EP1751274A1 - Methode zur herstellung von pluripotenten zellen aus monozyten - Google Patents

Methode zur herstellung von pluripotenten zellen aus monozyten

Info

Publication number
EP1751274A1
EP1751274A1 EP05761385A EP05761385A EP1751274A1 EP 1751274 A1 EP1751274 A1 EP 1751274A1 EP 05761385 A EP05761385 A EP 05761385A EP 05761385 A EP05761385 A EP 05761385A EP 1751274 A1 EP1751274 A1 EP 1751274A1
Authority
EP
European Patent Office
Prior art keywords
cells
cell
monocytes
differentiation
pluripotent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP05761385A
Other languages
English (en)
French (fr)
Inventor
Hinrich J. Peters
Dagmar Heinemann
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Peters Hinrich
Original Assignee
Peters Hinrich
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Peters Hinrich filed Critical Peters Hinrich
Priority to EP05761385A priority Critical patent/EP1751274A1/de
Publication of EP1751274A1 publication Critical patent/EP1751274A1/de
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • C12N5/0652—Cells of skeletal and connective tissues; Mesenchyme
    • C12N5/0653—Adipocytes; Adipose tissue
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/46—Cellular immunotherapy
    • A61K39/461—Cellular immunotherapy characterised by the cell type used
    • A61K39/4615—Dendritic cells
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/46—Cellular immunotherapy
    • A61K39/462—Cellular immunotherapy characterized by the effect or the function of the cells
    • A61K39/4622—Antigen presenting cells
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/46—Cellular immunotherapy
    • A61K39/464—Cellular immunotherapy characterised by the antigen targeted or presented
    • A61K39/4643—Vertebrate antigens
    • A61K39/4644—Cancer antigens
    • 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
    • C12N5/0639—Dendritic cells, e.g. Langherhans cells in the epidermis
    • 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
    • C12N5/0645—Macrophages, e.g. Kuepfer cells in the liver; Monocytes
    • 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
    • C12N5/0652—Cells of skeletal and connective tissues; Mesenchyme
    • C12N5/0654—Osteocytes, Osteoblasts, Odontocytes; Bones, Teeth
    • 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
    • C12N2500/00—Specific components of cell culture medium
    • C12N2500/30—Organic components
    • C12N2500/38—Vitamins
    • 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
    • C12N2500/00—Specific components of cell culture medium
    • C12N2500/30—Organic components
    • C12N2500/42—Organic phosphate, e.g. beta glycerophosphate
    • 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
    • C12N2501/01—Modulators of cAMP or cGMP, e.g. non-hydrolysable analogs, phosphodiesterase inhibitors, cholera toxin
    • 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
    • C12N2501/10—Growth factors
    • C12N2501/155—Bone morphogenic proteins [BMP]; Osteogenins; Osteogenic factor; Bone inducing factor
    • 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
    • C12N2501/22—Colony stimulating factors (G-CSF, GM-CSF)
    • 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]
    • 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
    • C12N2501/24—Interferons [IFN]
    • 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
    • C12N2501/25—Tumour necrosing factors [TNF]
    • 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
    • C12N2501/30—Hormones
    • C12N2501/33—Insulin
    • 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
    • C12N2501/30—Hormones
    • C12N2501/38—Hormones with nuclear receptors
    • C12N2501/39—Steroid hormones
    • 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
    • C12N2501/998—Proteins 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

Definitions

  • the present invention relates to methods for producing a cell population containing a majority of pluripotent intermediate cells or the pluripotent intermediate cells as such from monocytes, the pluripotent intermediate cells obtainable by said methods and their use for research purposes, diagnostic purposes, therapeutic purposes and/ or further differentiation.
  • Stem cells are cells found in all vertebrate animals, including human beings. They play a dominant role in the processes of normal development and regeneration or repair of damaged tissues. The reason for this is their capability of dividing to give rise to cells either identical to themselves or differentiated into particular types of cells. Cells having such developmental plasticity, i.e. cells not fixed as to their developmental destiny, are also referred to as pluripotent cells.
  • pluripotent stem cells may find use in research, diagnosis, and therapy.
  • Potential uses for pluripotent stem cells or their mature progeny include their application for studying fundamental processes of human development, such as differentiation, for toxicological testing and drug design, and for transplantation to replace cells or tissues damaged, e.g. by disease.
  • stem cells of fetal and/ or embryonic origin raises a number of ethical and legal questions. It would therefore be advantageous to use somatic stem cells, preferably from a readily accessible adult tissue.
  • somatic stem cells having a plasticity much higher than previously envisaged can be found in vertebrates.
  • somatic stem cells are monocytes.
  • the pluripotent nature of monocytes has been documented by their ability to be transdifferentiated in numerous types of differentiated cells, either of hematopoietic or non-hematopoietic lineages.
  • Monocytes are well-defined white blood cells originating from bone marrow. Upon certain stimuli, they migrate into the tissues and further develop into macrophages, myeloid dendritic cells, osteoclasts, or microglial cells. As amoeboid or phagocytic cells, they belong to the phylogenetically very ancient cells that can be found in primitive organisms lacking lymphocytes or other elements of a specific immune system. Monocytes thus represent immune cells as well as components of inflammation. Recently, information accumulated that monocytes also participate in regeneration.
  • monocytes are the precursors of macrophages. It was further demonstrated that monocytes have the potential of developing into myeloid dendritic cells (Peters et al., 1987). Monocytes were shown to represent the only nucleated cells in the blood failing to express nuclear lamine of the A/C variant, thus showing characteristics of precursor cells rather than of fully differentiated cells (Rober et al., 1990).
  • Fibrocytes which belong to the adherent fraction of blood mononuclear cells and express type I collagen. Fibrocytes could be produced from CD14+ cells (not referred to as monocytes here). As an inducer, conditioned me- dium from CD14- cells was used. When adding TGFbeta, the formation of collagen+ cells was enhanced. Anti-TGFbeta obliterated the effect, so that TGFbeta is regarded as a main inducer of fibrocyte development. In burn patients these cells occur at higher frequencies in the peripheral blood than in healthy donors, correlating with a higher level of TGFbeta in the blood.
  • fibroblastoid macrophages being positive for MAC-1 (CD11b/CD18), CD14, CD34, and CD45 were obtained. Diminished expression was found for HLA-DR, HLA-DQ, TNFRII, TNFalpha, leptin, PPARgammall, and lipid droplets.
  • the initial culture medium contained 10% fetal calf serum plus 10% horse serum, 10 "7 M cortisol, and the monoclonal CR3/43 antibody as inducers for transdifferentiation.
  • the CR3/43 antibody is directed against monomorphic regions of the human major histocompatibility complex (MHC)-class II antigens DP, DQ, and DR. Cortisol could be replaced by citrated human autologous plasma.
  • MHC human major histocompatibility complex
  • Cortisol could be replaced by citrated human autologous plasma.
  • the cells showed the following marker combination: CD34+, CD19-, CD45low, CD38+ or -, CD133 (c-Kit)+ or -. Under clonogenic test conditions, these cells formed colonies of all hematopoietic lineages, demonstrating their pluripotent nature.
  • MOMP monocyte-derived mesenchymal progenitors
  • monocytes were transdifferentiated into other cells either only from subpopulations of monocytes or under undefined culture conditions (i.e. in the presence of sera, conditioning factors, feeder cells), or both.
  • a method enabling a universal way of transdifferentiating monocytes has not been described so far.
  • the technical problem underlying the present invention is the provision of a method for producing cells containing a majority of pluripotent somatic cells or the pluripotent somatic cell as such.
  • this problem is solved by a method for producing a cell population containing a majority of pluripotent intermediate cells comprising the steps of a. culturing a highly purified preparation of monocytes in the presence of at least one retrodifferentiation inducing agent and optionally GM-CSF, until a majority of the monocytes has attained the state of an intermediate cell; and b. recovering the cell population containing a majority of pluripotent intermediate cells.
  • the problem is solved by a method for producing a pluripotent intermediate cell comprising the steps of a. culturing a highly purified preparation of monocytes in the presence of at least one retrodifferentiation inducing agent and optionally GM-CSF; and b. recovering a pluripotent intermediate cell.
  • monocytes may be reproducibly converted into an intermediate stage of pluripotency (pluripotent intermediate cells) under defined conditions and in a quantitative manner. That is, not only a subpopulation of monocytes but the majority of monocytes or even at least 80% of the monocytes may attain the state of an intermediate cell using the methods of the present invention.
  • the process of retro- differentiation may thus be induced in more of 50%, preferable in more than 60%, and even more preferably in more than 70%, 80% or even 90% of the monocytes.
  • pluripotent intermediate cell “intermediate cell” and “pluripotent cell” are used interchangeably for the purpose of this invention and refer to somatic stem cells having a distinct phenotype characterized by a marker combination shown in Table 1 below:
  • Table 1 Typical phenotypic markers for monocyte-derived pluripotent intermediate cells (determined for cells typically harvested after 10-15 days of culture)
  • the pluripotent intermediate cell of the invention thus phenotypically differs from all cell stages described in the state of the art up to date.
  • monocyte refers to cells of the monocyte-macrophage lineage, including mature monocytes, their descendants, and/or their precursors, carrying at least one marker of the myeloid lineage, i.e. CD14, CD68 (specific for mature cells) and/or CD33 (specific for their myeloid precursors).
  • transdifferentiation refers to the transformation of a differentiated cell of a given cell type to a differentiated cell of another cell type.
  • the first step in said transdifferentiation process leads to a less differentiated, pluripotent intermediate cell and is achieved by the method described above. This first step is also referred to as “retrodifferentiation” for the purpose of this invention. Retrodifferentiation may be followed by a second step, i.e. differentiation into any other cells accessible from the intermediate pluripotent cell.
  • retrodifferentiation of monocytes to produce pluripotent intermediate cells is achieved by culturing the monocytes in the presence of at least one retrodifferentiation inducing agent and optionally GM-CSF.
  • at least one means that up to 100 retrodifferentiation inducing agents may be used.
  • one, two or three, ten, 25 or 50 retrodifferentiation inducing agent(s) are combined.
  • the term “retrodifferentiation inducing agent” refers to an agent that induces retrodifferentiation in monocytes resulting in the pluripotent intermediate cells according to the invention.
  • the body's innate transmitters related to immunosuppression such as corticosteroids (e.g. cortisol, hydrocortisone), interleukin 10 (IL-10), transforming growth factor /? (TGF ), interferone ⁇ (VFN ⁇ ), and vascular endothelial growth factor (VEGF), as well as all factors that counteract the action of typical immune activators, may be used to induce retrodifferentiation.
  • corticosteroids e.g. cortisol, hydrocortisone
  • IL-10 interleukin 10
  • TGF transforming growth factor /?
  • VFN ⁇ interferone ⁇
  • VEGF vascular endothelial growth factor
  • immune activators examples include interieukin 1 (IL-1), interieukin 2 (IL-2), interieukin 12 (IL-12), interferon y (INFy), interieukin 8 (IL-8), IFN -inducing factor, tumor necrosis factor a (TNF ).
  • IL-1 interieukin 1
  • IL-2 interieukin 2
  • IL-12 interieukin 12
  • IFNy interferon y
  • IL-8 interieukin 8
  • IFN -inducing factor tumor necrosis factor a
  • TNF tumor necrosis factor a
  • the retrodifferentiation inducing agent is selected from the group consisting of
  • Immuno inhibitors are agents conferring immune inhibition and/or down regulation of the immune reaction and/or agents that counteract the action of immune activators.
  • the specific immune reaction is inhibited by inhibitors acting on generation, activity and survival of B- and T-lymphocytes including their products, and acting on generation, activity and survival of antigen-presenting cells, including their products.
  • the unspecific immune reaction is suppressed by agents that inhibit generation, activity and survival of unspecific immune cells such as monocytes, macrophages, granulocytes and their products, and a number of humoral nonspecific components such as complement.
  • immune inhibitors examples include interieukin 10 (IL-10), TGFbeta; interferons; hormones; receptors; immune inhibitory drugs; cytostatics; statins and microbial compounds such as cyclosporin.
  • IL-10 interieukin 10
  • TGFbeta TGFbeta
  • interferons hormones
  • receptors receptors
  • immune inhibitory drugs cytostatics
  • statins microbial compounds
  • Immune inhibitory drugs are prednisolone, dexamethasone, urocanic acid, cyclosporine- A, tacrolimus (FK 506), ursudeoxycholic acid (UDCA), desoxyspergualine (DSG), myco- phenolate mofetil (MMF).
  • cytostatics act through a general suppression of cell proliferation and by inducing cell death and thereby kill lymphocytes rather than monocytes and thus are also immune inhibitors.
  • Immune-inhibitory cytostatics such as cyclo- phosphamide, azathioprin and methotrexate are included.
  • Cytostatics have been designed to kill or to prevent proliferation of tumor cells.
  • non-tumor cells are kept alive.
  • these drugs are also immune-inhibitory in that they kill proliferating lymphocytes, while keeping alive other cells such as monocytic cells.
  • Actions on surviving cells can be summarized as the side effects of a drug. It appears that the monocyte system is programmed to react, as a side effect, by a genetically pre-programmed reaction pattern in the sense described herein, which can be summarized as the "regenerative program", developing along a pathway which is referred to as "retrodifferentiation” herein. This program appears to be activated generally in all cases, where an "activation" or "forward differentiation" of the monocytes is blocked.
  • immune response modifier is used synonymously with “immunomodulating agent” and “immune regulatory agent” and refers to the body's innate regulatory molecules and immunologically active drugs, the function of which cannot clearly be attributed to either immune activation or immune suppression in general.
  • Immunune response modifiers are agents that have been described to influence the direction of an immune response. The most prominent branching of an immune reaction known to occur within the T-helper cell system. The T-helper cells can either be polarized into the Th1 or into the Th2 direction. Signals to control this branching are mutally excluding each other, meaning that a signal that provokes one direction at the same time is inhibitory for the other direction.
  • interferon-gamma induces the Th1 polarization and inhibits the Th2 direction.
  • IL-4 IL-13
  • Th2 direction promotes the Th2 direction and inhibits the Th1 direction. It appears that every immunomodulating agent in parallel activates one and inhibits another developmental direction.
  • Immuno response modifiers include thymus peptides (such as Thym-Uvecal, Strath- mann), and endogenous mediators such as IL-4 or IL-13.
  • “Differentiation influencing agents” refer to agents which directly interfere with the process of differentiation. These agents either induce one defined process of "forward” differentiation, or they rather act on the cells to render them reprogrammable in a general sense. Most of them are typically used in combinations or cocktails with other inducers to induce a particular process of differentiation. Because they are not restricted to one particular type of differentiation, they are typically found in recipes of various differentiation protocols.
  • VEGF vascular endothelial growth as a differentiation inducing factor
  • heterogenous agents listed in Table 2 all exhibit more than one effect, most of them usually summarized as "side effects". None of these agents is only an activator or inhibitor; rather, they rather inhibit one system while activating another system. These polarities are reflected in columns 3 and 4 of Table 2. With respect to monocytes and the related cells of the "myeloid lineage" of bone marrow cells, it appears that these cells react on those manifold influences by a homogenous, genetically pre-determined program of "retrodifferentiation".
  • Prostaglandin System Prostaglan- PGE-2 lymphocytes macrophages, cAMP 78 ng/ml din-E-2 cGMP
  • Angiotensin-System Losartan Cozaar AT1-R-Antagonist Candesartan Atacand AT1-R-Antagonist Extracellular Matrix
  • two or more retrodifferentiation inducing agents may be used in combination.
  • the retrodifferentiation inducing agent is selected from interleukin-4 and interleukin-13.
  • IL-4 acts as an inducer of retrodifferentiation, attributed to its character as immune suppressor (regarded by some authors) or as immune response modifier (by its function to trigger a Th2-type of response). Because of their close relationship, IL-4 may be replaced by IL-13. IL-4 may be used either alone or in combination with IL-13.
  • dexamethasone sodium phosphate is used as the retrodifferentiation inducing agent.
  • Dexamethasone is an artificial analog of the natural hormone hydrocortisone.
  • hydrocortisone may be used.
  • the culture medium used for converting monocytes to pluripotent intermediate cells may optionally further contain granulocyte-macrophage colony stimulating factor (GM-CSF).
  • GM-CSF granulocyte-macrophage colony stimulating factor
  • GM-CSF is regarded as supporting the cell viability and the long-term survival of the cells.
  • GM-CSF can also be synthesized by the monocytes in an autocrine way, it does not necessarily have to be added to the culture.
  • the monocytes used in the methods according to the invention are derived from blood.
  • the blood is mammalian blood. Human blood is particularly preferred.
  • monocytes may be recovered as mature monocytes from bone marrow cells before they immigrate into the blood.
  • monocytes may be recovered from their natural precursors, i.e. from bone marrow cells of the "myeloid lineage". Beginning with the haematopoietic stem cell and continuing along the myeloid lineage, monocytes may be produced from any of their precursors using known growth factors such as GM- CSF and M-CSF.
  • the immune inhibitors and, if present, the GM-CSF are present in physiological concentrations.
  • physiological concentration refers to a concentration similar (i.e. deviating by no more than a factor of 5) to that found in blood.
  • the natural concentration in blood may easily be measured and compared to the concentration applied in cell culture. For instance, the level of corticosterone in human blood is about 10 microgram per liter blood, corresponding to 3x 10 ⁇ 8 M; the concentration of cortisol is about 100 microgram/liter, corresponding to 3x 10 ⁇ 7 M. During pregnancy, early childhood and certain conditions these levels may differ.
  • the cell culture concentration of dexamethasone used according to the invention is about 1x lO ⁇ M, i.e. only 3x higher than the physiological cortison level.
  • a typical dose of dexamethasone if applied therapeutically is 2 mg/liter blood, corresponding to 5x lO ⁇ M.
  • the concentration of dexamethasone used for retrodifferentiation according to the invention ranges within the physiological normal level of its natural counterpart and is even lower than the concentration used therapeutically.
  • cytokines such as IL-4
  • the concentration cannot be defined as "physiological blood concentration”, as cytokines function as short-range factors in the tissue, and are not normally released into the blood. Further, they are usually not therapeutically applied as drugs. Therefore, as far as cytokines such as interleukins (e.g. IL-4) are concerned, "physiological concentration” is to be understood in the sense that their concentration is much lower (i.e. by at least a factor of 10) and therefore more physiological, than the concentrations used in cell cultures previously described in the state of the art.
  • the concentrations used for producing the pluripotent intermediate cells in the first step of transdifferentiation are 25 U/ml for IL-4 and 3 U/ml for GM-CSF.
  • the culture medium used in the methods according to the invention is devoid of differentiation promoting factors.
  • differentiation promoting factor refers to any compound inducing the differentiation of monocytes and thus hindering the production of pluripotent intermediate cells from monocytes, e.g. factors contained in serum, factors that favor macrophage and/ or adipocyte development, and factors released by (activated) lymphocytes.
  • Factors that hinder the production of pluripotent intermediate cells from monocytes include macrophage colony stimulating factor (M- CSF), fungi, dead or vital microorganisms such as bacteria, lipopolysaccharides, teichoic acids or muramyl peptides and other factors released from microorganisms, granular material, immune complexes, dead cells, and cell fragments.
  • Factors that favor adipocyte development include lipids, liposomes, and chylomicrones. Lymphocytes, especially activated lymphocytes, which release immune activating factors such as inter- leukin-2 and interferone y are also inhibitory for the reaction and should therefore be omitted or suppressed.
  • the culture medium is preferably depleted of lymphocytes.
  • “Depleted of lymphocytes” means that lymphocytes are basically absent from the culture medium.
  • the lymphocytes may be removed by standard techniques in order to receive an at least 70% pure monocyte preparation, preferably an 80-90% pure monocyte preparation, more preferably a more than 95% or even a more than 99% pure monocyte preparation.
  • the present invention is related to a method for producing a differentiated cell comprising subjecting the cell population containing pluripotent intermediate cell(s) obtainable according to the method of the invention to differentiation by culturing the cell(s) in the presence of a differentiation inducing agent.
  • differentiation refers to a process in which a cell reaches a new state, associated with the acquisition of new properties. Differentiation may be induced by exogenous stimuli. After having reached the new state of differentiation, however, this state is maintained also in the absence of a further stimulus. In contrast, the process of activation leads to a shifting of a resting function to a higher metabolic activity, usually stimulated by exogenous stimuli. When omitting the stimulus, an activated cell falls back to the resting state within hours or maximally 3 days.
  • the differentiated state must not be a final state.
  • a differentiated cell may further differentiate into another state of differentiation.
  • Differentiation has so far been understood as a "forward"-process, i.e. cells develop away from the embryonic state and away from pluripotency or even totipotency. Recently, it is discussed in the literature that said process of "forward" differentiation may be reversible under physiological conditions. The reversing process is designated as “retrodifferentiation” or “reverse differentiation” and means that cells re-approach the state of pluripotency or even totipotency.
  • the intermediate pluripotent cell obtainable according to the methods of the present invention may be differentiated into both hematopoietic cells and non-hematopoietic cells (e.g. osteoblasts, follicular dendritic cells, osteoclasts, hepatocytes, fibroblasts, cartilage cells , endothelial cells, adipocytes, muscle cells, neural cells such as glial and nerve cells).
  • non-hematopoietic cells e.g. osteoblasts, follicular dendritic cells, osteoclasts, hepatocytes, fibroblasts, cartilage cells , endothelial cells, adipocytes, muscle cells, neural cells such as glial and nerve cells.
  • the present invention is related to a method for producing follicular dendritic cells (FDC) from monocytes comprising subjecting the pluripotent cells obtainable according to the methods of the present invention to differentiation by culturing the cell(s) in the presence of tumor necrosis factor alpha (TNF x) and/ or interferone gamma (INF ⁇ ).
  • TNF x tumor necrosis factor alpha
  • INF ⁇ interferone gamma
  • the phenotype of the mature FDCs which may be produced by the method of the present invention may be taken from Table 3. As shown in column six of said table, the monocyte-derived FDCs (MoDC) are positive for alkaline phosphatase, CD35, CD54, and CD106.
  • the monocyte-derived FDCs show further characteristics of FDCs, such as rosetting with B-lymphocytes, emperipolesis of B-lymphocytes, giant cell formation, antigen trapping, and expression of B-cell markers.
  • the present invention is further related to a method for producing osteoblasts from monocytes, comprising subjecting the pluripotent intermediate cell(s) obtainable according to the methods of the present invention to differentiation by culturing the cell(s) in the presence of at least one bone morphogenetic protein.
  • Bone morphogenetic protein-2 (BMP-2) is preferred.
  • BMP-3 and/or BMP-4 may be used.
  • the expression of osteo- calcin may be used as the primary marker for defining the osteoblast development.
  • the phenotype of the osteoblast derived by the method according to the present invention can be taken from Table 3 .
  • the present invention is related to a method for producing adipocytes from monocytes, comprising subjecting the pluripotent intermediate cell(s) obtainable according to the methods of the present invention to differentiation by culturing the cell(s) in the presence of isobutylmethylxanthin and/or insulin and/or dexamethasone.
  • iso- butylmethylxanthin, insulin, and dexamethasone are used in combination.
  • the differentiation into adipocytes may be supported by lipids, including cholesterol.
  • adipocytes may be highly specifically stained by the fat stain Oil-red-O.
  • any phenotype may be produced by subjecting the intermediate cell(s) according to the present invention to differentiation by culturing the cell in the presence of appropriate differentiation inducing agents.
  • the induction of forward differentiation from intermediate pluripotential cells to the following cells types may be achieved under the following conditions:
  • Osteoclasts are differentiated by adding RANK-L, GM-CSF, M-CSF, interferon gamma. Markers for osteoclasts are known in the art (e.g. tartrate-resistant acid phosphatase, vitronectin-receptor and calcitonin-receptor.) The function of osteoclasts may be tested by plating them on dentin plates or dentin-coated surfaces where they produce defects in the dentin. Inducers for the production of fibroblasts are fibroblast growth factor (FGF) (10 ng/ml) and/or TGFbeta (1-10 ng/ml). As a specific marker, alpha-1 -hydroxylase may be used.
  • FGF fibroblast growth factor
  • myocytes may be induced by basic fibroblast growth factor (4ng/ml), and/or 5-azacytidine (10 ⁇ M), and/or 50 mM hydrocortisone.
  • basic fibroblast growth factor (4ng/ml)
  • 5-azacytidine 10 ⁇ M
  • 50 mM hydrocortisone 50 mM hydrocortisone.
  • anti-myosin antibody may be used.
  • Inducers for endothelial cells are VEGF (1-10 ng/ml) and/or hydrocortisone (50 mM), equivalent to 1x10 "7 M dexamethasone. It may be advantageous to use TNF- ⁇ (7.5 ng/ml), additionally. As markers, van Willebrand factor, CD34, CD144, CD105, and/or VEGF-receptor-1 may be used.
  • hepatocyte growth factor 100 ng/ml
  • albumin immunostaining for albumin
  • the intermediate cell(s) according to the invention may further be induced to differentiate into nerve cells using embryonic stem cell medium supplemented with 0,1 M beta-2- mercaptoethanol, 1% non-essential amino acids and nerve-growth factor (200 ng/ml).
  • embryonic stem cell medium supplemented with 0,1 M beta-2- mercaptoethanol, 1% non-essential amino acids and nerve-growth factor (200 ng/ml).
  • nerve-growth factor 200 ng/ml
  • anti-glial fibrillary acidic protein-antibody may be used as a marker.
  • the present invention relates to a cell population containing a majority of pluripotent intermediate cells which may be obtained by the method according to the invention, according to which highly purified monocytes are cultured in the presence of at least one retrodifferentiation inducing agent and optionally GM-CSF, until a majority of the monocytes has obtained the state of an intermediate cell, and subsequently recovering the cell population.
  • a cell population contains at least 50% of pluripotent intermediate cells and preferably more than 50% of pluripotent intermediate cells.
  • the percentage of pluripotent intermediate cells is at least 60% or even 70%. In a particularly preferred embodiment, the percentage is more than 80% or 90%.
  • the pluripotent cells are characterized in that they have an AP+ phenotype.
  • the present invention further relates to a pluripotent intermediate cell obtainable by culturing highly purified monocytes in the presence of at least one retrodifferentiation inducing agent and optionally GM-CSF; and subsequently recovering the pluripotent intermediate cells.
  • the pluripotent cells are characterized in that they are having an AP+ phenotype.
  • AP positive cells may be harvested by standard cell culture techniques known in the art.
  • the pluripotent cell is characterized in that the cell is variable for CD35 and negative for interieukin 1 ⁇ and TNF ⁇ .
  • the present invention relates to the use of the pluripotent cell of the present invention obtainable by the methods according to the present invention in substi- tutional therapy.
  • substitutional therapy includes "cell substitution therapy” (adoptive cell therapy) and refers to a therapy comprising the transplantation of a recipient with cells, and/or tissue or tissue-like structures, wherein the transplanted cells and/or tissues complement a defect in the recipient.
  • the pluripotent cells of the invention may be expanded in vitro to form tissue-like structures which, after in vitro differentiation to e.g. follicular dendritic cells, chondrocytes, endothelial cells or osteoblasts, may be transplanted to a recipient to substitute for tissues such as cartilage, blood vessels or bone, respectively.
  • the intermediate pluripotent cells according to the invention can be used as somatic stem cells in adoptive cell therapy of several diseases to repair defects and to induce regeneration.
  • the intermediate pluripotent cells have reduced marker expression of the myeloid lineage and can even be negative for e.g. CD14 and CD68. They have also reduced expression of molecules of the major histocompatibility complex (MHC) class I and II. Therefore, it may be anticipated that they are less or not rejected when they are transplanted allo- or xenogenically.
  • MHC major histocompatibility complex
  • the intermediate pluripotent cell as well as all possible phenotypes derived from it carry the potential to be used for adoptive cell therapy.
  • cells may be developed in vitro according to the methods described herein and re-transplanted into the donor in order to repair defects.
  • cells from genetically intact individuals may be useful to repair defects in individuals having genetic disorders.
  • the intermediate pluripotent cells may migrate to the sites of defects and, induced by the local environment, further differentiate into the respective tissue relevant phenotypes.
  • the pluripotent cells of the present invention may thus further be used for preparing a medicament for treating diseases caused by genetic defects.
  • the genetic defect is cystic fibrosis, sickle cell anemia, hemophilia, Down's syndrome and/or Turner syndrome.
  • the present invention relates to the use of the follicular dendritic cells (FDCs) obtainable by the method according to the invention for research, diagnostic and therapeutic purposes.
  • the FDC developed from the pluripotent precursors (pluripotent intermediate cells) according to the invention may e.g. be used for immunological research such as studying the persistence of pathogens such as prions and HIV.
  • monocyte-derived FDCs may help to elucidate functioning of the immunological memory.
  • the extent of antigen trapping relevant for pathogenic organisms such as HIV may be investigated, as it is still open whether the virus can exist within FDCs in an infectious form or even may replicate within FDCs.
  • the follicular dendritic cells obtainable by the methods according to the invention may be used for diagnostic purposes.
  • FDCs from an uninfected donor may be incubated with blood or serum sample(s) of an individual to be tested. If present, infectious agents will be collected or even be amplified within the previously uninfected FDCs and may subsequently be identified by methods known in the art, such as agar culture or polymerase chain reaction. Further, different isolates of infectious agents may be added to separate cultures of FDCs and their trapping within the FDCs may be determined in order to compare their infectivity and their persistency.
  • the follicular dendritic cells obtainable by the method according to the invention may be used for therapeutic purposes other than gene therapy.
  • the follicular dendritic cells are used in substitutional therapy.
  • the FDCs obtained by the method according to the present invention may further be used for preparing a medicament for treated infectious diseases.
  • the infectious disease is caused by HIV.
  • the FDC is the last of the major immune cells who's origin was unclear so far. Facing the enormous impact of FDCs on the function of the immune memory, and their function as natural reservoir of pathogens (HIV, prions), the discovery of their ontogenesis is of high value because as a consequence, FDCs may be produced from their precursors in cell culture, their development may be influenced in vivo and thus immune reactions and vaccination strategies may be modified and improved. Regarding their value in infection research, using the FDCs according to the invention, it will be testable whether pathogens such as viruses (e.g. HIV), bacteria, protozoa and prions (e.g. BSE) are resident within these cells with a chance to remain pathogenic for a long time.
  • viruses e.g. HIV
  • bacteria e.g. BSE
  • a culture of FDCs obtained from a non-infected donor may for instance be treated with HIV-virus.
  • monocytes or macrophages from the same donor may be used. It will be tested how long the FDCs can entrap the infectious agent by harvesting material from the culture and testing it in an independent infection test, e.g. using polymerase chain reaction. Similarly, any other pathogen may be tested as well. The result provides information as to how far these pathogens use this cell to be protected against destruction.
  • the antigen is trapped by enrolling into membrane pockets and thereby protected against exogenous as well as cellular lytic events ( Habermannand Shlomchik, 2003).
  • FDCs generated by the method according to the invention are particularly useful for immunological research and for cell transplantation whether in an allogeneic, autologous or xenogeneic setting.
  • immunological diseases may be influenced.
  • FDCs obtained according to the methods of the invention may be charged with drugs, rendering them resistant against a given pathogen and subsequently may be injected in an individual suffering from an infectious disease to compensate for infected FDCs corrupted by a surviving pathogen.
  • the present invention relates to the use of osteoblasts obtainable by the methods according to the invention for research purposes, diagnostic purposes and therapeutic purposes.
  • the possibility to generate osteoblasts from monocytes is a recent finding, inasmuch as osteoblasts have so far been regarded to develop from mesenchymal stem cells or stromal cell within the bone marrow.
  • the osteoblasts obtained by the method according to the invention may be utilized to investigate the balance of regulation between osteoblasts and osteoclasts.
  • the signals which mediate the development into either direction may be tested.
  • diagnosis using the osteoblasts according to the invention, from patients suffering from bone disorders such as osteoporosis may be tested whether their monocytes already carry the preference in favour of osteoclastic reaction. It can be tested if there are signals in the patient's serum which induce an osteoclastic reaction.
  • the osteoblast obtained by the method according to the present invention are used in substitutional therapy.
  • monocytes from a patient may for instance be differentiated into osteoblasts in vitro, harvested by conventional cell culture techniques (as described), washed free of cell culture medium and of the differentiation inducing agent(s) and then injected into the recipient either systemically (e.g. intravenously) or locally at the site of a defect.
  • the osteoblasts obtainable by the method according to the invention may be used for preparing a medicament for treating osteoporosis and bone defects.
  • retrodifferentiation inducing agents are able to induce retrodifferentiation from monocytes to intermediate pluripotent (AP+) cells
  • this process may be used to test unknown substances for their retrodifferentiation-inducing potency.
  • pharmaceuticals in development may be subjected to this new test system.
  • the read out is performed by counting the percent of AP+ cells.
  • an AP reaction may be performed according to standard procedures resulting in a soluble end product which can then be quantitatively measured by an ELISA-reader.
  • the immune-suppressed state of a patient may be measured by adding his serum to the monocyte culture.
  • the present invention relates to a method for identifying new retrodifferentiation inducing agents comprising the steps of:
  • 70% of the cells are capable of transdifferentiation, more preferably over 90%, most preferably over 95% of the cells are capable of transdifferentiation.
  • agents inducing retrodifferentiation of monocytes such as chemical drugs, natural plant and animal products, human products such as cytokines and growth factors may be newly identified.
  • Fig. 1 Expression of phenotypes developed from human monocytes. Monocytes were treated either with IL-4 (IL-13) alone (upper left), with GM-CSF alone (lower left), with dexamethasone alone (upper right) and with IL-4 (IL-13), GM-CSF, and dexamethasone (lower right). Blue: alkaline-phosphatase.
  • Fig. 3 Monocyte-derived Osteoblasts. Osteocalcin demonstrated by immunocytochemi- cal reaction against osteocalcin in the nuclei (red). AP (blue), CD86 (brown).
  • AP alkaline phosphatase
  • monocyte cultures either obtained from ex-vivo or in-vitro induced granuloma, suggesting osteoblastic differentiation.
  • AP of the "osteoblast type” has furthermore been shown to be expressed in osteoblasts, activated endothelial cells as well as in follicular dendritic cells (FDCs; Rademakers).
  • FDCs follicular dendritic cells
  • Dexamethasone combined with IL-4 (IL-13) and GM-CSF prevents monocytes to develop into macrophages or DC. Instead, within two weeks, they developed into a novel cell type, the pluripotent intermediate cell which is phenotypically closely related to FDCs. Starting from this intermediate, an even more mature phenotype of FDCs as well as osteoblasts and adipocytes can be differentiated using appropriate physiological stimuli.
  • Monocytes were obtained by leukapheresis from healthy blood donors. Mononuclear cells were prepared by standard Ficoll-Hypaque gradient sedimentation (density 1.077p, Lymphoprep, Nyegard, Oslo, Norway). Alternatively, the gradient was used at 1.068p.
  • the monocyte content was measured from unstained cells by forward/scatter analysis using a flow cytometer.
  • Mononuclear cells were seeded into microwells at 30 000 mono- cytes/well, centrifuged at 500g for 1 min. to enhance sedimentation, and allowed to attach for a one hour incubation time.
  • wells were filled up with culture medium to form a convex meniscus, the microplates were then gently tilted top-down and cultured 2-18 hours in the inverted position. After reverse sedimentation was completed, the medium containing non-attached cells was snicked off, the cells washed once with PBS, and the adherent cells were further cultured in 100 ⁇ l of differentiation medium.
  • CellGro serum-free medium (CellGenix, Freiburg, Germany) was supplemented with N- acetyl-L-alanyl-L-glutamin (Ac-ala-gln) (Biochrom, Berlin, Germany), Penicillin- Streptomycin (PAN Biotech, Aldenbach, Germany).
  • serum-containing RPMI 1640 medium was used.
  • Inducers of retrodifferentiation were Dexamethasone, IL-4, and GM-CSF.
  • Dexamethasone was used at 10 "8 - 10 "5 M, preferably at 5x10 "7 M - 1x10 "6 M.
  • IL-4 was used at 5-100 U/ml, preferably at 25-50 U/ml.
  • IL-13 was used at 250-500 U/ml.
  • GM-CSF was used at 1-20 U/ml, preferably at 1-5 U/ml.
  • the cells are harvested according to standard cell culture techniques: they are deprived of calcium-ions by incubating them in phosphate buffered saline lacking Ca++ and Mg++, containing further 0.02 % EDTA, a calcium chelating agent. In order to improve the detachement of the cells, they are kept in the cold (in order to depolymerize microtubuli). Furthermore, they may be treated with 0.01% xylocaine (Lidocain), a local anaestetic, which has been shown to induce detachment of cells.
  • xylocaine Lidocain
  • enzymes such as trypsin (0.25% or trypsin 0.05% w/v in EDTA 0.02%), collagenase (0.1-0.2% w/v) / dispase (0.6-2.4 U/ml) may be used at standard conditions. After the cells have been detached (as controlled by phase contrast microscopy), they are collected in a centrifuge tube, centrifuged down at low speed (350xg, 5 min), the buffer removed, and the pelleted cells resuspended in a sterile buffer or medium, depending on the further use. Monocytes obtained from a proliferating culture
  • monocytes derived from a proliferating culture were used. Monocytes were put into culture as describe above. For inducing monocyte proliferation, GM-CSF was added at 25 U/ml. During the following 14 days the proliferating cells detached from the surface and were washed. Next, they were transferred into new wells. After omitting the proliferation-inducing concentration of GM-CSF, the cells were subjected to the above described "retrodifferentiation'-protocol in order to stop proliferation and to start retrodifferentiation.
  • the AP+ intermediate cells were subjected to tumor- necrosis factor alpha (TNFalpha) at 0.1-40U/ml, preferably 5-20U/ml and/or interferon- gamma at 1-300 U/ml, preferably 5-100 U/ml and kept in culture for 1-5 days. They were then fixed as above and stained for FDC markers. Alternatively, they remained in culture and were tested for their function.
  • TNFalpha tumor- necrosis factor alpha
  • FDCs were identified using a combination of markers and functions (Table 3). Characteristic functions of FDC that can be tested in vitro are: spontaneous homogeneous clustering, rosetting with B-lymphocytes, and emperipolesis, i.e. engulfing of B-cells which remain inside the FDC for longer time.
  • Raji cells (a permanent human B-lymphocyte line) were added to test for rosette formation. After 4 hours the cultures were stopped, fixed and stained for relevant markers. The same set-up was used to test for emperipolesis, which follows the rosetting and can be observed 4-10 hours later. Again, the cells were fixed and stained for relevant markers.
  • HRPO horse raddish peroxidase
  • HRPO/human IgG immune complexes containing HRPO-conjugated mouse-anti human Ig, compexed with aggregated human Ig and human serum (0.1 ⁇ g/ml final concentration of HRPO) was added, washed out after 15 min and the cells were further cultured for up to 16 days.
  • Fig. 2b shows monocyte-derived cells cultured for 14 days to rosette with Raji cells as well as engulfed Raji cells (Fig. 2c).
  • Antigen trapping is a most interesting function of FDC.
  • peroxidase as a reference antigen is taken up by monocyte-derived FDC (MoFDC) and stays enzymatically active for 16 days (Fig. 2 da).
  • macrophages degraded the enzyme within 4 hours (Table 3 and Fig. 2db).
  • the AP+ intermediates were subjected to bone morphogenetic protein 2 (BMP-2) at 10ng/ml, 10-1000 nM (preferably 100 nM) dexamethasone, 1-100 mM (preferably 10 mM) beta-glycerophosphate and 1-250 ⁇ g/ml (preferably 50 ⁇ g/ml) ascorbic acid for 14 days. They were fixed as above and stained for expression of osteocalcin according to standard procedures.
  • Fig. 3 demonstrates the positive reaction for osteocalcin.
  • AP+ intermediates were further cultured in human serum rich of lipids, or alternatively in medium containing 0.1-50mM (preferably 0.5 mM) isobutylmethylxanthin, 0.1-10 ⁇ g/ml insulin (preferably 1 ⁇ g/ml) and 0.025-2.5 ⁇ M dexamethasone (preferably 0.25 ⁇ M) for another 3-10 days to induce differentiation of adipocytes. Subsequently, they were fixed and specifically stained with Red Oil O.
  • FDCs are not characterized by exclusive markers and not uniformly described in the literature.
  • the authors decided to use expression of alkaline phosphatase as an arbitrary marker for FDCs which is negative in monocytes, macrophages and monocyte-derived dendritic cells.
  • AP expression can be induced in monocytic cells under various conditions such as in vitro induced granuloma, and AP expression was detected in ex- vivo cultured foreign body granulomas, suggesting AP expression as an indicator of monocytes' developmental plasticity (Heinemann et al.2000). Therefore, as a first goal we have attempted to convert monocytes into (AP+) pluripotent intermediate cells.
  • IL-4 (IL-13) was found to be inductive for AP expression in large adherent cells which were flat with fine dendritic protrusions and co-stained for the monocyte marker CD68. This morphology as well as AP expression were further enhanced and stabilized by addition of dexamethasone which is known to stabilize the phenotype of osteoblast cultures and was initially used by us in order to inhibit macrophage differentiation.
  • monocytes, macrophages and dendritic cells belong to a continuum of interconvertable cells, all of them equipped with the property of being developmentally plastic.
  • the pluripotent nature of these cells is demonstrated by the fact that osteoclasts and osteoblasts, can be as well differentiated from the AP positive intermediate described here.
  • Peripheral blood fibrocytes differentiation pathway and migration to wound sites: J Immunol, v. 166, p. 7556-62.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Cell Biology (AREA)
  • Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Microbiology (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biotechnology (AREA)
  • Organic Chemistry (AREA)
  • Mycology (AREA)
  • Epidemiology (AREA)
  • Medicinal Chemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Biochemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
EP05761385A 2004-05-27 2005-05-27 Methode zur herstellung von pluripotenten zellen aus monozyten Withdrawn EP1751274A1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP05761385A EP1751274A1 (de) 2004-05-27 2005-05-27 Methode zur herstellung von pluripotenten zellen aus monozyten

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP04012622A EP1600500A1 (de) 2004-05-27 2004-05-27 Methode zur Herstellung von pluripotenten Zellen aus Monozyten
EP05761385A EP1751274A1 (de) 2004-05-27 2005-05-27 Methode zur herstellung von pluripotenten zellen aus monozyten
PCT/EP2005/005721 WO2005118779A1 (en) 2004-05-27 2005-05-27 Method for producing pluripotent cells from monocytes

Publications (1)

Publication Number Publication Date
EP1751274A1 true EP1751274A1 (de) 2007-02-14

Family

ID=34925162

Family Applications (2)

Application Number Title Priority Date Filing Date
EP04012622A Withdrawn EP1600500A1 (de) 2004-05-27 2004-05-27 Methode zur Herstellung von pluripotenten Zellen aus Monozyten
EP05761385A Withdrawn EP1751274A1 (de) 2004-05-27 2005-05-27 Methode zur herstellung von pluripotenten zellen aus monozyten

Family Applications Before (1)

Application Number Title Priority Date Filing Date
EP04012622A Withdrawn EP1600500A1 (de) 2004-05-27 2004-05-27 Methode zur Herstellung von pluripotenten Zellen aus Monozyten

Country Status (2)

Country Link
EP (2) EP1600500A1 (de)
WO (1) WO2005118779A1 (de)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2006202318A1 (en) * 2005-06-02 2006-12-21 Wing-Yee Chan The preparation of multipotent stem cells and the use thereof
EP2171455A4 (de) 2007-07-06 2010-11-24 Vaxdesign Corp Schnelle erzeugung von t-zellen-unabhängigen antikörper-reaktionen auf t-zellen-abhängige antigene
US20120282228A1 (en) * 2009-07-15 2012-11-08 Vishal Bhasin Method of producing progenitor cells from differentiated cells
EP2553449A2 (de) * 2010-03-26 2013-02-06 Westfälische Wilhelms-Universität Münster Ersatztherapie für glucocorticoide
JP2023516484A (ja) 2020-03-11 2023-04-19 ビット バイオ リミテッド 肝細胞作製方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI288779B (en) * 2002-03-28 2007-10-21 Blasticon Biotech Forschung Dedifferentiated, programmable stem cells of monocytic origin, and their production and use
CA2505394C (en) * 2002-11-07 2014-05-13 University Of Chicago Human stem cell materials and methods

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2005118779A1 *

Also Published As

Publication number Publication date
EP1600500A1 (de) 2005-11-30
WO2005118779A1 (en) 2005-12-15

Similar Documents

Publication Publication Date Title
JP6526130B2 (ja) 間葉系間質細胞及びその関連用途
Gao et al. Effects of mesenchymal stem cells from human induced pluripotent stem cells on differentiation, maturation, and function of dendritic cells
KR101218663B1 (ko) 줄기세포 및 전구세포 분화의 조절, 측정 및 이들의 용도
KR20040029311A (ko) 다능성 줄기 세포의 동종이식편의 내성화
US9388382B2 (en) Isolation of CD14 negative, CD45 positive and CD117 positive embryonic-like stem cells free of monocytes from human umbilical cord blood mononuclear cells
WO2005097979A2 (en) Methods and compositions for obtaining hematopoietic stem cells derived from embryonic stem cells and uses thereof
US20180216065A1 (en) Method for Inducing Differentiation of Myeloid-Derived Suppressor Cells from Cord - Blood CD34 Positive Cells and Proliferating Same, and use of Myeloid-Derived
JP2018134086A (ja) 免疫調節活性を有する細胞集団、その調製方法、及び、その使用
EP1751274A1 (de) Methode zur herstellung von pluripotenten zellen aus monozyten
JP2017165757A (ja) 間葉系間質細胞集団およびそれを作成する方法
EP1941031A2 (de) Isolierte embryonenstammzellen aus menschlichem nabelschnurblut
JP2022513475A (ja) Ｈｌａ－ｅを発現する肝臓前駆細胞を含む細胞組成物
WO2024009226A1 (en) Cryopreserved intermediate and potency assay for same
TW202421780A (zh) T細胞的製造方法
AU2015201121A1 (en) Modulation of stem and progenitor cell differentiation, assays, and uses thereof
Donders Mesenchymal stem cells derived from umbilical cord tissue: a therapeutic option for multiple sclerosis?
Taqvi Notch ligand functionalized microheads for T cell differentiation of stem cells

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20061121

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU MC NL PL PT RO SE SI SK TR

RTI1 Title (correction)

Free format text: METHOD FOR PRODUCING PLURIPOTENT CELLS FROM MONOCYTES

17Q First examination report despatched

Effective date: 20070502

DAX Request for extension of the european patent (deleted)
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20101201