHC etc. and culturing the resulting transformant.

[0115] As the host, for example, bacteria of the genus Escherichia, animal cells, etc. are used. Examples of Escherichia bacteria that can be used include K12 DH1 [Proc. Natl. Acad. Sci. USA, Vol. 60, p. 160 (1968)], JM103 [Nucleic Acids Research, Vol. 9, p. 309 (1981)], JA221 [Journal of Molecular Biology, Vol. 120, p. 517 (1978)], HB101 [Journal of Molecular Biology, Vol. 41, p. 459 (1969)], and C600 [Genetics, Vol. 39, p. 440 (1954)].

[0116] Examples of animal cells include monkey COS-7 cells, monkey Vero cells, Chinese hamster ovary cells (hereinafter abbreviated as CHO cells), and dhfr gene-deficient CHO cells (hereinafter abbreviated as CHO(dhfr - ) cells), mouse L cells, mouse AtT-20 cells, mouse myeloma cells, rat GH3 cells, human FL cells, etc. are used.

[0117] Transformation can be carried out according to known methods depending on the type of host.

[0118] Bacteria of the genus Escherichia can be transformed, for example, according to the methods described in Proc. Natl. Acad. Sci. USA, vol. 69, 2110 (1972) or Genee, vol. 17, 107 (1982).

[0119] Animal cells can be transformed according to the methods described in, for example, Saibo Kogaku Supplement 8, New Saibo Kogaku Jikken Protocol, pp. 263-267 (1995) (published by Shujunsha), and Virology, vol. 52, 456 (1973).

[0120] The transformant can be cultured according to a known method depending on the type of host.

[0121] When the host is a bacterium of the genus Escherichia, a preferred medium is, for example, M9 medium containing glucose and casamino acids [Miller, Journal of Experiments in Molecular Genetics, 431-433, Cold Spring Harbor Laboratory, New York 1972]. If necessary, a drug such as 3β-indolylacrylic acid may be added to the medium to allow the promoter to function efficiently.

[0122] The transformant, whose host is a bacterium of the genus Escherichia, is usually cultured at about 15 to about 43° C. for about 3 to about 24 hours. Aeration or stirring may be performed as necessary.

[0123] When the host is an animal cell, a medium for culturing a transformant may be, for example, a minimum essential medium (MEM) containing about 5 to about 20% fetal bovine serum [Science, Vol. 122, 501 (1952)], Dulbecco's modified Eagle's medium (DMEM) [Virology, Vol. 8, 396 (1959)], RPMI1640 medium [The Journal of the American Medical Association, Vol. 199, 519 (1967)], or 199 medium [Proceeding of the Society for the Biological Medicine, Vol. 73, 1 (1950)]. The pH of the medium is preferably about 6 to about 8. The culture is usually performed at about 30°C to about 40°C for about 15 to about 60 hours. Aeration or stirring may be performed as necessary.

[0124] In this manner, MHC and the like can be produced intracellularly or extracellularly in the transformant.

[0125] MHC and the like can be separated and purified from the culture obtained by culturing the transformant according to a method known per se.

[0126] For example, when extracting MHC and the like from cultured bacteria or the cytoplasm of cells, a method is appropriately used in which bacteria or cells collected from the culture by a known method are suspended in an appropriate buffer, and the bacteria or cells are disrupted by ultrasonic waves, lysozyme and / or freeze-thawing, and then a crude extract of soluble proteins is obtained by centrifugation or filtration. The buffer may contain a protein denaturant such as urea or guanidine hydrochloride, or Triton X-100. TM In addition, when MHC and the like are secreted outside the bacterial body (cell), a method is used in which the culture supernatant is separated from the culture by centrifugation, filtration, or the like.

[0127] The soluble fraction thus obtained, and MHC and the like contained in the culture supernatant can be isolated and purified according to a method known per se. Examples of such methods include methods that utilize solubility, such as salting out and solvent precipitation; methods that mainly utilize differences in molecular weight, such as dialysis, ultrafiltration, gel filtration, and SDS-polyacrylamide gel electrophoresis; methods that utilize differences in charge, such as ion exchange chromatography; methods that utilize specific affinity, such as affinity chromatography; methods that utilize differences in hydrophobicity, such as reversed-phase high performance liquid chromatography; and methods that utilize differences in isoelectric point, such as isoelectric focusing. These methods can also be combined as appropriate.

[0128] The MHC / antigen peptide complex obtained as described above may be a multimer. By multimerizing the MHC / antigen peptide complex, a higher agonistic effect on TCR can be expected. Methods for multimerizing the MHC / antigen peptide complex of the present invention are known, and for example, a biotin-modified MHC / antigen peptide complex can be tetramerized via an avidin or streptavidin tetramer. Alternatively, the MHC / antigen peptide complex can be multimerized by linking it to dextran.

[0129] Furthermore, when the CD3 / TCR complex agonist used in step (I) of the present invention (or the above step (3)) is an MHC / superantigen complex, the MHC / superantigen complex is a complex of MHC class II and a superantigen. Examples of superantigens include staphylococcal enterotoxin, streptococcal pyrogenic exotoxin, and toxic shock syndrome toxin. The MHC or superantigen may be produced by the same method as that described above for MHC, etc. Furthermore, the MHC / superantigen complex may be a multimer, like the MHC / antigen peptide complex. The method for multimerizing the MHC / superantigen complex of the present invention is the same as the method for multimerizing the MHC / antigen peptide complex.

[0130] The CD3 / TCR complex agonist used in step (I) of the present invention may be present in any form as long as it is capable of contacting the CD3 / TCR complex on the surface of CD3-positive cells during culture. For example, it may be contained in the medium during culture or may be immobilized on a culture vessel, but is preferably immobilized on a culture vessel.

[0131] When the CD3 / TCR complex agonist is contained in the medium, the medium is not particularly limited as long as it can culture CD3 positive cells, and includes, for example, Glasgow's Minimal Essential Medium (GMEM) medium, IMDM medium, Medium 199 medium, Eagle's Minimum Essential Medium (EMEM) medium, αMEM medium, Dulbecco's modified Eagle's Medium (DMEM) medium, Ham's F12 medium, RPMI 1640 medium, Fischer's medium, Neurobasal Medium (Life Technologies), and mixed media thereof. The medium may contain serum or may be serum-free. When serum is contained, the concentration of serum (e.g., fetal bovine serum (FBS), human serum, etc.) may be, as a lower limit, usually 1% or more, preferably 5% or more, and, as an upper limit, usually 20% or less, preferably 15% or less. Furthermore, if necessary, the medium may contain one or more serum substitutes, such as, for example, Knockout Serum Replacement (KSR) (a serum substitute for FBS during ES cell culture), N2 supplement (Invitrogen), B27 supplement (Invitrogen), albumin, insulin, transferrin, selenium compounds (e.g., sodium selenite), vitamin C (e.g., ascorbic acid), apotransferrin, fatty acids, collagen precursors, trace elements, 2-mercaptoethanol, 3'-thiolglycerol, and may also contain one or more substances, such as lipids, amino acids, L-glutamine, L-alanyl-L-glutamine (e.g., Glutamax (registered trademark)), non-essential amino acids, vitamins, growth factors, low molecular weight compounds, antibiotics (e.g., penicillin, streptomycin), antioxidants, pyruvic acid, buffers, inorganic salts, selenium acid, progesterone, and putrescine. Furthermore, when a CD3 / TCR complex agonist is contained in the culture medium, the concentration of the CD3 / TCR complex agonist may be, at the lower limit, 0.3 ng / ml or more, preferably 3 ng / ml or more, and at the upper limit, 10,000 ng / ml or less, preferably 1,000 ng / ml or less.In particular, when the CD3 / TCR complex agonist is an anti-CD3 agonist antibody, the concentration of the anti-CD3 agonist antibody in the medium is, for example, 10 ng / ml to 1000 ng / ml. The culture can be performed, for example, in a CO2 incubator under an atmosphere of about 1 to about 10%, preferably about 2 to about 5%, at about 30 to about 40°C, preferably about 37°C. In addition, a person skilled in the art can appropriately determine the culture period in a medium containing a CD3 / TCR complex agonist while monitoring the number of CD3 positive cells, etc. As long as CD3 positive cells are obtained, the number of days is not particularly limited, but is, for example, at least 6 hours or more, 12 hours or more, 16 hours or more, 24 hours or more, 48 hours or more, 72 hours or more, and preferably 16 to 72 hours. In addition, 14 days or less is preferable, and 7 days or less is more preferable.

[0132] When vitamin C is used, it is preferable to add (supplement) vitamin C every 4 days, every 3 days, every 2 days, or every day, and more preferable to add every day. In one embodiment, the vitamin C is added in an amount equivalent to 5 ng / ml to 500 ng / ml in the culture solution (e.g., an amount equivalent to 5 ng / ml, 10 ng / ml, 25 ng / ml, 50 ng / ml, 100 ng / ml, 200 ng / ml, 300 ng / ml, 400 ng / ml, or 500 ng / ml). In another embodiment, the vitamin C is added in an amount equivalent to 5 μg / ml to 500 μg / ml in the culture medium (e.g., an amount equivalent to 5 μg / ml, 10 μg / ml, 25 μg / ml, 50 μg / ml, 100 μg / ml, 200 μg / ml, 300 μg / ml, 400 μg / ml, or 500 μg / ml).

[0133] The medium used in step (I) of the present invention may further contain a cytokine. The cytokine contained in the medium is not particularly limited, but may include at least one selected from IL-7, IL-15, IL-18, and IL-21, and preferably contains all of IL-7, IL-15, IL-18, and IL-21. The lower limit of the concentration of the cytokine may be 0.1 ng / mL or more, preferably 10 ng / mL or more, and the upper limit may be 1000 ng / mL or less, preferably 300 ng / mL or less. When these cytokines are used, the concentrations in the medium are, for example, 1 to 100 ng / ml for IL-7, 1 to 100 ng / ml for IL-15, 5 to 500 ng / ml for IL-18, and 2 to 200 ng / ml for IL-21. The medium used in step (I) of the present invention may further contain TL1A and / or IL-12, in which the concentration of TL1A in the medium is 5 to 500 ng / ml, and the concentration of IL-12 in the medium is 5 to 500 ng / ml.

[0134] The medium used in step (I) of the present invention may contain a TNF family cytokine as a cytokine. Examples of TNF family cytokines include TNF-α, TNF-β, lymphotoxin α, Fas ligand, TRAIL, TWEAK, TL1A, RANK ligand, OX40 ligand, APRIL, AITRL, BAFF, 4-1BBL, and CD40 ligand, and TL1A is preferred. When TL1A is used, its concentration in the medium may be 5 to 500 ng / ml.

[0135] The apoptosis inhibitor used in step (I) of the present invention includes a protease inhibitor, such as a caspase inhibitor. A preferred caspase inhibitor is the Pan Caspase FMK inhibitor Z-VAD (N-benzyloxycarbonyl-Val-Ala-Asp(O-Me) fluoromethylketone), and its concentration in the medium may be 1 to 1000 μM.

[0136] In addition, when the CD3 / TCR complex agonist is immobilized on a culture vessel, the culture vessel is not particularly limited as long as it is a culture vessel capable of culturing CD3-positive cells, and a vessel, a slide, beads, or a combination of these may be used. Examples of culture vessels include flasks, flasks for tissue culture, dishes, Petri dishes, dishes for tissue culture, multi-dishes, microplates, microwell plates, multi-plates, multiwell plates, microslides, chamber slides, petri dishes, tubes, trays, culture bags, roller bottles, and microbeads.

[0137] The CD3 / TCR complex agonist can be immobilized on the culture vessel by known means. For example, the CD3 / TCR complex agonist can be immobilized on the culture vessel by dissolving the CD3 / TCR complex agonist in a solvent (e.g., PBS, etc.), adding the solution to the culture vessel, and then leaving the solution at 4°C overnight. The concentration of the CD3 / TCR complex agonist solution when immobilizing the CD3 / TCR complex agonist on the culture vessel may be appropriately determined by a person skilled in the art depending on the type of the CD3 / TCR complex agonist. In one embodiment of the present invention, for example, when the CD3 / TCR complex agonist is an anti-CD3 agonist antibody or a binding fragment thereof, a solution of the anti-CD3 agonist antibody or a binding fragment thereof at 0.3 to 10,000 ng / ml can be contacted with the culture vessel, and 3 to 5,000 ng / ml is more preferable, 3 to 3,000 ng / ml is even more preferable, and 3 to 600 ng / ml is particularly preferable. In another embodiment of the present invention, the concentration of the anti-CD3 agonist antibody or binding fragment thereof in solution is, for example, 10 ng / ml to 10,000 ng / ml, preferably 50 ng / ml to 5,000 ng / ml, and more preferably 200 ng / ml to 4,000 ng / ml. In yet another embodiment of the present invention, the concentration of the anti-CD3 agonist antibody or binding fragment thereof in solution is, for example, 1 to 50,000 ng / ml, preferably 3 to 30,000 ng / ml, more preferably 30 to 30,000 ng / ml, and even more preferably 300 to 30,000 ng / ml. When the anti-CD3 agonist antibody or binding fragment thereof is an antibody (OKT3) produced from an OKT3 clone or a binding fragment thereof, its concentration in the solution is, for example, 1 ng / ml to 50,000 ng / ml, preferably 10 ng / ml to 10,000 ng / ml, more preferably 50 ng / ml to 5,000 ng / ml, and even more preferably 200 ng / ml to 4,000 ng / ml.When the anti-CD3 agonist antibody or binding fragment thereof is an antibody (UCHT1) produced from the UCHT1 clone or a binding fragment thereof, its concentration in the solution is, for example, 1 ng / ml to 50,000 ng / ml, preferably 3 ng / ml to 30,000 ng / ml, more preferably 30 ng / ml to 30,000 ng / ml, and even more preferably 300 ng / ml to 30,000 ng / ml.

[0138] In step (I) of the present invention, the fibronectin is not particularly limited as long as it is a molecule capable of binding to CD3 positive cells. The modified fibronectin is not particularly limited as long as it is a molecule capable of binding to VLA-5 and VLA-4 on the surface of CD3 positive cells, and an example of the modified fibronectin is Retronectin (registered trademark).

[0139] As with the CD3 / TCR complex agonist, the fibronectin or its variant used in step (I) of the present invention may be present in any form so long as it is capable of contacting CD3-positive cells during culture. For example, it may be contained in the medium during culture or may be immobilized on a culture vessel, but is preferably immobilized on a culture vessel.

[0140] When fibronectin or a variant thereof is contained in the medium, the medium may be the same as the medium containing the CD3 / TCR complex agonist. In addition, the presence or absence of serum, additives, etc. may be the same as the medium containing the CD3 / TCR complex agonist. When fibronectin or a variant thereof is contained in the medium, the concentration of fibronectin or a variant thereof may be 10 ng / ml or more as the lower limit, preferably 100 ng / ml or more, and 10000 μg / ml or less as the upper limit, preferably 1000 μg / ml or less.

[0141] In addition, when fibronectin or a variant thereof is solid-phased in a culture vessel, the culture vessel may be the same as the culture vessel in which the CD3 / TCR complex agonist is solid-phased. In addition, the solidification of fibronectin or a variant thereof in a culture vessel may be the same as the solidification of the CD3 / TCR complex agonist. The concentration of the solution of fibronectin or a variant thereof when solidifying fibronectin or a variant thereof in a culture vessel may be appropriately determined by a person skilled in the art depending on the fibronectin or variant thereof. For example, when the fibronectin or a variant thereof is Retronectin (registered trademark), it is preferable to contact the culture vessel with a solution of Retronectin (registered trademark) at 0.1 to 10000 μg / mL. In this case, the concentration of the Retronectin solution is more preferably 0.1 to 1000 μg / mL, more preferably 1 to 300 μg / mL, and particularly preferably 1 to 150 μg / mL.

[0142] In step (I) of the present invention, the CD30 agonist is not particularly limited as long as it is a molecule that can transmit a signal from CD30 into a cell by specifically binding to CD30. Examples of the CD30 agonist include at least one selected from the group consisting of an anti-CD30 agonist antibody or a binding fragment thereof, and a CD30 ligand or a binding fragment thereof.

[0143] The anti-CD30 agonist antibody and its binding fragment used in step (I) of the present invention may be similar in type, production method, etc. to the anti-CD3 agonist antibody and anti-TCR antibody.

[0144] The CD30 ligand or its binding fragment used in step (I) of the present invention may be, for example, CD153. The CD30 ligand or its binding fragment may be produced by a method similar to the method for producing MHC and / or antigen peptides.

[0145] The CD30 agonist used in step (I) of the present invention may be present in any form as long as it is capable of contacting CD30 during culture, similar to the CD3 / TCR complex agonist. For example, it may be contained in the medium during culture or may be immobilized on a culture vessel, but is preferably contained in the medium.

[0146] When the CD30 agonist is contained in the medium, the medium may be the same as the medium containing the CD3 / TCR complex agonist. In addition, the presence or absence of serum, additives, etc. may be the same as the medium containing the CD3 / TCR complex agonist. When the CD30 agonist is contained in the medium, the concentration of the CD30 agonist in the medium may be appropriately determined by those skilled in the art depending on the type of the CD30 agonist. For example, when the CD30 agonist is an anti-CD30 agonist antibody or a binding fragment thereof, the concentration of the anti-CD30 agonist antibody or a binding fragment thereof in the medium may be usually 1 ng / ml to 10000 ng / ml, preferably 1 ng / ml to 1000 ng / ml, more preferably 3 ng / ml to 300 ng / ml, and even more preferably 30 ng / ml to 300 ng / ml.

[0147] In addition, when the CD30 agonist is solid-phased in the culture vessel, the culture vessel may be the same as the culture vessel in which the CD3 / TCR complex agonist is solid-phased. In addition, the method of solidifying the CD30 agonist in the culture vessel may be the same as the method of solidifying the CD30 agonist in the culture vessel. The concentration of the CD30 agonist solution when solidifying the CD30 agonist in the culture vessel may be 0.1 ng / ml or more as the lower limit, preferably 1 ng / ml or more, and 10000 ng / ml or less as the upper limit, preferably 1000 ng / ml or less.

[0148] The production method or expansion culture method of the present invention may further include a step of culturing the CD3-positive cells cultured in step (I) of the present invention in the absence of a CD3 / TCR complex agonist, and fibronectin or a variant thereof, and in the presence of a CD30 agonist (hereinafter referred to as step (II) of the present invention).

[0149] The medium used in step (II) of the present invention may be the medium used in step (I) above, and may contain serum or may be serum-free. When serum is contained, the concentration of serum (e.g., fetal bovine serum (FBS), human serum, etc.) may be usually 1% or more, preferably 5% or more, as a lower limit, and usually 20% or less, preferably 15% or less, as an upper limit. If necessary, the medium may contain one or more serum substitutes such as, for example, Knockout Serum Replacement (KSR) (a serum substitute for FBS during ES cell culture), N2 supplement (Invitrogen), B27 supplement (Invitrogen), albumin, insulin, transferrin, selenium compounds (e.g., sodium selenite), vitamin C (e.g., ascorbic acid), apotransferrin, fatty acids, collagen precursors, trace elements, 2-mercaptoethanol, 3'-thiolglycerol, and may also contain one or more substances such as lipids, amino acids, L-glutamine, Glutamax (Invitrogen), non-essential amino acids, vitamins, growth factors, small molecule compounds, antibiotics, antioxidants, pyruvic acid, buffers, inorganic salts, selenium acid, progesterone, and putrescine. The culture can be carried out, for example, in a CO2 incubator under an atmosphere of CO2 concentration of about 1 to about 10%, preferably about 2 to about 5%, at about 30 to about 40°C, preferably about 37°C. In addition, a person skilled in the art can appropriately determine the culture period while monitoring the number of CD3 positive cells, etc. As long as CD3 positive cells are obtained, the number of days is not particularly limited, but is, for example, at least 3 days or more, 5 days or more, 7 days or more, 10 days or more, 14 days or more, 21 days or more, and preferably 7 days or more and 15 days or less. In addition, 30 days or less is preferable, and 21 days or less is more preferable.

[0150] When vitamin C is used, it is preferable to add (supplement) vitamin C every 4 days, every 3 days, every 2 days, or every day, and more preferable to add every day. In one embodiment, the vitamin C is added in an amount equivalent to 5 ng / ml to 500 ng / ml in the culture solution (e.g., an amount equivalent to 5 ng / ml, 10 ng / ml, 25 ng / ml, 50 ng / ml, 100 ng / ml, 200 ng / ml, 300 ng / ml, 400 ng / ml, or 500 ng / ml). In another embodiment, the vitamin C is added in an amount equivalent to 5 μg / ml to 500 μg / ml in the culture medium (e.g., an amount equivalent to 5 μg / ml, 10 μg / ml, 25 μg / ml, 50 μg / ml, 100 μg / ml, 200 μg / ml, 300 μg / ml, 400 μg / ml, or 500 μg / ml).

[0151] The medium used in step (II) of the present invention may further contain a cytokine. The cytokine is not particularly limited, but includes at least one selected from IL-7, IL-15, IL-18, and IL-21, and preferably includes all of IL-7, IL-15, IL-18, and IL-21. The concentration of the cytokine may be 0.1 ng / ml or more, preferably 10 ng / ml or more, as a lower limit, and 1000 ng / ml or less, preferably 300 ng / ml or less, as an upper limit. When using these cytokines, the concentrations in the medium may be, for example, 1 ng / ml to 100 ng / ml for IL-7, 1 ng / ml to 100 ng / ml for IL-15, 5 ng / ml to 500 ng / ml for IL-18, and 2 ng / ml to 200 ng / ml for IL-21. The medium used in step (II) of the present invention may further contain TL1A and / or IL-12. In this case, the concentration of TL1A in the medium may be 5 ng / ml to 500 ng / ml, and the concentration of IL-12 in the medium may be 5 ng / ml to 500 ng / ml.

[0152] The medium used in step (II) of the present invention may further contain an apoptosis inhibitor. Examples of the apoptosis inhibitor include protease inhibitors, such as caspase inhibitors. A preferred caspase inhibitor is Pan Caspase FMK inhibitor Z-VAD (N-benzyloxycarbonyl-Val-Ala-Asp(O-Me) fluoromethylketone) (hereinafter sometimes referred to as "Z-VAD-FMK"), and the concentration of the inhibitor in the medium may be 1 μM to 1000 μM, preferably 1 μM to 500 μM, more preferably 1 μM to 200 μM, and particularly preferably 1 μM to 50 μM.

[0153] In one embodiment of the present invention, the above steps (I) and (II) may be repeated in this order.

[0154] The present invention also provides CD3-positive cells obtained by the production method or expansion method of the present invention (hereinafter, referred to as the CD3-positive cells of the present invention). The CD3-positive cells of the present invention are identical to the CD3-positive cells obtained by the production method or expansion method of the present invention.

[0155] The present invention also provides a kit for expanding CD3-positive cells (hereinafter referred to as the kit of the present invention), comprising: (1) CD3 / TCR complex agonists, and Fibronectin or its modified form A culture vessel having the immobilized (2) Medium containing a CD30 agonist

[0156] The CD3 / TCR complex agonist, fibronectin or a variant thereof, CD30 agonist, culture vessel and medium contained in the kit of the present invention may be the same as those described in the production method or expansion culture method of the present invention.

[0157] The present invention also provides a method for maintaining CD3-positive cells as CD3-positive CD197-positive cells (hereinafter referred to as the maintenance method of the present invention), which comprises the step of stimulating a CD30 signal in CD3-positive cells. Normally, when naive T cells derived from peripheral blood are stimulated by antigens presented by dendritic cells, intracellular signals are activated in the naive T cells, which then undergo repeated proliferation and maturation, and differentiate into stem cell memory T cells, central memory T cells, effector memory T cells, and effector T cells. Effector T cells, CD3+CD4+CD8-negative cells (helper T cells), produce cytokines, while CD3+CD4-negative CD8-negative cells (cytotoxic T cells) kill target cells via antigens, but cannot survive for long periods of time. However, by stimulating the CD30 signal in T cells, it is possible to maintain them as self-proliferating naive T cells or stem cell memory T cells (CD197+, CD45RA+) or central memory T cells (CD197+, CD45RA-negative) that can differentiate into effector T cells.

[0158] In the maintenance method of the present invention, the CD3-positive cells cultured may be the same as the CD3-positive cells cultured in the production method or expansion method of the present invention. Preferably, the CD3-positive cells are CD3-positive CD197-positive cells.

[0159] The maintenance method of the present invention includes a step of stimulating a CD30 signal in a CD3-positive cell. The method of stimulating a CD30 signal in a CD3-positive cell is not particularly limited as long as the signal can be transmitted downstream via the intracellular domain of CD30. Such a method includes, for example, a method including a step of culturing a CD3-positive cell in the presence of a CD30 agonist (hereinafter, referred to as the maintenance method (1) of the present invention). The maintenance method (1) of the present invention allows the CD3-positive cell to be maintained as a CD3-positive CD197-positive cell. In one embodiment of the maintenance method (1) of the present invention, CD3-positive cells can be maintained as CD3-positive, CD197-positive, CD45RA-negative cells. The CD30 agonist and culture conditions used in the maintenance method (1) of the present invention may be the same as the CD30 agonist and culture conditions used in the production method or expansion method of the present invention.

[0160] The present invention also provides a kit for maintaining CD3-positive cells into CD3-positive CD197-positive cells, which comprises a CD30 agonist (hereinafter referred to as the maintenance kit of the present invention).

[0161] The CD30 agonist contained in the maintenance kit of the present invention may be the same as the CD30 agonist used in the maintenance method (1) of the present invention.

[0162] Furthermore, in the maintenance method of the present invention, another method for stimulating the CD30 signal in CD3-positive cells includes a method comprising a step of culturing CD3-positive cells expressing a chimeric antigen receptor containing the intracellular domain of CD30 in the presence of an antigen that stimulates the chimeric antigen receptor (hereinafter referred to as maintenance method (2) of the present invention). By stimulating the chimeric antigen receptor containing the intracellular domain of CD30, it becomes possible to transmit a signal downstream via the intracellular domain of CD30, and CD3-positive cells expressing a chimeric antigen receptor containing the intracellular domain of CD30 can be maintained as CD3-positive CD197-positive cells. In one embodiment of the maintenance method (2) of the present invention, CD3-positive cells expressing a chimeric antigen receptor comprising the intracellular domain of CD30 can be maintained as CD3-positive, CD197-positive, CD45RA-negative cells. The culture conditions used in the maintenance method (2) of the present invention may be the same as the culture conditions used in the production method or expansion method of the present invention.

[0163] The antigen that stimulates the chimeric antigen receptor used in the maintenance method (2) of the present invention is not particularly limited as long as it can transmit a signal downstream via the intracellular domain of CD30 contained in the chimeric antigen receptor. The antigen that stimulates the chimeric antigen receptor may be, for example, the same as the antigen targeted by the chimeric antigen receptor of the chimeric antigen receptor-expressing CD3-positive cells cultured in the production method or expansion culture method of the present invention.

[0164] The present invention also provides a chimeric antigen receptor comprising an antigen-binding domain, a transmembrane domain, and an intracellular signaling domain, wherein the intracellular signaling domain comprises the intracellular domain of CD30 or a modified form thereof (hereinafter referred to as the chimeric antigen receptor of the present invention).

[0165] The antigen-binding domain contained in the chimeric antigen receptor of the present invention may be identical to the antigen-binding domain contained in the chimeric antigen receptor expressed in CD3-positive cells cultured in the production method or expansion method of the present invention.

[0166] The transmembrane domain contained in the chimeric antigen receptor of the present invention may be the same as the transmembrane domain contained in the chimeric antigen receptor expressed in CD3-positive cells cultured in the production method or expansion method of the present invention.

[0167] The intracellular signaling domain contained in the chimeric antigen receptor of the present invention comprises the intracellular domain of CD30 or a modified version thereof. The intracellular domain of CD30 is not particularly limited as long as it retains the function of transmitting the recognition signal into the cell after the antigen-binding domain contained in the chimeric antigen receptor of the present invention recognizes an antigen, and an example of the intracellular domain is a peptide comprising the amino acid sequence shown in SEQ ID NO:6.

[0168] Modified forms of the intracellular domain of CD30 are not limited as long as they retain the above-mentioned functions, and examples thereof include peptides comprising an amino acid sequence having about 90% or more, preferably about 95% or more, more preferably about 97% or more, particularly preferably about 98% or more, and most preferably about 99% or more homology to the amino acid sequence shown in SEQ ID NO: 6. Here, "homology" may be the same as the homology in the amino acid sequence of "IL-15 / IL-15Rα".

[0169] Furthermore, examples of modified forms of the intracellular domain of CD30 include: (1) an amino acid sequence in which one or two or more (preferably about 1 to 100, preferably about 1 to 50, more preferably about 1 to 10, and particularly preferably one or several (2, 3, 4, or 5)) amino acids have been deleted from the amino acid sequence shown in SEQ ID NO: 6; (2) an amino acid sequence in which one or two or more (preferably about 1 to 100, preferably about 1 to 50, more preferably about 1 to 10, and particularly preferably one or several (2, 3, 4, or 5)) amino acids have been added to the amino acid sequence shown in SEQ ID NO: 6; (3) an amino acid sequence in which one or two or more (preferably about 1 to 50, preferably about 1 to 10, and more preferably one or several (2, 3, 4, or 5)) amino acids have been inserted into the amino acid sequence shown in SEQ ID NO: 6; and (4) Also included are (5) amino acid sequences in which one or more (preferably about 1 to 50, preferably about 1 to 10, and more preferably one to several (2, 3, 4 or 5)) amino acids in the amino acid sequence shown in SEQ ID NO:6 have been substituted with other amino acids, or amino acid sequences that are a combination thereof. When an amino acid sequence has been inserted, deleted or substituted as described above, the position of the insertion, deletion or substitution is not particularly limited as long as the function of the intracellular domain of CD30 is maintained.

[0170] The intracellular signaling domain contained in the chimeric antigen receptor of the present invention may further contain an intracellular domain derived from another protein in addition to the intracellular domain of CD30 or a modified version thereof. The further intracellular domain may be the same as the intracellular domain contained in the intracellular signaling domain contained in the chimeric antigen receptor expressed in the CD3-positive cells cultured in the production method or expansion culture method of the present invention. The further intracellular domain is not particularly limited, but is preferably an intracellular domain derived from CD28 or CD3 ζ chain.

[0171] The chimeric antigen receptor of the present invention may incorporate a spacer between the antigen-binding domain and the transmembrane domain, or between the intracellular signaling domain and the transmembrane domain. The spacer may be the same as the spacer contained in the chimeric antigen receptor expressed in the CD3-positive cells cultured in the production method or expansion method of the present invention.

[0172] Specific examples of the chimeric antigen receptor of the present invention include chimeric antigen receptors that include an scFv that recognizes CD19 as the antigen-binding domain, a CD8 transmembrane domain as the transmembrane domain, and an intracellular domain derived from CD28, an intracellular domain derived from CD30, and an intracellular domain derived from CD3ζ chain as the intracellular signaling domain. The order of the above-mentioned intracellular domains included in the intracellular signaling domain is not particularly limited, and may be, for example, the intracellular domain derived from CD28, the intracellular domain derived from CD30, and the intracellular domain derived from CD3ζ chain. More specifically, the chimeric antigen receptor of the present invention consists of, for example, the amino acid sequence represented by SEQ ID NO:7.

[0173] The chimeric antigen receptor of the present invention may be a protein that is chemically synthesized or biochemically synthesized in a cell-free translation system, or may be a recombinant protein produced from a transformant into which a nucleic acid having a nucleotide sequence encoding the chimeric antigen receptor of the present invention has been introduced. The chimeric antigen receptor of the present invention can be produced, isolated and purified in the same manner according to the method for producing MHC and / or antigen peptide used in the production method or expansion culture method of the present invention.

[0174] The present invention also provides a nucleic acid (hereinafter referred to as the nucleic acid of the present invention) comprising a polynucleotide encoding the chimeric antigen receptor of the present invention.

[0175] The nucleic acid of the present invention may be DNA or RNA, or may be a DNA / RNA chimera. DNA is preferred. The nucleic acid may be double-stranded or single-stranded. If double-stranded, it may be double-stranded DNA, double-stranded RNA, or a DNA:RNA hybrid. If single-stranded, it may be a sense strand (i.e., coding strand) or an antisense strand (i.e., non-coding strand).

[0176] The nucleic acid of the present invention can be obtained by polymerase chain reaction (hereinafter abbreviated as "PCR method"). First, genomic DNA or cDNA encoding each domain of the antigen-binding domain, transmembrane domain, and intracellular signaling domain contained in the chimeric antigen receptor of the present invention is obtained. In the case of cDNA, it can also be directly amplified by PCR and Reverse Transcriptase-PCR (hereinafter abbreviated as "RT-PCR method") using total RNA or mRNA fraction prepared from cells as a template. Using the obtained genomic DNA or cDNA as a template, a nucleic acid encoding each domain can be amplified by PCR using synthetic DNA primers consisting of a part of the base sequence encoding each domain of the antigen-binding domain, transmembrane domain, and intracellular signaling domain and a base sequence encoding a spacer. The nucleic acid of the present invention can be obtained by repeating PCR using the synthetic DNA primers and using the obtained domains as templates.

[0177] The present invention also provides a chimeric antigen receptor gene transfer vector (hereinafter referred to as the gene transfer vector of the present invention) comprising the nucleic acid of the present invention.

[0178] The gene transfer vector of the present invention can be produced, for example, by linking the nucleic acid of the present invention downstream of a promoter in an appropriate gene transfer vector. The gene transfer vector, promoter, and other elements may be the same as the vector, promoter, and other elements used when introducing an exogenous TCR into pluripotent stem cells in the production method or expansion culture method of the present invention.

[0179] The present invention also provides a chimeric antigen receptor-expressing cell (hereinafter referred to as the chimeric antigen receptor-expressing cell of the present invention) comprising the gene transfer vector of the present invention.

[0180] The chimeric antigen receptor-expressing cell of the present invention can be produced by introducing the gene transfer vector of the present invention into a cell and culturing it. The cell into which the gene transfer vector of the present invention is introduced can be a CD3 positive cell or its precursor cell (hematopoietic stem cell, common lymphoid precursor cell, lymphoblast, etc.) or a pluripotent stem cell. Examples of the pluripotent stem cell include ES cells, iPS cells, EC cells, and EG cells, with ES cells or iPS cells being preferred.

[0181] The gene transfer vector of the present invention can be introduced into cells by techniques such as lipofection, liposome, and microinjection.

[0182] The chimeric antigen receptor-expressing cells of the present invention are preferably CD3 positive cells. The CD3 positive cells are preferably CD3 positive CD8 positive cells (CD3 positive CD8 positive CD4 positive cells or CD3 positive CD8 positive CD4 negative cells), more preferably CD3 positive CD8 positive CD4 negative cells. Another preferred example of the CD3 positive cells is CD3 positive CD4 positive cells (CD3 positive CD4 positive CD8 positive cells or CD3 positive CD4 positive CD8 negative cells).

[0183] When the chimeric antigen receptor-expressing cells of the present invention are cells produced by introducing the gene transfer vector of the present invention into pluripotent stem cells, the pluripotent stem cells can be differentiated into CD3-positive cells according to a method known per se. The specific method for differentiating pluripotent stem cells into CD3-positive cells may be the same as the method for differentiating the cultured CD3-positive cells into pluripotent stem cells in the production method or expansion culture method of the present invention.

[0184] The thus obtained chimeric antigen receptor-expressing cells of the present invention are endowed with specificity for an antigen of interest by the chimeric antigen receptor, and therefore can exhibit cytotoxic activity against tumors expressing the antigen of interest. Furthermore, since the chimeric antigen receptor can directly recognize antigen molecules independent of HLA class I or class II, the chimeric antigen receptor-expressing cells of the present invention can induce a strong immune response even against tumors with reduced expression of HLA class I or class II genes. Therefore, the present invention also provides a pharmaceutical comprising the chimeric antigen receptor-expressing cell of the present invention as an active ingredient (hereinafter, referred to as the pharmaceutical of the present invention). The pharmaceutical comprising the chimeric antigen receptor-expressing cell of the present invention can be used for the prevention or treatment of a tumor expressing an antigen recognized by the chimeric antigen receptor of the present invention, and can be administered to, for example, a mammal (e.g., mouse, rat, hamster, rabbit, cat, dog, cow, sheep, monkey, human), preferably human. Thus, in one aspect of the present invention, the pharmaceutical of the present invention is provided for use in the prevention or treatment of a tumor expressing an antigen recognized by the chimeric antigen receptor of the present invention. Also provided is a method for preventing or treating a tumor expressing an antigen recognized by the chimeric antigen receptor of the present invention, which comprises administering the chimeric antigen receptor-expressing cell of the present invention, preferably in the form of a pharmaceutical comprising the cell.

[0185] Tumors to be prevented or treated by the medicament of the present invention or the chimeric antigen receptor-expressing cell of the present invention are not particularly limited as long as they express an antigen recognized by the chimeric antigen receptor of the present invention. Here, tumors are described, for example, in "Daniel Baumhoer et al., Am J. Clin Pathol, 2008, 129, 899-906" and include benign tumors, malignant tumors (also called "cancer"), and tumors that can be diagnosed or determined as benign or malignant. Specific examples of tumors include, but are not limited to, liver cancer (e.g., hepatocellular carcinoma), ovarian cancer (e.g., ovarian clear cell adenocarcinoma), childhood cancer, lung cancer (e.g., squamous cell carcinoma, small cell lung carcinoma), testicular cancer (e.g., non-seminomatous germ cell tumor), soft tissue tumor (e.g., liposarcoma, malignant fibrous histiocytoma), uterine cancer (e.g., cervical intraepithelial neoplasia, cervical squamous cell carcinoma), melanoma, adrenal tumor (e.g., adrenal adenoma), neural tumor (e.g., Schwannoma), gastric cancer (e.g., gastric adenocarcinoma), kidney cancer (e.g., Grawitz tumor), breast cancer (e.g., invasive lobular carcinoma, mucinous carcinoma), thyroid cancer (e.g., medullary carcinoma), laryngeal cancer (e.g., squamous cell carcinoma), and bladder cancer (e.g., invasive transitional cell carcinoma).

[0186] The chimeric antigen receptor-expressing cells of the present invention may be cultured and / or stimulated using an appropriate medium and / or stimulatory molecules before being administered to a subject. Stimulatory molecules include, but are not limited to, cytokines, appropriate proteins, and other components. Examples of cytokines include IL-2, IL-7, IL-12, IL-15, IFN-γ, and the like, and IL-2 can be preferably used. The concentration of IL-2 in the medium is not particularly limited, but is preferably, for example, 0.01 U / ml to 1×10 5 U / ml, more preferably 1 U / ml to 1×10 4U / ml. Examples of suitable proteins include antigens recognized by chimeric antigen receptors, CD3 ligands, CD28 ligands, and anti-IL-4 antibodies. In addition, lymphocyte stimulatory factors such as lectins can also be added. Furthermore, serum or plasma may be added to the medium. The amount of these to be added to the medium is not particularly limited, but is exemplified as 0% by volume to 20% by volume, and the amount of serum or plasma used can be changed depending on the culture stage. For example, the serum or plasma concentration can be reduced stepwise. The serum or plasma may be derived from either autologous or non-autologous sources, but from the viewpoint of safety, it is preferable to use autologous sources.

[0187] The pharmaceutical agent of the present invention is preferably administered parenterally to a subject. Examples of parenteral administration methods include intravenous, intraarterial, intramuscular, intraperitoneal, and subcutaneous administration. The dosage is appropriately selected depending on the condition, weight, age, and the like of the subject, but the number of cells is usually 1×10 per administration for a subject weighing 60 kg. 6 ~1×10 10 Preferably 1×10 7 ~1×10 9 10, more preferably 5×10 7 ~5×10 8 The pharmaceutical composition of the present invention is administered so that the number of cells is one. The pharmaceutical composition may be administered once or multiple times. The pharmaceutical composition of the present invention may be in a known form suitable for parenteral administration, such as an injection or infusion. The pharmaceutical composition of the present invention may also contain physiological saline, phosphate buffered saline (PBS), a medium, etc., in order to stably maintain the cells. The medium is not particularly limited, but includes, but is not limited to, RPMI, AIM-V, X-VIVO10, and the like. The pharmaceutical composition may also contain a pharmacologic acceptable carrier (e.g., human serum albumin), a preservative, etc., for the purpose of stabilization.

[0188] Furthermore, since the chimeric antigen receptor-expressing cells of the present invention can kill cells expressing an antigen recognized by the chimeric antigen receptor of the present invention, they can be used as an agent for killing cells expressing the antigen. Such an agent for killing can be prepared and used in the same manner as the above-mentioned pharmaceutical.

[0189] The present invention also encompasses an embodiment of using the chimeric antigen receptor-expressing cell of the present invention in the manufacture of a preventive or therapeutic agent for a tumor expressing an antigen recognized by the chimeric antigen receptor of the present invention, similar to a pharmaceutical comprising the chimeric antigen receptor-expressing cell of the present invention. The preventive or therapeutic agent for a tumor can be manufactured by a method known per se. For example, similar to the above-mentioned method for preparing the pharmaceutical of the present invention, it can be manufactured in a known form suitable for parenteral administration, such as an injection or infusion.

[0190] The present invention will be described in more detail below with reference to examples, but these are merely illustrative and the present invention is not limited to these. EXAMPLES

[0191] [Example 1] 1. iPS Cell Preparation The iPS cells used were the Ff-I01s04 line provided by the Center for iPS Cell Research and Application (CiRA), Kyoto University. iPS cell culture was performed according to the protocol "Feeder-free culture of human iPS cells" distributed by CiRA.

[0192] 2.Transduction of T cell receptor (TCR) genes into iPS cells The TCR gene used was the TAK1-derived, HLA-A*24:02-restricted WT1-specific TCR (WT1-TCR) gene provided by Professor Masaki Yasukawa of the Ehime University Graduate School of Medicine. The gene was introduced into iPS cells by incorporating it into the CS-UbC-RfA-IRES2-hKO1 lentiviral vector provided by the RIKEN Institute and infecting the iPS cells.

[0193] 3. Differentiation of iPS cells carrying the WT1-TCR gene into CD8 positive T cells (CTL) The iPS cells into which the WT1-TCR gene was introduced were differentiated into CD8-positive T cells (CTLs) according to a known method (WO2017 / 221975). The cells were CD3-positive and CD8-positive. In the following, the cells were used as iPS cell-derived T cells.

[0194] 4. Reagents and antibodies RetroNectin (registered trademark) was purchased from Takara Bio. Anti-CD3 agonist antibodies used were anti-human CD3 functional grade purified (Clone: ​​OKT3) purchased from eBioscience or CD3 antibody (Clone: ​​UCHT1) purchased from GeneTex. OKT3 was used unless otherwise stated. Anti-CD30 agonist antibodies used were CD30 agonist antibodies purchased from R&D.

[0195] 5. Immobilization of anti-CD3 agonist antibody and RetroNectin® on culture plates Anti-CD3 agonist antibody and RetroNectin (registered trademark) dissolved in PBS at the required concentrations were added to a 96-well plate at 50 μL / well, and then the plate was left to stand overnight at 4° C. After washing with PBS, the plate was subjected to the test.

[0196] 6. ELISA for detecting immobilized anti-CD3 agonist antibody and immobilized RetroNectin® For detection of the immobilized anti-CD3 agonist antibody, HRP Conjugated Goat anti-Mouse IgG2a Detection Antibody included in the Mouse IgG2a ELISA Quantitation Set purchased from Bethyl Laboratories was used. For detection of immobilized RetroNectin (registered trademark), peroxidase-labeled anti-RetroNectin antibody included in the RetroNectin EIA kit purchased from Takara Bio was used. After adding each detection antibody to the immobilized plate, it was left to stand at room temperature for 1 hour. After washing with PBS containing 0.05% Tween-20, 1-Step TM Ultra TMB-ELISA Substrate Solution (ThermoFisher) was added, and the plate was left to stand at room temperature for 15 minutes, after which 1 M sulfuric acid was added to stop the reaction, and the absorbance at 450 nm was measured using a plate reader.

[0197] 7. Proliferation Test iPS cell-derived T cells were prepared at 100,000 cells / 200 μL in α-MEM medium containing 15% FBS to which the cytokines listed in Table 1 were added. The T cells were seeded onto plates immobilized with anti-CD3 agonist antibody (3, 30, 300, 3000 ng / ml) and RetroNectin (registered trademark) (0, 1.85, 2.25, 16.7, 50, 150 μg / ml) and cultured for 3 days under 5% CO2 at 37°C. On the third day of culture, the cells were collected from the plate, the number of cells was counted using TC20 (Bio-Rad), and the cells were suspended in an appropriate amount of α-MEM medium containing 15% FBS to which the cytokines in Table 2 were added, and the cells were added to a non-solid-phase 96-well plate and cultured under 5% CO2 / 37°C. Thereafter, the cells were collected from the plate once each on the 5th, 6th, 7th, 8th, 9th, 10th, 12th, 14th, and 16th days of culture, for a total of 4 to 7 times, and the number of cells was counted, and the cells were suspended in an appropriate amount, and the cells were added to a non-solid-phase plate and cultured under 5% CO2 / 37°C.

[0198] [Table 1]

[0199] [Table 2]

[0200] 8.ATP Test ATP in the cells and culture supernatant on day 12 of the proliferation test was measured using CellTiter-Glo(R) Luminescent Cell Viability Assay purchased from Promega according to the standard protocol.

[0201] 9. Measurement of WT1 antigen-specific cytotoxicity HLA-A*24:02 positive LCL cells were purchased from the RIKEN Bioresource Center. They were cultured in RPMI1640 medium containing 10% FBS. The synthesis of the WT1 antigen peptide (CMTWNQMNL: sequence number: 3) was outsourced to Scrum Co., Ltd. Cytotoxicity tests were performed using the DELFIA immunoassay purchased from PerkinElmer Co., Ltd. according to standard protocols.

[0202] 10. Proliferation test with anti-CD30 agonist antibody Anti-CD30 agonist antibody diluted to final concentrations of 0, 30, 100, and 300 ng / mL was added to the culture medium at the time of cell suspension. The rest of the experiment was performed in the same manner as in "7. Proliferation test". In addition, in the proliferation test of iPS cell-derived T cells in response to multiple stimulations with immobilized anti-CD3 agonist antibody / Retronectin (registered trademark) and anti-CD30 agonist antibody, anti-CD30 agonist antibody diluted to a final concentration of 100 ng / mL was added to the culture medium at the time of cell suspension. The rest of the test was performed in the same manner as in "7. Proliferation test".

[0203] 11. Detection of CD197 and CD45RA on the Cell Membrane Surface On day 7 of culture, the cells were harvested and stained with the antibodies listed in Table 3. TMDetection was performed using X-20 (BD Bioscience) flow cytometry.

[0204] [Table 3]

[0205] [Test Example 1] 1. Determination of the concentration of anti-CD3 agonist antibody and RetroNectin (registered trademark) suitable for immobilization on a culture plate The ELISA method was used to measure the suitable concentrations of anti-CD3 agonist antibody and RetroNectin (registered trademark) for immobilization on culture plates (Figure 1). Concentration-dependent immobilization of anti-CD3 agonist antibody was confirmed between 3 ng / mL and 3000 ng / mL. Concentration-dependent immobilization of RetroNectin (registered trademark) was confirmed between 16.7 μg / mL and 150 μg / mL.

[0206] 2. Verification of the concentration range of anti-CD3 agonist antibody and RetroNectin® required for immobilized anti-CD3 agonist antibody and RetroNectin® suitable for proliferation of iPS cell-derived T cells iPS cell-derived T cells were stimulated for 3 days on plates coated with anti-CD3 agonist antibody (0, 3, 30, 300, 3000 ng / mL) and RetroNectin (registered trademark) (0, 1.85, 5.56, 16.7, 50, 150 μg / mL), respectively, and then cultured for 9 days on non-coated plates, after which the amount of ATP was measured (Figure 2).

[0207] 3. Proliferation test of iPS cell-derived T cells stimulated with solid-phase anti-CD3 agonist antibody / RetroNectin® iPS cell-derived T cells, prepared at 100,000 cells / 200 μL, were stimulated for 3 days on a 96-well plate immobilized with anti-CD3 agonist antibody (3000 ng / mL) and RetroNectin (registered trademark) (150 μg / mL), or with anti-CD3 / CD28 beads (Dynabeads) added so that the number of iPS cell-derived T cells and the number of bead particles were 1:1, and then the number of cells was measured over time when cultured without stimulation (Figure 3). iPS cell-derived T cells proliferated more when stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) than with anti-CD3 / CD28 beads.

[0208] 4. Proliferation test of iPS cell-derived T cells stimulated multiple times with solid-phase anti-CD3 agonist antibody / RetroNectin® The cell proliferation response of iPS cell-derived T cells to multiple stimulations with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) was confirmed. One proliferation test was performed by stimulating iPS cell-derived T cells on a solid-phase plate for 3 days, followed by culturing on a non-solid-phase plate for 11-15 days. After the test, the cell number was adjusted and the cells were subjected to the next test. The iPS cell-derived T cells proliferated in response to the fourth stimulation with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) (Figure 4).

[0209] 5. Verification of WT1 antigen-specific cytotoxic activity of T cells derived from WT1-TCR gene-transduced iPS cells expanded by stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark) The WT1 antigen-specific cytotoxic activity of T cells derived from WT1-TCR gene-introduced iPS cells expanded by stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark) was evaluated. The WT1 antigen-specific cytotoxic activity was evaluated based on the difference in cytotoxic activity against LCLs to which WT1 antigen peptide had been added and against LCLs to which no WT1 antigen peptide had been added. The WT1-TCR gene-introduced iPS cell-derived T cells had almost no nonspecific cytotoxic activity and only showed WT1 antigen-specific cytotoxic activity (Figure 5).

[0210] 6. Proliferation test of iPS cell-derived T cells stimulated with anti-CD30 agonist antibody We examined whether the addition of anti-CD30 agonist antibody (0, 30, 100, 300 ng / mL) during stimulation with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) had any effect on the proliferation of iPS cell-derived T cells. The immobilized 96-well plate used had anti-CD3 agonist antibody (3000 ng / mL) and RetroNectin (registered trademark) (150 μg / mL) immobilized on it. The iPS cell-derived T cells proliferated more when anti-CD30 agonist antibody was added. Furthermore, proliferation was dependent on the concentration of the added anti-CD30 agonist antibody (Figure 6).

[0211] 7. Proliferation test of iPS cell-derived T cells in response to multiple stimulations with solid-phase anti-CD3 agonist antibody / Retronectin® and anti-CD30 agonist antibody We verified whether iPS cell-derived T cells show a proliferation response to stimulation with multiple immobilized anti-CD3 agonist antibodies / Retronectin® and anti-CD30 agonist antibodies. T cells were seeded on a plate immobilized with anti-CD3 agonist antibodies (3000 ng / ml) and Retronectin® (150 μg / ml) and cultured for 3 days under 5% CO2 / 37℃. On the third day of culture, the cells were collected from the plate, the number of cells was counted using TC20 (Bio-Rad), and the cells were suspended in an appropriate amount of α-MEM medium containing 15% FBS and the cytokines in Table 2 were added, added to a plate not solid-phased, and cultured under 5% CO2 / 37°C. Thereafter, the cells were collected from the plate once each at the timing of the 6th, 7th, 9th, 10th, 14th, and 16th days of culture, the number of cells was counted, and the cells were suspended in an appropriate amount, added to a plate not solid-phased, and cultured under 5% CO2 / 37°C. The culture medium used was one containing anti-CD30 agonist antibody diluted to a final concentration of 100 ng / mL, and one not containing anti-CD30 agonist antibody. The above stimulation from the 0th to the 16th day of culture was repeated twice. Even in the second stimulation, iPS cell-derived T cells proliferated more when stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) and anti-CD30 agonist antibody than when stimulated with immobilized anti-CD3 agonist antibody / RetroNectin (registered trademark) alone (Figure 7).

[0212] 8. Detection of CD197 and CD45RA on the membrane surface of iPS cell-derived T cells after stimulation with immobilized anti-CD3 agonist antibody / Retronectin® and anti-CD30 agonist antibody After stimulation with immobilized anti-CD3 agonist antibody / RetroNectin® or with immobilized anti-CD3 agonist antibody / RetroNectin® and anti-CD30 agonist antibody, the expression of CD197 and CD45RA on the membrane surface of iPS cell-derived T cells on day 7 was measured using a flow cytometer. In the cell group stimulated with anti-CD3 agonist antibody / RetroNectin® and anti-CD30 agonist antibody, CD197-positive, CD45RA-negative central memory-like iPS cell-derived T cells accounted for the majority (FIG. 8).

[0213] 9. Verification of WT1 antigen-specific cytotoxic activity of T cells derived from WT1-TCR gene-transduced iPS cells expanded by stimulation with solid-phase anti-CD3 agonist antibody / retronectin and anti-CD30 agonist antibody T cells derived from WT1-TCR gene-transduced iPS cells expanded by stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark) and anti-CD30 agonist antibody were applied to HLA-A*24:02-positive LCL cells in the presence or absence of WT1 antigen peptide, and WT1 antigen-specific cytotoxic activity was evaluated. T cells derived from WT1-TCR gene-transduced iPS cells showed almost no nonspecific cytotoxic activity and only WT1 antigen-specific cytotoxic activity (Figure 9). Furthermore, the WT1 antigen-specific cytotoxic activity was maintained even after expansion by the second stimulation (Figure 9).

[0214] [Example 2] 1. Preparation of Human Peripheral Blood-derived CD8+ T Cells Human peripheral blood was purchased from Precision Bioservices as peripheral blood mononuclear cells derived from healthy individuals. CD8+ T cells were isolated using a CD8+ T cell isolation kit, human (Milteny).

[0215] 2. Proliferation test of CD8 positive T cells derived from human peripheral blood [Example 1] 7. Proliferation test The test was carried out in the same manner as described above.

[0216] 3. Culture of human peripheral blood-derived CD8+ T cells for mouse engraftment tests Human peripheral blood-derived CD8 positive T cells were suspended at a final concentration of 100,000 cells / mL in three types of media containing α-MEM medium containing 15% FBS and the additives shown in Table 4, and Dynabeads T-Activator CD3 / CD28 (Gibco) adjusted to three times the number of cells was added and cultured for 3 days under 5% CO2 / 37°C. On the third day of culture, the cells were collected from the plate, suspended in an appropriate amount in α-MEM medium containing 15% FBS and the cytokines and other substances listed in Table 5 were added, and cultured under 5% CO2 / 37°C. After that, on the 10th day of culture, the cells were collected from the plate, the cell number was counted, and the cells were suspended in an appropriate amount and administered to mice. In addition, on the 6th, 10th, 13th, and 17th days of culture, the cells were collected from the plate, suspended in an appropriate amount, and subjected to CD197 expression experiments.

[0217] [Table 4]

[0218] [Table 5]

[0219] 4. Administration of human peripheral blood-derived CD8+ T cells to mice and recovery of engrafted cells Eight-week-old male NSG mice (Charles River Japan) were used, which had been irradiated with 2 Gy of gamma rays before the same day of cell administration. Five million cells, prepared by culturing human peripheral blood-derived CD8 positive T cells used in the mouse engraftment test in [Example 2] 3, were administered intravenously to the mice, and the mice were then kept for four weeks. The mice were then euthanized, and bone marrow cells, splenocytes, and white blood cells in the blood were collected.

[0220] 5. Detection of human peripheral blood-derived CD8+ T cells engrafted in mouse tissues The collected cells were stained with the antibodies in Table 3 and then incubated with LSRFortessa TM Detection was performed using X-20 (BD Bioscience) flow cytometry.

[0221] [Test Example 2] 1. Proliferation test of CD8+ T cells derived from human peripheral blood by stimulation with anti-CD30 agonist antibody We confirmed whether the addition of an anti-CD30 agonist antibody during stimulation with solid-phase anti-CD3 antibody / Retronectin (registered trademark) had any effect on the proliferation of CD8-positive T cells derived from human peripheral blood. The addition of an anti-CD30 agonist antibody enhanced the proliferation of CD8-positive T cells in human peripheral blood (Figure 10).

[0222] 2. Detection of CD197 on the membrane surface of human peripheral blood-derived CD8+ T cells after stimulation with anti-CD3 / CD28 beads and anti-CD30 agonist antibody CD197 expression on the cell membrane surface of human peripheral blood-derived CD8+ T cells stimulated with anti-CD3 / CD28 beads in IL-2-containing medium, IL-7 / IL-15-containing medium, or IL-7 / IL-15 / anti-CD30 antibody-containing medium was measured by flow cytometer on days 6, 10, 13, and 17 of culture. CD197 expression was confirmed in all groups on day 6, but CD197 expression almost disappeared on day 13 in the IL-2-containing medium group and on day 17 in the IL-7 / IL-15-containing medium group, whereas CD197 expression was maintained even on day 17 in the IL-7 / IL-15 / anti-CD30 antibody-containing medium group (Figure 11).

[0223] 3. Evaluation of engraftment of human peripheral blood-derived CD8+ T cells after stimulation with anti-CD3 / CD28 beads and anti-CD30 agonist antibody Human peripheral blood-derived CD8+ T cells on day 10 of culture stimulated with anti-CD3 / CD28 beads were administered intravenously to immunodeficient mice in IL-2-containing medium, IL-7 / IL-15-containing medium, or IL-7 / IL-15 / anti-CD30 antibody-containing medium, and engraftment in the blood and immune tissues was confirmed. Blood, spleen, and bone marrow were collected from the mice on day 28 after administration, and human CD8+ T cells contained therein were detected by flow cytometry. In either organ, human CD8+ T cells were hardly detected in the IL-2-containing medium group, whereas human CD8+ T cells were detected in the IL-7 / IL-15-containing medium group and the IL-7 / IL-15 / anti-CD30 antibody-containing medium group. Furthermore, a larger number of human CD8+ T cells were detected in the IL-7 / IL-15 / anti-CD30 antibody-containing medium group. Therefore, it was shown that human peripheral blood-derived CD8+ T cells cultured in a medium containing IL-7 / IL-15 / anti-CD30 antibody were not only able to maintain CD197 expression for a long period during culture, but also were able to survive for a long period in the body (Figure 12).

[0224] [Example 3] 1. Proliferation test of iPS cell-derived anti-CD19-CART cells iPS cell-derived anti-CD19-CART cells prepared at 100,000 cells / 200 μL in α-MEM medium containing 15% FBS plus cytokines and the like listed in Table 1 were seeded on a plate on which anti-CD3 antibody and RetroNectin (registered trademark) were solid-phased, and cultured for 3 days under 5% CO2 / 37°C. On the third day of culture, the cells were collected from the plate, the number of cells was counted using TC20 (BioRat), and the cells were suspended in an appropriate amount of α-MEM medium containing 15% FBS plus cytokines and the like listed in Table 2, added to a plate on which the cells were not solid-phased, and cultured under 5% CO2 / 37°C. Thereafter, the cells were collected from the plate 4-7 times on the 5th, 6th, 7th, 8th, 9th, 10th, 12th, 14th, and 16th days of culture, the number of cells was counted, and the cells were suspended in an appropriate amount, added to a plate on which the cells were not solid-phased, and cultured under 5% CO2 / 37°C.

[0225] 2. Anti-CD19-CAR gene The anti-CD19-CAR gene was artificially synthesized using an oligo DNA encoding a polypeptide (sequence number 5) designed to be arranged in the order of Table 6 from the N-terminus.

[0226] [Table 6]

[0227] 3. Preparation of retroviral vector carrying anti-CD19-CAR gene [Example 3] The artificial oligo DNA synthesized in 2. was inserted into the multicloning site of the pMEI-5 retrovirus vector. The virus vector production was outsourced to Unitech Co., Ltd.

[0228] 4. Production of iPS cell-derived anti-CD19-CART cells The retroviral vector carrying the anti-CD19-CAR gene prepared in [Example 3] 3. was infected into the iPS cell-derived T cells prepared in [Example 1] 3. to produce iPS cell-derived anti-CD19-CAR T cells.

[0229] [Test Example 3] 1. Proliferation test of iPS cell-derived anti-CD19-CART cells stimulated with solid-phase anti-CD3 agonist antibody / RetroNectin® The iPS cell-derived T cells prepared in [Example 1] 3. and the iPS cell-derived anti-CD19-CART cells prepared in [Example 3] 4. were stimulated with immobilized anti-CD3 antibody / RetroNectin (registered trademark) for 3 days, and then the number of cells was measured over time when cultured without stimulation. The iPS cell-derived anti-CD19-CART cells proliferated by stimulation with immobilized anti-CD3 antibody / RetroNectin (registered trademark) to the same extent as the iPS cell-derived T cells (Figure 13).

[0230] 2. Proliferation test of iPS cell-derived anti-CD19-CART cells stimulated with anti-CD30 agonist antibody We confirmed whether the addition of an anti-CD30 agonist antibody during stimulation with immobilized anti-CD3 antibody / RetroNectin (registered trademark) had an effect on the proliferation of iPS cell-derived anti-CD19-CART cells. The addition of an anti-CD30 agonist antibody enhanced the proliferation of iPS cell-derived anti-CD19-CART cells (Figure 14).

[0231] 3. Detection of CD197 on the cell membrane surface of iPS cell-derived anti-CD19-CART cells after stimulation with immobilized anti-CD3 agonist antibody / Retronectin® and anti-CD30 agonist antibody CD197 expression on the cell membrane surface of iPS cell-derived anti-CD19-CART cells was measured using a flow cytometer on days 3 and 7 after stimulation with immobilized anti-CD3 antibody / RetroNectin (registered trademark) or stimulation with immobilized anti-CD3 antibody / RetroNectin (registered trademark) / anti-CD30 agonist antibody. CD197 expression was confirmed in both groups on day 3, but on day 7, CD197 expression almost disappeared in the anti-CD3 antibody / RetroNectin (registered trademark) stimulation group, whereas CD197 expression was maintained in the anti-CD3 antibody / RetroNectin (registered trademark) + anti-CD30 agonist antibody stimulation group ( FIG. 15 ).

[0232] 4. Verification of Raji cytotoxic activity of iPS cell-derived anti-CD19-CART cells after stimulation with solid-phase anti-CD3 agonist antibody / Retronectin® and anti-CD30 agonist antibody [Test Example 3] The cytotoxic activity of iPS cell-derived anti-CD19-CART cells obtained by proliferation in 1 against CD19-positive cancer cells was evaluated based on their cytotoxic activity against CD19-positive Raji cells. The iPS cell-derived anti-CD19-CART cells exhibited cytotoxic activity against CD19-expressing Raji cells (Figure 16).

[0233] [Example 4] 1.Anti-CD19-CAR gene containing CD30-derived intracellular domain The anti-CD19-CAR gene was artificially synthesized using an oligo DNA encoding a polypeptide (sequence number 7) designed to be arranged in the order of Table 7 from the N-terminus.

[0234] [Table 7]

[0235] 2. Construction of retroviral vector carrying anti-CD19-CAR gene containing CD30-derived intracellular domain [Example 4] The artificial oligo DNA synthesized in 1 was inserted into the multicloning site of the pMY retrovirus vector. A viral vector was produced using FRY-RD18 cells for producing retrovirus vectors.

[0236] 3. Production of iPS cell-derived anti-CD19-CART cells (iCD19-CD30-CART) containing CD30-derived intracellular domain The retroviral vector carrying the anti-CD19-CAR gene prepared in [Example 4] 2. was infected into the iPS cell-derived T cells prepared in [Example 1] 3. to produce iPS cell-derived anti-CD19-CART cells (iCD19-CD30-CART) containing a CD30-derived intracellular domain.

[0237] [Test Example 4] [Example 4] The cytotoxic activity of iCD19-CD30-CART obtained in 3. against CD19-positive cancer cells was evaluated based on its cytotoxic activity against CD19-positive Raji cells. iCD19-CD30-CART showed cytotoxic activity against CD19-expressing Raji cells (Figure 17).

[0238] [Example 5] 1. iPS Cell Preparation The iPS cells used were the Ff-I01s04 strain provided by the Center for iPS Cell Research and Application (CiRA) of Kyoto University, as in Example 1. The iPS cells were cultured according to the protocol "Feeder-free culture of human iPS cells" distributed by CiRA.

[0239] 2. Differentiation of iPS cells into γδTCR-positive T cells (γδT cells) Differentiation of iPS cells into γδTCR positive T cells (γδT cells) was performed according to a known method (WO2017 / 221975) in the same manner as in [Example 1]. 3000 ng / mL UCHT1 (GeneTex) was used as the anti-CD3 antibody in the differentiation process. The obtained CD3 positive cells were γδT cells (hereinafter referred to as "iPS cell-derived γδT cells (iγδT cells)").

[0240] 3. Expansion of iPS cell-derived γδ T cells [Example 5] The iγδT cells obtained in 2. were suspended at 2,000,000 cells / mL in α-MEM medium containing 15% FBS and the cytokines in Table 8, and seeded on a plate on which anti-CD3 antibody (UCHT1) and RetroNectin (registered trademark) were solidified, and cultured for 3 days under 5% CO2 / 37°C. On the third day of culture, the cells were collected from the plate, the cell count was counted using a NucleoCounterNC-200 (ChemoMetec), and an appropriate amount of the cells were suspended in a medium containing α-MEM medium containing 15% FBS and the cytokines in Table 9, added to a non-solid-phase G-Rex 6-well plate (WILSONWOLF), and cultured under 5% CO2 / 37°C. Thereafter, some of the cells were collected from the plate and the cell count was counted 4-6 times on the 5th, 6th, 7th, 8th, 9th, 10th, 11th, 14th, and 17th days of culture. Anti-CD3 antibody and RetroNectin (registered trademark) were immobilized on the culture plate by the following method. Anti-CD3 antibody (UCHT1, final concentration 3000 ng / mL) and RetroNectin (registered trademark) (final concentration 150 μg / mL) dissolved in PBS at the required concentration were added to the plate, and the plate was left to stand overnight at 4° C. After washing with PBS, the plate was subjected to the test.

[0241] [Table 8]

[0242] [Table 9]

[0243] [Test Example 5] 1. Proliferation test of iPS cell-derived γδ T cells stimulated with anti-CD30 agonist antibody In [Example 5] 3, we examined whether the addition of anti-CD30 agonist antibody (300 ng / ml) to the stimulation method using solid-phase anti-CD3 agonist antibody / RetroNectin (registered trademark) had an effect on the proliferation of iPS cell-derived γδ T cells. iPS cell-derived T cells proliferated more when anti-CD30 agonist antibody was added ( FIG. 18 ).

[0244] [Example 6] 1.IL-15Rα / IL-15 gene The IL-15Rα / IL-15 gene was prepared by artificially synthesizing an oligoDNA encoding a polypeptide (SEQ ID NO: 8) designed to be arranged in the order of Table 10 from the N-terminus.

[0245] [Table 10]

[0246] 2. Construction of retroviral vector carrying IL-15Rα / IL-15 gene [Example 6] The artificial oligo DNA synthesized in 1 was inserted into the multicloning site of the pMY retrovirus vector. A viral vector was produced using FRY-RD18 cells for producing retrovirus vectors.

[0247] 3. Production of iPS cell-derived anti-CD19-CAR / IL-15γδ T cells The retroviral vector carrying the anti-CD19-CAR gene prepared in [Example 3] 3. and the retroviral vector carrying the IL-15Rα / IL-15 genes prepared in [Example 6] 1. were infected into the iPS cell-derived γδ T cells (iγδ T cells) prepared in [Example 5] 2. to produce iPS cell-derived anti-CD19-CAR / IL-15γδ T cells (iCD19CAR / IL-15γδ T cells).

[0248] 4. Expansion of iPS cell-derived anti-CD19-CAR / IL-15γδ T cells Expansion culture of iCD19CAR / IL-15γδT cells was carried out in the same manner as in [Example 5] 3., except that IL-2 was not added.

[0249] [Test Example 6] 1. Proliferation test of iPS cell-derived anti-CD19-CAR / IL-15γδT cells stimulated with anti-CD30 agonist antibody In [Example 6] 4., we verified whether the addition of anti-CD30 agonist antibody (300 ng / mL) during stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark) had an effect on the proliferation of iCD19CAR / IL-15γδT cells. The addition of anti-CD30 agonist antibody resulted in greater proliferation (Figure 19).

[0250] 2. Examination of the cytotoxic activity of iPS cell-derived anti-CD19-CAR / IL-15γδ T cells after stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark) and anti-CD30 agonist antibody [Example 6] The cytotoxic activity of iCD19CAR / IL-15γδT cells obtained in 4. was evaluated. CD19-positive Raji cells and CD19-negative CCRF-CEN cells were used as target cells, and iCD19CAR / IL-15γδT cells were mixed at a ratio of 0.5, 1, 2, 4, 8, and 16 times the target cells, and the cytotoxic activity of iCD19CAR / IL-15γδT cells was evaluated based on the target cell death after 2 hours. It was shown that iCD19CAR / IL-15γδT cells expanded in a medium containing an anti-CD30 agonist antibody had cytotoxic activity against CD19-positive Raji cells, but not against CD19-negative CCRF-CEN cells (Figure 20).

[0251] 3. Effect of extending survival time by iPS cell-derived anti-CD19-CAR / IL-15γδ T cells after stimulation with solid-phase anti-CD3 agonist antibody / Retronectin (registered trademark) and anti-CD30 agonist antibody 5x10 NOD / Shi-scid,IL-2RγKO (NOG) mice (Central Institute for Experimental Animals, female, 7-8 weeks old) 5 Nalm6 cells (ATCC) were transplanted into the tail vein to generate Nalm6 xenograft mice. Four days after transplantation, iCD19CAR / IL-15γδT cells (5×10 6A suspension of 100 cells (1000 cells) in 0.1 mL of HBSS-buffer or an equal volume of HBSS-buffer was administered via the tail vein, and the survival time was confirmed. All mice in the control group that received CD19-positive Nalm6 cancer cells via the tail vein died within 3 weeks, whereas all mice in the group that received iCD19CAR / IL-15γδT cells expanded in a medium containing an anti-CD30 agonist antibody survived for at least 6 weeks (Figure 21).

[0252] [Example 7] 1. Production of iPS cell-derived anti-CD19-CAR / IL-15αβ T cells The iPS cell-derived anti-CD19-CAR T cells produced by the method in [Example 3], 4. were infected with the retroviral vector carrying the IL15Rα / IL-15 gene produced in [Example 6], 2., to produce iPS cell-derived anti-CD19-CAR / IL-15αβ T cells (iCD19CAR / IL-15αβ T cells).

[0253] 2. Expansion of iCD19CAR / IL-15αβ T cells using solid-phase anti-CD3 agonist antibody / Retronectin® The iCD19CAR / IL-15αβT cells obtained in [Example 7] 1 were cultured until day 7 in the same manner as in [Example 6] 4. However, anti-human CD30 antibody was not added.

[0254] [Test Example 7] 1. In vivo antitumor effect of iCD19CAR / IL-15αβ T cells after stimulation with solid-phase anti-CD3 agonist antibody / Retronectin® 5x10 NOD / Shi-scid,IL-2RγKO (NOG) mice (Central Institute for Experimental Animals, female, 7-8 weeks old) 5 Luciferase-expressing Nalm6 cells (ATCC) were transplanted into the tail vein to generate luciferase-expressing Nalm6 xenograft mice. Four days after transplantation, the iCD19CAR / IL-15αβT cells (5×10 6A suspension of Nalm6 cells (1000 cells) in 0.1 mL of HBSS-buffer or an equal volume of HBSS-buffer was administered via the tail vein. Luciferin was administered via the tail vein every week after administration, and the activity of luciferase expressed by Nalm6 cells was measured using IVIS. In the control administration group, luminescence from Nalm6 cells was confirmed throughout the body two weeks after administration, and all animals died by the third week after administration, whereas in the iCD19CAR / IL-15αβT cell administration group, luminescence was not detected until six weeks after administration (Figure 22).

[0255] [Example 8] 1. Production of iPS cell-derived γδ T cells [Example 5] iPS cell-derived γδ T cells (iγδ T cells) were produced in the same manner as in 1. and 2.

[0256] [Test Example 8] 1. Measurement of the concentration of anti-CD3 agonist antibody (UCHT1) and RetroNectin (registered trademark) suitable for immobilization on a culture plate Anti-CD3 agonist antibody (UCHT1) and RetroNectin (registered trademark) were mixed and immobilized on a culture plate in the same manner as in [Example 1] 5. Then, the amount of immobilization on the culture plate was measured using ELISA (Figure 23). The anti-CD3 agonist antibody not mixed with RetroNectin (registered trademark) was confirmed to be immobilized in a concentration-dependent manner between 3 ng / mL and 30,000 ng / mL (0.003 μg / mL and 30 μg / mL), but the amount of immobilization of the anti-CD3 agonist antibody decreased as the concentration of RetroNectin (registered trademark) mixed was increased. On the other hand, RetroNectin (registered trademark) was confirmed to be immobilized in a concentration-dependent manner between 16.7 μg / mL and 150 μg / mL.

[0257] 2. Verification of the concentration range and mixing ratio of anti-CD3 agonist antibody and RetroNectin® required for immobilized anti-CD3 agonist antibody and RetroNectin® suitable for proliferation of iγδ T cells iγδT cells were adjusted to 100,000 cells / 200μL in IMDM medium containing 15% FBS, the cytokines in Table 1, and anti-CD30 agonist antibodies diluted to final concentrations of 0, 3, 30, and 300 ng / ml. The iγδT cells were seeded onto plates immobilized with anti-CD3 agonist antibodies (0, 300, 3000, 30000 ng / ml (0, 0.3, 3, 30 μg / ml)) and RetroNectin (registered trademark) (0, 2, 15, 150 μg / mL), and cultured for 3 days under 5% CO2 / 37℃. On the third day of culture, the cells were collected from the plate, suspended in an appropriate amount of medium containing 15% FBS and the cytokines listed in Table 2, seeded on a non-solid-phase 96-well plate, and cultured under 5% CO2 / 37°C. Thereafter, the cells were collected from the plate once each on the fifth, sixth, seventh, eighth, nineth, tenth, and twelfth days of culture, a total of four to seven times, suspended in an appropriate amount of medium, seeded on a non-solid-phase plate, and cultured under 5% CO2 / 37°C. On the thirteenth day of culture, the number of cells was counted using a hemocytometer, and the proliferation rate was measured in comparison with the number of cells on the th day of culture (FIG. 24). In the plates on which anti-CD3 agonist antibody and RetroNectin (registered trademark) were mixed and solidified at 0.3 μg / mL and 2 μg / mL, 3 μg / mL and 15 μg / mL, and 30 μg / mL and 150 μg / mL, respectively, the equivalent induction of iγδT cell proliferation was observed. Furthermore, cell proliferation was confirmed to be dependent on the concentration of anti-CD30 agonist antibody added. [Industrial Applicability]

[0258] By culturing CD3 positive cells in the presence of a CD3 / TCR complex agonist, fibronectin or its modified form, and a CD30 agonist, T cells can be efficiently and repeatedly expanded. In addition, when the CD3 positive cells to be cultured are CD3 positive CD8 positive cells or CD3 positive CD8 positive CD30 positive cells, the produced or expanded cells can easily shift to effector T cells and exert cytotoxic activity, and therefore can be applied to T cell therapy. This application is based on Japanese Patent Application No. 2018-151580 (filing date: August 10, 2018), Japanese Patent Application No. 2019-042666 (filing date: March 8, 2019), and Japanese Patent Application No. 2019-117878 (filing date: June 25, 2019), the contents of which are incorporated in their entirety herein.

Claims

[Claim 1] (I) culturing CD3 positive cells in the presence of a CD3 / TCR complex agonist, fibronectin or a variant thereof, and a CD30 agonist; and (II) culturing the CD3 positive cells cultured in step (I) in the absence of a CD3 / TCR complex agonist and fibronectin or a variant thereof, and in the presence of a CD30 agonist; A method for producing CD3 positive cells, comprising repeating the steps (I) and (II) in this order.

Images