Patent Application
20240254445
This application contains a sequence listing submitted in Computer Readable Form (CRF). The CRF file containing the sequence listing entitled “10-PK6386507-SequenceListing.txt”, which was created on Nov. 28, 2023, and is 3,945 bytes in size. The information in the sequence listing is incorporated herein by reference in its entirety.
The present invention relates to a composition for proliferating natural killer cells, comprising feeder cells and a method for proliferating natural killer cells. Specifically, the present invention relates to a method for proliferating natural killer cells by using feeder cells that are transformed to express at least one gene selected from the group consisting of B7H6, CD137L, IL-15, and IL-15Rα.
Natural killer cell (NK cell) is a representative cell responsible for innate immunity and is a type of lymphocyte that possesses large granules and is cytotoxic to various types of tumor cells and virus-infected cells. NK cells make up 5-10% of human peripheral blood lymphocytes, and unlike T cells, they mature in the liver or bone marrow. In general, immune cells eliminate infected cells by detecting infected cells through major histocompatibility complex (MHC) proteins presented on their surface and secreting various cytokines and chemicals that induce apoptosis. However, NK cells can induce an immediate immune response because they can recognize and eliminate abnormal cells even without the major histocompatibility complex bound to the antigen.
Defects in the function of NK cells have been reported in many diseases, and it is known that most NK cells are inactivated, especially in patients with cancer. Some researchers conducted research on methods to proliferate and activate NK cells in vitro, and demonstrated that NK cells amplified in vitro showed excellent cytotoxicity when reacted against various carcinomas.
Therefore, methods for proliferation of NK cells are being studied, and research is being conducted using feeder cells as one of the efficient methods for selective amplification of NK cells. However, the clear mechanism of how to amplify NK cells is unknown.
Allogeneic or autologous peripheral blood mononuclear cells (PBMC) and cancer cell lines are used as feeder cells for the amplification of NK cells. As cancer cell lines, HFWT, a Wilms tumor-derived cell line, EBV-LCL (EBV transformed lymphoblastoid cells), and the like are known.
The present inventors discovered that feeder cells expressing B7H6 have an excellent NK cell proliferation effect, and also discovered that, in addition to previously known feeder cells, ARH77 cells are excellent feeder cells and have an NK cell proliferation effect. Based on the above, the present inventors completed the present invention.
(Non-Patent Document 1) Hiroyuki Fujisaki, Harumi Kakuda, Noriko Shimasaki, Chihaya Imai, Jing Ma, Timothy Lockey, et al. (2009) EXPANSION OF HIGHLY CYTOTOXIC HUMAN NATURAL KILLER CELLS FOR CANCER CELL THERAPY. Cancer Res. Author manuscript. 2009 May 1; 69(9): 4010-4017
(Non-Patent Document 2) Denman CJ, Senyukov VV, Somanchi SS, Phatarpekar PV, Kopp LM, et al. (2012) Membrane-Bound IL-21 Promotes Sustained Ex Vivo Proliferation of Human Natural Killer Cells. PLoS ONE 7(1): e30264
An object of the present invention is to provide a composition for proliferating natural killer cells, comprising feeder cells that are transformed to express at least one gene selected from the group consisting of B7H6, CD137L, IL-15, and IL-15Rα.
In addition, another object of the present invention is to provide a feeder cell line that is transformed to express at least one gene selected from the group consisting of B7H6, CD137L, IL-15, and IL-15Rα and a method for proliferating natural killer cells using the same.
The present invention provides a composition for proliferating natural killer cells, comprising feeder cells that are transformed to express B7H6 gene.
The present invention provides a composition for proliferating natural killer cells, comprising feeder cells that are transformed to express at least one gene selected from the group consisting of B7H6, CD137L, IL-15, and IL-15Rα.
The composition of the present invention may comprise feeder cells that express B7H6, and the feeder cells may further express at least one selected from the group consisting of CD137L, IL-15, and IL-15Rα.
Preferably, the composition of the present invention may comprise feeder cells that express B7H6, CD137L, and IL-15.
More preferably, the composition of the present invention may comprise feeder cells that express B7H6, CD137L, IL-15, and IL-15Rα.
The feeder cells of the present invention may be ARH77 or K562 cells, and preferably the feeder cells may be ARH77 cells.
The present invention provides a feeder cell line that expresses B7H6.
The feeder cells of the present invention line may further express at least one selected from the group consisting of CD137L, IL-15, and IL-15Rα.
The feeder cell line of the present invention may be ARH77 or K562 cell line.
In addition, the present invention provides a method of producing feeder cells that express B7H6, comprising the steps of:
The transgene of the present invention may further include at least one gene selected from the group consisting of CD137L, IL-15, and IL-15Rα.
The virus of the present invention may be a lentivirus or a retrovirus.
The feeder cells of the present invention may be ARH77 or K562 cells.
In addition, the present invention provides a method for proliferating natural killer cells, comprising the step of culturing feeder cells that express B7H6 and peripheral blood mononuclear cells.
The feeder cells of the present invention may further express at least one selected from the group consisting of CD137L, IL-15, and IL-15Rα.
The feeder cells of the present invention may be ARH77 or K562 cells.
The culture solution of the present invention may comprise at least one selected from the group consisting of penicillin, streptomycin, glutamine, gentamicin, fetal bovine serum, human serum, mercaptoethanol, ethanolamine, ascorbic acid, and sodium selenite. Preferably, the culture solution of the present invention may comprise at least one selected from the group consisting of glutamine, gentamicin, human serum, mercaptoethanol, ethanolamine, ascorbic acid, and sodium selenite.
The proliferation method of the present invention may further comprise the step of adding at least one selected from the group consisting of recombinant human interleukin-2, recombinant human interleukin-21, and recombinant human interleukin-15.
Preferably, the method may further comprise the steps of (a) adding recombinant human interleukin-2 and recombinant human interleukin-21, and (b) adding recombinant human interleukin-2 and recombinant human interleukin-15.
In addition, the present invention may provide a natural killer cell line produced by the proliferation method of the present invention.
The feeder cells that express at least one gene selected from the group consisting of B7H6, CD137L, IL-15, and IL-15Rα according to the present invention have the effect of obtaining NK cells with higher levels of expansion rate, purity, and cytotoxicity when the feeder cells according to the present invention are used to proliferate natural killer cells (NK cells) compared to the method using the previously known feeder cells. Therefore, the feeder cells according to the present invention can be very useful in various immune cell therapies using NK cells, etc.
Hereinafter, with reference to the accompanying drawings, embodiments and examples of the present disclosure will be described in detail so that those of ordinary skill in the art to which the present invention belongs can easily practice the present invention. However, the present disclosure may be implemented in various forms and is not limited to the embodiments and examples described herein.
Throughout the present specification, when a certain part “includes” a certain component, it means that other components may be further included, rather than excluding other components, unless otherwise stated.
The present invention relates to a composition for proliferating natural killer cells, comprising feeder cells that are transformed to express B7H6 gene and a method for proliferating natural killer cells.
The present invention relates to a composition for proliferating natural killer cells, comprising feeder cells that are transformed to express at least one gene selected from the group consisting of B7H6, CD137L, IL-15, and IL-15Rα and a method for proliferating natural killer cells.
As used herein, the term “B7H6” refers to the ligand of the natural killer cell receptor NKp30.
The B7H6 gene according to the present invention may be composed of the nucleotide sequence of SEQ ID NO: 1, and homologs of the nucleotide sequence are included within the scope of the present invention. Specifically, the gene may comprise a nucleotide sequence having sequence homology of at least 70%, preferably at least 80%, more preferably at least 90%, and most preferably at least 95% with the nucleotide sequence of SEQ ID NO: 1.
As used herein, the term “CD137L” refers to the ligand of CD137.
The CD137L gene according to the present invention may be composed of the nucleotide sequence of SEQ ID NO: 2, and homologs of the nucleotide sequence are included within the scope of the present invention. Specifically, the gene may comprise a nucleotide sequence having sequence homology of at least 70%, preferably at least 80%, more preferably at least 90%, and most preferably at least 95% with the nucleotide sequence of SEQ ID NO: 2.
As used herein, the term “IL-15” refers to interleukin-15, which is a cytokine produced in epithelial cells.
The IL-15 gene according to the present invention may be composed of the nucleotide sequence of SEQ ID NO: 3, and homologs of the nucleotide sequence are included within the scope of the present invention. Specifically, the gene may comprise a nucleotide sequence having sequence homology of at least 70%, preferably at least 80%, more preferably at least 90%, and most preferably at least 95% with the nucleotide sequence of SEQ ID NO: 3.
As used herein, the term “IL-15Rα” refers to interleukin 15 receptor α-chain.
The IL-15Rα gene according to the present invention may be composed of the nucleotide sequence of SEQ ID NO: 4, and homologs of the nucleotide sequence are included within the scope of the present invention. Specifically, the gene may comprise a nucleotide sequence having sequence homology of at least 70%, preferably at least 80%, more preferably at least 90%, and most preferably at least 95% with the nucleotide sequence of SEQ ID NO: 4.
As used herein, the term “feeder cell (supporting cell)” refers to a cell that does not have the ability to divide and proliferate, but is metabolically active and produces various metabolites to help the proliferation of target NK cells. The feeder cells that can be used in the present invention include animal cell lines into which genes have been introduced, peripheral blood leukocytes (PBL) treated with various cytokines or compounds, one's own or another person's peripheral blood leukocytes, T cells, B cells, or monocytes, etc. Preferably, animal cell lines into which genes have been introduced can be used. More preferably, the feeder cells may be ARH77 cells, but are not limited thereto. Other feeder cells known to be commonly available in the technical field to which the present invention belongs can also be used without limitation as long as they meet the purpose of the present invention.
As used herein, the term “expression vector” is a vector capable of expressing a target protein or target RNA in a suitable host cell, and refers to a gene construct comprising essential regulatory elements operably linked to express the gene insert.
As used herein, the term “operably linked” refers to a functional linkage between a nucleic acid expression control sequence and a nucleic acid sequence encoding a desired protein or RNA to perform a general function. For example, a promoter and a nucleic acid sequence encoding a protein or RNA can be operably linked to affect expression of the encoding nucleic acid sequence. Operably linking with a recombinant expression vector can be achieved using genetic recombination techniques well known in the art, and site-specific DNA cleavage and ligation can be achieved using enzymes commonly known in the art.
Expression vectors that can be used in the present invention include, but are not limited to, plasmid vectors, cosmid vectors, bacteriophage vectors, viral vectors, and the like. Preferably, the vector may be a viral vector, and more preferably a lentiviral or retroviral vector, but is not limited thereto. In addition, suitable expression vectors can be prepared in various ways depending on the purpose, including a signal sequence or a leader sequence for membrane targeting or secretion, in addition to an expression control sequence such as a promoter, an operator, an initiation codon, a termination codon, a polyadenylation signal, and an enhancer. The promoter of an expression vector can be constitutive or inducible. In addition, the expression vector includes a selection marker for selecting host cells containing the vector, and, in the case of an expression vector capable of replication, includes an origin of replication.
As used herein, the term “peripheral blood mononuclear cell (PBMC)” refers to a cell with a spherical nucleus present in the blood. The peripheral blood mononuclear cells include immune cells such as B cells, T cells, macrophages, dendritic cells, and natural killer cells (NK cells).
“IL-2 (interleukin-2)” as used herein has been reported to have the function of enhancing the proliferation and activation of mature NK cells. There are reports that the number of NK cells is significantly reduced in humans and mice deficient in IL-2. On the other hand, there are also studies showing that IL-2 and IL-2Ra deficiency indirectly affects the number and activation of NK cells. The IL-2R chain is known to be involved in forming the IL-15 receptor.
Regarding “IL-15 (interleukin-15)” as used herein, it was found that NK cells were not found in mice deficient in IL-15 or IL-15Rα. In addition, it was found that NK cells were deficient in mice deficient in transcription factor interferon (IFN)-regulatory factor 1 that is required for IL-15 production. Accordingly, it is known that IL-15 is involved in NK cell differentiation and that IL-15 directly promotes the growth and differentiation of NK cells through the IL-15 receptor expressed on NK cells.
“IL-21 (interleukin-21)” as used herein is known to increase the telomere length of NK cells by stimulating transcription-3 (STAT-3) and to play an important role in the activation, growth, and amplification of NK cells. In particular, it has been reported that IL-21 helps the growth of NK cells in human CD34+ hematopoietic stem cells through combination with IL-15. It was confirmed that when NK cells are amplified through membrane-bound (mb) IL-21, the expression and cytotoxicity of interferon gamma (IFN-γ) are increased. In addition, it has been reported that a single initial injection of IL-21 is more effective in amplifying NK cells than continuous injection of IL-21 into the culture solution.
Hereinafter, the present invention will be described in more detail through the examples, but the following examples are for illustrative purposes only and are not intended to limit the scope of the present invention.
The genes for B7H6, CD137L, IL-15, and IL-15Rα were cloned, and then the cDNA of each gene was transferred to the pLVX-EF1α-IRES-Puro (Takara, Japan) plasmid, a lentivirus expression vector, to produce a lentivirus.
As shown in
In order to transduce each gene into feeder cells, ARH77 cells and K562 cells were dispensed at 2×105 cells per well in a 24 well plate, and then the recombinant lentivirus was added to each well along with polybrene (8 μg/mL). The mixture was centrifuged at 1,500 g for 2 hours at 25° C. and then cultured for 48 hours in an incubator at 37° C. and 5% CO2 conditions. Thereafter, the culture solution was removed, and culture was maintained while replacing with fresh culture solution (2 mL/well). One week after transduction, all cells were individually recovered, and then only fluorescence-positive cells were isolated using a cell sorting device, BD FACSAria™MIII, and these cells were continued to be cultured in RPMI1640 culture solution containing 10% FBS.
In the same manner as above, each gene was introduced into ARH77 cells and K562 cells in the order shown in
The nucleotide sequences of B7H6, CD137L, IL-15, and IL-15Rα are listed in Table 1 below.
In order to confirm the NK cell activation effect by B7H6 or CD137L expression, the expansion rate of NK cells was evaluated using K562 cells, B7H6 expressing K562 (K562-B7H6) cells, and CD137L expressing K562 (K562-CD137L) cells.
PBMCs were isolated from the peripheral blood of healthy blood donors using density gradient centrifugation and washed twice with PBS, and then 3×106 PBMCs were co-cultured with 5×105 respective feeder cells (K562 cells, K562-B7H6 cells, or K562-CD137L cells) irradiated with 100 Gy of gamma radiation in a 24 well plate with 2 mL/well of culture solution in an incubator at 37° C. and 5% CO2 conditions.
As a culture solution, RPMI1640 culture solution containing 10% fetal bovine serum (FBS), 100 U·mL penicillin, 100 μg/mL streptomycin, and 4 mmol/L L-glutamine was used. For one week from the start of culture, 10 U/mL recombinant human interleukin (rhIL)-2 and 5 ng/ml rhIL-21 were added to the culture solution, and after 1 week of culture, 100 U/mL rhIL-2 and 5 ng/mL rhIL-15 were added to the culture solution, and cultured for 28 days. The culture solution was replaced with new culture solution every 1 to 2 days.
On days 14, 21, and 28 of culture, the cultured cells were recovered, and the ratio (purity) of NK cells (CD3−, CD56+ cells) in the recovered cells was evaluated by flow cytometry. The total number of NK cells was calculated by multiplying the total number of viable cells among the recovered cells by the ratio of NK cells. The total number of NK cells in PBMCs prior to culture was calculated in the same manner. The expansion rate of NK cells was calculated by dividing the total number of NK cells on days 14, 21, and 28 of culture by the number of NK cells prior to culture, respectively.
The experimental results are shown in Tables 2 and 3 below and
As shown in Table 2 above and
In addition, as shown in Table 3 above and
Therefore, B7H6 expressing K562 (K562-B7H6) cells exhibited an expansion rate of 4 times or more compared to K562 cells, and CD137L expressing K562 (K562-CD137L) cells exhibited an expansion rate of 11 times or more, and thus, it can be seen that the cells have a more excellent NK cell expansion effect.
In order to confirm the NK cell activation effect by B7H6 or CD137L expression, the purity of NK cells was evaluated using K562 cells, B7H6 expressing K562 (K562-B7H6) cells, and CD137L expressing K562 (K562-CD137L) cells.
In the same manner as in Example 1-1 above, PBMCs were isolated and co-cultured with each feeder cell irradiated with radiation. PBMC prior to culture and each cell recovered on days 14, 21, and 28 of culture were stained with fluorescent-conjugated human CD3 and CD56 monoclonal antibodies, and then the purity of NK cells was evaluated by flow cytometry. The ratio of CD3− CD56+ NK cells in each cell was evaluated as the purity of NK cells.
The experimental results are shown in Tables 4 and 5 below and
As shown in Tables 4 and 5 above and
Therefore, it can be seen that both B7H6 expressing K562 (K562-B7H6) cells and CD137L expressing K562 (K562-CD137L) cells can proliferate NK cells with high purity.
In order to confirm the NK cell activation effect by B7H6 or CD137L expression, the cytotoxicity capability against cancer cells of NK cells that were proliferated using K562 cells, B7H6 expressing K562 (K562-B7H6) cells, and CD137L expressing K562 (K562-CD137L) cells was evaluated.
The killing ability of NK cells proliferated in the same manner as in Example 1-1 above against K562 cells was measured by a highly sensitive colorimetric assay using WST-8 (Biotool, USA). K562 cells (1×105 cells/100 μL of culture solution), which are cancer cells targeted by NK cells, were dispensed in a 96 well plate, and then 2.5×104 proliferated NK cells were added and mixed (effector:target ratio=0.25:1). Thereafter, the cells were centrifuged at 1,500 rpm for 3 minutes and cultured in an incubator at 37° C. and 5% CO2 conditions. After 3 hours of culture, 10 μL of WST-8 was added to each well and then cultured for another hour. Thereafter, the absorbance (A450) was measured using SpectraMax (Molecular Devices, USA) at a wavelength of 450 nm, and the ratio (%) of cancer cells killed by NK cells was calculated using the following calculation formula.
The experimental results are shown in Tables 6 and 7 below and
As shown in Tables 6 and 7 above and
Therefore, it can be seen that B7H6 expressing K562 (K562-B7H6) cells and CD137L expressing K562 (K562-CD137L) cells can proliferate NK cells exhibiting a higher level of cytotoxicity.
In order to confirm the NK cell activation effect by IL15Rα expression, the expansion rate of NK cells was evaluated using ARH77 cells and IL15Rα expressing ARH77 (ARH77-IL15Rα) cells.
The experiment was conducted in the same manner as in Example 1-1 above, and only IL-2 and IL-15 were added to the culture solution, and the cells were cultured and evaluated for 3 weeks. The experimental results are shown in Table 8 below and
As shown in Table 8 above and
Therefore, IL15Rα expressing ARH77 (ARH77-IL15Rα) cells exhibited an expansion rate of 1.5 times or more compared to ARH77 cells, and thus, it can be seen that the cells have a more excellent NK cell expansion effect.
In order to confirm the NK cell activation effect by IL15Rα expression, the purity of NK cells was evaluated using ARH77 cells and IL15Rα expressing ARH77 (ARH77-IL15Rα) cells.
The experiment was conducted in the same manner as in Example 1-2 above and evaluated for 3 weeks. The experimental results are shown in Table 9 below and
As shown in Table 9 above and
Therefore, it can be seen that NK cells obtained through IL15Rα expressing ARH77 (ARH77-IL15Rα) cells have higher purity, and IL15Rα expressing ARH77 (ARH77-IL15Rα) cells can proliferate NK cells with higher purity.
In order to confirm the NK cell activation effect by IL15Rα expression, the cytotoxicity capability against cancer cells of NK cells that were proliferated using ARH77 cells and IL15Rα expressing ARH77 (ARH77-IL15Rα) cells was evaluated.
The experiment was conducted in the same manner as in Example 1-3 above and evaluated for 3 weeks. The experimental results are shown in Table 10 below and
As shown in Table 10 above and
Therefore, it can be seen that IL15Rα expressing ARH77 (ARH77-IL15Rα) cells can proliferate NK cells exhibiting a higher level of cytotoxicity.
In order to confirm the NK cell stimulating effect of ARH77 cells, the expansion rate of NK cells was evaluated using ARH77 cells and K562 cells.
In the same manner as in Example 1-1 above, PBMCs were isolated and co-cultured with ARH77 cells or K562 cells irradiated with radiation. PBMC prior to culture and each cell recovered on days 14, 21, and 28 of culture were stained with fluorescent-conjugated human CD3 and CD56 monoclonal antibodies, and then the purity of NK cells (CD3− CD56+ cells) was evaluated by flow cytometry. The total number of NK cells was calculated by multiplying the total number of viable cells among the recovered cells by the ratio of NK cells. The total number of NK cells in PBMCs prior to culture was calculated in the same manner, and the expansion rate of NK cells was calculated by dividing the total number of NK cells on days 14, 21, and 28 of culture by the number of NK cells prior to culture, respectively.
The experimental results are shown in Table 11 below and
As shown in Table 11 above and
Therefore, it can be seen that ARH77 cells have a more excellent NK cell expansion effect by 2 times or more.
In order to confirm the NK cell stimulating effect of ARH77 cells, the purity of NK cells obtained using ARH77 cells and K562 cells was evaluated.
The purity was evaluated by measuring the ratio of CD3− CD56+ NK cells in the cell by flow cytometry in the same manner as in Example 1-2 above, and the experimental results are shown in Table 12 below and
As shown in Table 12 above and
Therefore, it can be seen that NK cells obtained through ARH77 cells have higher purity.
In order to confirm the NK cell stimulating effect of ARH77 cells, the cytotoxicity of NK cells obtained using ARH77 cells and K562 cells was evaluated.
In the same manner as in Example 1-3 above, the cytotoxicity capability against cancer cells of NK cells obtained using ARH77 cells or K562 cells was measured, and the experimental results are shown in Table 13 below and
As shown in Table 13 above and
Therefore, it can be seen that ARH77 cells can proliferate NK cells exhibiting a similar level of cytotoxicity to K562 cells.
In order to confirm the NK cell stimulating effect of ARH77 cells, the receptor expression of NK cells obtained using ARH77 cells and K562 cells was evaluated, and the results are shown in Tables 14 to 20 below and
As shown in Tables 14 to 20 above and
Therefore, it can be seen that ARH77 cells have a more excellent NK cell stimulating effect as feeder cells compared to K562 cells.
In order to confirm the NK cell stimulating effect by B7H6, CD137L, IL15, and IL15Rα expressing feeder cells, the following experiment was conducted by expressing each gene using ARH77 cells and K562 cells.
In order to confirm the NK cell stimulating effect by B7H6, CD137L, IL15, and IL15Rα expressing feeder cells, the expansion rate of NK cells was evaluated using ARH77 cells and K562 cells expressing the above genes.
In the same manner as in Example 1-1 above, PBMCs were isolated and co-cultured with each feeder cell irradiated with radiation. In PBMC prior to culture and each cell recovered on days 14, 21, and 28 of culture, the purity of NK cells (CD3− CD56+ cells) was evaluated by flow cytometry, and then the expansion rate of NK cells was calculated in the same manner as above.
The experimental results are shown in Table 21 below.
As shown in Table 21 above, it was confirmed that B7H6, CD137L, and IL-15 expressing ARH-77 (ARH77-B7H6-CD137L-IL15) cells, B7H6, CD137L, IL-15, and IL-15Rα expressing ARH77 (ARH77-B7H6-CD137L-IL15-IL15Rα) cells, and B7H6, CD137L, IL-15, and IL-15Rα expressing K562 (K562-B7H6-CD137L-IL15-IL15Rα) cells exhibit the most excellent expansion rate of NK cells at 3 weeks.
In order to confirm the NK cell stimulating effect by B7H6, CD137L, IL15, and IL15Rα expressing feeder cells, the purity of NK cells was evaluated using ARH77 cells and K562 cells expressing the above genes.
The purity was evaluated by measuring the ratio of CD3− CD56+ NK cells in the cell by flow cytometry in the same manner as in Example 1-2 above, and the experimental results are shown in Table 22 below.
As shown in Table 22 above, it was confirmed that NK cells obtained through B7H6, CD137L, and IL-15 expressing ARH-77 (ARH77-B7H6-CD137L-IL15) cells, B7H6, CD137L, IL-15, and IL-15Rα expressing ARH77 (ARH77-B7H6-CD137L-IL15-IL15Rα) cells, B7H6, CD137L, and IL-15 expressing K562 (K562-B7H6-CD137L-IL15) cell, and B7H6, CD137L, IL-15, and IL-15Rα expressing K562 (K562-B7H6-CD137L-IL15-IL15Rα) cells exhibit a purity of about 90% or more by the fourth week.
In order to confirm the NK cell stimulating effect by B7H6, CD137L, IL15, and IL15Rα expressing feeder cells, the cytotoxicity against cancer cells of NK cells that were proliferated using ARH77 cells and K562 cells expressing the above genes was evaluated.
In the same manner as in Example 1-3 above, the cytotoxicity capability against cancer cells of NK cells that were proliferated using each gene expressing feeder cell was measured, and the experimental results are shown in Table 23 below.
As shown in Table 23 above, it was confirmed that NK cells obtained through B7H6, CD137L, and IL-15 expressing ARH-77 (ARH77-B7H6-CD137L-IL15) cells, B7H6, CD137L, IL-15, and IL-15Rα expressing ARH77 (ARH77-B7H6-CD137L-IL15-IL15Rα) cells, and B7H6, CD137L, IL-15, and IL-15Rα expressing K562 (K562-B7H6-CD137L-IL15-IL15Rα) cells maintain toxicity by the fourth week, but NK cells using the remaining cells have reduced toxicity.
Therefore, it can be seen that B7H6, CD137L, and IL-15 expressing ARH-77 (ARH77-B7H6-CD137L-IL15) cells, B7H6, CD137L, IL-15, and IL-15Rα expressing ARH77 (ARH77-B7H6-CD137L-IL15-IL15Rα) cells, and B7H6, CD137L, IL-15, and IL-15Rα expressing K562 (K562-B7H6-CD137L-IL15-IL15Rα) cells have an excellent NK cell stimulating effect as feeder cells.
The following experiment was conducted using B7H6, CD137L, and IL-15 expressing ARH-77 (ARH77-B7H6-CD137L-IL15) cells, B7H6, CD137L, IL-15, and IL-15Rα expressing ARH77 (ARH77-B7H6-CD137L-IL15-IL15Rα) cells, and B7H6, CD137L, IL-15, and IL-15Rα expressing K562 (K562-B7H6-CD137L-IL15-IL15Rα) cells, which have an excellent NK cell stimulating effect as feeder cells in Example 3 above.
In order to confirm the NK cell stimulating effect by the three genetically modified feeder cells, the expansion rate of NK cells was evaluated using a medium optimized for NK cells.
In the same manner as in Example 1-1 above, PBMCs were isolated and co-cultured with each feeder cell irradiated with radiation. As a culture solution, DMEM culture solution containing 30% HAM'S F12, 10% human serum (HS), 10 μg/mL gentamicin, 1× Glutamax, 10 μM β-mercaptoethanol, 50 μM ethanolamine, 20 μg/mL ascorbioc acid, and 5 ng/mL sodium selenite was used. For one week from the start of culture, 10 U/mL recombinant human interleukin (rhIL)-2 and 5 ng/mL rhIL-21 were added to the culture solution, and after 1 week of culture, 100 U/mL rhIL-2 and 5 ng/mL rhIL-15 were added to the culture solution, and cultured for 28 days.
The culture solution was replaced with new culture solution every 1 to 2 days. On days 14, 21, and 28 of culture, the cultured cells were recovered, and the ratio (purity) of NK cells (CD3−, CD56+ cells) in the recovered cells was evaluated by flow cytometry. The total number of NK cells was calculated by multiplying the total number of viable cells among the recovered cells by the ratio of NK cells.
The total number of NK cells in PBMCs prior to culture was calculated in the same manner, and the expansion rate of NK cells was calculated by dividing the total number of NK cells on days 14, 21, and 28 of culture by the number of NK cells prior to culture, respectively.
The experimental results are shown in Table 24 below and
As shown in Table 24 above and
Specifically, it was confirmed that NK cells obtained through B7H6, CD137L, IL-15, and IL-15Rα expressing ARH77 (ARH77-B7H6-CD137L-IL15-IL15Rα) cells have an expansion rate by about 3.5 times higher compared to NK cells obtained through B7H6, CD137L, IL-15, and IL-15Rα expressing K562 (K562-B7H6-CD137L-IL15-IL15Rα) cells after 4 weeks of culture.
In order to confirm the NK cell stimulating effect by the three genetically modified feeder cells of Example 4-1 above, the purity of NK cells was evaluated using a medium optimized for NK cells.
The purity was evaluated by measuring the ratio of CD3− CD56+ NK cells in the cell by flow cytometry in the same manner as in Example 1-2 above, and the experimental results are shown in Table 25 below and
As shown in Table 25 above and
In order to confirm the NK cell stimulating effect by the three genetically modified feeder cells, the cytotoxicity of NK cells was evaluated using a medium optimized for NK cells.
The cytotoxicity against cancer cells of NK cells that were proliferated using each gene expressing feeder cell was measured in the same manner as in Example 1-3 above, and the experimental results are shown in Table 26 below and
As shown in Table 26 above and
Ultimately, from the above experimental results, it can be seen that B7H6, CD137L, IL-15, and IL-15Rα expressing ARH77 (ARH77-B7H6-CD137L-IL15-IL15Rα) cells have the most excellent NK cell stimulating effect as feeder cells.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2021-0070778 | Jun 2021 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2022/007782 | 5/31/2022 | WO |
