Patent Application
20240366673
The present invention relates to a method for treating cells for administration to humans, such as highly active NK cells.
NK cells are important in injuring tumor cells and virus-infected cells. In August 2017, chimeric antigen receptor (CAR) T-cell therapy was approved in the United States for the treatment of relapsed and refractory B-cell acute lymphoblastic leukemia (B-ALL) in children and young adults, and in recent years, clinical application of CAR-NK has been expanding in place of CAR-T (see Non-patent document 1).
When attempting to administer cells to a patient, the first consideration is to use cells harvested from the patient himself/herself to avoid rejection. However, depending on the patient's condition, it may be difficult to collect the necessary amount of cells for treatment. In addition, the degree to which cells can be activated and proliferated in vitro varies among individuals, and there are also cases in which proliferation and activation are difficult. In addition, it takes a certain period of time for cells to be activated and proliferated, posing a problem that it is difficult to start treatment immediately. In this respect, it would be desirable if cells could be activated in advance and stored for preparation of administration.
As a method for preserving cells, it is known to preserve cells in suspension without freezing for short-time preservation (e.g., Patent document 1), and to freeze cells for long time preservation (e.g., Patent document 2). Furthermore, use of a solution for freezing containing a sodium salt, potassium salt, sugar, cryoprotectant, and hydrogencarbonate and/or carbonate has been investigated, since use of such a solution may provide cells that maintain high viability even after freeze-thawing (Patent document 3).
Also known is a method for preserving cells that are difficult to preserve, such as NK cells, in which the cells are stored in a solution containing a sodium salt, potassium salt, sugar, and protein as active ingredients (Patent document 4). Further, a cell preservation solution for refrigerated preservation containing potassium ions and lactate ions, and having an osmolarity of 200 to 350 mOsm/kg and pH of 6.0 to 8.0 is known (Patent document 5), and this preservation solution contains 0.5 to 150 mM of sugars and 1 to 4 mM of calcium ions. Furthermore, there is also known a cell or tissue preservation solution having an osmolarity of 270 to 450 mOsm/l and pH of 7 to 8, and containing K+ and organic acid anions (Patent document 6). In this reference, lactic acid is exemplified as the organic acid. Furthermore, it is known to use a physiological aqueous solution as a solution for suspending mammalian cells such as NK cells, and it is known that isotonic (250 to 380 mOsm/l) aqueous solutions such as Ringer's solution (lactated Ringer's solution) can be used as the physiological aqueous solution (Patent document 7). In an example of this reference, a lactated Ringer's solution (“Lactec Injection” produced by Otsuka Pharmaceutical Factory) is used (paragraph 0038), which contains potassium and lactic acid, has a pH of 6.0 to 7.5, and does not contain glucose.
However, conventional freezing methods using protective agents such as dimethyl sulfoxide can preserve T-cell lines and primary NK cells, but are not sufficient for NK cells with high cytotoxic activity, whose activity and viability are significantly reduced by freeze-thaw operations. This problem could not be solved by use of a programmed freezer, cell density control, addition of dextran, albumin, carboxylated poly-L-lysine, etc. In addition, if cells for administration are packaged on the assumption that a certain amount of the cells will die, a step for reactivation culture is required after thawing, and the resulting cells must be further washed. Therefore, frozen and stocked highly active NK cells currently require use of facilities for cell culture and processing that meet certain criteria for handling cells for clinical use (Cell Processing Center, CPC).
By the way, the inventors of the present invention have studied methods for freezing and thawing highly active NK cells (Patent document 8). In these studies, it was found that even if viability of thawed cells is maintained high, high cytotoxic activity may not be maintained. It was also suggested that if thawed cells maintain high cytotoxic activity, viability may also be high, and it was found that high cytotoxic activity evaluated by a given method is a useful evaluation criterion for thawed cells.
An object of the present invention is to provide a thawing method effective for highly active cells. More specifically, it is to provide a method for thawing frozen highly active NK cells so that the cells maintain a cytotoxic activity of 60% or higher, preferably 80% or higher, as evaluated by a given method.
The inventors of the present invention found that composition of a solution used for dilution at the time of thawing frozen cells is particularly important. They also found that the composition of the solution used for such dilution can consist of only the ingredients used in infusion solutions etc. approved under the Act on Securing Quality, Efficacy and Safety of Products Including Pharmaceuticals and Medical Devices (Act No. 145 of 1960) in Japan, and accomplished the present invention.
The present invention provides the followings.
The present invention also provides the followings.
Albumin/K.C.L./physiological saline/Amizet/water/MEYLON, and (5) Pasma-Lyte A as a positive control, all of which were prepared so as to have an osmolarity of 300 mOsm. The solution of (2) showed a good activity-maintaining ability, and the solutions of (1) and (3) showed markedly good results.
In the explanations of the present invention, mM is used with the same meaning as mmol/L, unless especially noted. When a numerical range is expressed as x to y, the range includes the values x and y at both ends.
The present invention relates to a method for thawing or unfreezing frozen cells for administration to humans. For the present invention, thawing or unfreezing means a thawing frozen material, except as otherwise noted. During thawing or unfreezing, a solution may be added to dilute frozen material.
The present invention can be applied to a variety of cells. One class of the cells to which the present invention can be preferably applied are cells to be administered to humans, preferably cells to be administered to humans that have undergone an activation operation by using some cytokine in vitro, such as NK cells with high cytotoxic activity (highly active NK cells). The activation operation is typically based on incubating the cells with a medium containing interleukin (IL)-2. In the following descriptions, the present invention may be explained by exemplifying cases of applying it to NK cells or highly active NK cells, but those skilled in the art can also appropriately understand the application of the present invention to other types of cells on the basis of such explanations.
In general, NK cells are large granular lymphocytes that are not expressing the T cell receptor (TCR), the universal T cell marker, CD3, and the membrane immunoglobulin, B cell receptor, and they are usually CD16-positive and CD56-positive in humans. Whether or not cells are NK cells can be easily determined by those skilled in the art on the basis of expression patterns of cell surface markers, and so forth. NK cells have cytotoxic activity, and the presence or absence and degree of cytotoxic activity can be measured by various known methods. NK cells can include peripheral blood NK cells, cord blood NK cells, primary NK cells, cultured NK cells, and highly active NK cells.
Raw material of highly active NK cells and so forth to which the present invention can be preferably applied may be peripheral blood, cord blood, bone marrow and/or lymph nodes, and blood collected by apheresis method (apheresis blood). The raw material may also be those prepared from at least one kind of cells selected from hematopoietic stem cells derived from any stem cells selected from the group consisting of embryonic stem cells, somatic stem cells, and induced pluripotent stem (iPS) cells, hematopoietic stem cells derived from cord blood, hematopoietic stem cells derived from peripheral blood, hematopoietic stem cells derived from bone marrow blood, cord blood mononuclear cells, and peripheral blood mononuclear cells. The donor of the raw material may be a patient himself/herself who will receive an immunotherapy using highly active NK cells or the like, a close relative of the patient, or a healthy person genetically unrelated to the patient. The donor may consist of a plurality of donors.
Examples of the culture medium used for culturing highly active NK cells and so forth include the KBM501 medium (Kojin Bio, containing 1,750 JRU/mL of IL-2), Cosmedium 008 (Cosmo Bio, containing 1,750 JRU/mL of IL-2), FKCM101 (Fukoku, containing no IL-2 or 175 IU/mL of IL-2), CellGro SCGM medium (CellGenix, Iwai Chemical), X-VIVO15 medium (Lonza, Takara Bio), Gibco (registered trademark) CTS (registered trademark) AIM V (registered trademark) Medium (Thermo Fisher Scientific, serum-free medium of known composition for growth and manipulation of T cells and dendritic cells), CTS OpTmizer T Cell Expansion Basal Medium (Thermo Fisher Scientific, for growth and proliferation of human T lymphocytes), IMDM, MEM, DMEM, RPMI 1640, and so forth, but not limited to these. Preferred examples are the KBM501 medium, FKCM101, and Cosmedium 008. For the present invention, the expression that culture of cells (cells are cultured) means to maintain cells in a medium or a similar solution for a certain period of time for any purpose selected from the group consisting of maintaining cell viability, amplifying cells, and activating cells, unless especially stated. To carry out a treatment at a specific temperature for a certain period of time may be sometimes referred to as incubation (to incubate).
IL-2 may be added to the medium at such a concentration that the purpose of the invention can be achieved. The concentration of IL-2 may range from 2500 to 2813 IU/mL. IL-2 should preferably have a human amino acid sequence thereof, and be produced by a recombinant DNA technique for safety reasons. IL-2 concentration may be expressed in the national standard unit (Japan Reference Unit, JRU) and international unit (IU). 1 IU is approximately 0.622 JRU, and therefore 1,750 JRU/mL of the existing media is equivalent to approximately 2813 IU/mL.
Together with or instead of IL-2 described above, one selected from the group consisting of IL-12, IL-15, and IL-18 may be added at such a concentration that the purpose of the present invention can be achieved (Non-patent document 2, Leong JW et al., Biol. Blood Marrow Transplant, 20 (2014) 463-473). The concentration of each may be 1 pg/mL to 1 μg/mL irrespective of presence or absence or concentration of other cytokines. IL-2 preferably has a human amino acid sequence thereof, and be produced by recombinant DNA technique for safety reasons.
The medium may be supplemented with the subject's autologous serum, human type AB serum available from Bio Whittaker and others, or donated blood human serum albumin available from the Japanese Red Cross Society. Autologous serum and human AB serum are preferably added at a concentration of 1 to 10%, and donated blood human serum albumin is preferably added at a concentration of 1 to 10%. Human platelet lysate (HPL) may be added together with or instead of serum. HPL is commercially available, and those of the UltraGRO™ series (AventaCell BioMedical), and so forth are commercially available. Sodium heparin may be further added to the medium, when HPL is used.
The medium may contain appropriate proteins, cytokines, antibodies, compounds, and other components, on condition that they do not impair the effectiveness of the NK cell culture. Cytokines may be IL-2, IL-12, IL-15, and IL-18 described above, as well as IL-3, IL-7, IL-21, stem cell factor (SCF), and/or FMS-like tyrosine kinase 3 ligand (Flt3L). All of these should preferably have human amino acid sequences thereof, and be produced by recombinant DNA technique for safety reasons.
The medium should preferably be a serum-free medium. The serum-free medium should preferably contain serum albumin, transferrin, and insulin. Serum-free media for culturing lymphocytes have been developed, and are commercially available, and they can be used for the present invention. One preferred example of serum-free medium is a basic medium supplemented with CTS Immune Cell SR (Thermo Fisher Scientific), which is commercially available as a composition that supports the proliferation of human T cells.
The medium may be replaced or replenished at any time after the start of culture, on condition that the desired culture effect is obtained, but the medium is preferably replaced or replenished every 3 to 5 days.
Culture vessels used for the culture include, but are not limited to, commercially available dishes, flasks, plates, and multi-well plates. Culture conditions are not particularly limited, so long as the culture effect of NK cells is not impaired, but culture conditions of 37° C., 5% CO2, and saturated water vapor atmosphere are generally used. Culture period is not particularly limited, on condition that the desired culture effect is obtained.
Highly active NK cells, and so forth to which the present invention can be preferably applied include the following [1], [2], [3] and [4].
The highly active NK cells of [1] may show high CD16 expression. The highly active NK cells of [1] may also have the following characteristics, regardless of whether or not they show high CD16 expression;
The highly active NK cells of [1] can also be expressed as follows:
NK cells obtained by eliminating CD3-positive cells from peripheral blood mononuclear cells derived from a healthy human using CD3 beads (e.g., CliniMACS CD3, Miltenyi Biotech, catalog no. 130-017-601), LD column (e.g., Miltenyi Biotech, catalog no. 130-042-901), and a separation buffer (e.g., PBS containing 0.5% human AB serum (inactivated), and 2 mM EDTA), and culturing the obtained cell population for 14 days in an appropriate medium (e.g., Cosmedium 008 supplemented with 5% human AB serum (inactivated)), and having the following characteristics (1) and (3):
For details of the characteristics, and more specific production methods of the highly active NK cells of [1], Japanese Patent Publication (Kokai) No. 2018-193303 can be referred to.
The cells of [2] may also show high CD11c expression.
The cells of [2] can also be expressed as follows
CCR5-positive, CCR6-positive, CXCR3-positive, integrin α1-positive, integrin α3-positive, integrin β3-negative, and CD3-negative cells. Alternatively, CCR5-positive, CCR6-positive, CXCR3-positive, highly CD11a-expressing, highly CD11c-expressing, and CD3-negative cells, of which high expressions are determined by comparison with the expressions in a population of NK cells obtained from peripheral blood that have not been substantially cultured.
According to the studies of the inventors of the present invention, the cells of [2] show extremely high cytotoxic activity against solid tumors forming tumor masses. For details of the characteristics, and more specific production methods of the highly active NK cells of [2], Japanese Patent Publication (Kokai) No. 2019-170176 can be referred to.
For the specific production method of the highly active NK cells of [3], the section of Examples in this description can be referred to.
In the following explanations, the present invention may be explained with reference to the case of using highly active NK cells as an example, but those skilled in the art can also understand other cases using cells subjected to an in vitro activation operation using some cytokine in accordance with the explanations.
For the present invention, the term activity or cytotoxic activity used for highly active NK cells, and so forth refers to an ability of subject cells (effector cells, E) to lyse target cells (T), unless especially stated. Cytotoxic activity can be expressed as the percentage of target cells killed by effector cells, and is calculated in accordance with the following equation.
(Cell death observed in co-culture with effector cells−Spontaneous cell death (negative control))/(Maximum cell death (positive control)−Spontaneous cell death (negative control))×100
When cytotoxic activity is measured, in general, the mixing ratio of the effector cells to the target cells (E:T) and the time of co-culture of effector cells and target cells can be appropriately determined according to the degree of cytotoxic activity of the effector cells, etc., and depending on the types and the intensity of the activity of cells to be used. When NK cells are used as the effector cells, target cells may be, but are not limited to, K562 cells, acute myeloid leukemia cells, and chronic myeloid leukemia cells. The effector cells and target cells, and live cells and dead cells can be distinguished and quantified by using reagents such as antibodies labeled with a radioactive substance, fluorescent dye, or the like. When NK cells are used as the effector cells, the cytotoxic activity can be measured by using K562 cells as the target cells with the conditions of, for example, E:T of 1:0.05 to 10, preferably 1:0.1 to 5, and an incubation time of 0.5 to 18 hours, preferably 1 to 12 hours.
For the present invention, the expression that the activity of NK cells or the like is high means that the cytotoxic activity is 50% or higher when the target cells are K562 cells, and the cells are mixed at E:T of 2:1 and co-cultured for 1 to 3 hours, more specifically 2 hours, unless especially stated. The activity should be preferably 60% or higher, more preferably 70% or higher.
According to the present invention, prior to the freezing step described later, highly active NK cells or the like to be frozen are collected from the culture system. Collection can be performed by centrifuging the culture to separate the cells from the culture medium. If necessary, EDTA may be added at an appropriate concentration to the culture system to detach adhered cells from the surface of the culture vessel. The surface of the culture vessel may also be washed with an appropriate solution after the cells were detached to further obtain remaining cells. The obtained cells are washed with an appropriate solution and suspended in an appropriate solution, if necessary.
In the collection step, solutions such as culture medium, isotonic solution, and buffer may be used to detach and wash the cells. Examples of usable media include KBM501 medium, Cosmedium 008, FKCM101, CellGro SCGM medium, X-VIVO15 medium, Gibco (registered trademark) CTS (registered trademark) AIM V (registered trademark) Medium, CTS OpTmizer T Cell Expansion Basal Medium, IMDM, MEM, DMEM, and RPMI 1640. Isotonic solution refers to a solution with an osmolarity approximately equal to the osmolarity of body fluid (plasma) (285±5 mOsm/L), and for the present invention, a solution with an osmolarity of 285±13 mOsm/L. For example, the osmolality of Plasma-Lyte A is 294 mOsm/L, and that of PBS(−) is 280±4 mOsm/L (freezing point depression method). Examples of usable isotonic solutions include Plasma-Lyte A (Baxter), saline (physiological saline), Ringer's solution (lactated Ringer's solution, acetated Ringer's solution, hydrogencarbonated Ringer's solution, etc.) and 5% glucose aqueous solution. Examples of buffers that can be used include phosphate-buffered saline (PBS), Tris-hydrochloric acid buffer, Tris-acetic acid buffer, and HEPES buffer.
One of the preferred examples of the solution used in the collection step is a culture medium, more preferably a culture medium for human lymphocytes. The culture medium for human lymphocytes may contain human serum albumin, human transferrin, recombinant human insulin, and recombinant human IL-2. Preferred examples of such a medium are KBM501 medium, FKCM101, and Cosmedium 008. The KBM501 medium contains human serum albumin, human transferrin, recombinant human insulin, and recombinant human IL-2, but no other proteins. The KBM501 medium also contains antibiotics (kanamycin), NaHCO3, L-glutamine, and pH adjuster.
In the collection step, use of PBS(−) may be undesirable, because it may reduce cell viability after thawing. PBS(−) typically contains 136.9 mM sodium chloride, 2.68 mM potassium chloride, 8.1 mM disodium hydrogenphosphate, and 1.47 mM potassium dihydrogenphosphate.
For the present invention, prior to the freezing step described later, the highly active NK cells or the like to be frozen may be subjected to a pretreatment. The pretreatment means suspending the collected cells in a solution containing an additive. The pretreatment includes collecting the cells with a solution containing an additive.
The additive used for the pretreatment can be one selected from the group consisting of a bile acid and phenylbutyric acid. Examples of bile acid are tauroursodeoxycholic acid (TUDCA), ursodeoxycholic acid (UDCA), kenodeoxycholic acid, cholic acid, hyodeoxycholic acid, deoxycholic acid, 7-oxolithocholic acid, lithocholic acid, iododeoxycholic acid, iocholic acid, taurokenodeoxycholic acid, taurodeoxycholic acid, glycoursodeoxycholic acid, taurocholic acid, glycocholic acid, and analogues and derivatives thereof. Examples of phenylbutyric acid are 4-phenylbutyric acid (4-PBA), glyceryl tri-(4-PBA), phenylacetic acid, 2-POAA-OMe, 2-POAA-NO2, 2-NOAA, pharmaceutically acceptable salts, analogues, derivatives and prodrugs thereof. Particularly preferred examples of the additive used for the pretreatment are any selected from the group consisting of TUDCA and 4-PBA.
When a bile acid is used as the additive for the pretreatment, the concentration thereof may be appropriately determined, but it is preferably 100 to 5000 μM, more preferably 200 to 2500 μM, further preferably 400 to 1000 μM. A concentration in such a range is particularly suitable when TUDCA is used. When a phenylbutyric acid is used as the additive for the pretreatment, the concentration thereof may be appropriately determined, but it is preferably 1 to 1000 μM, more preferably 5 to 500 μM, even more preferably 10 to 100 μM. A concentration in such a range is particularly suitable when 4-PBA is used.
Another example of the additive for the pretreatment is dimethyl sulfoxide (DMSO). The concentration thereof may be appropriately determined, but it is preferably 0.5 to 15%, more preferably 1 to 12.5%, further preferably 2 to 10%.
The solution for the pretreatment can be a solution such as medium, isotonic solution, and buffer, like the solution used for the collection. One preferred example of the solution used in the pretreatment is a culture medium, more preferably a medium for culture of human lymphocyte, further preferably KBM501 medium, FKCM101 or Cosmedium 008. The medium used for the pretreatment may also contain human serum albumin, human transferrin, recombinant human insulin, and recombinant human IL-2, and may contain antibiotics (kanamycin), NaHCO3, L-glutamine, and pH adjuster.
The time for the pretreatment is not particularly limited. After the cells are suspended for the pretreatment, the suspension may be allowed to stand for several minutes to several hours, for example, 5 minutes to 4 hours, more preferably 30 minutes to 3 hours. The suspension may be allowed to stand at ambient temperature (e.g., 1 to 30° C., typically 15 to 25° C.), and may be allowed to stand in a CO2 incubator (e.g., 36 to 42° C., typically 37° C.).
The cell density during the pretreatment may be appropriately determined, but should be a cell density suitable for cell maintenance. Specifically, the cell density is 1×105 to 1×107 cells/mL, preferably 2×105 to 5×106 cells/mL, more preferably 5×105 to 2×106 cells/mL.
In a particularly preferred embodiment, the pretreatment consists of suspending the cells in the KBM501 medium, FKCM101 or Cosmedium 008 supplemented with 400 to 1000 μM TUDCA or 10 to 100 μM 4-PBA at a cell density of 5×105 to 2×106 cells/mL. For this treatment, the cells are preferably incubated at 37° C. and 5% CO2 for 30 minutes to 3 hours.
Although the pretreatment is not essential for the present invention, the pretreatment of highly active NK cells or the like with the KBM501 medium supplemented with 4-PBA or TUDCA before freezing can improve the viability (also called recovery rate) after the cells are thawed compared with the case of not performing the pretreatment.
According to the present invention, the collected and preferably pretreated cells are frozen by normal procedures. Specifically, the cell count and viability are checked as required, the supernatant is removed by centrifugation, and then the cells are suspended in a cryopreservation solution at an appropriate cell density. After dispensing the cell suspension into cryopreservation containers, it is frozen in a deep freezer at −80° C., and stored. If necessary, it is cryopreserved in a liquid nitrogen tank.
Cryopreservation solutions that can be used in the present invention can contain a sodium salt, potassium salt, sugar, hydrogencarbonate, carbonate, and cryoprotectant.
Sodium salts that can be used are not particularly limited so long as a sodium salt that produces sodium ion when it is dissolved in a solvent is used, and it can be an oxoacid salt, halide, oxide, hydroxide, inorganic salt, organic acid salt, or the like. One kind or a combination of two or more kinds of sodium salts may be used. For the present invention, sodium chloride is preferably used when one kind of salt is used, and sodium chloride and sodium citrate are preferably used when multiple kinds of salts are used. The sodium salt content is not particularly limited, but is preferably 0.01 to 5000 mM, more preferably 0.1 to 1000 mM, further preferably 1 to 300 mM, as the final concentration of total sodium ions contained in the cryopreservation solution.
Potassium salts that can be used are not particularly limited so long as a potassium salt that produces potassium ions when it is dissolved in a solvent is used, and it can be an oxoacid salt, halide, oxide, hydroxide, inorganic salt, organic acid salt, or the like. One kind of potassium salt may be used, or two or more kinds of potassium salts may be used in combination. Potassium chloride is preferably used in the present invention. The potassium salt content is not particularly limited, but as a final concentration of total potassium ions contained in the cryopreservation solution, it is preferably 0.01 to 5000 mM, more preferably 0.1 to 1000 mM, further preferably 1 to 100 mM.
Hydrogencarbonates that can be used are not particularly limited so long as a hydrogencarbonate that produces hydrogencarbonate ions when it is dissolved in a solvent is used, and salts with various cations can be used. Examples include, for example, ammonium hydrogencarbonate, potassium hydrogencarbonate, calcium hydrogencarbonate, sodium hydrogencarbonate, magnesium hydrogencarbonate, and so forth. Carbonates that can be used are not particularly limited so long as a carbonate that produces carbonate ions when it is dissolved in a solvent is used, and salts with a variety of cations can be used. Examples include ammonium carbonate, potassium carbonate, calcium carbonate, sodium carbonate, barium carbonate, magnesium carbonate, and so forth. One kind of these hydrogencarbonates and/or carbonates may be used, or two or more kinds of them may be used in combination. Sodium hydrogencarbonate is preferably used in the present invention. The content of hydrogencarbonate and/or carbonate is not particularly limited, but it is preferably 0.01 to 1000 mM, more preferably 0.1 to 500 mM, further preferably 1 to 100 mM, as the final concentration of total hydrogencarbonate and carbonate ions contained in the cryopreservation solution.
The concentration ratio of sodium ions to potassium ions (sodium ions/potassium ions) in the cryopreservation solution is preferably 1/1000 to 1000/1, more preferably 1/100 to 100/1, further preferably 1/10 to 100/1, further preferably 1/1 to 100/1, further preferably 10/1 to 50/1.
Usable sugars include monosaccharides, oligosaccharides, and sugar alcohols, such as glucose, galactose, fructose, mannose, xylose, arabinose as monosaccharides, trehalose, sucrose, maltose, lactose, cellobiose as oligosaccharides, xylitol, and sorbitol as sugar alcohols. One kind or a combination of two or more kinds of these sugars may be used. For the present invention, the sugar preferably consists of at least one kind of sugar selected from the group consisting of glucose, galactose, fructose, mannose, xylose, and arabinose, more preferably glucose. The content of the sugar in the cryopreservation solution is preferably 0.01 to 100 g/L, more preferably 0.1 to 100 g/L, further preferably 0.25 to 50 g/L.
Examples of usable cryoprotectants include dimethyl sulfoxide (DMSO), hydroxyethyl starch (HES), ethylene glycol, glycerol, and so forth. One kind or a combination of two or more kinds of cryoprotectants may be used. For the present invention, any selected from the group consisting of DMSO and hydroxyethyl starch is preferably used. When DMSO and hydroxyethyl starch are used together as the cryoprotectants, it is preferred that the total content thereof should be in the aforementioned range, and as for the respective concentrations, DMSO concentration is preferably 0.01 to 50%, more preferably 1 to 30%, further preferably 2 to 15%, and hydroxyethyl starch concentration is preferably 0.01 to 50%, more preferably 1 to 30%, further preferably 2 to 15%.
In a preferred embodiment of the present invention, in addition to the essential ingredients of the solution used in the method for cryopreservation of cells described above, the solution may further contain ingredients selected from the group consisting of proteins, magnesium salts and calcium salts. Proteins that can be used include, specifically, serum albumin, serum globulin, and so forth. Serum albumin includes human serum albumin, and bovine serum albumin. For the present invention, human serum albumin is preferred. The protein content in the cryopreservation solution is preferably 0.01 to 50%, more preferably 1 to 30%, further preferably 2 to 15%. Magnesium salts that can be used are not particularly limited so long as a magnesium salt that produces magnesium ions when it is dissolved in a solvent is used, and an oxoacid salt, halide, oxide, hydroxide, inorganic salt, organic acid salt, and so forth can be used. One kind of magnesium salt may be used, or two or more kinds of magnesium salts may be used in combination. Magnesium chloride is preferably used in the present invention. The magnesium salt content of the cryopreservation solution is not particularly limited, but it is preferably 0.01 to 10 mM, more preferably 0.1 to 5 mM, as the final concentration of total magnesium ions in the cryopreservation solution. Calcium salts that can be used are not particularly limited so long as a calcium salt that produces calcium ions when it is dissolved in a solvent is used, and an oxoacid salt, halide, oxide, hydroxide, inorganic salt, organic acid salt, or the like can be used. One kind of calcium salt may be used, or two more kinds of calcium salts may be used in combination. Calcium chloride is preferably used in the present invention. The calcium salt content of the cryopreservation solution is not particularly limited, but is preferably 0.01 to 10 mM, more preferably 0.1 to 5 mM, as the final concentration of total calcium ions in the cryopreservation solution. In addition to the above ingredients, the cryopreservation solution may also contain additional substances that are not injurious to cells, for example, vitamins, amino acids, and so forth. In addition to the above ingredients, the cryopreservation solution may also contain phosphate ions from the viewpoint of pH adjustment and buffering.
The osmolarity of the cryopreservation solution should be within such a range that the cells are not damaged during freezing. The osmolarity is, for example, 500 o 8000 mOsm/L, and may be 1000 to 7500 mOsm/L, 1500 to 7000 mOsm/L, or 1800 to 5000 mOsm/L, from the viewpoints of increasing the penetration of the ingredients into cells during freezing, and inhibition of ice crystal formation. The pH of the cryopreservation solution should be in such a range that the cells are not damaged, for example, 3.0 to 10.0, more preferably 4.5 to 9.0.
For the present invention, commercially available cryopreservation solutions may be used. Examples of products that can be used include the cryopreservation solutions for cells and tissues of the CellBanker series (STEM-CELLBANKER (registered trademark)), more specifically, STEM-CELLBANKER (ZENOAQ, CB045).
The cells are preferably in the logarithmic growth phase at the time of freezing.
The cell density at the time of freezing can be appropriately determined, but it is specifically 1×106 to 2×108 cells/mL, preferably 2×106 to 1×108 cells/mL, more preferably 1×107 to 5×107 cells/mL. In one of the preferred embodiments, the cells are stored at a cell density of 4×107 cells/mL in a 5-mL volume container. The characteristic of the highly active NK cells that they can be frozen at a high density at the time of freezing for shipping allows to make the product more compact, and contributes to lower shipping costs.
In the present invention, cryopreserved cells can be thawed by various procedures. For example, such cells can be quickly thawed by incubating the cryopreservation container containing the cells in a warm bath at 37° C. or the like, with shaking the container as required. Alternatively, cryopreserved cells can be spontaneously thawed by leaving them at room temperature without any active heating after they are taken out from the freezer. At the time of or after thawing, the thawing cell cryoproduct can be diluted with an appropriate solution.
The present invention provides a solution for suspending cells for administration to humans, more specifically, a solution for diluting a cell cryoproduct, which satisfies the following criteria:
For the present invention, the expression that a solution does not contain a certain ingredient means that the ingredient is not detected by ordinary measurement methods, unless otherwise stated.
The concentration of potassium ions in the solution for dilution is preferably 0.50 to 8.0 mM, more preferably 1.0 to 7.0 mM, further preferably 2.5 to 6.0 mM. Alternatively, it is preferred that the solution contains 0.496 to 5.96 mM potassium chloride.
In one preferred embodiment, the concentration of potassium ions in the solution for dilution is 4.0 mEq/L or higher. The maximum concentration is not particularly limited, but is, for example, 18.0 mEq/L or lower, preferably 15.0 mEq/L or lower, more preferably 10.0 mEq/L or lower, further preferably 7.50 mEq/L or lower.
In another preferred embodiment, the solution for dilution does not contain calcium ions, irrespective of the presence or absence of the other ingredients and concentrations thereof. In another preferred embodiment, the solution for dilution does not contain glucose, irrespective of the presence or absence of the other ingredients and concentrations thereof. In further another preferred embodiment, pH of the solution for dilution is 7.0 to 8.3, preferably 7.2 to 8.1, more preferably 7.3 to 7.9.
The ions contained in the solution for dilution may be derived from salts that can be used as pharmaceuticals. Such salts may be carbonates, hydrogencarbonates, oxoates, halides, oxides, hydroxides, inorganic salts or organic acid salts. One type of salt or a combination of two or more types of salts may be used.
The solution for dilution may contain a sodium salt, gluconate, and acetate. It may also contain a magnesium salt. The concentration of sodium ions in the solution for dilution is preferably 14.0 to 200 mM, more preferably 28.0 to 182 mM, further preferably 70.0 to 168 mM. Or the solution for dilution preferably contains 9.00 to 108 mM sodium chloride, 2.0 to 27.7 mM sodium gluconate, and 2.7 to 32.5 mM sodium acetate. The concentration of gluconate ions in the solution for dilution is preferably 2.3 to 32.3 mM, more preferably 4.6 to 29.9 mM, further preferably 12.5 to 27.7 mM. The concentration of acetate ions in the solution for dilution is preferably 2.7 to 37.8 mM, more preferably 5.4 to 35.1 mM, further preferably 13.5 to 32.5 mM.
The solution for dilution can be constituted by approved pharmaceuticals. Examples of such pharmaceuticals are listed below.
One particularly preferred embodiment of the solution for dilution is the followings.
Another preferred composition consists of the followings.
Another preferred composition consists of the followings.
Cells suspended along with the solution for cryopreservation in the solution for dilution can be used as they are for administration. From the viewpoint of use for administration, it is preferred that the mixture of the cryopreservation solution and the solution for dilution should be isotonic (i.e., it has an osmolarity approximately equal to that of body fluid, specifically 285±13 mOsm/L). Since the solution for cryopreservation is a hypertonic solution (e.g., 1500 to 7000 mOsm/L) in a preferred embodiment, the solution for dilution may be a low osmotic solution. Those skilled in the art can appropriately determine concentrations of the ingredients of the solution for dilution in consideration of the magnitude of dilution of the solution for cryopreservation with the solution for dilution.
In any composition of the solution for dilution, it is preferred that the solution for dilution does not contain serum at a concentration of 40% or higher, and it is more preferred that it does not contain serum at all. This is because if the solution for dilution contains serum, cell viability may be reduced.
Although the density of the cells suspended in the solution for dilution can be optionally chosen, it may be a cell density suitable for maintenance of the cells or cell density suitable for administration. Specifically, it is 1×105 to 1×107 cells/mL, preferably 2×105 to 5×106 cells/mL, more preferably 5×105 to 2×106 cells/mL.
The cells can be maintained in the solution for dilution for a relatively long period of time. After suspending the cells in the solution for dilution, the suspension may be allowed to stand for several minutes to several hours, e.g., 5 minutes to 6 hours, more preferably 30 minutes to 4 hours. They may be allowed to stand at ambient temperature (e.g., 1 to 30° C., typically 15 to 25° C.), or in a CO2 incubator (e.g., 36 to 42° C., typically 37° C.).
The present invention provides a pharmaceutical composition containing highly active NK cells, which have been collected by an appropriate method, pretreated as required, and cryopreserved, and so forth.
The pharmaceutical composition provided by the present invention can be used for the treatment and/or prevention of various diseases susceptible to highly active NK cells, and so forth. Examples of such diseases are cancers and infectious diseases, and specifically, they include, but not limited to, skin cancer, oral cancer, gallbladder cancer, bile duct cancer, lung cancer, liver cancer, stomach cancer, colon cancer, pancreatic cancer, kidney cancer, ovarian cancer, bladder cancer, prostate cancer, neuroblastoma, leukemia, and infectious diseases caused by viruses, bacteria or the like. The inventors of the present invention confirmed the effect of use of cells frozen and thawed by the method of the present invention on animal models of colon cancer, which should otherwise die within 30 days without any treatment. A cell therapy using the pharmaceutical composition of the present invention may be performed solely, or in combination with surgical therapy, chemotherapy, radiation therapy, antibody drugs, and so forth.
The characteristics of one embodiment of the pharmaceutical composition provided by the present invention are shown below.
The frozen composition is thawed in a thermostatic bath at 37° C. or the like until it is completely thawed. Immediately after the thawing, the cells are aseptically suspended in a separately prepared isotonic solution acceptable as a pharmaceutical additive.
The shelf life of the composition after thawing is 6 hours, preferably 4 hours, when it is stored at room temperature.
A) Method for culturing highly active NK cells GAIA-102
Frozen apheresis blood (HemaCare/Cellero) as the raw material was thawed, and then the cells were washed and concentrated by using Lovo Cell Processing System (Fresenius Kabi) to obtain PBMCs.
CD3-Positive and CD34-positive cells were removed from the resulting PBMCs by using CliniMACS Prodigy (registered trademark, Miltenyi Biotec), and the cells were eluted with KBM501 medium*1. The numbers of the cells in the eluate was counted, and the total cell count was calculated. The culture was performed by using an adhesion culture bag 640 cm2, to which 200 mL per bag of a cell suspension prepared in the KBM501 medium at a density of 5×105 cells/mL was inoculated, in a CO2 incubator (37° C., 5% CO2). On day 9 of the culture, the KBM501 medium was further added to make the final volume 650 mL per bag, and the incubation was continued until day 14. *1: KBM501 (Kohjin Bio) supplemented with 5% UltraGRO (AventaCell, HPCPLCRL10) and 2 U/mL heparin sodium (Nipro).
On day 14 of the culture, the culture medium was collected, and 1 mM EDTA was added to the culture bag to detach the adhered cells. The total volume of the collected culture medium and the detached cells were centrifuged, and the cells were washed and resuspended in the KBM501 medium.
The number of viable cells of GAIA-102 obtained by the procedures described as the methods for culturing and collecting highly active NK cells was counted, and 2×108 cells were suspended in 5 mL of HSC-BANKER (ZENOAQ, CB071) and frozen at −80° C.
The GAIA-102 cells thawed under each condition were prepared on a 96-well plate (IWAKI, 4870-800SP) at a density of 1×105 cells/well, and centrifuged, the supernatant was removed, then a 7-AAD solution (Beckman Coulter, A07704) diluted with PBS was added to suspend the cells, and the plate was incubated at room temperature for 20 minutes. After the staining, measurement of the cells was performed by using a flow cytometer (BD LSR Fortessa, BD Biosciences), the results were analyzed with FlowJo software, and the viability was calculated from the 7-AAD-positive rate.
For the measurement of cytotoxic activity, a group of the NK cells reacted with the K562 cells, a group solely consisting of the K562 cells as a negative control, and a group of the K562 cells fixed with 10% formalin as a positive control were prepared.
The GAIA-102 cells were thawed and diluted under each condition, and a necessary amount of the cells were taken on the basis of the number of viable cells at the time of freezing, and then prepared at a density of 1×106 cells/mL in 10% FBS/RPMI 1640.
The K562 cells were suspended in serum-free RPMI 1640 medium, stained with PKH26 Red Fluorescent Cell Linker Kit, and then prepared at a density of 2×106 cells/mL in 10% FBS/RPMI 1640.
The GAIA-102 cells and K562 cells were added and mixed in wells of 96-well plate (IWAKI, 4870-800SP) at a cell ratio of 2:1, and allowed to react at 37° C. for 2 hours under 5% CO2. After the reaction, the plate was centrifuged (500×g, 5 minutes), the supernatant was removed, then a 7-AAD solution diluted with PBS was added to suspend the cells, and the suspension was incubated at room temperature for 20 minutes. Measurement was performed by using a flow cytometer, and the results were analyzed with the FlowJo software to calculate the cytotoxic activity rate (% Lysis)*2. 2*: Cytotoxic activity rate=(K562 Cell dead cell rate−Negative control dead cell rate)/(Positive control dead cell rate—Negative control dead cell rate)×100
The following reagents and infusion agents were used in the verification of solutions for thawing.
The GAIA-102 cells frozen for 48 hours or longer were thawed on a water bath at 37° C. and then allowed to stand at room temperature for up to 3.5 hours. Viability measurement based on 7-AAD staining and cytotoxic activity measurement were performed 30 minutes and 3 hours after the thawing.
After the thawing, the cells were diluted 41-fold with the solutions (1) to (6) shown in the following table. There were set a group of (1) a solution having a composition based on the concentrations of the ingredients of Plasma-Lyte A, but not containing sodium gluconate, a group of (2) a solution having a composition based on the concentrations of the ingredients of Plasma-Lyte A, but not containing sodium gluconate, and containing the other ingredients increased by 16% each to adjust osmolarity, a group of (3) a solution having a composition based on the concentrations of the ingredients of Plasma-Lyte A, but not containing sodium gluconate and having an osmolarity adjusted with NaCl, a group of (4) Plasma-Lyte A as a positive control, a group of (5) physiological saline, and a group of (6) physiological saline containing sodium gluconate at the same concentration as that of Plasma-Lyte A. The osmolarities were obtained by calculation for all the cases unless especially noted.
No decrease in viability was observed after the thawing for all the groups. However, a marked decrease in the activity was observed in the groups of (5) physiological saline, and (6) physiological saline to which sodium gluconate was added at the same concentration of as Plasma-Lyte A (
Verification was performed for the ingredients other than sodium gluconate. The GAIA-102 cells frozen for 48 hours or longer were thawed on a water bath at 37° C. and then allowed to stand at room temperature up to 3.5 hours. Viability measurement based on 7-AAD staining and cytotoxic activity measurement were performed 30 minutes and 3.5 hours after the thawing.
After the thawing, the cells were diluted 41-fold with the solutions shown in the following table. There were set groups of (1) to (3) solutions having a composition based on the concentrations of the ingredients of Plasma-Lyte A, but not containing sodium gluconate, from which each of Mg2+, K+, and CH3COO− (acetate) was excluded, respectively, and groups of (4) to (6) physiological saline supplemented with each of the ingredients, respectively.
In terms of viability, a slight decrease was observed only in the group of K+-free (2) at 3 hours after the thawing and dilution. On the other hand, decrease in the activity was observed in groups of (2) and (3) wherein K+ and CH3COONa were excluded, respectively, but not in the group (1) in which Mg+ was removed. Further, the experiments of the groups (4) to (6), in which one of the ingredients was added to physiological saline, respectively, showed that only K+ was an ingredient that contributes to the activity all by itself (
The GAIA-102 cells frozen for 48 hours or longer were thawed on a water bath at 37° C. and then allowed to stand at room temperature for up to 3.5 hours. Viability measurement based on 7-AAD staining and cytotoxic activity measurement were performed 30 minutes and 3.5 hours after the thawing.
After the thawing, the cells were diluted 41-fold with the solutions shown in the following table. There were prepared (1) Plasma-Lyte A as a positive control, (2) physiological saline as a negative control, and (3) to (6) solutions having a composition based on the concentrations of the ingredients of Plasma-Lyte A, but not containing sodium gluconate and magnesium chloride, and having osmolarity ratios to physiological saline of 0.80, 0.95, 1.0, and 1.10, respectively. There was also set a group of (7) a solution having a composition based on the concentrations of the ingredients of Plasma-Lyte A, of which osmolarity ratio was adjusted to 1.0 with the content of NaCl alone.
No decrease in viability was observed for all the concentrations up to 3.5 hours after the thawing and dilution. No effect on the activity was observed for the groups (3) to (6), but a decreasing tendency was observed for the group (7) in which the osmolarity ratio was adjusted to 1.0 with the content of NaCl alone (
The GAIA-102 cells frozen for 48 hours or longer were thawed on a water bath at 37° C. and then allowed to stand at room temperature for up to 3 hours. Cytotoxicity activity was measured 3 hours after the thawing.
After the thawing, the cells were diluted 41-fold with the solutions shown in the following table. There were set groups of (1) Plasma-Lyte A as a positive control, and (2) physiological saline as a negative control, and (3) phosphate buffer supplemented with K+ for a group of phosphate buffer having a K+ concentration of 5 mEq/L, (4) THAM Injection, (6) a solution containing physiological saline/MEYLON/KCl, and (7) a solution containing water/MEYLON/KCl/NaCl were prepared. In addition, there were also prepared (5) a solution containing THAM/MEYLON prepared so as to have a K+ concentration of 2.5 mEq/L, and (8) a solution containing water/CH3COONa/KCl/NaCl.
For the group of (3) phosphate buffer supplemented with K+ to achieve a K+ concentration of 5 mEq/L, an increase in the activity was observed compared with (2) physiological saline, but it could not satisfactorily maintain the activity. The maintenance of the activity was also insufficient with (5) the solution containing THAM/MEYLON prepared so as to have a K+ concentration of 2.5 mEq/L and (8) the solution containing water/CH3COONa/KCl/NaCl, (
The GAIA-102 cells frozen for 48 hours or longer were thawed on a water bath at 37° C. and then allowed to stand at room temperature for up to 3 hours. Cytotoxicity activity was measured 3 hours after the thawing.
After the thawing, the cells were diluted 41-fold with the solutions shown in the following table. There were set groups of (1) Plasma-Lyte A as a positive control, and (2) physiological saline as a negative control, and there were prepared (7) SOLMALT (SOLMALT Infusion), as well as (3) a solution containing SOLMALT/MEYLON, and (4) a solution containing SOLMALT/THAM, for groups of solutions based on SOLMALT of which pH is adjusted. In addition, there were also prepared (5) a solution having the same composition as Plasma-Lyte A except that sodium gluconate and Mg2+ were both excluded, in which the concentrations of the other ingredients were the same as those in Plasma-Lyte A, and (6) a solution having the same composition as Plasma-Lyte A except that sodium gluconate and Mg2+ were both excluded, and only NaCl was contained in a decreased amount so that the solution had the same osmolarity as the solution of (5). Further, there was additionally set a group of (8) SOLMALT having a pH adjusted with THAM, and an osmolarity reduced by adding water after the pH adjustment. The pH values of the prepared solutions were also measured.
Although the activity could not be maintained with (7) SOLMALT, an activity-improving tendency was observed for (3) the solution containing SOLMALT/MEYLON, and (4) the solution containing SOLMALT/THAM, which were based on SOLMALT, and of which pH values were adjusted. This tendency was confirmed with reproducibility, and similar results were obtained for the group of (8) SOLMALT having a pH adjusted with THAM, and an osmolarity reduced by adding water after the pH adjustment. From these results, it was also experimentally confirmed that it becomes difficult to maintain the activity when the pH decreases to 6.0, and acceptable results can be obtained up to pH 8.8 (
For the groups for which dilution was performed with the solutions described in 2-5), viability measurement based on 7-AAD staining and cytotoxic activity measurement were performed 1 and 3 hours after the thawing, and viability of the GAIA-102 cells was also analyzed after the reaction for the cytotoxic activity measurement.
It was found that decrease in viability, which was not observed immediately after the thawing and dilution, was observed after replacement with RPMI. After the replacement with RPMI, decrease in viability was observed over time, and it was found that the extent of the decrease was highly correlated with the activity (
The GAIA-102 cells frozen for 48 hours or longer were thawed on a water bath at 37° C. and then allowed to stand at room temperature up to 3 hours. Cytotoxicity activity was measured 3 hours after the thawing. After the thawing, the cells were diluted 41-fold with the solutions shown in the following table. There were set groups of (1) Plasma-Lyte A as a positive control, and (2) physiological saline as a negative control, and there were prepared (3) a solution consisting of SOLMALT and MEYLON at a ratio of 20:1, (4) a solution consisting of SOLMALT and MEYLON at a ratio of 10:1, and (5) a solution containing SOLMALT/MEYLON/water for groups of solutions prepared based on SOLMALT with pH adjustment with MEYLON, as well as (6) Klinisalz, and (7) a solution containing Klinisalz/MEYLON for a group of a solution prepared based on Klinisalz with pH adjustment with MEYLON. There were also prepared (8) a solution containing Plasma-Lyte A+140,000 IU/mL Imunace and (9) a solution containing Plasma-Lyte A+875 μM tauroursodeoxycholic acid (TUDCA). The pH values of the prepared solutions were also measured.
For the groups in which the cells were thawed with the described solutions, viability measurement based on 7-AAD staining and cytotoxic activity measurement were performed 1 and 3 hours after the thawing, and viability of the GAIA-102 cells was also analyzed after the reaction for the cytotoxic activity measurement.
It was found that the activity could be maintained with (3) the solution consisting of SOLMALT and MEYLON at a ratio of 20:1, which was prepared on the basis of SOLMALT with pH adjustment with MEYLON. The activity-maintaining ability observed for the group (8) was comparable to that observed with (1) Plasma-Lyte A, and it was found that the addition of Imunace does not contribute to at least the activity for K562. (6) Klinisalz having a low pH, and (7) the solution containing Klinisalz/MEYLON, of which pH was adjusted, but which has a high osmolarity, could not maintain the activity (
The GAIA-102 cells frozen for 48 hours or longer were thawed on a water bath at 37° C. and then allowed to stand at room temperature up to 3 hours. Cytotoxicity activity was measured 3 hours after the thawing. After the thawing, the cells were diluted 41-fold with the solutions shown in the following table. There were prepared solutions of which pH was adjusted to 7.6 to 8.0 with MEYLON, and which was prepared to have a K+concentration of 5 mEq/L, (1) a solution containing Albumin/K.C.L./physiological saline/MEYLON, and (2) a solution containing Albumin/K.C.L./physiological saline/MEYLON, further, for groups of a solution of which Cl− concentration was further adjusted to 80 mMq/L, (3) a solution containing Albumin/K.C.L./physiological saline/Amizet/water/MEYLON, and (4) a solution containing K.C.L./physiological saline/Amizet/water/MEYLON, as well as (6) Pasma-Lyte A as a positive control. The pH values of the prepared solutions were also measured.
The solutions of (2) and (4) showed good activity-maintaining ability, and the solution of (3) showed markedly good results (
The GAIA-102 cells frozen for 48 hours or longer were thawed on a water bath at 37° C. and then allowed to stand at room temperature up to 4 hours. Cytotoxicity activity was measured 3 hours after the thawing, and viability measurement based on 7-AAD staining was performed 4 hours after the thawing. After the thawing, the cells were diluted 41-fold with the solutions shown in the following table. There were prepared (1) a solution containing Albumin (Albumin 25% I.V.-BENESIS, Japan Blood Products Organization)/K.C.L./physiological saline/Amizet/water/MEYLON, (2) a solution containing K.C.L./physiological saline/Amizet/water/MEYLON, (3) a solution containing Albumin/K.C.L./physiological saline/Amizet/water/MEYLON, and (5) Pasma-Lyte A as a positive control, all of which were prepared so as to have an osmolarity of 300 mOsm. The pH values of the prepared solutions were also measured.
The solution of (2) showed a good activity-maintaining ability, and the solutions of (1) and (3) showed markedly good results.
The data of the experiments conducted to date by the inventors of the present invention were compiled and statistically analyzed by using JMP (registered trademark) Pro 15 (SAS Institute Inc.). The results of the statistical analysis suggested that Cl concentration and pH significantly affect maintenance of the activity, and that there may be a threshold value for K+ (
The thawed GAIA-102 cells were diluted 41-fold with Plasma-Lyte A and the conditioned solution mentioned in the following table, and left to stand for 3 hours at room temperature, and cytotoxic activity against K562 and viability based on 7-AAD staining were measured.
The conditioned solution outperformed Plasma-Lyte A (
The thawed GAIA-102 cells were diluted 45-fold with Plasma-Lyte A, and the conditioned solution mentioned in the following table, which supposes addition of albumin upon use, and left to stand for 3 hours at room temperature, and then cytotoxic activity against K562 and viability based on 7-AAD staining were measured. The conditioned solution outperformed Plasma-Lyte A (
Frozen GAIA-102 cells were thawed on a water bath at 37° C. for 2 minutes and 40 seconds, and then diluted 10-fold with each of the solutions for dilution.
After standing at room temperature for 3 hours, cytotoxic activity against K562 was evaluated. According to the method described in the section “E) Method for measuring cytotoxic activity against tumor cells”, cytotoxic activity was measured with mixing the GAIA-102 cells (E) and K562 cells (T) at an ET ratio of 0.5:1, 1:1, or 2:1. From the cytotoxic activity ratios calculated for ET ratios at 4 points (including 0), the calculated value for E: T=1:1 was obtained by nonlinear regression analysis using JMP (registered trademark) Pro statistical analysis software.
High cytotoxic activity was maintained with the solutions for dilution having a glucose concentration not higher than 26 g/L, especially not higher than 16 g/L (
| Number | Date | Country | Kind |
|---|---|---|---|
| 2021-146461 | Sep 2021 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2022/033487 | 9/7/2022 | WO |
