WO1998006823A2 - Culture sans cytokines, de cellules dendritiques - Google Patents

Culture sans cytokines, de cellules dendritiques Download PDF

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Publication number
WO1998006823A2
WO1998006823A2 PCT/US1997/013759 US9713759W WO9806823A2 WO 1998006823 A2 WO1998006823 A2 WO 1998006823A2 US 9713759 W US9713759 W US 9713759W WO 9806823 A2 WO9806823 A2 WO 9806823A2
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cells
culture
antigen
cell
dendritic
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PCT/US1997/013759
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WO1998006823A3 (fr
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Mona Vachula
Dennis E. Van Epps
Mortimer T. Alzona
Frederick M. Aono
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Nexell Therapeutics Inc.
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Priority claimed from US08/904,124 external-priority patent/US6458585B1/en
Application filed by Nexell Therapeutics Inc. filed Critical Nexell Therapeutics Inc.
Priority to CA002263722A priority Critical patent/CA2263722A1/fr
Priority to AU40521/97A priority patent/AU4052197A/en
Priority to EP97938120A priority patent/EP0918847A2/fr
Publication of WO1998006823A2 publication Critical patent/WO1998006823A2/fr
Publication of WO1998006823A3 publication Critical patent/WO1998006823A3/fr

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    • C12N2501/50—Cell markers; Cell surface determinants
    • C12N2501/515—CD3, T-cell receptor complex

Definitions

  • This invention is in the field of ex vivo culture of hematopoietic cells, more specifically in the culture of human dendritic cells and T-cells for therapeutic purposes.
  • Dendritic cells play an important role in immune responses. They provide the immune system with an effective means of antigen presentation, unlike that of any other cell. Dendritic cells are the most potent antigen presenting cells in the immune system. They have been characterized to have a unique morphology and cell surface phenotype that may contribute to their potency in initiating cellular immune responses, specifically T cell dependent responses. Therefore, dendritic cells have been proposed as a valuable component in cellular based therapies that require presentation of antigen to effector cells. Dendritic effector cells can be primed ex vivo to create activated cells to be reintroduced into the body in order to combat disease. However, dendritic cells comprise less than 1% of leukocytes circulating in peripheral blood, which makes it difficult to obtain an amount sufficient to use in therapy.
  • DC Dendritic Cells
  • APC professional antigen- presenting cells
  • Caux et al . Immunology Today 16: 2-4, 1995; Steinman, Annu . Re . Immunol . 9: 271- 296, 1991; Young, JW, et al . , Stem Cells 14:376-387, 1996; Steinman, RM, Exptl Hematol 24:859-882, 1996) .
  • antigen-presenting cells take in, process, and present antigen to T lymphocytes, they serve different immune functions.
  • DC are the most potent initiators of the immune response and are the APCs responsible for the induction of primary antigen-specific immune reactions (Bhardwaj et al., . Exp . Med . 175: 267-273, 1992; Bhardwaj et al . , . Exp . Med. 178: 633-642, 1993).
  • the DC as are all hematopoietic cells, are derived from CD34+ stem cells. These hematopoietic cells arise in the bone marrow and as they mature traffic to the peripheral blood where they circulate
  • T cells make a detour to the thy us
  • the differentiation pathway from a CD34+ cell to a DC is not completely understood (Santiago-Schwarz et al., J. Leukoc. Biol. 52: 274-281, 1992; Galy et al . , Immunity 3: 459-473, 1995; Rosenzwajg et al . , Blood 87: 535-544, 1996) .
  • DC are found in very low levels in peripheral blood ( ⁇ 1%) compared to other white blood cells (WBC) or leukocytes (neutrophils about 60%, lymphocytes about 35%, monocytes about 5%, eosinophils about 2%, basophils ⁇ 1%) ;
  • WBC white blood cells
  • leukocytes neurotrophils about 60%, lymphocytes about 35%, monocytes about 5%, eosinophils about 2%, basophils ⁇ 1%
  • DC have been identified by a bundle of criteria that cover different features of DC -- morphology, phenotype, and their function in mixed lymphocyte reactions
  • DC are identified by their cytoplasmic processes or “veils” that extend from the surface of the cells .
  • the unusual morphology of DC has been described in many publications and illustrated in photomicrographs. For example, Young and Steinman describe DC thusly: "DC extend long processes, easily 10 ⁇ in length, in many directions from the cell body. In the living state, these processes are sheet-like "veils” or lamellipodia and are actively motile. When spun onto glass, slides, the DC processes are numerous and spiny". (Young, JW, et al . , Stem Cells 14:376- 387, 1996.)
  • DC constitutively express CD80 and CD86, the costimulatory molecules that bind CD28 on T cells.
  • the ability to stimulate T-cells in an allogeneic mixed lymphocyte reaction is a functional capacity attributed to DC. It has recently been shown that DC are very efficient presenters of antigen and can result in potent CD8+ cytotoxic T cell responses (Bender et al . , J . Exp . Med . 182: 1663-1671, 1995; Tjoa et al . , The Prostate 28: 65-69, 1996) .
  • DC can be culture derived from renal cell carcinoma patients (Radmayr et al . , Int. J. Cancer 63: 627-632, 1995) .
  • the DC are functional after being in culture ex vivo (Tjoa et al . , The Prostate 27: 63-69, 1995).
  • cytokines such as granulocyte/macrophage-colony stimulating factor (GM-CSF) , interleukin-4 (IL-4) , tumor necrosis factor- ⁇ (TNF-o;) , and stem cell factor (SCF) .
  • GM-CSF granulocyte/macrophage-colony stimulating factor
  • IL-4 interleukin-4
  • TNF-o tumor necrosis factor- ⁇
  • SCF stem cell factor
  • Vitamin D2 was reported to increase differentiation of monocytes in a cell line, while retinoic acid did not (Howell, et al . 1994 Blood Coagulation and Fibrinolvsis 5:445-453) .
  • Leukemia cell lines were reported to increase their differentiation to mature granulocytes, or monocytes/macrophages, or erythroid cells upon stimulation with tubulin disruptors, TPA, retinoids, or hemin (Nakajima, et al . 1994 Biol . Pharm. Bull. 17:742- 744) .
  • the HL60 cell line was reported to show increased differentiation towards neutrophils or monocytes upon stimulation with retinoids and Vitamin D3 (Bunce et al. 1995 Leukemia 9:410-418).
  • Figure 1 shows a Wright-Giemsa-stained dendritic cell (DC; solid arrow) produced by the method of the invention.
  • the hollow arrows indicate processes or "veils" typical of DC.
  • the hollow diamonds indicate lymphocytes which remained in the DC culture.
  • Figure 2 shows a clump of DC produced by a positive-control method using animal serum (RPMI + 10%FCS) ; the DC are stained with an antibody to CD86. Hollow arrows indicate processes and veils typical of DC.
  • Figure 3 shows a DC (solid arrow) in a culture produced by the method of the invention and stained with an antibody to CD86.
  • the hollow arrow indicates typical DC processes.
  • Figure 4 shows a DC (solid arrow) produced by the method of the invention and stained with an antibody to CD80.
  • the hollow arrows indicate typical DC processes.
  • FIG. 5 shows DC (solid arrows) produced by the method of the invention and stained with S100 antibody. Hollow arrows indicate processes typical of DC. This photo suggests how DC may contact and interact with lymphocytes, which in this culture were lymphocytes remaining in the DC culture .
  • Figure 6 shows DC (solid arrows) produced from a commercially-available research source, using the commercially available method, as a positive control.
  • the cells are stained with an antibody to CD86.
  • Hollow arrows indicate processes typical of DC.
  • Figure 7 shows a clump of DC produced from the same commercially-available source as in Figure 6.
  • the cells are stained with an S100 antibody.
  • the hollow arrow indicates a process typical of DC.
  • FIG 8 depicts results of mixed- lymphocyte reactions (MLRs) using dendritic cells produced by the method of the invention, as well as control methods, as stimulators of allogeneic T-cells.
  • Figure 9 shows dendritic cells produced by the method of the invention which were pulsed with tetanus toxin antigen peptide (TT) , then co-cultured with autologous T-cells according to the method of the invention for seven days.
  • Solid arrows indicate two dendritic cells which are prominently stained by an antibody to TT using immunohistochemistry .
  • Hollow diamonds indicate T-cells.
  • the invention provides a method for producing human dendritic cells (DC) for therapeutic purposes by culturing mononuclear cells in a medium containing at least one agent selected from the group consisting of calcium ionophores, theophylline, prostaglandin El, dibutyryl cyclic AMP, Vitamin D3 , Vitamin E, retinoic acid, and fatty acids, and maintaining the culture until it is enriched for DC.
  • the culturing and maintaining comprise about 4- 14 days in duration.
  • an enriched population of DC can be culture- derived from adherent cells.
  • mononuclear cells are first incubated in the culture container for a time sufficient to allow a subset of cells to adhere to the polystyrene inner surface of the container.
  • the incubation time is at least 1 hour, more preferably 2 hours, but could be up to 18 hours.
  • the non-adherent cells are removed, and those cells which adhere to the polystyrene inner surface are further cultured as described above.
  • Enrichment for DC is evidenced by at least about 2.5% of total cells exhibiting DC morphology, namely DC processes.
  • the identity of DC can also be evidenced by expression of at least one antigen selected from CD80, CD86, and CDla, on at least 2.5% of the total cell culture population.
  • the invention further provides a method to produce antigen- pulsed dendritic cells for therapeutic use by culturing mononuclear cells as described above, and then contacting the cells with an antigen.
  • the antigen may be a viral antigen, a tumor antigen, or any other antigen to which an immune response is desired.
  • the invention also provides a method for producing antigen-specific T-cells by co-culturing antigen-pulsed dendritic cells with T-cells to produce antigen-specific T-cells.
  • the method begins with providing mononuclear cells (MNC) from the blood or bone marrow of the patient or an HLA- matched donor.
  • MNC mononuclear cells
  • the term MNC includes monocytes, lymphocytes, stem and progenitor cells, including CD34+ cells.
  • MNC excludes granulocytes (neutrophils, basophils, acidophils) , platelets, and red blood cells.
  • HLA-matched refers to an individual who expresses at least several major histocompatibility complex (MHC) genes in common with the intended recipient. Each individual expresses at least seven different MHC proteins on his cells. Allogeneic MHC molecules are highly immunogenic and will trigger rejection of the grafted cells if there are too many mismatches.
  • MHC major histocompatibility complex
  • HLA-matched donor is defined as an individual chosen by a clinician, on the basis of HLA tissue typing, as an appropriate donor for the individual patient.
  • MNC can be derived from bone marrow, peripheral blood, or umbilical cord blood. Since obtaining bone marrow cells entails general anesthesia, it is preferable to obtain peripheral blood cells via leukapheresis, which is a non- invasive procedure performed without anesthesia.
  • the patient or donor may undergo a treatment with cytokines and/or chemotherapeutic agents prior to cell collection, which agents mobilize CD34+ stem cells from the bone marrow into the peripheral blood.
  • cytokines and/or chemotherapeutic agents prior to cell collection, which agents mobilize CD34+ stem cells from the bone marrow into the peripheral blood.
  • it is not absolutely necessary to administer mobilizing agents to the donor sufficient DC can ultimately be produced from non-mobilized peripheral blood, using the method of the invention.
  • MNC are isolated by density gradient centrifugation and can be used directly in the culture system of the invention.
  • CD34+ stem cells can be pre-selected from the MNC population using an antibody against CD34 in combination with various selection means to form the starting population for DC production.
  • various means for CD34+ cell selection are described in the following patent documents: WO 95/34817; EP 438 520; WO 95/24969; U.S. 5,536,475; WO 91/16116; U.S. 5,240,856; WO 92/07243; WO 95/05843; WO 95/02685; U.S. 5,411,863.
  • MNC or pre-selected CD34+ cells are first suspended in medium containing at least one agent selected from the group consisting of calcium ionophores, theophylline, prostaglandin El, dibutyryl cyclic AMP, Vitamin D3 , Vitamin E, retinoic acid, and fatty acids.
  • An example of a useful calcium ionophore is A23187.
  • a fatty acid can be selected from the group consisting of linoleic acid, palmitic acid, stearic acid, eicosanoic acid, palmitoleic acid, oleic acid, linolenic acid, and arachidonic acid.
  • any of the above mentioned agents can also be used in combination or serially with one or more cytokines or hematopoietic growth factors.
  • the advantage of the invention is that it provides a means to substitute a common molecule for an individual cytokine which may be too expensive, unavailable, or otherwise unsuitable for clinical use.
  • a cytokine can be selected from IL-4, GM- CSF, TNF-C-, or any other cytokines known to be active in the hematopoeitic system.
  • IL-4 is thought to promote the proliferation of dendritic cells by supressing the growth of monocytes, thus leaving more space and resources for the proliferation of DC, and possibly leaving more progenitors free to differentiate along the DC line.
  • GM-CSF increases the growth and differentiation of DC along with granulocytes and macrophages. If it is desired to first select CD34+ cells, they can be cultured initially with GM- CSF to cause their proliferation, and subsequently cultured with one or more of the above named agents to promote differentiation into DC.
  • TNF- ⁇ suppresses the growth of myeloid progenitors, such as granulocytic and macrophage progenitors, while allowing the growth of DC.
  • suitable base medium is preferably chosen from among the commercially available serum-free, animal protein-free base media such as X-VIVO 10TM or X-VIVO 15TM (BioWhittaker, Walkersville, MD) , Hematopoietic Stem Cell-SFM media (GibcoBRL, Grand Island, NY) or can be of any formulation which is favorable to hematopoietic cells.
  • Serum-free media are described in the following patent documents: WO 95/00632; U.S. 5,405,772; PCT US94/09622.
  • the serum-free base medium will generally contain clinical grade human serum albumin in a concentration of about 0.5 - 5.0%, usually about 1.0% (w/v) .
  • Clinical grade albumin derived from human serum such as Buminate ® (Baxter Hyland, Glendale, CA) , is so highly purified and isolated from other serum components that it is herein considered serum-free.
  • the MNC or CD34+ cell suspension is preferably cultured in a container having at least one inner growing surface of polystyrene.
  • an enriched population of DC can be culture- derived by first allowing the starting cell suspension to incubate in the container for about 1 to 2 hours, or even up to about 18 hours. Then, cells which do not adhere to the polystyrene inner surface are removed, and the adherent cells are further cultured as described below.
  • a gas-permeable culture container offers the advantages of a closed fluid path culture system whereby the cell suspension may be added to the culture container via a sterile-connect port.
  • the entire cell collection, and preselection if desired is conducted in a closed fluid path system such as the CS3000 ® /Isolex ® 300i (Baxter Immunotherapy, Irvine, CA) which then is aseptically connected to the gas -permeable container for the transfer of cells into the container.
  • the culture media can then be continuously perfused through the container, or periodically refreshed, via sterile connect ports and sterile tubing systems.
  • the cell culture within the gas- permeable container can be maintained in the gas-regulated atmosphere of the incubator without exposure to environmental hazards such as microorganisms which could otherwise be introduced into the culture when the cells are originally introduced to the container or when the medium is refreshed.
  • samples of the cultured cells can be aseptically drawn off from the container through sterile-connect ports for analysis.
  • antigens and/or T-cells can be added to the DC culture via sterile-connect ports.
  • the DC culture, plus or minus T-cells is ready for harvest, the cells can be aseptically drawn off for closed- system washing and further processing.
  • concentration into an infusible medium such as Plasma- Lyte ® A (Baxter IV Systems, Round Lake, IL) can be carried out aseptically via sterile-connect ports, and the washed and concentrated DC/T-cells can be infused directly via the patient's intravenous line without exposing the cells to the environment, or the health-care workers to the cells.
  • the term "closed fluid path system” refers to an assembly of components, each of which is closed to the ambient environment, and each of which is provided with means for effecting sterile connections among the components .
  • the cells are maintained within the culture system until the culture is enriched for DC.
  • a culture is considered enriched for DC when at least about 2.5% of the total cells are DC. This represents about a 25 -fold enrichment over the normal cellular composition of peripheral blood, where the percentage of DC is about 0.1%.
  • the culture is maintained for about 4 - 14 days, preferably about 7 days, to achieve the desired degree of DC enrichment.
  • the absolute number of DC in the enriched culture will depend on the number of starting MNC in the culture, and the duration of culture. When cells are obtained by leukapheresis, a 1.5 hour procedure yields about 1-3 X 10 9 MNC from a non-mobilized donor.
  • An apheresis product from a mobilized donor can yield about 2- 6 X 10 10 MNC, about 1.0% - 7.0% of which are CD34+ cells.
  • a number of DC appear in the DC-enriched culture which is equal to one- tenth the starting number of MNC which were originally placed in culture. In other words, if two million DC are desired, 20 million MNC are provided in the starting culture.
  • Dendritic cells possess characteristic processes which are evident on their surfaces upon inspection under a microscope when the cells are stained with a common histological stain. Samples of the culture are prepared on cytospin slides and stained with any conventional stain that enables visualization of the processes, such as Wright-Giemsa, hematoxylin, or an immunohistochemical stain. Examples of dendritic-cell processes are indicated with hollow arrows in figures 1-6. In figures 1-4 and 6-7, these processes take the form of "veils", which are feathery, barely outlined projections which usually appear to be more lightly stained than the cytoplasm. Such veils on dendritic cells are also shown in prominent publications such as the cover of Blood Volume 87, January 15, 1996.
  • dendritic cell refers to a cell which exhibits dendritic cell processes.
  • enrichment of a culture for DC is evidenced by at least about 2.5% of the total cells exhibiting dendritic cell processes.
  • the identity of DC in the culture can also be evidenced by the expression of at least one antigen selected from CD80, CD86, and CDla, on at least 2.5% of the cultured cell population.
  • CD80 also known as B7-1
  • B7-1 is a highly glycosylated single-chain protein of about 60kDa which is constitutively expressed on DC, activated B cells and monocytes (In: Schlossman, SF, et al . , eds . , Leukocyte Typing V, Oxford University Press, Oxford, 1995, p.682-684; Larsen, CP, et al . , J Immunol 152:5208-5219, 1994; Hathcock, KS, et al .
  • CD86 also known as B7-2, is an 80kDa glycoprotein which is constitutively expressed on DC as well as on activated B cells and monocytes (In: Schlossman, SF ibid p. 703-705; Larsen, CP et al . , supra ; Hathcock, KS, et al., supra) .
  • CD80 and CD86 may have other functions, they are known as ligands for the T-cell CD28 antigen. Interaction of CD80 and/or CD86 on antigen-presenting cells with CD28 on T-cells allows the close association of the two cell types required for internal signaling and activation of the T-cell.
  • CDla is a 49kDa glycoprotein associated with B2- microglobulin which is not present on peripheral blood T and B lymphocytes, monocytes, or normal bone marrow mononuclear cells, but is present on cortical thymocytes and on Langerhans cells, which are considered DC of the epidermis (Bounsell L, et al . , In: Reinherz EL et al . , eds, Leukocyte Typing II: Human, T Lymphocytes. New York Springer-Verlag; 1986:289-302; Martin LH, et al . , PNAS USA 1987; 84 :9189) .
  • Antibodies to CD80, CD86, and CDla suitable for immunohistochemical staining and phenotyping by flow- cytometry, are widely available from companies such as Immunotech (Westbrook, ME) , Coulter (Hialeah, FL) , Becton Dickinson (San Jose, CA) , Ancell (Bayport, MN) , BioSource (Camarillo, CA) , and Serotec (Indianapolis, IN) .
  • the function of a DC culture may be confirmed by conducting a mixed-lymphocyte-reaction (MLR) in which a number of cells from a culture containing DC is mixed with allogeneic T-cells, and the subsequent proliferation of the T-cells is assayed.
  • MLR mixed-lymphocyte-reaction
  • a given ratio of putative DC to allogeneic T-cells is said to be 30-100 times more active in a MLR, as assessed by 3 H-thymidine incorporation in the T-cells, when compared with a comparable ratio of MNC to allogeneic T-cells.
  • the DC can be "pulsed” with an antigen.
  • antigen-pulsed dendritic cells refers to DC which have been contacted with an antigen. It is generally believed that dendritic cells require a few hours, or up to a day, to process the antigen for presentation to naive and memory T-cells. It may be desirable to pulse the DC with antigen again after a day or two in order to enhance the uptake and processing of the antigen.
  • an antigen-primed DC Once the DC has engulfed and processed the antigen, it is termed an "antigen-primed DC".
  • Evidence of antigen-priming can be seen in DC which have been in the presence of the antigen for some time, then processed through immunohistochemistry for staining with an antibody to the specific antigen used for pulsing.
  • the antigen is located throughout the cytoplasm of the DC, and may be especially concentrated along the plasma membrane of the DC (see Figure 9) .
  • Antigens are chosen for a specific purpose such as preparing an antigen-specific DC or T-cell composition as a vaccine or a therapeutic agent against a specific cancer cell and/or virus or a bacterial infection.
  • antigens of hepatitis B virus (HBV) hepatitis C virus
  • Antigen- primed DC can be infused directly to the patient where they are expected to interact with T-cells in vivo to induce the desired immune response (Hsu, FJ, et al . , supra) .
  • Antigen- primed DC can also be co-cultured with T-cells, • the co- culture product will be antigen-specific T-cells useful for infusion to a patient to prevent or ameliorate infection by the specific pathogen.
  • antigens of Epstein-Bar virus which causes lymphomas
  • papilomavirus which causes cervical cancer
  • antigens of Epstein-Bar virus which causes lymphomas
  • papilomavirus which causes cervical cancer
  • Antigens of HER2/neu or chorio- embryonic antigen (CEA) can be used to produce antigen- specific DC and/or T-cells for treatments against cancers of the breast, ovary, pancreas, colon, prostate, and lung which express these antigens.
  • mucin-type antigens such as MUC-1 can be used against various carcinomas; the MAGE, BAGE, and Mart-1 antigens can be used against melanomas.
  • the antigen-pulsed DC population can then be washed, concentrated, and infused directly into the patient as a type of vaccine or treatment against the pathogen or tumor cells from which the antigen originated.
  • This type of use is exemplified by reports from the Ronald Levy group on their treatment for B-cell lymphoma wherein an immune reaction to the B-cell antigen was induced by as few as two to three million antigen-pulsed DC after only one infusion (Hsu, FJ, et al., supra) .
  • the antigen-pulsed DC are expected to interact with naive and/or memory T- lymphocytes in vivo, thus causing them to recognize and destroy cells displaying the antigen on their surfaces.
  • DC can be genetically modified ex vivo by infection or transfection using a viral vector, for instance, carrying a foreign or corrective gene.
  • DC can be genetically modified to express cytokines, or increased co-stimulatory molecules or adhesion molecules.
  • the genetically modifed DC are then infused to the patient, and are expected to express the transfected gene in vivo, thereby enhancing their therapeutic effect.
  • the antigen-pulsed DC culture may be co-cultured with T- lymphocytes to produce antigen-specific T-cells.
  • antigen-specific T-cells refers to T-cells which have been contacted by an antigen-primed DC and thus caused to proliferate as well as to develop the ability to attack cells having the specific antigen on their surfaces.
  • T-cells known as cytotoxic T-cells, lyse target cells by releasing toxic enzymes such as granzymes and perforin onto the surface of the target cells or by effecting the entrance of these lytic enzymes into the target cell interior.
  • Cytotoxic T-cells may express the protein antigen known as CD8 on their surface membranes.
  • the CD8 antigen is a determinant on the 32-kDa ⁇ -subunit of a disulfide- linked bimolecular complex (In: Knapp W, D ⁇ rken B, Gilks WR, et al . , eds. Leucocyte Typing IV: White Cell Differentiation Antigens. Oxford: Oxford University Press; 1989:342-346) .
  • the CD8 antigenic determinant on a cytotoxic T-cell binds to a Class I major histocompatibility (MHC) molecule in association with a target antigen on a cancer cell or virally infected cell, thus increasing adhesion of the T-cell to the target cell and facilitating lysis of the target cell.
  • MHC major histocompatibility
  • T-cells which express the antigen CD4 can also help promote specific cytotoxic activity.
  • the CD45RO antigen is present on certain memory T-cells within the CD4 and CD8 populations, and is thought to be essential for lymphocyte activation (In: Schlossman, SF, et al . , eds., Leucocyte Typing V, Oxford University Press, Oxford, 1995, p. 386-399; Trowbridge, LS, et al . , Annu Rev. Immunol 12:85-116, 1995).
  • the T-cells can be derived from the same donor whose MNC yielded the DC, which can be the patient or an HLA-matched individual as described above.
  • the T-cells and DC can be derived from two different HLA-matched individuals.
  • a second portion of antigen-pulsed DC can be added to the co-culture after one or several days of the original co-culture.
  • the antigen-specific T-cells in the co-culture have proliferated to the desired number, they can be washed, concentrated and infused to the patient.
  • certain sub-populations of T-cells can be selected from the co-culture prior to infusion.
  • Well known means for selecting cells displaying a specific antigen on their surfaces have been described above for CD34+ cells. The same principles can be applied to selecting sub-populations of CD8+, CD4+, and/or CD45RO+ cells. These selected cells can then be washed, concentrated, and infused to the patient to fight the specific virally infected or cancer cells.
  • the number of antigen-pulsed DC needed is in the range of about two to about 100 million. This range is based on the assumption that a ratio of 1:50 to 1:10 DC:T- cells is required for efficient activation of the T-cells. It is estimated that about 100 million to 1 billion antigen-specific T-cells are required to achieve the desired cell-killing activity in vivo, and that activated T-cells will comprise about 10% of the total T-cells in a co-culture. Therefore, about one billion to ten billion T- cells are needed in the final co-culture.
  • PI proliferation index
  • Example 1 Dendritic cells culture-derived from mononuclear cells. Whole blood from healthy human donors was obtained from several sources. Mononuclear cells from apheresis products were obtained from the Fenwal Division, Baxter, Round Lake, IL. When CD34+ cell pre-selection was employed, certain donors with cancer conditions had been pre- treated with chemotherapeutic agents or G-CSF, or both, to mobilize stem cells into their peripheral blood. For CD34+ cell preselection, healthy volunteers also received pre-treatment with G-CSF in order to mobilize stem cells from their marrows into their peripheral blood for collection.
  • FACSort or FACScan TM flow cytometer, Becton Dickinson, San
  • Mouse IgGl FITC Mouse IgGl PE, Goat anti-mouse IgG FITC,
  • Anti-CD3 FITC Anti-CD3 PE, Becton Dickinson.
  • Anti-HLA-DR PE Becton Dickinson.
  • Anti-CDl* FITC Biosource, Camarillo, CA. Anti-CD80, Immunotech.
  • Anti-CD86 PE Ancell, Bayport , MN.
  • Anti-CD45 PE Coulter, Hialeah, FL.
  • HA Human Albumin
  • Ficoll-Paque ® Pharmacia, Uppsala, Sweden. L-glutamine, Sigma, St. Louis, MO.
  • Anti-CD3 mAb (MT-301) ; Anti-CD4 mAb (MT-415) ; Anti-CD8 mAb
  • Blood was diluted 1:2 with phosphate-buffered saline, calcium- and magnesium-free (PBS-CMF) and aliquoted into 50 ml polypropylene centrifuge tubes (40 ml each) .
  • PBS-CMF phosphate-buffered saline, calcium- and magnesium-free
  • Each tube was provided an underlayer of 10 ml ficoll, then centrifuged at 400 x g for 20 min. at room temperature.
  • the interface was removed from each tube and placed into 50 ml tubes, then washed with PBS-CMF at 400 x g for 10 min. at room temperature.
  • the washed mononuclear cells (MNC) were then resuspended into the desired volume.
  • Preselection of CD34+ cells was conducted using an Isolex ® apparatus (Baxter Immunotherapy, Irvine, CA) per manual instructions .
  • Either non-selected MNC or pre-selected CD34+ cells were cultured in either RPMI 1640 supplemented with 10% fetal calf serum (FCS) and 2 M L-glutamine, or X-VIVO 15TM serum- free medium, or X-VIVO 15TM serum-free medium containing 1% HA. Cultures were initiated at 5 x 10 s cells/ml.
  • GM-CSF was used at concentrations ranging from 500 to 5000 U/ml .
  • IL-4 was used at concentrations of 1000 U/ml and 1400 U/ml .
  • TNF-Cf was used at 100 ng/ml and SCF was used at a concentration of 25 ng/ml.
  • Cells were cultured in polystyrene tissue culture flasks (75 cm 2 ) or polystyrene tissue culture plates (collectively both polystyrene flasks and plates will be denoted as "flasks") . Cells were also cultured in PL732 ® Lifecell ® flasks or PL2417 gas permeable containers.
  • the PL732 ® Lifecell ® flasks are composed of a polyolefin blend of EVA, polypropylene, and Kraton.
  • the PL2417 containers are composed of a multilayer, gas-permeable film, with a thin layer of polystyrene on the inner surface.
  • Culture containers were filled with cell cultures by either spiking inlet ports with sample site couplers then aseptically injecting cultures into the bags using a syringe and needle (PL2417) or a syringe with its plunger removed from the barrel was attached to the female sample tubing (PL732 ® flasks) and cultures were then aseptically poured into the bag, using the syringe as a funnel.
  • Cells were cultured for up to 7 or 8 days in 5% C0 2 , ambient 0 2 , 37° humidified incubator.
  • a solution tranfer pump such as the Lifecell® Solution Transfer Pump sold by the Baxter IV Systems division in Round Lake, Illinois, can be used for the efficient transfer of solutions.
  • MNC were prepared from whole blood. MNC were resuspended to a concentration of 5 x 10 7 cells/ml in PBS-CMF containing 1% HA and 0.1% Human immunoglobulin (HIg) (PBS/1% HA/01% HIg) . Anti-CD4 and anti-CD8 or anti-CD3 monoclonal antibodies (mAb) were added to a final concentration of 10 ug/ml each. Cells were rotated at 4° C for 30 minutes then washed 3 times in PBS-CMF in a centrifuge. Cells were resuspended to 5 x 10 7 cells/ml in PBS/1% HA/01% HIg.
  • HIg Human immunoglobulin
  • mAb monoclonal antibodies
  • Sheep anti-mouse Ig magnetic beads were washed by placing them in a 15 ml polypropylene tube then placing the tube next to a magnet. The beads were allowed to adhere to the side of the tube closest to the magnet, then the supernatant was removed. Fresh PBS-CMF was added, the tubes were vortexed and then placed next to the magnet again. The supernatant was decanted. The number of beads to be used was calculated as follows:
  • GAM used was either whole IgG (Becton Dickinson) or F(ab) ' 2 (Immunotech) .
  • the pure antibodies were added first, and the tubes were incubated for 15 minutes on ice.
  • Step A One ml of PAB was added to each tube and the tubes were vortexed to mix.
  • the cells were collected by centrifugation for 3 min at room temperature at HIGH setting using the SERO-FUGE II, then the supernatants were decanted, the excess fluid was blotted off and the tubes were vortexed gently to loosen the pellets.
  • step A was repeated.
  • the PE conjugated antibodies were added and the tubes were incubated on ice for 15 min. Then step A was repeated.
  • the cells were resuspended in 500 ul PAB. The cells were held on ice until they were analyzed with the flow cytometer . Viability Determination: Prior to acquisition, 5 ul propidium iodide (PI) was added to each tube for use as a viability check. The cells were vortexed and acquired within 10 min of PI addition.
  • PI propidium iodide
  • the FL1 versus FL2 dot plot of the FITC and PE stained cells was displayed.
  • the quadrants described above were copied.
  • the %FITC+/PE+ cells were determined by subtracting the %FL1+/FL2+ of the isotype control (upper right quad) from the %FL1+/FL2+ (upper right quad) of the FITC/PE stained sample. This was subsequently done with any FITC/PE combinations needed by subtracting the % positive in the isotype control.
  • Cytospin Slides and Wright-Giemsa staining were attached to microscope slides. 50,000 to 100,000 cells were removed from each culture and resuspended in approximately 100 to 200 ul of PBS-CMF. Slides were placed in the Cytospin ® 2 centrifuge and spun at 100 rpm for 4 min. Cytofunnels were removed from the slides and the slides were air dried for 1 minute. Ten drops of Wright-Geimsa stain were placed onto each slide and allowed to fix for 1 to 2 minutes. Ten drops of water were added to each slide and allowed to sit for 2 to 4 minutes. The slides were rinsed and air dried.
  • Reading of Cytospin Slides Slides were read under phase contrast microscopy, 40x and 60x oil magnification. One hundred cells were identified and characterized morphologically as either dendritic cells or non-dendritic cells (lymphocytes and monocyte, or CD34 + -derived cells in those cases) . Digital images were taken using a color monitor and color video printer.
  • MLR's were setup using T cells as responders and dendritic cell enriched cultures as antigen presenters. Sheep red blood cells were prepared and used to erythrocyte rosette T cells from a MNC preparation as described in "Current Protocols in Immunology", John Wiley & Sons Inc, 1995. Vol. 2, 7.2.1-7.2.4. Erythrocyte+ (E+) T cells were resuspended to 1 x 10 6 cells/ml in RPMI 1640/10% FCS. Dendritic cells were resuspended to 1 x 10 6 cells/ml in RPMI 1640/10% FCS and mitomycin C was added at 25 ug/ml to inhibit proliferation. The tubes were incubated at 37° C for 30 min.
  • PL2417 culture containers were evaluated for their ability to support dendritic cells.
  • PL2417 containers are a newly developed product of Baxter Healthcare Corporation which are made from a flexible, gas-permeable multilayer film, with a thin layer of polystyrene on the inner growing surface. These PL2417 containers are compatible with a closed fluid path culture system.
  • MNC's were cultured in X-VIVO 15TM/1% HA containing 2500 U/ml GM- CSF and 1000 U/ml IL-4 in PL732 ® Lifecell ® Flasks, PL2417 culture containers, and polystyrene tissue culture flasks.
  • Table 1 represents the mean percentage of each phenotype
  • MNC were depleted of CD3+ cells using magnetic bead technology.
  • the cells were cultured in X-
  • VIVO 15TM plus 1000 U/ml IL-4 and 1000 U/ml GM-CSF in PL732 ® and PL2417 culture containers were compared to CD3+ depleted cells cultured in RPMl/10% FCS plus cytokines in a polystyrene tissue culture flask. The cultures were assessed for expression of CDla, HLA-DR, HLA-ABC, and CD14.
  • Cytospins were prepared from each culture and differentials were read. The percentage of CDla+/HLA-DR+ peaked at day 1 for all cultures. Viability at day 1 for all cultures was over 90%, however by day 7, only the X-VIVO 15TM PL2417 culture had a viability over 80% (Tables 2 and 3) .
  • CD34+ cells The source of CD34+ cells was Isolex ® selected products received from Baxter Immunotherapy, Irvine, California, previously frozen and thawed for culture, or utilized fresh.
  • the CD34+ cells were selected from apheresis products from the peripheral blood of healthy volunteers who had been pre-treated with G-CSF to mobilize their CD34+ stem cells from their marrows to their peripheral circulation.
  • Mouse IgGl FITC Mouse IgGl PE, Becton Dickinson Goat anti-mouse F(ab)'2 IgG (H & L chains) FITC; Goat anti- mouse F(ab)'2 IgG (H & L chains) PE, Immunotech
  • Anti-CD34 PE Anti-CD14 FITC
  • Anti-HLA-DR Anti-HLA-DR
  • Frozen CD34+ cells were removed from liquid nitrogen in 1 ml vials of 5 X 10 6 . Vials were thawed rapidly in warm tap water and immediately transferred to a 50 ml polypropylene tube containing X-VIVO 15TM media. Cells were pelleted by centrifugation at 400g for 7 min. , washed twice with X-VIVO 15TM media, and resuspended in a final volume of 10 ml . Cells were counted using Coulter counter, 10 ml cetrimide and 20 ul of sample cells, washed a final time in 50 ml X-VIVO 15TM, and resuspended in 1 ml PBS. Aliquots of this final cell suspension were then added to appropriate volumes of media, plus growth factors chosen to drive preferential differentiation of dendritic cells .
  • PL2417 containers were filled using a 250 ml conical tube, pouring the appropriate cell suspension into a 60 ml syringe barrel attached as a funnel to an injection port of the PL2417 container via a needle .
  • Fresh CD34+ cells were processed in a similar manner except for the thaw and subsequent washings. Cell samples were counted on a Coulter counter in 10 ml cetrimide + 20ul of sample cells. Viability and CD34+ percentages were assessed prior to setting up the experiment via PI exclusion of dead cells, anti-CD34 PE staining, and acquisition on FACSort .
  • Flask and bag cultures were set up as described above for the frozen sources.
  • Poietic Technologies commercial source: Cells received were frozen day 7 cells termed intermediate progenitors by Poietic Technologies, thawed and cultured in the following manner. RPMI/10%FCS media was warmed. The vial of frozen cells was quickly thawed in a 37°C water bath and the outside of the vial was cleaned with 70% ethanol. A maximum of 2 ml of cell suspension was aseptically transferred to a 50 ml conical tube. The vial was rinsed with 1 ml of media and added dropwise to the cells while gently swirling after each addition. Enough medium was slowly added dropwise to the cells until the total volume was 5 ml, while gently swirling after each addition of several drops.
  • the volume was slowly brought up to 50 ml by adding 1 ml to the 2 ml volumes of media dropwise, gently swirling after each addition of media. Tubes were centrifuged at 200g at room temp for 20 min. 45 ml of the wash was carefully removed by pipet . The pellet was gradually suspended in the remaining 5 ml of media and the cells were transferred to a 15 ml conical tube. The tube was rinsed with 5 ml of media and the rinse was slowly added dropwise to the cell suspension in 15ml conical tubes, gently swirling each addition of several drops of media. The tube was rinsed a second time with 4 ml of media and the rinse was slowly added to the 15 ml conical tube, as above. The tubes were then centrifuged at 200g for 20 min. 12 ml of wash was carefully removed by pipet. The pellet was gently resuspended in the remaining 2ml of media and counted.
  • the cells were allowed to rest for 1 hour at 37°C and 5% C0 2 . They were counted a second time and 5 X 10 6 cells + 50 ml QBSF ® 58 media + Cytokine A (70ul) were placed in each T175 flask. Media and Cytokine A was provided by Poietic Technologies; their composition was unknown to the present inventors. Considering the state of the art, it is very likely that the media contained FCS, since if it were serum- free, this would have been a remarkable advance that Poietic Technologies would surely have advertised. These cells were used as a positive control since Poetic Technologies advertises this system as a source of dendritic cells.
  • the cells were placed in an incubator at 37°C, 5% C0 2 . Cultures were fed 3 days post-thaw (day 10) by adding 25 ml QBSF ® 58 media + 25 ul Cytokine B (again, provided by Poietic Tech., composition unknown. The cells were harvested day 7 post thaw (day 14) by agitating the flask, then removing and saving the cell suspension. Adherent cells were treated with 5mM EDTA for 10 min at 37°C. Diluted 2X with 1%HA/PBS to buffer the EDTA.
  • Cells were centrifuged at 400g for 10 min. and resuspended in RPMI/10.FCS, used for phenotyping, cytospin/morphological identification, and MLR.
  • Phenotyping of Cultured Cells Staining of Cells Approximately 1 x 10 ⁇ cells were transferred into multiple 12 x 75 mm polypropylene tubes. One ml of PAB was added to each tube, and cells were collected by centrifugation for 3 minutes at room temperature at HIGH setting (1,000 x g) using a SERO-FUGE II. The supernatants were poured off, the excess liquid was blotted on absorbent paper and the tubes were gently vortexed to loosen the cell pellets. The cells were stained by adding conjugated and pure antibodies as follows
  • PBS phosphate buffered saline
  • PBS phosphate buffered saline
  • PBS phosphate buffered saline
  • Endogenous peroxidase activity was blocked by treating slides with hydrogen peroxide/PBS (2ml 30% H 2 0 2 + 30 ml PBS) for 10 min.
  • Slides were rinsed with PBS one time.
  • Non-specific binding sites were blocked by incubating with normal serum matching source of secondary antibody (i.e. if secondary antibody is biotinylated goat-anti-mouse, used normal goat serum) at room temp. for 15 min. in a humidified environment.
  • Chromagen solution was made with 5ml millipore water + 2 drops of chromagen buffer + 1 drop of concentrated chromagen + 1 drop of substrate, and 4 -5 drops were added to each slide. Slides were incubated for 2-10 min., until the cells showed positive red color, then rinsed with distilled water. Slides were counterstained with hematoxylin for about 5 min, or until cell nuclei were stained purple. Cells were rinsed with tap water and allowed to air dry. Slides were covered with crystal mount and oven dried at 80 degrees for 15 min. Slides were allowed to cool, then coversliped with mounting medium.
  • CD34+Cell -derived Dendritic Cells Serum-containing media in a Flask vs. Serum-free media in a PL2417 Container.
  • Tables 7 and 8 show the average phenotype, morphology, and MLR values of 3 experiments designed to test the feasibility of culture deriving dendritic cells from thawed CD34+ cells, using serum-free conditions and PL2417 containers .
  • Each experiment consisted of two cultures at I X 10 5 cells/ml in 100 ml media + 100 U/ml GM-CSF + lOOU/ml TNF-cr.
  • culture 1 was grown in RPMI supplemented with 10% FCS, a condition typically cited in literature as conducive to dendritic cell growth.
  • Culture 2 contained serum- free X-VIVO 15TM in PL2417 containers.
  • 1% HA was used as a supplement in the serum- free culture, without significant improvement in cell growth, phenotype or stimulatory capacity (data not shown) .
  • Phenotypic analysis over the 14 day culture shows the following trends in surface expression: decreased expression of CD34, expected as the cells differentiate as a result of culture; increased CD80 expression in both cultures, again higher in the serum- free culture; and an increase in the CD86 expression that seemed equivalent in both cultures.
  • CDla expression showed slight fluctuations, but no consistent increase.
  • Dendritic cells displaying dendritic cell morphology increased to an average of 25% for RPMI culture and 32% for serum-free by day 14, as evidenced by Wright -Geimsa staining.
  • Dendritic cells were identified by cytoplasmic processes or "veils" that extend from the surface of the cells. The S100 antibody was used in the immunohistochemical staining of the cells of cytospins and seems to correlate best with the CD80 phenotyping. MLR's performed showed a moderate proliferative response when stimulated with 10,000 cells from dendritic cell enriched cultures.
  • Tables 9 and 10 summarize preliminary data from one experiment using conditions similar to those above.
  • Fresh CD34 + cells were utilized at a higher concentration, 3 X 10 5 cells/ml, under the same media/flask/cytokine conditions. Phenotyping was changed to exclude CD14/HLA-DR, and included CD4/CD3. Dendritic cells are reputed to be CD3 negative, but CD4 positive.
  • the CDla stain was also changed to a new PE-conjugated antibody that made a more easily resolved population because of brighter fluorescence. This culture follows similar trends as the previous, with the addition that a high percentage of the populations were CD3-/CD4+. In addition, the new antibody to CDla resulted in a clear population of CDla positive cells. These data are again reinforced by the morphologic and MLR data. Interestingly, cells derived from the serum- free culture seem to have a much greater stimulatory capacity at day 7.
  • Cytospin slides from this culture were also stained immunohistochemically on day 14 using a panel of 5 antibodies chosen on the basis of positive staining of a commercially available source of dendritic cells (under results, Dendritic cells derived from Poietic Technologies) .
  • Table 11 summarizes the percentages positive of each antibody.
  • the X-VIVO 15TM condition has more positive cells, correlating with the greater stimulatory capacity indicated above.
  • CD80 expression increased by Day 14 in all but the PROGENitorTM-34 media.
  • CD86 expression increased substantially at Day 14 in cultures in X-VIVO 15TM and RPMI/10%FCS, and to a lesser degree in X-VIVO 15TM/1%HA and PROGENitorTM-34. Again, there was a high percentage by day 7 of CD4+/CD3- cells, except in the PROGENitorTM-34 media. There was no upregulation of CDla expression. Two other CDla antibodies were also evaluated in these experiments from alternate sources Biosource and Serotec (data not shown), but there was little or no staining.
  • Progenitor 34 37 63 30 70 17,430 8,584 4,827 4,918
  • Dendritic Cells Derived from Poietic Technologies The source of cells bought from Poietic Technologies is CD34+ cells isolated from bone marrow. Three separate experiments were set up with these cells. The first experiment was to culture the cells as instructed by Poietic Technologies as a positive control for the methods of the invention. The cells received were frozen at day 7 culture, subsequently thawed and cultured in-house for another 7 days, for a total of 14 days. The cells were stained with a panel of fluorescent antibodies, stained for morphology, and set up in an MLR. Phenotype showed an increase in CD80 expression. These day 14 cells also showed increased expression of CDla.
  • Morphology data also confirms the presence of dendritic cells in the culture, but not the 90% expected from the advertising of Poietic Technologies.
  • the cultured cells are not very effective at stimulating T-cells, however this may be a reflection of the poor day 7 viabilities, possibly attributed to the 5mM EDTA treatment to remove the adherent cells from the flask.
  • Cytospin slides were also prepared from the two cultures reported above, including both Wright-Geimsa and acetone- fixed for immunohistochemical analysis.
  • Six different antibodies were chosen based on literature citations and results of phenotypic analysis above: CD86, S100, CD35, CD80 (Immunotech), CD80-PE (BD),and CDla (Coulter).
  • Various dilutions of antibodies were used in the assay, from 1:10 to 1:1000, to determine the optimal titration for immunohistochemical staining, as shown in Tables 18 and 19. This determination was based on intensity of staining of individual positive cells and the lack of background, or non-specific staining.
  • CD35 showed approximately 4 positive cells (data not shown) and CD80-PE showed none, and was not used in subsequent staining.
  • DC-2 36 64 The purpose of this series of experiments was to determine the feasibility of culture deriving dendritic cells utilizing selected CD34+ cells in serum-free media in PL2417 containers. To this end, a number of different media/culture conditions were evaluated to determine possible effects on dendritic cell differentiation, as evidenced by phenotype, morphology, immunohistochemistry, and MLR data. Efforts were made to correlate expression of some of the commonly cited surface molecules with the positive identification by morphology (Wright-Geimsa staining) , immunohistochemistry and stimulatory capacity in MLR. CDla is commonly cited as a dendritic cell marker, yet expression was not always consistent in these cultures. The most consistent results are increased expression of CD80 and CD86, T-cell costimulatory molecules whose presence on the cell surface is consistent with the role of the dendritic cell as a professional antigen presenting cell.
  • the preliminary data comparing fresh cells in serum vs. PL2417/serum-free shows a noticeable difference in stimulatory capacity, especially at the 1,000 stimulators/well condition (approx. 8,000 vs. 31,000 on day 7, and 2,000 vs. 15,000 on day 14) .
  • Poietic Technologies cells were used as a positive control to test various antibodies for flow cytometric analysis and immunohistochemistry. Based on the panel of flow cytometry antibodies screened, the best correlation of positive staining on dendritic cells and minimal reactivity to non-dendritic cells is with the following antibodies: CDla-PE, Coulter; CD86-PE, Ancell; and CD80-PE, BD.
  • dendritic cells can be culture derived from CD34+ cells cultured serum- free in culture containers having a polystyrene growing surface.
  • Example 3 Co-culturing and immunostaining of tetanus toxin antigen-pulsed DC.
  • CD34+ cell selection was performed using Isolex ® , per Manual instructions.
  • Cell sources 1) DC culture derived from CD34+ cells/T-cells from non- targeted (non-CD34-selected) fraction.
  • Fresh CD34+ cells and the non-CD34 -selected fraction were counted on Coulter counter in 10 ml cetrimide + 20ul of sample cells. Viability and CD34+ percentages were assessed prior to setting up the experiment via PI exclusion of dead cells, anti-CD34 PE staining, and acquisition on FACSort .
  • the appropriate volume of non- CD34 -selected cell suspension was added to make a concentration of 5 X 10 5 cells/ml in 300ml of X-VIVO 15TM, plus 50ng/ml OKT-3 and lOOU/ml IL-2, and cultured in the PL2417 container.
  • the PL2417 container was filled using a 250 ml conical tube, pouring the appropriate cell suspension into a 60 ml syringe barrel attached as a funnel to an injection port of the PL2417 container via a needle.
  • DC/T-cell co-cultures were set up by adding the autologous T-cells to the PL2417 "window" container at a T- cells:DC ration of 10:1. Cytospin slides were made after 7 days of co-culture.
  • Phenotyping and morphological analysis were performed as described in Examples 1 and 2 above.
  • T-cells were isolated via sheep red blood cell rosetting as follows. Sheep red blood cells were prepared and used to erythrocyte rosette T-cells as described in Current Protocols in Immunology, John Wiley and Sons Inc., 1995. Vol. 2, 7.2.1 - 7.2.4.
  • the Ficoll interface (non-T-cell- MNC) was retained as starting source for culture-deriving dendritic cells. These were set up in 20 ml cultures, plate/RPMl/lO%FCS, and 2417container/X-VIVO 15TM at a concentration of 3 X 10 5 cells/ml, stimulated with 100 U/ml GM-CSF and 1000 U/ml IL-4.
  • T-cells from the rosetting step were set up in 40ml X-VIVO 15TM in 2417 container at a concentration of 5 X 10 5 cells/ml, stimulated with 50ng/ml OKT-3 and lOOU/ml IL-2.
  • each dendritic cell-enriched culture was split 3 ways and stimulated with different concentrations of Tetanus Toxin C fragment (TTC) , lOOug/ml, lOug/ml and lug/ml for overnight.
  • TTC Tetanus Toxin C fragment
  • T-cells from the above described culture were added at a T- cell-.DC ratio of 5:1.
  • Co-cultures were maintained for 21 days, with cytospin slides made at days 7, 14, and 21.
  • Cytospin slides were prepared and Wright-Giemsa stained as described in Example 1 above .
  • Phenotyping and morphological analysis were performed as described in Examples 1 and 2 above.
  • PBS phosphate buffered saline
  • PBS phosphate buffered saline
  • Chromagen solution was made by mixing 5ml millipore water + 2 drops of chromagen buffer + 1 drop of concentrated chromagen + 1 drop of substrate, and 4 -5 drops were added to each slide. Slides were incubated for 2-10 min., until cells showed positive red color, then rinsed with distilled water. Slides were counter-stained with hematoxylin for about 5 min, or until cell nuclei were stained purple. Slides were rinsed with tap water and let air dry. Slides were rinsed with crystal mount and oven dried at 80 degrees for 15 min, cooled, and coversliped with mounting medium. RESULTS: Cells which were prominently stained for tetanus toxoid antigen also displayed characteristic DC processes (see Figure 9) . Cells with lymphocyte morphology appeared unstained by the tetanus toxoid antigen antibody.
  • Example 4 Culture of DC from umbilical cord blood.
  • CD34+ cells from umbilical cord blood offer certain advantages over cells obtained from bone marrow or peripheral blood in that the CB CD34+ cells are naive, highly proliferative, and the risk of culturing and reinfusing tumor cells is diminished.
  • CB mononuclear cells were obtained from CB samples using a 1.2% hetastarch solution in sodium chloride (HESPAN ® , DuPont) .
  • CD34+ cells were isolated using the Isolex ® magnetic bead CD34 cell selection method described above. The average viability and CD34 purity, post-selection, was 7.19% and 67.50% respectively.
  • Cells were fed with 200 U/ml GM-CSF and 50 U/ml TNF- ⁇ or with 200 U/ml GM-CSF, 50 U/ml TNF- ⁇ , 10 ng/ml SCF, and 50 U/ml IL-3. Cells were counted and analyzed at days 0, 11, and 25 for the presence of DC.
  • DC were identified by their expression of CDla, CD80, and CD86 by flow cytometric methods, immunohistochemically using an anti-SlOO antibody, and morphologically by Wright-Geimsa staining.
  • the highest average percent of cells displaying DC characteristics was obtained in cultures containing only GM-CSF and TNF- ⁇ with no added autologous plasma. Morphologically, 51% of these cells were DC.
  • the highest average amount of proliferation (32 fold) at day 11 was obtained in cultures containing GM-CSF, TNF- ⁇ , SCF, and IL-3 with 10% plasma
  • the average percent of characterized DC was not greatly enhanced and morphologically only 5% of the cells were DC. Viability averaged over 90% throughout the culture period in all culture conditions.
  • the addition of autologous plasma did not significantly increase the purity of DC and although addition of SCF and IL-3 to the GM-CSF and TNF-c. combination did induce greater proliferation, the purity and overall number of characterized DC was not significantly enhanced.
  • Example 5 Producing clinically useful numbers of DC and antigen-specific T-lymphocytes.
  • Antigen-specific T-lymphocytes can be infused into a patient in order to combat cancer cells, for instance.
  • stimulated T-lymphocytes can be administered as a cancer vaccine to prevent recurrence of a specific cancer for which the patient is known to be at risk.
  • the entire culture of cells would contain about 10 billion (10 10 ) total cells, of which only about 10% would be antigen-specific T-cells.
  • a lower dose of antigen-specific T-cells might be useful for this indication; as few as 100 million antigen- specific T-cells could be effective.
  • vaccine use it is expected that higher numbers of antigen-specific T-cells will be necessary.
  • sufficient DC can be culture-derived to produce the required number of antigen- specific T-cells.
  • the PL2417 gas-permeable culture bags used in the above experiments have a growing surface area of 75cm 2 , which is designed for a volume of about 20ml of culture medium.
  • two million T-cell depleted MNC originally seeded in a 20 ml culture yielded two million DC.
  • this small-scale culture is sufficient.
  • 20 million DC are required, for instance, a total of 20 million MNC can be originally seeded in a total volume of 200 ml of culture medium, which can be contained in five clinical-scale culture bags of 150cm 2 surface area each.
  • the seeding cell concentration can be increased to 3 - 5 X 10 5 cells/ml, and the media volumes and culture surface areas adjusted accordingly.
  • the culture bags can be manufactured to higher surface areas, as required for a given clinical need.
  • Antigen-pulsing and addition of the requisite number of T-cells can be carried out aseptically in the originally seeded culture bag(s) once the culture has become enriched for DC.
  • DC cultures can be split aseptically by directing a portion of the culture in the original bag to other aseptically attached bags using sterile connections and tubes. Antigen-pulsing and T-cell co-culture can then be performed aseptically in the split DC cultures.
  • Example 6 Dendritic cells culture-derived from adherent cells. PBMNC were placed into PL2417 gas-permeable containers and allowed to adhere to the container over a 2 hour incubation period. Non-adherent cells were removed and placed into a separate container. For comparison, PBMNC or MNC were also cultured without preadherence, as described above, in both PL2417 gas-permeable containers and Teflon ® cell culture bags .
  • Adherent cells, non-adherent cells, and bulk MNC were all cultured in X-VIVO 15 serum free media supplemented with 2 mM L-glutamine, 50 ng/ml granulocyte/macrophage-colony stimulating factor (GM-CSF) , and 1000 U/ml interleukin-4
  • IL-4 Analysis for the presence of DC were performed on days 0 and 7 of the culture period, as described above. These analyses included phenotyping for cell surface markers CDla, CD14 , CD80, and CD86 using flow cytometric techniques, immunohistochemical staining for the S100 protein, morphological identification after Wright-Geimsa staining, and in some cases, functional capacity of cultured cells to induce T cell proliferation in an allogeneic mixed lymphocyte reaction (MLR) .
  • MLR allogeneic mixed lymphocyte reaction
  • Teflon ® Cell Culture Bags were purchased from American Flouroseal Co., Silverspring, MD. All other materials were as described above.
  • Mononuclear cells were prepared from whole blood or apheresis product, as described above.
  • PBMNC cells were cultured in X-VIVO 15TM supplemented with 2 mM L- glutamine . Cultures were initiated at 5 x 10 5 cells/ml in PL2417 gas-permeable containers (20 ml) or Teflon ® cell culture bags (30 ml) .
  • GM-CSF and IL-4 were added to the cultures at final concentrations of 50 ng/ml and 1000 U/ml, respectively.
  • Addition and subtraction of cells, media, and growth factors to and from PL2417 gas-permeable containers was accomplished by spiking a Sampling Site Coupler into the sample port of the container followed by use of syringes and needles.
  • Addition and subtraction of cells, media, and growth factors to and from Teflon ® cell culture bags was accomplished by attaching a syringe (without needle) to the female connectors of the sample ports. Cells were cultured in a 5% C0 2 , ambient 0 2 , 37° C humidified incubator for 7 days .
  • PBMNC were resuspended in culture media (X-VIVO 15TM ) at 2 x 10 6 cells/ml.
  • Cells were placed into PL2417 gas-permeable containers (20 ml) or Teflon ® cell culture bags (30 ml) and incubated for 2 hours in a 5% C0 2 , ambient 0 2 , 37° C humidified incubator.
  • Non-adherent cells were removed from the containers and set aside, then containers were rinsed with PBS-CMF. The rinse from each container was then removed and also set aside.
  • Cells remaining in the containers were adherent cells. These cells were cultured by adding 20 ml of X-VIVO 15TM to the PL2417 containers or 30 ml X-VIVO 15TM to the Teflon ® cell culture bags then adding GM-CSF and IL-4 at final concentrations of 50 ng/ml and 1000 U/ml, respectively. For analysis purposes only, duplicate containers were made and adherent cells were removed by adding 20 ml (PL2417) or 30 ml (Teflon ® ) of lx trypsin to each container. Containers were placed in a 5% C0 2 , ambient 0 2 , 37° C humidified incubator for 5 minutes.
  • the trypsinized cells were removed and then immediately placed into tubes containing cold culture media. Containers were rinsed with culture media. This rinse was removed and placed into the tubes containing the cells.
  • Adherent cells were washed by centrifugation, then resuspended in culture media. Cells were counted using the Coulter Counter.
  • Non-adherent cells were washed by centrifugation at 400 x g for 7 minutes at room temperature, then resuspended to 5 x 10 5 cells/ml in X-VIVO 15TM.
  • Non-adherent cells were placed into fresh PL2417 gas-permeable containers or fresh Teflon ® cell culture bags (depending in which container they originated from) then cultured in the presence of GM-CSF (50 ng/ml) and IL-4 (1000 U/ml) for 7 days in a 5% C0 2 , ambient 0 2 , 37° C humidified incubator.
  • GM-CSF 50 ng/ml
  • IL-4 1000 U/ml
  • MLR mixed lymphocyte reactions
  • Table 34 shows the average percent phenotype of cells present in the 4 culture conditions at days 0 and 7. By day 7, the average percent of CD14+ cells decreased in all cultures. Furthermore, the PL2417 adherent culture contained the highest average percent of CDla+ , CD80+, and CD86+ cells. Table 35 shows the average total number of cells in the 4 culture conditions expressing certain phenotypic markers. These total cell numbers were calculated by multiplying the percents m Table 34 by the proliferation index and starting cell numbers from Table 33.
  • Tables 36 and 37 show the morphological data and tables 38 and 39 show the immunohistochemical data.
  • Tables 36 and 38 are the percent of cells identified as DC morphologically under Wright-Geimsa staining and the percent of cells that were positive for the S100 protein, respectively.
  • Table 37 Average of Total Number of Cells in Culture Displaying DC Morphology.
  • Example 7 Cytokine-free culture of dendritic cells. Whole blood from healthy human donors was obtained and mononuclear cell preparations were made as described above in Example 1. Equipment, materials and methods were as described above. Sources for additional materials were:
  • Cyclic Adenosine Monophosphate cAMP
  • Vitamin D3 Sigma, Cat. No. C-9756
  • PBMNC Polystyrene Tissue Culture Plates
  • PBMNC were resuspended in culture media (X-VIVO 15TM + 10% autologous serum) at 2 x 10 6 cells/ml.
  • Cells were placed into 48 well polystyrene tissue culture plates (2 ml per well) and incubated for 2 hours in a 5% C0 2 , ambient 0 2 , 37° C humidified incubator.
  • Non-adherent cells were removed from the plates then wells were rinsed with X-VIVO 15TM containing no serum. Cells remaining in the wells were adherent cells.
  • PBMNC cells were cultured in X-VIVO 15TM supplemented with 2 mM L- glutamine. Cultures were initiated at 5 x IO 5 cells/ml in PL2417 gas-permeable containers (20 ml) .
  • GM-CSF and IL-4 were added to the cultures at final concentrations of 50 ng/ml and 1000 U/ml or non-cytokine additives such as Vitamin D3 at 2.5 uM, Vitamin E at 0.1%, Linoleic Acid at 5 ug/ml, or Ca +t Ionophore at 10 m .
  • the percentage of S100+ cells was also the highest in the GM-CSF/IL-4 wells (26%) while Vitamin E, Linoleic Acid and Ca ++ Ionophore containing wells possessed 19%, 20%, and 17% S100+ cells, respectively.
  • the percentage of morphologically identified DC cells was again highest in the GM-CSF/IL-4 containing wells (8%) while all other conditions contained less than 4% DC. Table 42. Day 4 Results Without GM-CSF.
  • the percent viable cells was higher than the non-cytokine alone cultures at day 4 (Table 43) . Furthermore, the percentage of S100+ cells was higher in more non-cytokine additive conditions when GM-CSF was added with the highest in the GM-CSF/cAMP wells (41%) . The percent of morphologically identified DC was also enhanced when GM-CSF is added. The wells with the highest percent DC were ones with GM-CSF/IL-4, GM-CSF/Linoleic Acid and GM-CSF/Ca ++ Ionophore.
  • Vrt D3 1 95E+05 9586% 800% 300%
  • the GM-CSF/IL-4 wells contained the highest percentage of S100+ cells (46%) and morphologically identified DC (9.5%).
  • the Linoleic Acid and Ca" Ionophore conditions possessed the next highest percentages of S100+ cells and morphologically identified DC.
  • the SlOO protein is a nerve cell protein that has been associated with dendritic cells.
  • Table 47 at day 7 of culture, the highest percent of S100+ cells was present in the GM-CSF/IL-4 culture (13%) .
  • the Ca ++ Ionophore, Vitamin E, and Linoleic Acid cultures contained equivalent average percentages of S100+ cells while Vitamin D3 contained the lowest average percent .
  • the table also shows the average total number of cells projected in culture positive for the SlOO protein.
  • day 0 cells showed averages of 3.7% CDla, 11.3% CD14 , 0.6% CD80 and 9.3% CD86 expression (Table 49) .
  • day 7 dropped (except for CD80) below what is normally expected in the GM-CSF/IL-4 cultures, although the highest percentage of CDla, CD80, and CD86 expression was seen in these cultures when compared to the non-cytokine containing cultures.
  • VIT D3 0.10% 0.53% 2.65% 262%

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Abstract

L'invention porte sur un procédé de production de cellules dendritiques humaines à des fins thérapeutiques à partir de cultures sans cytokines ou avec peu de cytokines. Ledit procédé consiste à cultiver des cellules mononucléaires sanguines ou médullaires dans un milieu contenant au moins un agent tel que: un ionophore de calcium, (par exemple l'A23187), de la théophylline, de la prostaglandine E1, de l'AMP cyclique dibutyryle, de la vitamine D3, de la vitamine E, de l'acide rétinoïque, ou un acide gras. La culture est maintenue pendant un temps suffisant, par exemple de 4 à 14 jours, pour la production d'une culture enrichie en cellules dendritiques au moins 2,5 % du total des cellules présentant le processus des cellules dendritiques, ou un antigène de cellules dendritiques tel que le CD80, le CD86, ou le CD1a. L'invention porte également sur un procédé de production de cellules T humaines spécifiques d'un antigène qui consiste à pulser les cellules dendritiques obtenues par le susdit procédé à l'aide d'un antigène viral, tumoral ou bactérien ou de la surface de cellules, puis à co-cultiver les cellules T et les cellules dendritiques à impulsion antigénique. Les cellules dendritiques ainsi obtenues sont utiles pour le traitement d'infections virales ou bactériennes, en tant que vaccin contre le cancer, ou pour l'induction de tolérance aux allo ou xéno-greffes.
PCT/US1997/013759 1996-08-14 1997-08-13 Culture sans cytokines, de cellules dendritiques WO1998006823A2 (fr)

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US6010905A (en) * 1995-01-27 2000-01-04 The United States Of America As Represented By The Department Of Health & Human Services Method for inducing monocytes to exhibit the phenotype of activated myeloid dendritic cells
WO2001027245A2 (fr) * 1999-10-08 2001-04-19 Dendreon Corporation Generation et caracterisation d'une cellule dendritique isolee des cellules mononucleaires du sang peripherique humain
WO2001051617A1 (fr) * 2000-01-11 2001-07-19 Maxygen, Inc. Sous-ensembles de cellules dendritiques dérivées de monocytes
US6358736B1 (en) 1995-01-27 2002-03-19 The United States Of America As Represented By The Department Of Health And Human Services Method for increasing the antigen presenting ability of leukemia cells
WO2004056397A1 (fr) * 2002-05-29 2004-07-08 Demao Yang Stimulation de l'hematopoiese au moyen de cellules immunitaires activees ex vivo
EP1647256A1 (fr) * 2003-07-09 2006-04-19 Oncorex, Inc. Composition activant la capacite de filtration de cellules dentritiques et activateur immunitaire
US7332158B2 (en) 2002-05-29 2008-02-19 Demao Yang Compositions and treatments for myelosuppression by ex vivo activated immune cells
KR101309894B1 (ko) 2011-07-07 2013-09-17 인제대학교 산학협력단 수지상세포 분화 유도용 조성물 및 이의 분화 유도방법
US9969979B2 (en) 2012-08-31 2018-05-15 The Governors Of The University Of Alberta Methods for producing cells having a phenotype of a primary human hepatocytes and compositions

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WO1994002156A1 (fr) * 1992-07-16 1994-02-03 The Board Of Trustees Of Leland Stanford Junior University Procedes d'utilisation de cellules dendritiques pour activer des lymphocytes t
WO1996023060A1 (fr) * 1995-01-27 1996-08-01 The Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services Procede pour isoler des cellules dendritiques

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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6010905A (en) * 1995-01-27 2000-01-04 The United States Of America As Represented By The Department Of Health & Human Services Method for inducing monocytes to exhibit the phenotype of activated myeloid dendritic cells
US6358736B1 (en) 1995-01-27 2002-03-19 The United States Of America As Represented By The Department Of Health And Human Services Method for increasing the antigen presenting ability of leukemia cells
WO1999000137A3 (fr) * 1997-06-30 2000-01-06 Us Health Induction d'un phenotype de cellules dendritiques myeloides activees
WO2001027245A2 (fr) * 1999-10-08 2001-04-19 Dendreon Corporation Generation et caracterisation d'une cellule dendritique isolee des cellules mononucleaires du sang peripherique humain
WO2001027245A3 (fr) * 1999-10-08 2001-12-13 Dendreon Corp Generation et caracterisation d'une cellule dendritique isolee des cellules mononucleaires du sang peripherique humain
WO2001051617A1 (fr) * 2000-01-11 2001-07-19 Maxygen, Inc. Sous-ensembles de cellules dendritiques dérivées de monocytes
WO2004056397A1 (fr) * 2002-05-29 2004-07-08 Demao Yang Stimulation de l'hematopoiese au moyen de cellules immunitaires activees ex vivo
US7048922B2 (en) 2002-05-29 2006-05-23 Demao Yang Stimulation of hematopoiesis by ex vivo activated immune cells
US7332158B2 (en) 2002-05-29 2008-02-19 Demao Yang Compositions and treatments for myelosuppression by ex vivo activated immune cells
EP2011863A1 (fr) * 2002-05-29 2009-01-07 Demao Yang Stimulation de l'hématopoïèse par des cellules immunitaires activées ex vivo
US7758857B2 (en) 2002-05-29 2010-07-20 Demao Yang Stimulation of hematopoiesis by ex vivo activated immune cells
EP1647256A1 (fr) * 2003-07-09 2006-04-19 Oncorex, Inc. Composition activant la capacite de filtration de cellules dentritiques et activateur immunitaire
EP1647256A4 (fr) * 2003-07-09 2007-10-31 Oncorex Inc Composition activant la capacite de filtration de cellules dentritiques et activateur immunitaire
KR101309894B1 (ko) 2011-07-07 2013-09-17 인제대학교 산학협력단 수지상세포 분화 유도용 조성물 및 이의 분화 유도방법
US9969979B2 (en) 2012-08-31 2018-05-15 The Governors Of The University Of Alberta Methods for producing cells having a phenotype of a primary human hepatocytes and compositions

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