Methods for reprogramming fibroblasts or fibroblast-like cells into conventional type 2 dendritic cells

Abstract

Provided is a method for producing a conventional type-2 dendritic cell (cDC2)-like cell from a fibroblast or a fibroblast-like cell, the method including a step for introducing a nucleic acid encoding PU.1, a nucleic acid encoding KLF4, a nucleic acid encoding IRF4 and a nucleic acid encoding C / EBP into the fibroblast or the fibroblast-like cell.

Description

[Technical Field]

[0001] The present invention relates to methods and compositions for preparing conventional type 2 dendritic cells from fibroblasts or fibroblast-like cells by direct reprogramming. [Background technology]

[0002] Pancreatic cancer has a 5-year relative survival rate of less than 10%, making it a known intractable cancer with an extremely poor prognosis compared to other cancers. One of the characteristics of intractable cancers such as pancreatic cancer is the large amount of stroma surrounding cancer cells. The stroma contains many cells that promote angiogenesis and cancer cell proliferation and invasion, and the quantitatively dominant cells among these are cancer-associated fibroblasts (CAFs). CAFs not only promote cancer cell proliferation by producing growth factors, but also harden cancer tissue by excessively producing extracellular matrix such as collagen. As a result, intractable cancers exhibit strong resistance to conventional chemotherapy and radiation therapy.

[0003] Immunotherapy, which aims to activate antitumor immune responses, has been attempted as a treatment for intractable cancers. DC vaccine therapy, which activates antitumor immune responses by sensitizing autologous dendritic cells with cancer antigens in vitro and then infusing them into the patient, has attracted attention due to its high safety. However, because dendritic cells and their precursor cells, monocytes, are present in extremely low amounts in peripheral blood and cannot be expanded in culture, preparing therapeutically effective DC vaccines is difficult. To address this issue, methods for preparing dendritic cells by reprogramming are currently being developed. Techniques for generating induced pluripotent stem cells (iPSCs) from somatic cells and then inducing them into dendritic cells are already being tested in clinical trials. However, the time-consuming, expensive, and technically challenging process of iPSC generation has prevented the clinical application of iPSC-derived DCs.

[0004] Therefore, there is growing expectation for direct reprogramming technology, which can directly induce differentiated cells into different types of differentiated cells without going through iPSCs. In particular, if dendritic cells could be directly induced from fibroblasts, DC vaccines could be prepared easily, quickly, and at low cost. It has now been demonstrated that direct reprogramming from mouse embryonic fibroblasts (MEFs) into dendritic cells is possible (Patent Documents 1 and 2, Non-Patent Document 1). However, it has not yet been possible to directly induce dendritic cells from adult human fibroblasts with high efficiency. [Prior art documents] [Patent documents]

[0005] [Patent Document 1] International Publication No. 2018 / 185709 [Patent Document 2] International Publication No. 2021 / 105234 [Non-patent literature]

[0006] [Non-Patent Document 1] Rosa FF et al., Sci. Immunol., 2018 Dec 7;3(30):eaau4292 Summary of the Invention [Problem to be solved by the invention]

[0007] The present invention was made with the aim of providing a new therapeutic strategy for intractable cancers and an easy and efficient method for preparing DC vaccines. [Means for solving the problem]

[0008] As a result of extensive research, the present inventors have succeeded in transdifferentiating various fibroblasts or fibroblast-like cells into conventional type 2 dendritic cell (cDC2)-like cells by introducing a combination of four specific transcription factors.

[0009] That is, according to one embodiment, the present invention provides a method for generating conventional type 2 dendritic cell (cDC2)-like cells from fibroblasts or fibroblast-like cells, the method comprising the step of introducing a nucleic acid encoding PU.1, a nucleic acid encoding KLF4, a nucleic acid encoding IRF4, and a nucleic acid encoding C / EBP into the fibroblasts or fibroblast-like cells.

[0010] The C / EBP is preferably C / EBP alpha or C / EBP beta.

[0011] The fibroblasts or fibroblast-like cells are preferably cancer-associated fibroblasts.

[0012] The fibroblasts or fibroblast-like cells are preferably mesenchymal stem cells.

[0013] Furthermore, according to one embodiment, the present invention provides a pharmaceutical composition for preventing or treating cancer in a subject, comprising conventional type 2 dendritic cell (cDC2)-like cells prepared by the above-described method.

[0014] The cDC2-like cells are preferably loaded with a cancer antigen.

[0015] Preferably, the cDC2-like cells are autologous to the subject.

[0016] The cDC2-like cells may be immortalized.

[0017] Furthermore, according to one embodiment, the present invention provides a composition for transdifferentiating fibroblasts or fibroblast-like cells into conventional type 2 dendritic cell-like cells, comprising a nucleic acid encoding PU.1, a nucleic acid encoding KLF4, a nucleic acid encoding IRF4, and a nucleic acid encoding C / EBP. [Effects of the Invention]

[0018] According to the method of the present invention, fibroblasts or fibroblast-like cells can be directly transdifferentiated into cDC2-like cells, and therefore, according to the method of the present invention, DC vaccines can be prepared easily and efficiently. [Brief explanation of the drawings]

[0019] [Figure 1] FIG. 1 shows the results of flow cytometry gating of MEFs into which four mouse transcription factors were introduced, based on the expression of CD45, CD11b, CD11c, and MHC class II. [Figure 2] FIG. 2 shows the expression of cDC2-specific markers (CLEC10A, SIRPα, and CCR7) in CD45+CD11b+MHC-II+CD11c+ cells. [Figure 3] FIG. 3 shows the expression of C-type lectins (SIGNR1 and DC-SIGN) in CD45+CD11b+MHC-II+CD11c+ cells. [Figure 4] FIG. 4 shows the expression of macrophage-specific markers (CD115 and F4 / 80) and monocyte-specific marker (Ly6C) in CD45+CD11b+MHC-II+CD11c+ cells. [Figure 5] FIG. 5 is a graph showing the results of quantification by RT-qPCR of the expression of Zbtb46, a cDC-specific transcription factor, in icDC2. [Figure 6] FIG. 6 is a graph showing the results of quantification by RT-qPCR of the expression of macrophage-specific tyrosine kinase MerTK in icDC2. [Figure 7] FIG. 7 is a graph showing the time course of transdifferentiation of immortalized MEFs into which four mouse transcription factors were introduced into cDC2-like cells. [Figure 8] FIG. 8 is a graph showing the proliferation of cDC2-like cells induced from immortalized MEFs. [Figure 9]FIG. 9 is a graph showing the transdifferentiation efficiency of MEFs into icDC2s introduced with a combination of mouse PU.1 and one or more transcription factors selected from mouse KLF4, IRF4, and C / EBP alpha. [Figure 10] FIG. 10 is a schematic diagram showing the construction of a polycistronic vector that expresses four mouse transcription factors under the control of the TRE promoter. [Figure 11] FIG. 11 shows the results of flow cytometry gating of MEFs into which four mouse transcription factors were introduced using individual vectors, based on the expression of CD45, CD11b, CD11c, and MHC class II. [Figure 12] FIG. 12 shows the results of flow cytometry gating of MEFs into which four transcription factors were introduced by a single polycistronic vector, based on the expression of CD45, CD11b, CD11c, and MHC class II. [Figure 13] FIG. 13 shows the results of flow cytometry gating of MRC-5 cells into which four human transcription factors have been introduced, based on the expression of CD45 and CD11b. [Figure 14] FIG. 14 shows enhanced expression of HLA-DR in CD45+CD11b+ cells. [Figure 15] FIG. 15 shows increased expression of CD11c in CD45+CD11b+ cells. [Figure 16] FIG. 16 is a plot showing the increase in the number of CD3 epsilon-positive cells in a mixed cell population of MEFs, MSCs, 3T3, and CD4-positive T cells transfected with four mouse transcription factors. [Figure 17] FIG. 17 shows enhanced expression of CD69 in CD4-positive T cells mixed with MEFs into which four mouse transcription factors had been introduced. [Figure 18] FIG. 18 is a graph comparing tumor size in model mice administered with or without MEFs into which four mouse transcription factors have been introduced. DETAILED DESCRIPTION OF THE INVENTION

[0020] The present invention will be described in detail below, but the present invention is not limited to the embodiments described in this specification.

[0021] According to a first embodiment, the present invention provides a method for generating conventional type 2 dendritic cell (cDC2)-like cells from fibroblasts or fibroblast-like cells, the method comprising the step of introducing a nucleic acid encoding PU.1, a nucleic acid encoding KLF4, a nucleic acid encoding IRF4, and a nucleic acid encoding C / EBP into the fibroblasts or fibroblast-like cells.

[0022] "Fibroblasts" refer to spindle-shaped cells present in the interstitium that produce extracellular matrix-constituting proteins and their decomposing enzymes. On the other hand, "fibroblast-like cells" refer to cells that are defined only by their spindle shape, similar to that of fibroblasts, and do not have specific functions such as differentiation potential. Morphologically, fibroblasts and fibroblast-like cells cannot be distinguished. The method of this embodiment can use either fibroblasts or fibroblast-like cells.

[0023] The fibroblasts or fibroblast-like cells in this embodiment may be derived from any vertebrate, preferably from mammals such as mice, rats, guinea pigs, rabbits, dogs, sheep, pigs, cattle, horses, goats, monkeys, or humans, and are particularly preferably derived from humans. Furthermore, the fibroblasts or fibroblast-like cells in this embodiment may be derived from any fetal or adult tissue, and the tissue may be either normal tissue or cancer tissue.

[0024] Therefore, in this embodiment, fibroblasts or fibroblast-like cells include, but are not limited to, for example, mouse embryonic fibroblasts (MEFs), immortalized mouse embryonic fibroblasts (3T3), adult mouse tail tip fibroblasts (TTFs), human embryonic fibroblasts (HEFs), cancer-associated fibroblasts (CAFs), adipose-derived mesenchymal stem cells (AD-MSCs), bone marrow mesenchymal stem cells (BM-MSCs), and the like.

[0025] Methods for preparing fibroblasts or fibroblast-like cells are well established and can be prepared according to methods known in the art. Alternatively, established fibroblast or fibroblast-like cell lines may be obtained from, for example, the RIKEN BioResource Center (RIKEN BRC), the American Type Culture Collection (ATCC), etc.

[0026] In the method of this embodiment, nucleic acids encoding PU.1, KLF4, IRF4 and C / EBP are introduced into fibroblasts or fibroblast-like cells.

[0027] "PU.1," "KLF4," "IRF4," and "C / EBP" are all transcription factors. The C / EBP family consists of C / EBP alpha, C / EBP beta, C / EBP gamma, C / EBP delta, C / EBP epsilon, and CHOP (C / EBP zeta). The C / EBP in this embodiment may be any of these, but is preferably C / EBP alpha or C / EBP beta. PU.1, KLF4, IRF4, and C / EBP in this embodiment may be derived from any vertebrate, but are preferably derived from mammals such as mice, rats, guinea pigs, rabbits, dogs, sheep, pigs, cows, horses, goats, monkeys, and humans, and are particularly preferably derived from humans.

[0028] The genes encoding PU.1, KLF4, IRF4, and C / EBP have already been cloned, and their nucleic acid sequence information is available from designated databases. For example, NM_003120 for human PU.1, NM_011355 for mouse PU.1, NM_004235 for human KLF4, NM_010637 for mouse KLF4, NM_002460 for human IRF4, NM_013674 for mouse IRF4, NM_004364 for human C / EBP alpha, NM_007678 for mouse C / EBP alpha, NM_005194 for human C / EBP beta, and NM_009883 for mouse C / EBP beta (all available from the NCBI Nucleotide Database).

[0029] PU.1, KLF4, IRF4, and C / EBP in this embodiment may also include their variants and homologs that have equivalent transcriptional regulatory activity. In other words, PU.1, KLF4, IRF4, and C / EBP in this embodiment may encompass proteins consisting of amino acid sequences that share 80% or more, preferably 90% or more, and more preferably about 95% or more identity with the amino acid sequences registered in the database, as long as the transcriptional regulatory activity is maintained. Amino acid sequence identity can be calculated using sequence analysis software or programs commonly used in the art (e.g., FASTA, BLAST, etc.). PU.1, KLF4, IRF4, and C / EBP in this embodiment may also encompass proteins consisting of amino acid sequences in which one to several amino acids have been substituted, deleted, inserted, and / or added to the amino acid sequences registered in the database, as long as the transcriptional regulatory activity is maintained. Here, "one to several" refers to, for example, "1 to 30," preferably "1 to 10," and particularly preferably "1 to 5."

[0030] Nucleic acids encoding PU.1, KLF4, IRF4, and C / EBP can be introduced into fibroblasts or fibroblast-like cells by methods well known in the art. For example, these nucleic acids may be cloned into an expression vector and then introduced into the cells. The type of expression vector can be selected appropriately depending on the target fibroblasts or fibroblast-like cells. Examples of suitable vectors include, but are not limited to, viral vectors such as retroviruses, lentiviruses, adenoviruses, and Sendai viruses, as well as plasmid vectors such as pCMV. Furthermore, the nucleic acids encoding PU.1, KLF4, IRF4, and C / EBP may be expressed from separate vectors or from a single polycistronic vector.

[0031] In the method of this embodiment, the expression vector can be introduced into cells by methods well known in the art depending on the type of vector. Non-viral vectors can be introduced by, for example, lipofection, electroporation, microinjection, etc. Viral vectors can be introduced by infecting cells with an appropriate titer or multiplicity of infection (MOI).

[0032] Upon expression of PU.1, KLF4, IRF4, and C / EBP, fibroblasts or fibroblast-like cells transdifferentiate into conventional type 2 dendritic cell (cDC2)-like cells. Here, "transdifferentiation (or direct reprogramming)" refers to the direct conversion of one mature (differentiated) cell type into another mature (differentiated) cell type without passing through a pluripotent cell state.

[0033] In this embodiment, "conventional type 2 dendritic cell (cDC2)-like cells" refer to cells that express cDC2-specific markers and have antigen-presenting ability. Dendritic cells (DCs) are classified into three major subsets: conventional type 1 dendritic cells (cDC1), conventional type 2 dendritic cells (cDC2), and plasmacytoid dendritic cells (pDC), and the markers characterizing each subset are well known. In this embodiment, cDC2-like cells may be defined by any combination of well-known blood cell markers, myeloid cell markers, and cDC2-specific markers. However, they are preferably defined as, for example, CD45+, CD11b+, CD11c+, and MHC class II (HLA-DR)+. Significant expression of MHC class II (HLA-DR) indicates that the cDC2-like cells of this embodiment have antigen-presenting ability. In this embodiment, the cDC2-like cells preferably further express CLEC10A, SIRPα, and / or CCR7 in addition to the above-mentioned markers, and more preferably further express a C-type lectin such as SIGNR1 or DC-SIGN. The cDC2-like cells in this embodiment may further express not only cDC2-specific markers, but also macrophage-specific markers such as CD115 and monocyte-specific markers such as Ly6C. Marker expression can be analyzed by known techniques such as RT-PCR, Western blotting, and flow cytometry.

[0034] According to the method of this embodiment, cDC2-like cells can be generated directly from fibroblasts or fibroblast-like cells without going through a pluripotent cell state. Because fibroblasts can be easily obtained and expanded, the method of this embodiment is useful for preparing DC vaccines.

[0035] According to a second embodiment, the present invention provides a pharmaceutical composition for preventing or treating cancer in a subject, comprising cDC2-like cells prepared by the above-described method.

[0036] In this embodiment, "preventing" refers not only to preventing the onset of cancer in a subject at risk of developing cancer, but also to reducing the risk of cancer onset, or to treating a subject before the onset of cancer, thereby delaying the progression of symptoms or reducing the severity of the symptoms if the subject does develop cancer. "Treating" refers not only to completely curing cancer, but also to ameliorating or alleviating cancer symptoms, delaying or halting the progression of cancer, and improving cancer prognosis.

[0037] The "subject" in this embodiment may be any vertebrate, but is preferably a mammal such as a mouse, rat, rabbit, sheep, pig, cow, goat, monkey, or human, and is particularly preferably a human. The subject may be of any age, including infants, juveniles, adolescents, adults, and elderly subjects.

[0038] The cDC2-like cells in this embodiment are the same as those defined in the first embodiment, and may be prepared from fibroblasts or fibroblast-like cells derived from any tissue of any vertebrate. The cDC2-like cells in this embodiment may be prepared from fibroblasts or fibroblast-like cells that are preferably allogeneic or autologous to the subject, more preferably autologous.

[0039] The cDC2-like cells in this embodiment may optionally be immortalized. Here, "immortalized" cells means that the cells maintain a proliferative state even after a certain number of divisions, i.e., the cells have the ability to proliferate indefinitely. Methods for immortalizing cells have already been established, and known techniques can be used. For example, cells can be immortalized by introducing an immortalizing gene such as the SV40 T antigen gene or the telomerase reverse transcriptase (TERT) gene into the cells using a retroviral vector.

[0040] The cDC2-like cells of this embodiment are preferably loaded with a cancer antigen. Methods for loading dendritic cells with cancer antigens have been well established, and the cDC2-like cells of this embodiment can be loaded with a cancer antigen according to methods known in the art. For example, cDC2-like cells can be cultured for 12 hours to several days in a medium containing a full-length or partial fragment of a cancer antigen peptide or tumor lysate. Alternatively, a nucleic acid encoding a full-length or partial fragment of a cancer antigen peptide can be introduced into the cells using a viral or non-viral vector.

[0041] Cancer antigens that can be used in this embodiment are not particularly limited, but may be, for example, HER2 / NEU, TERT, WT1, MAGE-A3, NY-ESO-1, PAP, PSA, etc.

[0042] The pharmaceutical composition of this embodiment contains the above-mentioned cDC2-like cells as an active ingredient. The pharmaceutical composition of this embodiment may consist of only the active ingredient, but may further contain, as optional ingredients, known pharmaceutically acceptable carriers, buffers, and other ingredients (for example, Toll-like receptor ligands such as CpG DNA, STING agonists such as synthetic cyclic nucleotides, cytokines / chemokines such as GM-CSF, CCL19, and FLT3L). For example, the pharmaceutical composition of this embodiment can be prepared as an injectable formulation using a carrier such as phosphate-buffered saline that can maintain the viability of the cells that are the active ingredient. In this case, the cDC2-like cells are administered in an amount of, for example, 1 x 10 6 ~1×10 8 The cells may be suspended in the carrier at a concentration of 1000 cells / mL.

[0043] The pharmaceutical composition of this embodiment can be administered by an appropriate method, such as injection, infusion, or implantation. Preferably, the pharmaceutical composition of this embodiment can be injected intravenously, subcutaneously, intradermally, or into a lymph node. The dosage of the pharmaceutical composition of this embodiment may vary depending on the age, weight, and severity of cancer of the subject, but is typically 1×10 5 ~1×10 10The dose may be in cells / kg body weight. The dose may be administered in one dose or multiple doses.

[0044] The pharmaceutical composition of this embodiment can safely and effectively activate anti-tumor immune responses, and is therefore useful for treating intractable cancers that are difficult to treat with conventional chemotherapy or radiation therapy.

[0045] According to a third embodiment, the present invention provides a composition for transdifferentiating fibroblasts or fibroblast-like cells into conventional type 2 dendritic cell-like cells, comprising a nucleic acid encoding PU.1, a nucleic acid encoding KLF4, a nucleic acid encoding IRF4, and a nucleic acid encoding C / EBP. In this embodiment, the cDC2-like cells, fibroblasts, fibroblast-like cells, PU.1, KLF4, IRF4, and C / EBP-encoding nucleic acids are the same as those defined in the first embodiment, and can be prepared and used as described in the first embodiment. [Example]

[0046] The present invention will be further described below with reference to examples, which should not be construed as limiting the scope of the present invention.

[0047] <1.4 Transdifferentiation of MEFs into dendritic cells by transcription factors> The coding sequences of the mouse PU.1 gene (RefSeq ID: NM_011355, SEQ ID NO: 1), KLF4 gene (RefSeq ID: NM_010637, SEQ ID NO: 2), IRF4 gene (RefSeq ID: NM_013674, SEQ ID NO: 3), and C / EBP alpha gene (RefSeq ID: NM_007678, SEQ ID NO: 4) were amplified by PCR and subcloned into the pMXs vector (Kitamura et al., Exp. Hematol., 2003). These vectors were cotransfected with the VSV-G plasmid and the gag / pol plasmid (Addgene) into HEK293 cells to produce retroviral particles. The culture supernatant was collected and ultracentrifuged at 6,000 × g for 20 minutes at 4°C. The supernatant, from which the insoluble fraction was removed, was mixed with 1 / 4 of the volume of 40% (w / v) PEG-8000, 1.2 M NaCl / PBS solution and incubated overnight at 4°C. The mixture was then ultracentrifuged at 1,600 × g for 60 minutes at 4°C, and the supernatant was removed. The pellet was suspended in 50 μL of DMEM per 1 mL of the original culture supernatant and stored at -80°C.

[0048] Mouse embryonic fibroblasts (MEFs) were obtained from 13.5-day-old embryos according to standard methods. MEFs were seeded onto 24-well plates (4 × 10 cells per well). 4 The next day, 100 μL of virus suspension was added per well. The next day (day 1), the cells in one well were subcultured into three wells and maintained until measurement. DMEM containing 10% FCS was used for culture. After 13 days, the cells were harvested and immunostained for marker proteins. To stain the marker proteins, trypsinized and harvested cells were suspended in antibody solution and incubated at 37°C for 20 minutes, followed by 15 minutes at 4°C. The stained cells were observed using a FACS Verse (BD Biosciences).

[0049] Table 1. Antibodies used for marker staining [Table 1]

[0050] Figure 1 shows the results of cell gating by flow cytometry based on the expression of the blood cell marker CD45, myeloid cell marker CD11b, dendritic cell marker CD11c, and antigen-presenting cell marker MHC class II (MHC-II). In the figure, "4TF" indicates cells transfected with four transcription factors: PU.1, KLF4, IRF4, and C / EBP alpha, while "mock" indicates cells that were not transfected. It was confirmed that dendritic cell-like cells expressing the blood cell marker CD45, myeloid cell marker CD11b, dendritic cell marker CD11c, and antigen-presenting cell marker MHC class II were obtained from cells transfected with the four transcription factors.

[0051] Figures 2–4 show the results of comparing the expression of cDC2-specific markers and other monocyte-lineage cell markers between CD45+CD11b+MHC-II+CD11c+ cells and CD45- cells. CD45+CD11b+MHC-II+CD11c+ cells were found to express the cDC2-specific markers CLEC10A, SIRPα, and CCR7 (Figure 2). CD45+CD11b+MHC-II+CD11c+ cells also expressed the C-type lectins SIGNR1 and DC-SIGN, which are expressed on dendritic cells (Figure 3). On the other hand, CD45+CD11b+MHC-II+CD11c+ cells differed from cDC2s in that they expressed macrophage-specific markers (CD115 and F4 / 80) and the monocyte-specific marker Ly6C. Based on these results, we concluded that the cells obtained by introducing the four transcription factors PU.1, KLF4, IRF4, and C / EBP alpha were cDC2-like cells, and named them "induced cDC2 (icDC2)."

[0052] Next, the expression of the cDC-specific transcription factor Zbtb46 and the macrophage-specific tyrosine kinase MerTK in icDC2s was evaluated by RT-qPCR. GM-CSF-induced bone marrow-derived dendritic cells (GM-DCs) were prepared as a positive control using the following procedure. Bone marrow cells were collected from the femur of a mouse. Bone marrow cells from one animal were suspended in 24 mL of GM-CSF medium (RPMI 1640 medium containing 10 ng / mL GM-CSF (Peprotech), 3.5 μL 2-mercaptoethanol (Nacalai Tesque), and 10% FCS) and seeded at 1 mL per well in a 24-well plate. Half of the culture supernatant was replaced with fresh medium every two days. Six days after the start of culture, floating cells were collected and used as GM-DCs.

[0053] RNA was extracted from cells using TRI reagent (Molecular Research Center) according to the manufacturer's instructions, and cDNA was synthesized using ReverTra Ace qPCR RT Master Mix with gDNA Remover (Toyobo) according to the manufacturer's instructions. qPCR was performed using this cDNA as a template using THUNDERBIRD SYBR qPCR Mix (Toyobo) and a LightCycler 96 (Roche). The primers used are listed below. The expression level in mock cells was set to 1, and the fold change in expression induction was calculated.

[0054] Table 2. Primers used for qPCR [Table 2]

[0055] The results are shown in Figures 5 and 6. Expression of the Zbtb46 gene and Mertk gene was increased in icDC2. These results demonstrate that icDC2 are novel cDC2-like cells that possess characteristics of cDC2 but also have characteristics distinct from cDC2.

[0056] 2.4 Timeline of transdifferentiation of MEFs into cDC2-like cells by transcription factors MEFs were immortalized by transfection with the SV40 T antigen-expressing plasmid pBSSVD2005 (Addgene, plasmid #21826). The four transcription factors were introduced using the same procedure as in 1 above, and marker expression was monitored. The time course of transdifferentiation was analyzed based on the percentage of CD45+CD11b+MHC-II+CD11c+ cells.

[0057] The results are shown in Figure 7. It was confirmed that transdifferentiation began about three days after the introduction of the four transcription factors, peaked on day 7, and then decreased.

[0058] 3. Proliferation of immortalized MEF-derived icDC2 The cells from step 2 were then subcultured every 7 days, and the number of CD45+CD11b+MHC-II+CD11c+ cells was counted. The results are shown in Figure 8. The number of CD45+CD11b+MHC-II+CD11c+ cells increased with increasing culture days, indicating that these cells themselves were proliferating. These results indicate that icDC2 derived from immortalized cells can sustain proliferation, suggesting their potential application in drug discovery.

[0059] 4. Combination of transcription factors required for transdifferentiation of MEFs into cDC2-like cells We investigated whether PU.1, KLF4, IRF4, or C / EBP alpha is required for the transdifferentiation of MEFs into cDC2-like cells. Because CD45+ cells were not induced by any combination of other transcription factors in the absence of PU.1 (data not shown), we introduced PU.1 in combination with one or more transcription factors selected from KLF4, IRF4, and C / EBP alpha into MEFs, and evaluated the efficiency of transdifferentiation into icDC2s using the same procedure as above (1).

[0060] The results are shown in Figure 9. In the figure, "P" indicates the transduction of PU.1 alone; "PC" indicates the transduction of PU.1 and C / EBP alpha; "PK" indicates the transduction of PU.1 and IRF4; "PI" indicates the transduction of PU.1 and IRF4; "PCK" indicates the transduction of PU.1, C / EBP alpha, and KLF4; "PCI" indicates the transduction of PU.1, C / EBP alpha, and IRF4; "PIK" indicates the transduction of PU.1, IRF4, C / EBP alpha, and KLF4. The lack of IRF4 induced almost no transdifferentiation into icDC2 cells. The lack of KLF4 or C / EBP alpha induced transdifferentiation into icDC2 cells, but the transduction efficiency was significantly reduced compared to the transduction of all four transcription factors. These results demonstrate that the transduction of MEFs into cDC2-like cells requires the transduction of all four transcription factors: PU.1, KLF4, IRF4, and C / EBP alpha.

[0061] We then compared the transdifferentiation efficiency of other C / EBP family members: C / EBP beta (RefSeq ID: NM_009883, SEQ ID NO: 13), C / EBP delta (RefSeq ID: NM_007679, SEQ ID NO: 14), and C / EBP epsilon (RefSeq ID: NM_207131, SEQ ID NO: 15). Using the same procedure as in 1 above, retroviral vectors expressing each C / EBP family member were prepared and transfected into MEFs in combination with PU.1, KLF4, and IRF4. The transdifferentiation efficiency was evaluated. C / EBP beta exhibited a transdifferentiation efficiency comparable to that of C / EBP alpha, whereas C / EBP delta or C / EBP epsilon exhibited a lower transdifferentiation efficiency (data not shown). These results suggest that the optimal combination of PU.1, KLF4, IRF4, and C / EBP alpha or C / EBP beta is optimal for transdifferentiation of MEFs into cDC2-like cells.

[0062] 5.4 Transdifferentiation of MEFs into cDC2-like cells by polycistronic expression of transcription factors from lentiviral vectors A fusion gene containing four transcription factors, PU.1, KLF4, IRF4, and C / EBP alpha, connected by a 2A peptide was subcloned into the FUW-tetO-MCS vector (Hockemeyer et al., Cell Stem Cell, 2008) to generate a vector construct expressing the four transcription factors polycistronically under the control of the tetracycline response element (TRE) promoter (Figure 10). The resulting vector was cotransfected into HEK293 cells with pMD2.G (Addgene, plasmid #12259) and psPAX2 (Addgene, plasmid #12260) to generate lentiviral particles. Viral concentrates were prepared using the same procedure as above (1) and stored at -80°C. Lentiviral particles for each transcription factor were also generated using the same procedure, except that the fusion gene was replaced with the PU.1, KLF4, IRF4, or C / EBP alpha gene. MEFs were seeded into 24-well plates (4 × 10 per well). 4 The next day, 100 μL of virus suspension was added per well. The following day, 1 μg / mL doxycycline (Sigma-Aldrich) was added, and the medium was changed every other day. After 13 days, marker expression was monitored using the same procedure as in 1 above.

[0063] The results of introducing the four transcription factors using individual vectors are shown in Figure 11, and the results of introducing them using a polycistronic vector are shown in Figure 12. In both cases, it was confirmed that icDC2 was obtained by adding doxycycline (Dox+).

[0064] <6.4 Examination of starting cells transdifferentiated into cDC2-like cells by transcription factors> To investigate the type of starting cells that could be transdifferentiated into cDC2-like cells by the introduction of four transcription factors, we performed the same analysis as described above using mouse melanoma cell line B16F1 (RIKEN), mouse lung cancer cell line 3LL (National Institute of Biomedical Innovation), mouse breast cancer cell line e0771 (CH3 BioSystems), mouse lymphoma cell line EL4 (RIKEN), adult mouse tail tip fibroblasts (TTF), and mouse adipose-derived mesenchymal stem cells (AD-MSCs). TTFs were prepared from C57BL / 6 mice by standard methods (Takahashi et al., Nat. Protocol, 2007). AD-MSCs were prepared by digesting white adipose tissue isolated from C57BL / 6 mice with collagenase solution (RPMI 1640 medium containing 100 U / mL collagenase (Wako) and 5% FCS) and then isolating adherent cells. All cells were cultured in DMEM containing 10% FCS.

[0065] As a result, TTF and AD-MSCs were transdifferentiated into cDC2-like cells, whereas B16F1, 3LL, e0771, and EL4 did not (data not shown). These results indicate that fibroblasts and fibroblast-like cells can be used to generate cDC2-like cells by introducing the four transcription factors.

[0066] 7. Transdifferentiation of human fibroblasts into cDC2-like cells by human transcription factors Retroviruses were prepared using the same procedures as in 1 above, except that the coding sequences of the human PU.1 gene (RefSeq ID: NM_003120, SEQ ID NO: 5), KLF4 gene (RefSeq ID: NM_004235, SEQ ID NO: 6), IRF4 gene (RefSeq ID: NM_002460, SEQ ID NO: 7), and C / EBP alpha gene (RefSeq ID: NM_004364, SEQ ID NO: 8) were used in place of the coding sequences of the mouse PU.1 gene (SEQ ID NO: 1), KLF4 gene (SEQ ID NO: 2), IRF4 gene (SEQ ID NO: 3), and C / EBP alpha gene (SEQ ID NO: 4). Using the human fibroblast cell line MRC-5 (ATCC) instead of MEFs, marker expression was monitored 13 days after infection using the same procedures as in 1 above.

[0067] The results are shown in Figures 13 to 15. Introduction of the four transcription factors resulted in the generation of CD45+CD11b+ cells (Figure 13, MRC-5+4TF). Furthermore, HLA-DR and CD11c expression was upregulated in CD45+CD11b+ cells compared with CD45-CD11b- cells (Figures 14 and 15). Similarly, when the human immortalized AD-MSC line SCRC-4000 (ATCC) was used instead of MRC-5, CD45+CD11b+HLA-DR+CD11c+ cells were also observed (data not shown). These results demonstrate that icDC2 can be generated from human fibroblasts or fibroblast-like cells using the four transcription factors human PU.1, KLF4, IRF4, and C / EBP alpha.

[0068] On the other hand, when a similar analysis was performed using the human lung epithelial cell line A549 (RIKEN), the human pancreatic cancer cell line Capan-1 (ATCC), and the human cervical cancer cell line HeLa (ATCC) instead of MRC-5, no CD45+CD11b+HLA-DR+CD11c+ cells were observed (data not shown).

[0069] <8.4 Induction of adaptive immune responses by cDC2-like cells transdifferentiated by transcription factors> The four transcription factors were introduced into MEFs using the procedure described above, and the antigen-presenting ability of the resulting cDC2-like cells was examined. Spleens were collected from OT-II mice (chicken ovalbumin 323-339 epitope-specific T cell receptor transgenic mice), digested in collagenase buffer, and then crushed on a glass slide to collect splenocytes. CD4+ T cells were isolated from the splenocyte population using a CD4+ T Cell Isolation Kit for mice (Miltenyi Biotec Inc.) according to the kit's instructions. Four transcription factor-introduced MEFs, AD-MSCs, or immortalized mouse embryonic fibroblasts (hereinafter referred to as "3T3") prepared by the 3T3 method (Todaro and Green, J. Cell Biol., 1962), MEFs (negative control), or GM-DCs (positive control) (2 × 10 cells each) were used. 4 pcs) and 2 x 10 4 CD4+ T cells were mixed with 1000 CD4+ T cells or were mixed with nothing (mock, negative control) and seeded in a round-bottom 96-well plate. CD4+ T cells were cultured for 7 days with or without the addition of 10 μg / mL chicken ovalbumin 323-339 peptide. Total cell count, CD3 epsilon-positive cell count, and CD69 expression were monitored using a FACS Verse (BD Biosciences).

[0070] The results are shown in Figures 16 and 17. The number of CD3 epsilon-positive cells was increased in the cell populations obtained by mixing T cells with MEFs transfected with the four transcription factors (MEF + 4TF), T cells with MSCs transfected with the four transcription factors (MSC + 4TF), and T cells with 3T3s transfected with the four transcription factors (3T3 + 4TF), confirming an increase in T cells (Figure 16). Furthermore, the expression of the activated T cell marker CD69 was also increased in the cell population obtained by mixing T cells with MEFs transfected with the four transcription factors (MEF + 4TF) (Figure 17). These results indicated that cDC2-like cells transdifferentiated from MEFs by the four transcription factors possess antigen-presenting ability.

[0071] 9.4 Induction of antitumor immune responses in mouse cancer models by cDC2-like cells transdifferentiated by transcription factors The following describes the procedure for evaluating whether cDC2-like cells transdifferentiated by the four transcription factors can be pulsed with cancer antigens and used as DC vaccines using a mouse cancer model.

[0072] (9-1) Preparation of tumor-bearing mouse models B16F1 melanoma cells (1 × 10 6 The tumors were subcutaneously transplanted into C57BL / 6 mice. One week later, tumor size was measured and the mice were used as tumor-bearing models.

[0073] (9-2) Preparation and administration of pulsed cDC2-like cells cDC2-like cells were induced from fibroblasts derived from C57BL / 6 CD45.1 mice by introducing four transcription factors according to the same procedure as in 1 above. The cDC2-like cells were loaded with B16F1 melanoma cell lysate and cultured for 16 hours. The cDC2-like cells were then intravenously administered to the above-mentioned tumor-bearing mouse model, and tumor size was measured weekly.

[0074] The results are shown in Figure 18. In the figure, "days" indicates the number of days since subcutaneous implantation of B16F1 melanoma cells. The tumor sizes of the group administered MEFs transfected with the four transcription factors (MEF + 4TF) and the group administered nothing (mock, negative control) were measured and compared. A significant difference was observed 21 days after subcutaneous implantation (i.e., 14 days after MEF + 4TF administration) (p<0.05, Student's t-test). These results demonstrate that cDC2-like cells transdifferentiated from MEFs by the four transcription factors have the effect of reducing tumor size.

Claims

1. A method for generating conventional type 2 dendritic cell (cDC2)-like cells from fibroblasts or fibroblast-like cells, comprising the step of introducing a nucleic acid encoding PU.1, a nucleic acid encoding KLF4, a nucleic acid encoding IRF4, and a nucleic acid encoding C / EBP into the fibroblasts or fibroblast-like cells, wherein the cDC2-like cells are CD45+, CD11b+, CD11c+, MHC class II+, and further express CD115, Ly6C, and MerTK.

2. The method of claim 1, wherein the C / EBP is C / EBP alpha or C / EBP beta.

3. The method of claim 1 or 2, wherein the fibroblasts or fibroblast-like cells are cancer-associated fibroblasts.

4. The method of claim 1 or 2, wherein the fibroblasts or fibroblast-like cells are mesenchymal stem cells.

5. A composition for transdifferentiating fibroblasts or fibroblast-like cells into conventional type 2 dendritic cell-like cells, comprising a nucleic acid encoding PU.1, a nucleic acid encoding KLF4, a nucleic acid encoding IRF4, and a nucleic acid encoding C / EBP, wherein the cDC2-like cells are CD45+, CD11b+, CD11c+, MHC class II+, and further express CD115, Ly6C, and MerTK.

6. The composition of claim 5 , wherein the C / EBP is C / EBP alpha or C / EBP beta.

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