Kit containing medium for culturing natural killer cells and method of effectively culturing natural killer cells using the same

Abstract

Disclosed is a method of culturing natural killer cells (NK cells) applied to immunotherapy. More specifically, disclosed are a kit containing a medium for culturing NK cells (NKCM kit) that can efficiently amplify and activate NK cells effective for the treatment of malignant tumors by culturing lymphocytes derived from human peripheral blood, and a method of culturing natural killer cells using the kit. The method for amplifying NK cells of the present invention includes stimulating NK cells with lymphocytes separated from peripheral blood, culturing the NK cells in a medium containing IL-2, IL-12, IL-15, IL-17, IL-18, and IL-21, and isolating the NK cells. Provided is a pharmaceutical composition for cell therapy containing NK cells produced by the method of amplifying NK cells. The pharmaceutical composition for cell therapy is expected to be widely used to treat infections and/or cancer.

Claims

1. A method of culturing natural killer cells using a kit containing a medium for culturing cells comprising: a basic solution containing L-glutamine, IL-2 and a medium for cell culture; a C-1 solution containing IL-12 in the basic solution; a C-2 solution containing IL-15 in the basic solution; a C-3 solution containing IL-17 and IL-21 in the basic solution; a C-4 solution containing IL-18 in the basic solution; an A-1 solution containing an anti-CD16 antibody and an anti-CD-56 antibody in the basic solution; and an A-2 solution containing an anti-CD3 antibody in the basic solution, the method comprising: a first step comprising adding said basic solution and said A-1 solution to separated lymphocytes and further adding autologous plasma thereto to stimulate NK cells; a second step of adding said A-2 solution and autologous plasma thereto to accelerate initial proliferation of the NK cells; a third step of adding said C-1, C-2, C-3 and C-4 solutions and autologous plasma thereto to amplify culture of the NK cells; and a fourth step of amplifying and culturing the NK cells in the basic solution and the autologous plasma.

2. A method of preparing a pharmaceutical composition for treating an infection and cancer, the method comprising the respective steps of the method of culturing natural killer cells according to claim 1.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The above and other objects, features and other advantages of the present invention will be more clearly understood from the following detailed description taken in conjunction with the accompanying drawings, in which:

(2) FIG. 1 is a diagram illustrating a culture protocol of a kit for culturing NK cells according to the present invention; and

(3) FIG. 2 is a diagram showing the phenotypic change of activated lymphocytes obtained according to an embodiment of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

(4) It will be understood that the terms used herein are used only to describe certain embodiments and should not be construed as limiting the scope of the present invention. Singular forms are intended to include plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the term “comprises” or “has”, when used in this specification, specify the presence of stated features, numbers, steps, operations, elements, components or combinations thereof, but does not preclude the presence or addition of one or more other features, numbers, steps, operations, elements, components, or combinations thereof.

(5) It will be understood that the terms “first”, “second”, etc. may be used herein to describe various elements and should not be construed as limiting the elements. The terms are used only to distinguish one element from another element. For example, within the scope defined by the present invention, a “first” element may be referred to as a “second” element, and similarly, a “second” element may be referred to as a “first” element.

(6) Unless differently defined herein, all terms used herein including technical or scientific terms have the same meanings as generally understood by those skilled in the art. In addition, terms identical to those defined in generally used dictionaries should be interpreted as having meanings identical to contextual meanings in the related art, and are not to be interpreted as having abnormal or excessively formal meanings unless they are definitely defined herein.

(7) Hereinafter, the technical configuration of the present invention will be described in detail with reference to the attached drawings and preferred embodiments.

(8) However, the present invention is not limited to the embodiments, and will be embodied in different forms. Like reference numbers refer to like elements throughout the description of the figures.

(9) The technical feature of the present invention is directed to a kit containing a medium for culturing NK cells having a composition that is capable of proliferating NK cells in large quantities through stable amplification in the finally obtained lymphocyte-conditioned medium, without the cumbersome process of culturing lymphocytes (immune cells) for a certain period of time in the state in which anti-CD3 antibodies are immobilized in a culture vessel in order to stimulate the lymphocytes, and a method of culturing NK cells using the kit containing the medium.

(10) In other words, in the present invention, by first performing stimulation using an anti-CD16 antibody and an anti-CD56 antibody and, after 24 hours, simply adding an anti-CD3 antibody to the medium, the number of NK cells can be stably increased from at least 500 times up to 5000 times.

(11) As described above, the result of experimentation performed based on the principles developed in the present invention showed that, when immature progenitor cells are stimulated with an anti-CD16 antibody and an anti-CD56 antibody to induce differentiation of the progenitor cells into NK cells, mature NK cells are activated and T cells are stimulated with an anti-CD3 antibody to induce activation of the NK cells with the activated T cells, many NK cells were proliferated without any problem, even if stimulation was given, until the anti-CD3 antibody is degraded and removed in the culture medium. This proves that the culture method of the present invention is capable of culturing lymphocytes with a very high proportion of NK cells without the cumbersome process of culturing lymphocytes (immune cells) for a certain period of time in the state in which anti-CD3 antibodies are immobilized in a culture vessel in order to stimulate the lymphocytes.

EXAMPLE 1

Preparation of Culture Kit

(12) A basic solution was prepared in a final amount of 10L by adding 2,000 to 4,000 IU/mL of IL-2 and 100 mL of a 500 mM L-glutamine solution to a basic medium for culturing suspending cells (when IL-2 or L-glutamine was already contained in the basic medium, the added amounts were changed to adjust the final concentration).

(13) C-1 solution was prepared by dissolving IL-12 in the basic solution at a concentration of 0.5 to 3 ug/mL.

(14) C-2 solution was prepared by dissolving IL-15 in the basic solution at a concentration of 0.5 to 3 ug/mL.

(15) C-3 solution was prepared by dissolving each of IL-17 and IL-21 in the basic solution at a concentration of 0.1 to 2 ug/mL.

(16) C-4 solution was prepared by dissolving IL-18 in the basic solution at a concentration of 0.5 to 3 ug/mL.

(17) A-1 solution was prepared by dissolving each of an anti-CD16 antibody and an anti-CD56 antibody in the basic solution at a concentration of 0.5 to 5 ug/mL.

(18) A-2 solution was prepared by dissolving an anti-CD3 antibody in the basic solution at a concentration of 0.5 to 5 ug/mL.

EXAMPLE 2

Proliferation and Culture of Natural Killer Cells Using Culture Kit

(19) Lymphocytes and autologous plasma were prepared from the blood of patients and then natural killer cells were cultured using the kit containing a medium for culturing NK cells obtained in Example 1 as follows.

(20) 1. Lymphocyte Extraction and Autologous Plasma Preparation

(21) 30 ml of the peripheral blood of patient A was added to a 50 ml conical tube and centrifuged, and then the upper layer of autologous plasma was added to and treated with a heparin tube, and the result was added to a fresh 50 mL conical tube and was then centrifuged again to prepare the upper layer of plasma as autologous plasma.

(22) Then, PBS was added to the blood tube from which the plasma has been removed to adjust the volume to 30 ml, thoroughly mixed, transferred to a tube containing Ficoll-Paque Plus, and centrifuged at 800 xg for 15 minutes, and a buffy coat layer containing lymphocytes, that is, the second layer, was separated and collected in a 50 mL conical tube, and the volume was adjusted to 50 mL with PBS, and then mixing was conducted. Then, centrifugation was performed 2 to 3 times, and then the supernatant was discarded and lymphocytes were separated.

(23) 2. Initial Culture

(24) The basic solution, A-1 solution and autologous plasma were added to the separated lymphocytes, the result was incubated in a T25 or T75 flask in a CO.sub.2 incubator (37° C., 5% CO.sub.2) for 24 hours, and then A-2 solution was added thereto and incubated in the CO.sub.2 incubator (37° C., 5% CO.sub.2) for 48 hours (3 days in total).

(25) 3. Amplification Culture

(26) After initial culture, C-1 solution, C-2 solution and autologous plasma were added to a T75 flask every 24 hours for 2 days, and C-1, C-2, C-3 and C-4 solutions and autologous plasma were further transferred to a T175 flask every 24 hours for 2 days and continuously incubated in a CO.sub.2 incubator (37° C., 5% CO.sub.2) (4 days in total).

(27) 4. Mass Culture

(28) After amplification culture, the resulting entire culture solution was added to a 1L CO.sub.2 permeable culture bag containing a cell culture medium, 5 to 10 mL of autologous plasma was further added thereto, massaged to be mixed thoroughly with the culture solution, and then incubated in a CO.sub.2 incubator (37° C., 5% CO.sub.2) for 4 to 6 days and massaged every 24 hours to be thoroughly mixed with the culture solution.

(29) 5. Harvesting of Natural Killer Immune Cells

(30) The final culture solution obtained after culture was contained in a centrifuge tube, the cells were harvested through several rounds of centrifugation, and the harvested cells were packaged in a physiological saline bag and stored in a refrigerator or frozen.

Experimental Example 1 Immune Cell Proportion Analysis

(31) The percentage of cells proliferated using the blood of patient A was analyzed. The result is shown in FIG. 2. As can be seen from FIG. 2, the percentage of NK cells is 81.35%, the percentage of NKT cells is 2.11%, and the percentage of gdT cells is 1.13%. This proves that about 92% or more of proliferated cells are killing-active cells that can exhibit therapeutic effects.

Experimental Example 2 Reproducibility of Immune Cell Culture in Subjects

(32) An immune cell proliferation study was conducted using the above method, culture reproducibility was determined based on the following result of immune cell proliferation reproducibility, and the result is shown in Table 1 below.

(33) TABLE-US-00001 TABLE 1 Harvested Total blood Initial immune culture Final immune Item volume cell count day cell count Subject A 60 mL 0.53 × 10.sup.7 14 days 3.08 × 10.sup.9 Subject B 60 mL 1.44 × 10.sup.7 14 days 6.24 × 10.sup.9 Subject C 60 mL 1.82 × 10.sup.7 14 days 6.86 × 10.sup.9 Subject D 60 mL 0.88 × 10.sup.7 14 days 5.28 × 10.sup.9

Experimental Example 3 Comparative Study with Other Culture Method

(34) The culture method using IL-2, IL-12, IL-15, IL-17, IL-18, IL-21 and the anti-CD3 antibody, the anti-CD16 antibody and the anti-CD56 antibody (the kit of the present invention) was compared with other culture methods to determine the differentiation of the method using the kit of the present invention.

(35) A. Comparative Study with Kit for Mass-Culturing Cells of KOHJIN BIO

(36) The kit of the present invention was found to exhibit a higher immune cell count and a higher proportion of cells having killing activity when compared to culture using a known NK cell culture kit, specifically NK kit from KOHJIN BIO (NKCC-1, NKCC-2, NKCC-b, NKCC-c), for 14 days. The results are shown in Table 2 below.

(37) TABLE-US-00002 TABLE 2 Immune cell Immune cell count before count after NK cell Culture method Target culture culture proportion Kit of KOHJIN Health 0.58 × 10.sup.7 3.08 × 10.sup.9 42% BIO Patient 0.42 × 10.sup.7 1.71 × 10.sup.9 33% Kit of present Health 0.50 × 10.sup.7 6.04 × 10.sup.9 96% invention Patient 0.38 × 10.sup.7 4.27 × 10.sup.9 88%

(38) B. Comparative Experiment Between Kit of Present Invention and Combination Culture Method

(39) The kit of the present invention was found to exhibit a higher immune cell count and a higher proportion of cells having killing activity when compared to a culture method of adding 2 0 a single culture solution containing a mixture of all of IL-2, IL-12, IL-15, IL-17, IL-18, IL-21, the anti-CD3 antibody, the anti-CD16 antibody, and the anti-CD56 antibody (Culture method

(40) A). The results are shown in Table 3 below.

(41) TABLE-US-00003 TABLE 3 Immune cell Immune cell count before count after NK cell Culture method Target culture culture proportion Culture method A Health 0.50 × 10.sup.7 0.86 × 10.sup.9 24% Patient 0.36 × 10.sup.7 0.45 × 10.sup.9 27% Kit of present Health 0.48 × 10.sup.7 5.04 × 10.sup.9 92% invention Patient 0.38 × 10.sup.7 4.42 × 10.sup.9 89%

(42) C. Comparative Experiment Between Kit of Ppresent Invention and Culture Method Not Using Some Cytokines

(43) In order to compare the kit of the present invention with a culture method using the kit from which some cytokines are removed, a culture method, in which IL-17 and IL-21 are removed from the kit of the present invention (culture method B) was compared with the kit of the present invention. The kit of the present invention was found to exhibit a higher immune cell count and higher proportion of cells having killing activity when compared to the culture method B, and the results are shown in Table 4 below.

(44) TABLE-US-00004 TABLE 4 Immune cell Immune cell count before count after NK cell Culture method Target culture culture proportion Culture method B Health 0.55 × 10.sup.7 1.74 × 10.sup.9 42% Patient 0.41 × 10.sup.7 1.05 × 10.sup.9 43% kit of present Health 0.49 × 10.sup.7 5.31 × 10.sup.9 88% invention Patient 0.33 × 10.sup.7 4.22 × 10.sup.9 85%

(45) As is apparent from the foregoing, the kit containing a medium for culturing NK cells according to the present invention has a composition that is capable of proliferating NK cells in large quantities through stable amplification in the finally obtained lymphocyte-conditioned medium, while eliminating the cumbersome process of culturing lymphocytes (immune cells) for a certain period of time in the state in which anti-CD3 antibodies are immobilized in a culture vessel in order to stimulate the lymphocytes.

(46) The method of stably culturing NK cells is capable of providing activated lymphocytes having a low content of T cells and a high content of NK cells in the finally obtained lymphocyte-conditioned medium by sequentially using additives constituting a unit included in the kit containing the medium, that is, by setting a specific order of stimulation to the lymphocytes.

(47) Although the preferred embodiments of the present invention have been disclosed, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims.