Human haemopoietic maturation factor

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

Reexamination Certificate

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C514S008100, C514S012200, C424S085100, C435S325000, C435S377000

Reexamination Certificate

active

06790826

ABSTRACT:

FIELD OF THE INVENTION
This invention relates to newly identified polynucleotides, polypeptides encoded by such polynucleotides, the use of such polynucleotides and polypeptides, as well as the production of such polynucleotides and polypeptides. The polypeptides of the present invention have been putatively identified as a human haemopoietic maturation factor, sometimes hereinafter referred to as “HMF”. The invention also relates to inhibiting the action of such polypeptides.
BACKGROUND OF THE INVENTION
Various growth factors have been discovered, studied and utilized (cellular and molecular biology, edited by the Japanese Tissue Culture Association, Asakura Shoten (1987). Such cell growth factors include epidermal growth factor, platelet derived growth factor, acidic fibroblast growth factor and basic fibroblast growth factor among others. All these factors have been isolated based upon growth promotion of fibroblast cells. However, these factors have also been found to display widely ranging activity and poor specificity.
Accordingly, recent attempts have been made to search for growth factors specifically acting on functionally differentiated cells. As a result, growth factors such as keratinocyte growth factor and hepatocyte growth factor have been isolated, thus creating the possibility that these factors could be used to treat diseases vulnerable to their specific action spectra. Another growth factor which has been isolated is disclosed in European Patent Application No. 92102385.9 applied for by Takeda Chemical Industries, Ltd. disclosing a glia activating factor which has glial cell growth promoting activity, and the DNA encoding for that polypeptide.
Hematopoiesis is the production of blood cells. The major hematopoietic tissues are bone marrow, spleen, lymph nodes and thymus. Hematopoiesis in the human embryo begins in the second week of life. Bone marrow appears in the embryo in the second month, and it becomes the dominant hematopoietic organ in the latter half of gestation and throughout postnatal life. The bone marrow contains stem cells that give rise to all cells of the haemopoietic series. All of the blood cells except T-lymphocytes are produced in the marrow.
SUMMARY OF THE INVENTION
The polypeptides of the present invention has been putatively identified as a haemopoietic maturation factor polypeptide based on amino acid sequence homology to Human glia maturation factor polypeptides.
In accordance with one aspect of the present invention, there are provided novel polypeptides, as well as biologically and diagnostically active fragments, analogs and derivatives thereof. The polypeptides of the present invention is of human origin.
In accordance with another aspect of the present invention, there are provided isolated nucleic acid molecules encoding such polypeptides, including mRNAs, DNAs, cDNAs, genomic DNA, as well as biologically active and diagnostically or therapeutically useful fragments, analogs and derivatives thereof.
In accordance with still another aspect of the present invention, there are provided procedures for producing such polypeptides by recombinant techniques comprising culturing recombinant prokaryotic and/or eukaryotic host cells, containing a nucleic acid sequence encoding the polypeptide of the present invention, under conditions promoting expression of said protein and recovery of said protein.
In accordance with yet a further aspect of the present invention, there are also provided nucleic acid probes comprising nucleic acid molecules of sufficient length to specifically hybridize to the nucleic acid sequences of the present invention.
In accordance with yet a further aspect of the present invention, there is provided a process for utilizing such polypeptides, or polynucleotide encoding such polypeptide, for therapeutic purposes, for example, to treat leukemia, blood related disorders, to stimulate differentiation and proliferation of cells of hematopoietic or stromal origin, and to remove malignant cells.
In accordance with yet another aspect of the present invention, there are provided antibodies against such polypeptides.
In accordance with yet another aspect of the present invention, there are provided antagonists against such polypeptides, which may be used to inhibit the action of such polypeptides, for example, to treat auto-immune diseases by preventing expansion of certain T-cell populations.
In accordance with still another aspect of the present invention, there are provided diagnostic assays for detecting diseases or susceptibility to diseases related to mutations in the nucleic acid sequences and altered levels of the polypeptides of the present invention.
In accordance with yet a further aspect of the present invention, there is provided a process for utilizing such polypeptides, or polynucleotides encoding such polypeptides, for in vitro purposes related to scientific research, for example, synthesis of DNA and manufacture of DNA vectors.
These and other aspects of the present invention should be apparent to those skilled in the art from the teachings herein.


REFERENCES:
patent: 5270452 (1993-12-01), Lim et al.
patent: 5922572 (1999-07-01), Rosen et al.
patent: 5986069 (1999-11-01), Kirkness et al.
patent: 6346246 (2002-02-01), Kirkness et al.
patent: 92102385.9 (1992-03-01), None
patent: 0503297 (1992-09-01), None
patent: WO 91/16915 (1991-11-01), None
patent: WO 92/06712 (1992-04-01), None
Bosch et al., “Axonal signals regulate expression of glia maturation factor beta in Schwann cells; an immunohistochemical study of injured sciatic nerves and cultured Schwann cells,” The Journal of Neuroscience, 9(10):3690-3698 (1989).
Bowie et al., “Deciphering the message in protein sequences: tolerance to amino acid substitutions,” Science, 247:1306-1310 (1990).
Kaplan et al., “Molecular cloning and expression of biologically active human glia maturation factor-beta,” Journal of Neurochemistry, 57:483-490 (1991).
Keles et al., “Expression of glia fibrillary acidic protein in human medulloblastoma cells treated with recombinant glia maturation factor beta,” Oncology Research, 4(10):431-437 (1992).
Lim et al., “Antiproliferative function of glia maturation factor beta,” Cell Regulation, 1:741-746 (1990).
Lim et al., “Cell-surface expression of glia maturation factor beta in astrocytes,” The FASEB Journal, 4:3360-3363 (1990).
Lim et al., “Glia maturation factor beta regulates the growth of N18 neuroblastoma cells,” Developmental Biology, 137:444-450 (1989).
Lim et al., “Purification and characterization of glia maturation factor beta: a growth regulator for neurons and glia,” Proc. Natl. Acad. Sci. USA, 86:3901-3905 (1989).
Lim et al., “Sequential interaction of glia maturation factor with insulin,” Science, 1419-1420 (1984).
Lim et al., “Structure and function of glia maturation factor beta,” Plasticity and Regeneration of the Nervous System, 161-164 (1991).
Ngo et al., “Computational complexity, protein structure prediction, and the Levinthal paradox,” The Protein Folding Problem and Tertiary Structure Prediction, Merz et al., eds., Birkhauser, Boston, 491-5 (1994).
Nietro-Sampedro et al., “Early release of glia maturation factor and acidic fibroblast growth factor after rat brain injury,” Neuroscience Letters, 86:361-365 (1988).
Zaheer A. et al., “Expression of glia maturation factor beta mRNA and protein in rat organs and cells,” J. of Neurochem., 60(3):914-920 (1993).
George et al., “Current methods in sequence comparison and analysis,” Macromolecular Sequencing and Synthesis: Selected Methods and Applications, D.H. Schlesinger, ed. Alan R. Liss, Inc. NY, 127-149 (1988).
Lim et al., “Complete amino acid sequence of bovine glia maturation factor beta,” Proc. Natl. Acad. Sci. USA, 7:5233-5237 (1990).
Lim et al., “Glia maturation factor-beta promotes the appearance of large neurofilament-rich neurons in injured rat brains,” Brain Research, 504:154-158 (1989).
Wang et al., “Polyclonal antibody localizes glia maturation factor beta-like immunoreactivity in neurons and glia,” Brain Research, 591:1-7 (1992).
Genbank Accession No.

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