EP3853354A1 - Cellules nk dérivées de cellules mononucléaires - Google Patents

Cellules nk dérivées de cellules mononucléaires

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Publication number
EP3853354A1
EP3853354A1 EP19936966.1A EP19936966A EP3853354A1 EP 3853354 A1 EP3853354 A1 EP 3853354A1 EP 19936966 A EP19936966 A EP 19936966A EP 3853354 A1 EP3853354 A1 EP 3853354A1
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EP
European Patent Office
Prior art keywords
cells
mixture
antibody
feeding
mononuclear
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Pending
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EP19936966.1A
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German (de)
English (en)
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EP3853354A4 (fr
Inventor
Rohit Duggal
Ranjeet SINHA
Wenzhao Li
Jason ISAACSON
Karl MARQUEZ
Patrick Soon-Shiong
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Immunitybio Inc
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NantKwest Inc
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Application filed by NantKwest Inc filed Critical NantKwest Inc
Publication of EP3853354A1 publication Critical patent/EP3853354A1/fr
Publication of EP3853354A4 publication Critical patent/EP3853354A4/fr
Pending legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
    • C12N5/06—Animal cells or tissues; Human cells or tissues
    • C12N5/0602—Vertebrate cells
    • C12N5/0634—Cells from the blood or the immune system
    • C12N5/0646—Natural killers cells [NK], NKT cells
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2501/00—Active agents used in cell culture processes, e.g. differentation
    • C12N2501/20—Cytokines; Chemokines
    • C12N2501/23—Interleukins [IL]
    • C12N2501/2315—Interleukin-15 (IL-15)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2501/00—Active agents used in cell culture processes, e.g. differentation
    • C12N2501/50—Cell markers; Cell surface determinants
    • C12N2501/515—CD3, T-cell receptor complex
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2501/00—Active agents used in cell culture processes, e.g. differentation
    • C12N2501/50—Cell markers; Cell surface determinants
    • C12N2501/599—Cell markers; Cell surface determinants with CD designations not provided for elsewhere
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2506/00—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells
    • C12N2506/11—Differentiation of animal cells from one lineage to another; Differentiation of pluripotent cells from blood or immune system cells
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2509/00—Methods for the dissociation of cells, e.g. specific use of enzymes

Definitions

  • the present disclosure relates to compositions, methods, and devices to generate and cultivate immune competent cells, especially as it relates to cord blood (CB) or peripheral blood (PB) NK cells from whole blood.
  • CB cord blood
  • PB peripheral blood
  • Natural killer (NK) cells constitute a group of innate immune cells, which are often characterized as cytotoxic lymphocytes that exhibit antibody dependent cellular toxicity via target-directed release of granulysin and perforin. Most NK cells have a specific cell surface marker profile (e.g., CD3 . CD56 + , CD16 + , CD57 + , CD8 + ) in addition to a collection of various activating and inhibitory receptors. While more recently NK cells have become a significant component of certain cancer treatments, generation of significant quantities of NK cells (and especially autologous NK cells) has been a significant obstacle as the fraction of NK cells in whole blood is relatively low.
  • NK Natural killer
  • NK cells can be generated from various precursor cells.
  • various stem cell factors (SCF), FLT3 ligand, interleukin (IL)-2, IL-7 and IL-15 have been reported in various in vitro approaches to induce and expand cord blood-derived cytokine-induced killer (CIK) cells ( Anticancer Research 30: 3493-3500 (2010)).
  • CIK cord blood-derived cytokine-induced killer
  • CD34 + hematopoietic cells can be exposed to IL-12 and other agents as is reported in US 2018/0044636.
  • human hemangioblasts were sequentially exposed to two different cytokine cocktails as described in WO2011/068896, and different cytokine cocktails were used with post-embryonic hematopoietic stem cells as taught in WO2012/128622. While at least some of these methods provide a significant n-fold expansion of NK cells, methods and reagents for such expansion are both time and resource demanding. Still further, it should be noted that many of the known methods also require NK cell culture on a feeder cell layer, which is often problematic from a technical and a regulatory perspective.
  • AML acute myeloid leukemia
  • TpoR agonists to so induce the AML cells to form NK cells.
  • NK cells can be exposed to TpoR agonists to so induce the AML cells to form NK cells.
  • TpoR agonists to so induce the AML cells to form NK cells.
  • culturing peripheral blood cells in the presence of various interleukins, stem cell factors, and FLT3 ligands as is disclosed in WO 2011/103882.
  • US 2013/0295671 teaches methods of stimulating already existing NK cells with anti-CD 16 and anti-CD3 antibodies along with cytokines. While procedurally simpler, such methods still require elaborate manipulation of the cells and add significant costs due to the specific reagent required.
  • US 10,125,351 describes use of cord blood or peripheral blood as a source of cells that are subject to density gradient separation to isolate nucleated cells that are then cultivated with a medium that contains interferon, interleukin, a CD3 antibody and human albumin. Most advantageously, such method is amenable to perfusion culture in a bioreactor and as such significantly reduces operational difficulties. Unfortunately, however, the yield of NK cells is relatively low.
  • NK cells can be generated from blood mononuclear cells (MNCs) obtained from cord or whole blood without isolating either CD34+ hematopoietic stem cells (HSC) or NK cells, and without the use of a feeder layer, preferably by an enrichment process that uses N-803 and optionally an anti-CD16 agonist antibody and an anti-CD3 antibody.
  • MNCs blood mononuclear cells
  • HSC hematopoietic stem cells
  • NK cells preferably by an enrichment process that uses N-803 and optionally an anti-CD16 agonist antibody and an anti-CD3 antibody.
  • the inventors contemplate a method of producing NK cells that includes a step of isolating from a biological fluid a mixture of mononuclear cells, a step of contacting the mixture of the mononuclear cells with an anti- CD 16 antibody and N-803 to activate NK cells, and another step of sequentially feeding the activated NK cells with a medium containing N-803.
  • the step of isolating the mixture of the mononuclear cells is performed using density gradient centrifugation, and/or the biological fluid is whole blood or cord blood. Therefore, the mixture of mononuclear cells will generally include T cells, NK cells, NKT cells, and double negative (DN) T cells. While not categorically excluded, it is generally preferred that the mixture of mononuclear cells is not further processed to enrich NK cells.
  • contemplated anti-CD16 antibodies it is generally preferred that the antibody is a monoclonal antibody with specificity to human CD 16. Most typically, the anti- CD16 antibody is present at a concentration of between 0.05-0.5 mcg/ml, and/or the N-803 is present at a concentration of between 0.1-1.0 nM. Where desired, contemplated methods may also include a step of contacting the mixture further includes contacting the mixture of the mononuclear cells with an anti-CD3 antibody (e.g., at a concentration of between 0.1-1.0 ng/ml).
  • the mixture of the mononuclear cells contains about 100-500 x 10 6 cells, and/or the step of contacting the mixture is performed in a volume of between about 100-300ml or at a cell density of about 1 x 10 6 cells/ml.
  • the medium containing N-803 comprises human AB serum and/or NK MACSTM medium (commercially available from Mileny Biotech, Friedrich-Ebert-Strahe 68, 51429 Bergisch Gladbach, Germany) and hydrocortisone (0.1-5 uM).
  • the step of sequentially feeding is performed about every 72 hours, and/or that the step of sequentially feeding is performed until a total cell number of about 0.5- 5.0 x 10 9 cells is reached.
  • the step of sequentially feeding the activated NK cells may be performed in single container and the step of contacting the mixture of the mononuclear cells may be performed in the same container.
  • the step of sequentially feeding the activated NK cells is performed until NK cells are enriched to an at least 100-fold expansion, and/or until NK cells constitute at least about 80% or at least about 90% of all live cells.
  • the inventors also contemplate a method of expanding NK cells from a mixture of mononuclear cells that includes a step of providing a mixture of the mononuclear cells that contains equal or less than 5% NK cells.
  • the mixture of the mononuclear cells is then contacted with an anti-CD 16 antibody and N-803 to activate NK cells, and in a further step the activated NK cells are fed with a medium containing N-803.
  • the mixture of the mononuclear cells is obtained from whole blood or cord blood, or the mixture of the mononuclear cells is obtained from an MHC-matched autologous source relative to an individual that receives the NK cells.
  • the mixture of the mononuclear cells that contains equal or less than 3% NK cells and/or may further comprise T cells, NKT cells, and DN cells.
  • the medium, anti-CD16 antibody, the N-803, and the anti-CD3 antibody the same considerations as noted above apply.
  • the step of feeding comprises sequentially feeding at an interval of about every 72 hours, that the step of feeding is performed until a total cell number of about 0.5- 5.0 x 10 9 cells is reached, and/or that the step of feeding the activated NK cells is performed until NK cells are enriched to an at least 100-fold expansion.
  • the step of feeding the activated NK cells is performed in an automated manner, preferably in a single container.
  • the inventors also contemplate a method of expanding NK cells in an automated bioreactor.
  • Such method will typically include a step of incubating a mixture of mononuclear cells in an activation medium containing N-803 and an anti-CD 16 antibody for a time sufficient to activate NK cells, wherein the mixture of mononuclear cells is contained in a cell culture container while incubating the mixture.
  • growth of the cells is measured while the cells are in the container, and the cells are automatically fed with a medium containing N-803 according to a predetermined schedule and/or a result from the step of measuring growth of the cells.
  • feeding the cells is terminated according to a predetermined schedule and/or a result from the step of measuring growth of the cells.
  • suitable containers will have a volume of between about 200 ml and about 2,500 ml, and/or the step of measuring growth of the cells is performed through a wall of the container (e.g., using optical measurements).
  • the activation medium contains N-803 at a concentration of between 0.1-1.0 nM and an anti-CD16 antibody at a concentration of between 0.05-0.5 mcg/ml.
  • the medium containing N-803 contains N-803 at a concentration of between 0.1-1.0 nM.
  • the time sufficient to activate NK cells is between 24 hours and 96 hours, and the cells are fed until a total cell number of about 0.5- 5.0 x 10 9 cells is reached, and/or until NK cells are enriched to an at least 100-fold expansion.
  • the inventors also contemplate a cell culture container (e.g., having a volume of between about 200 ml and about 2,500 ml) that contains a medium with distinct types of immune competent cells.
  • the medium contains NK cells in an amount of at least 80% of all live cells, NKT cells in an amount of equal or less than 10 % of all live cells, T cells an amount of equal or less than 5 % of all live cells, and DN T cells an amount of equal or less than 3 % of all live cells.
  • at least one wall of the container has an optically transparent portion, and/or the NK cells are present in an amount of at least about 90% of all live cells.
  • Fig.1 depicts an exemplary schematic illustrating a process starting from cord blood through isolation of CBMCs that then make up the seed for the enrichment/expansion of NK cells.
  • Fig.2 depicts exemplary details of a representative process in an automated environment (‘GMP in a box’) and the schedule of addition of various ingredients.
  • Fig.3 depicts exemplary results for enrichment kinetics of the process of Fig. 2 for NK cells by number and selected flow cytometry properties.
  • Fig.4 depicts exemplary results for kinetics of various cell populations of the process of Fig. 2 along results for with marker expression, especially significant expression of the majority of NK activation receptors.
  • NK cells With the continuously increasing use of immune therapies in the treatment of cancer, production of sufficient quantities of NK cells, and especially autologous NK cells as therapeutic entities has become critical.
  • many of the current methods require use of feeder layers or differentiation of isolated CD34+ hematopoietic stem cells (HSCs), which is both time and resource intensive.
  • HSCs hematopoietic stem cells
  • NK cells In an effort to improve production methods for NK cells, the inventors have now discovered various systems, compositions, and methods to generate therapeutically meaningful quantities (e.g., at least 0.5 x 10 9 NK cells) from a biological fluid containing mononuclear cells (e.g., whole blood, cord blood) in a simple and effective manner that can even be fully automated once the mononuclear cells are obtained as is schematically illustrated in Fig.l.
  • a biological fluid containing mononuclear cells e.g., whole blood, cord blood
  • the bioreactor is a self-contained unit and will have a central processor and memory on board to execute a programmable protocol for various activities (e.g., operation of pumps for fluid movements, temperature and gas regulation, image processing, etc.) and to generate regulatory-ready reports, as well as a microscope (or other optical unit) for monitoring the cell culture.
  • a programmable protocol for various activities (e.g., operation of pumps for fluid movements, temperature and gas regulation, image processing, etc.) and to generate regulatory-ready reports, as well as a microscope (or other optical unit) for monitoring the cell culture.
  • whole peripheral blood or cord blood is used as a starting material that is processed to obtain mononuclear cells.
  • processing can be done using conventional density gradient centrifugation (e.g., using Ficoll-Paque PlusTM (a hydrophilic soluble polysaccharide, density 1.077 g/mL), commercially available from GE Lifesciences).
  • Ficoll-Paque PlusTM a hydrophilic soluble polysaccharide, density 1.077 g/mL
  • the mononuclear cells are separated from the centrifuge tube, the cells are washed and re-suspended in an activation medium (e.g., NK MACS supplemented with 10% human AB serum).
  • an activation medium e.g., NK MACS supplemented with 10% human AB serum.
  • the activation medium further comprises N-803 at a concentration of about 0.4 nM, and an anti-CD16 antibody at a concentration of about 1.0 mcg/ml.
  • the mononuclear cells have a density of 1-2 xlO 6 cells/ml in a total volume of about 200 ml, and the cells and medium are in a single container. After about 3-4 days, the cells are fed with fresh medium containing N-803, and further feed cycles are performed about every three days through recovery, rapid expansion, and culture culmination as exemplarily shown in Fig.2. Cells are harvested upon reaching a desired quantity, typically about 0.5- 5.0 x 10 9 total cells and/or upon reaching a desired expansion (e.g. at least 100- fold expansion).
  • the so obtained cell culture contains after about three weeks more than about 85% NK cells, with less than about 8% NKT cells, and with less than about 2.5% T cells, and less than about 1.2% double negative (DN) T cells.
  • the entire culture process may be performed in a single container within a self-contained bioreactor, which substantially reduces risk of contamination and eliminates reagent and cell handling during the cultivation step.
  • Fig.3 depicts exemplary results for an NK production that yielded an about 136-fold expansion of NK cells in 23 days with a total of 1.17 x 10 9 cells harvested from a final volume of about 480 ml.
  • Fig.4 depicts further experimental data that illustrate cell composition over time tracking T cells, NK cells, NKT cells, DN cells (along with CD 16 results; left panel). Results for the final phenotyping for the cells harvested in the process of Fig.2 and Fig.3 are shown in the right panel of Fig.4. As can be readily seen, the detected markers were indicative of NK cells.
  • the fluids could be autologous relative to the individual that will receive the NK cells isolated in the methods presented herein. Therefore, especially preferred biological fluids include fresh whole blood, cord blood (frozen or fresh), and cells separated in a leukapheresis procedure.
  • the biological fluid may also be any fluid that contains NK cells (typically among other cell types).
  • suitable alternative biological fluids include whole blood from allogenic donors, which may or may not be matched for a compatible MHC type. Therefore, samples in a blood bank that approach expiration date are deemed suitable for use, as well as freshly donated whole or stored cord blood by an individual other than the NK cell recipient.
  • mononuclear cells may vary considerably, and the person of ordinary skill in the art will be readily apprised of the most suitable methods of isolation and enrichment.
  • the biological fluid is whole blood or cord blood
  • the fluid is processed via gradient density centrifugation using any suitable medium (e.g., Ficoll-Hypaque).
  • mononuclear cells may be obtained directly from the patient by leukapheresis, or the biological fluid may be subjected to removal of red blood cells using antibodies.
  • mononuclear cells may be isolated using magnetic bead separation where the beads are coated or otherwise coupled to antibodies binding the mononuclear cells.
  • NK MACS medium all media known to support growth of NK cells are deemed suitable for use herein. Most preferably, however, defined media are used and may be supplemented with human AB serum.
  • Activation of the NK cells in the mixture of mononuclear cells is preferably performed with a combination of an anti-CD 16 antibody and N-803, and optionally an anti- CD3 antibody.
  • an anti-CD 16 antibody and N-803 There are various sources for anti-CD 16 antibodies known in the art/commercially available, and particularly preferred anti-CD 16 antibodies have agonist (activating) activity and are specific to human CD 16.
  • activators other than anti- CD 16 antibodies are also deemed suitable for use herein include anti-CD 16 antibody fragments and fusion proteins with anti-CD16 antibody fragments.
  • contemplated activators also include CD314 or NKG2D, the natural cytotoxicity receptors CD335 (NKp46), CD336 (NKp44) and CD337 (NKp30), CD226 (DNAM-1), CD244 (2B4), members of the CD 158 or killer immunoglobulin-like receptor (KIR) family that carry a short cytoplasmic tail (KIR2DS and KIR3DS) and CD94/NKG2C, among others.
  • CD314 or NKG2D the natural cytotoxicity receptors CD335 (NKp46), CD336 (NKp44) and CD337 (NKp30), CD226 (DNAM-1), CD244 (2B4), members of the CD 158 or killer immunoglobulin-like receptor (KIR) family that carry a short cytoplasmic tail (KIR2DS and KIR3DS) and CD94/NKG2C, among others.
  • concentrations of the anti-CD 16 antibody will typically follow those already known in the art for activation of NK cells. Therefore, suitable concentrations for anti-CD 16 antibodies will be between about 0.01-5.0 mcg/ml, and more typically between about 0.01- 0.3 mcg/ml, or between about 0.05-0.5 mcg/ml, or between about 0.1-1.0 mcg/ml, or between about 1.0-5.0 mcg/ml.
  • the mixture of mononuclear cells is exposed to only a single, two, or there doses of the anti-CD 16 antibody, most typically when the mononuclear cells are isolated and contacted with the activation medium for the first (and/second, and/or third) time.
  • the person of ordinary skill in the art will be readily able to recognize proper schedule and dosage to achieve NK cell activation.
  • exposure of the mononuclear cells to the anti-CD 16 antibody is contemporaneous with exposure of the mononuclear cells with the N-803.
  • exposure of the mononuclear cells to the anti-CD 16 antibody is sequentially to exposure of the mononuclear cells with the N-803 (with exposure of the mononuclear cells to the anti-CD 16 antibody first being the preferred sequence).
  • activation may also include contacting the cells with anti-CD3 antibody, typically at the same time of contacting the cells with anti-CD16 antibody.
  • concentrations of the anti-CD3 antibody will typically follow those already known in the art for activation of NK cells. Therefore, suitable concentrations for anti-CD3 antibodies will be between about 0.01-10.0 ng/ml, and more typically between about 0.01-0.1 ng/ml, or between about 0.1-0.5 ng/ml, or between about 0.3-1.0 ng/ml, or between about 1.0-5.0 ng/ml.
  • the mixture of mononuclear cells is exposed to only a single, two, or there doses of the anti-CD3 antibody, most typically when the mononuclear cells are isolated and contacted with the activation medium for the first (and/second, and/or third) time.
  • the person of ordinary skill in the art will be readily able to recognize proper schedule and dosage to achieve NK cell activation.
  • N-803 an IL-15N72D:IL-15RaSu/IgGl Fc complex with human sequences; see US 2019/0023766, commercially available from ImmunityBio
  • N-803 is preferred as an agent in the activation and feed medium.
  • various alternative agents with IL-15 activity are also deemed suitable for use herein.
  • IL-15 as isolated cytokine has a very short lifespan and signaling activity is typically very short.
  • N-803 also provides a physiological context (i.e., IL-15 R-alpha chain) and a N72D form that acts as a super agonist. Therefore, any stabilized IL-15 compound is also expressly deemed suitable for use herein.
  • IL-15 (recombinant, recombinantly expressed, or isolated) and/or N-803 may be at least in part replaced or supplemented by TxM type fusion protein complexes, especially preferred fusion protein complexes are described in WO 2018/165208, which is incorporated by reference herein.
  • contemplated TxM type fusion protein complexes will include at least one additional cytokine selected from the group consisting of IL-7, IL-18, and IL-21. Therefore, and among other suitable choices, contemplated TxM fusion complexes include an IL-18/IL-7 TxM and/or IL-18/IL-21 TxM.
  • the stabilized IL-15 compounds will include at least portions of human sequences for IL-15 and/or IL-15 Ra.
  • suitable compounds include P22339 (a complex of IL-15 and the Sushi domain of IL-15Ra chain with a disulfide bond linking the IL- 15/Sushi domain complex with an IgGl Fc to augment its half-life; see Nature, Scientific Reports (2016) 8:7675), and XmAb24306, which is a IL-15/IL-15Ra-Fc heterodimer (see e.g., WO 2018/071919).
  • the mixture of mononuclear cells is, after isolation from the biological fluid, placed into a cell culture container together with the medium containing the anti-CD 16 (and optionally anti-CD3) antibody and N-803 to activate the NK cells.
  • the container is a cell culture flask with at least one wall (or portion thereol) that is transparent to light such that cell shape, staining, and/or growth can be observed with a microscope or other optical instrument.
  • the cells can be continuously or periodically monitored in a bioreactor, and so obtained measurements (e.g., cell size, cell number, cell distribution, etc.) can be used to trigger or modify an automated feeding schedule in a control unit that is logically coupled to the bioreactor.
  • feeding fresh medium with N-803 can be performed using a predefined schedule, typically every three days, where preferably each feeding will include N-803 to maintain continuous signaling.
  • the specific volumes shown in Fig.2 are suitable for expanding the NK cells to cell densities consistent with cell growth, it should be appreciated that the volumes may be adjusted to accommodate particular growth patterns.
  • the feeding may be continuously or that predetermined volumes may be changed in response to the growth kinetic observed in the container.
  • the yield of the NK cells at the end of the cultivation will be typically at least 80%, or at least 82%, or at least 85%, or at least 88%, or at least 90%, or at least 92%, or at least 94% of all live cells with the remainder being NKT cells, DN T cells, and T cells.
  • remaining NKT cells will typically be equal or less than 10%, or equal or less than 8%, or equal or less than 7%, or equal or less than 6% of all live cells, while remaining T cells will typically be equal or less than 5%, or equal or less than 4%, or equal or less than 3%, or equal or less than 2% of all live cells, and remaining DN T cells will typically be equal or less than 3%, or equal or less than 2%, or equal or less than 1.5 %, or equal or less than 1% of all live cells.
  • NK cells capable of remarkably high expansion of NK cells, and typical expansions are at least 80-fold, or at least 100-fold, or at least 120-fold, or at least 130-fold, or at least 140-fold with respect to the number of NK cells originally present in the mixture of mononuclear cells.
  • Such expansion is particularly notable in view of the very simple manner of activation and cultivating (one-pot process). Indeed, once the mixture of mononuclear cells is placed into the cell culture container, the entire process con continue within the same container and will be sustained by addition of media only as schematically shown in Fig.2. Thus, complex handling and expensive reagents are entirely avoided, and the risk for contamination is significantly reduced.
  • the NK cells are expanded and/or activated in a culture environment that allows for continuous monitoring, continuous management of CO2 and O2 levels, and continuous monitoring to detect cell density (e.g., confluence).
  • a culture environment that allows for continuous monitoring, continuous management of CO2 and O2 levels, and continuous monitoring to detect cell density (e.g., confluence).
  • especially preferred environments are automated cell culturing and harvesting devices as are described, for example, in WO 2015/165700.
  • Such‘GMB-in-a-box’ systems beneficially allow control over feeding schedules, gas control, allow for real-time detection of cell density, growth (kinetics) and cell health, as well as dramatically reduce the possibility of contamination due to significantly reduced handling requirements.
  • the systems and methods presented herein advantageously also allow generation of CD56 dim and CD56 bnght NK cells, particularly where the NK cells are generated from peripheral blood. Depending on further culture conditions, CD56 bnght NK cells may then differentiate to CD56 dim cells. Such distinct NK cell populations can then be employed as for distinct therapeutic options due to their distinct maturation and cytotoxicity profile. Additionally, it should be appreciated that the compositions, systems and methods will also be suitable to generate NKT cells upon proper stimulation and culture.
  • one exemplary method entailed isolating CBMCs or PBMCs by a single Ficoll centrifugation step, which was followed by incubation of the cells with about 0.4 nM N-803 and about 0.1 mcg/ml of an anti-CD 16 antibody (e.g., clone B73.1, commercially available from BD Biosciences), and optionally about 0.5 ng/ml of an anti-CD3 antibody in NK MACS media with 10% human AB serum.
  • an anti-CD 16 antibody e.g., clone B73.1, commercially available from BD Biosciences
  • NK MACS media optionally about 0.5 ng/ml of an anti-CD3 antibody in NK MACS media with 10% human AB serum.
  • 150 mL of CBMCs at a million cells/ml were used as the starting material with above reagents.
  • Media was used for dilution with N-803 twice a week with a regimen of a 1:2 and 1
  • NK MACS medium with NK supplement staining antibodies for phenotyping (aCD3, aCD16, aCD56, aNKp30, aNKp44, aNKp46, aNKG2A, aNKG2D, aTIGIT, aCD34, aTRAIL, aCD57, aCXCR3, and aCCR5), Miltenyi Biotec San Diego, CA; Human AB serum, Access Biologicals, San Diego CA; N-803, GMP in a Box kit, Nantbio Inc Culver City CA.
  • MNCs were freshly isolated from cord blood or peripheral blood. It was washed twice with complete NKMACS medium (NKMACS+ Supplements+ 10% hu-AB-serum). MNCs were suspended in 150mL of medium with density of 1c10 L 6 cell/mL. 150mL cell suspension was supplemented with aCD16 antibody (lmcg/mL) and N-803 (0.4nM). Further GMP kit was installed in the box and protocol uploaded through VivaBio web portal. Cells suspension with complete cytokine and antibody were transferred to cell bag, and 150mL cell suspension was injected through cell injection port in Box-kit. GMP Box started imaging and cells were propagated according to steps written in protocol as mentioned in Fig2.
  • NK enrichment phenotype for CD3, CD56, and CD 16 expression
  • cell health cell number, viability, and cell density
  • administering refers to both direct and indirect administration of the pharmaceutical composition or drug, wherein direct administration of the pharmaceutical composition or drug is typically performed by a health care professional (e.g., physician, nurse, etc.), and wherein indirect administration includes a step of providing or making available the pharmaceutical composition or drug to the health care professional for direct administration (e.g., via injection, infusion, oral delivery, topical delivery, etc.).
  • a health care professional e.g., physician, nurse, etc.
  • indirect administration includes a step of providing or making available the pharmaceutical composition or drug to the health care professional for direct administration (e.g., via injection, infusion, oral delivery, topical delivery, etc.).
  • the cells or exosomes are administered via subcutaneous or subdermal injection.
  • administration may also be intravenous injection.
  • antigen presenting cells may be isolated or grown from cells of the patient, infected in vitro, and then transfused to the patient. Therefore, it should be appreciated that contemplated systems and methods can be considered a complete drug discovery system (e.g., drug discovery, treatment protocol, validation, etc.) for highly personalized cancer treatment.
  • drug discovery system e.g., drug discovery, treatment protocol, validation, etc.

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Abstract

La présente invention concerne du sang de cordon ombilical ou des cellules NK du sang périphérique qui sont préparés à partir de cellules mononucléaires de sang total sans avoir besoin d'isoler de cellules souches hématopoïétiques CD34+ ou de cellules NK et sans avoir besoin d'une couche d'alimentation. De manière avantageuse, les procédés de l'invention utilisent un procédé d'enrichissement qui utilise des anticorps agonistes anti-CD16, des anticorps anti-CD3 et N-803. De plus, les procédés envisagés sont appropriés pour une adaptation dans un processus de production entièrement automatisé (GMP dans une boîte).
EP19936966.1A 2019-07-08 2019-07-08 Cellules nk dérivées de cellules mononucléaires Pending EP3853354A4 (fr)

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PCT/US2019/040867 WO2021006875A1 (fr) 2019-07-08 2019-07-08 Cellules nk dérivées de cellules mononucléaires

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KR (1) KR20210080566A (fr)
CN (1) CN113166726A (fr)
AU (1) AU2019456283B2 (fr)
CA (1) CA3120695A1 (fr)
IL (1) IL283998A (fr)
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ES2763169T3 (es) * 2009-03-26 2020-05-27 Cellprotect Nordic Pharmaceuticals Ab Expansión de células NK
IN2012DN05053A (fr) 2009-12-04 2015-10-09 Stem Cell & Regenerative Medicine Internatioinal Inc
AU2010347018A1 (en) 2010-02-24 2012-09-20 Ingo Schmidt-Wolf Method for the generation of a CIK cell and NK cell population
CN107880136B (zh) 2010-09-21 2021-11-12 阿尔托生物科学有限公司 多聚体il-15可溶性融合分子与其制造与使用方法
EP2666466A4 (fr) * 2011-01-21 2014-11-05 Biotherapy Inst Of Japan Procédé pour la production de préparation du sang enrichi en cellules nk
DK2686421T3 (da) 2011-03-18 2021-03-08 Glycostem Therapeutics B V Generering af nk-celler og nk-celleforløbere
US20150010583A1 (en) 2012-02-08 2015-01-08 Ipd-Therapeutics B.V. Ex vivo nk cell differentiation from cd34+ hematopoietic cells
CN102988415B (zh) 2012-08-15 2014-11-19 中航（宁夏）生物有限责任公司 人异基因有核细胞工业化制备自然杀伤性细胞(nk)及注射液
WO2015154012A1 (fr) * 2014-04-03 2015-10-08 Memorial Sloan-Kettering Cancer Center Populations de cellules tueuses naturelles (nk) clonogéniques et procédés de production et d'utilisation de telles populations
US11773364B2 (en) 2014-04-28 2023-10-03 Vivabiocell S.P.A. Automated cell culturing and harvesting device
KR101683614B1 (ko) * 2016-02-15 2016-12-07 신동혁 Nk세포배양용 배지첨가키트 및 상기 키트를 이용한 nk세포배양방법
US20200179447A1 (en) * 2016-09-23 2020-06-11 The Regents Of The University Of California Autologous irradiated whole cell tumor vaccines lentivirally engineered to express cd80, il-15 and il-15 receptor alpha
PE20191034A1 (es) 2016-10-14 2019-08-05 Xencor Inc Proteinas de fusion heterodimericas biespecificas que contienen proteinas de fusion fc il-15/il-15r y fragmentos de anticuerpo pd-1
EA201991632A1 (ru) * 2017-02-28 2020-03-12 Аффимед Гмбх Комбинация антитела против cd16a с цитокином
KR20230170821A (ko) 2017-03-06 2023-12-19 알토 바이오사이언스 코포레이션 Il-12 및 il-18로의 il-15-기반 융합
EP3621647A1 (fr) * 2017-05-11 2020-03-18 Nantkwest, Inc. Compositions de cellules nk anti-egfr/haute affinité et procédés de traitement du chordome
US12060577B2 (en) * 2017-05-19 2024-08-13 Case Western Reserve University Compositions for expanding natural killer cells
CN108070556A (zh) * 2017-07-26 2018-05-25 深圳市北科生物科技有限公司 用于免疫细胞培养的方法和组合物
KR20200090742A (ko) * 2017-08-28 2020-07-29 알토 바이오사이언스 엘엘씨 Il-7 및 il-21에의 il-15 기반 융합

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WO2021006875A1 (fr) 2021-01-14
CN113166726A (zh) 2021-07-23
KR20210080566A (ko) 2021-06-30
SG11202104339WA (en) 2021-05-28
JP7213976B2 (ja) 2023-01-27
IL283998A (en) 2021-07-29
JP2022513614A (ja) 2022-02-09
AU2019456283B2 (en) 2023-06-08
AU2019456283A1 (en) 2021-05-20
CA3120695A1 (fr) 2021-01-14
JP2023040184A (ja) 2023-03-22
EP3853354A4 (fr) 2022-04-20

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