Modified galectin 9 proteins and methods of treatment using them
A recombinant galectin 9 (rGal 9) is provided which exhibits an immune system-mediated action and a direct action on tumor cells (i.e., activity of inducing the intercellular adhesion and apoptosis of the tumor cells), thereby potent in inducing the inhibition of cancer metastasis and reduction. Moreover, the rGal 9 exerts no efficacy on non-activated lymphocytes but can induce apoptosis in activated T cells, in particular, CD4-positive T cells causing an excessive immune response.
1. A pharmaceutical drug comprising:
an effective amount of a protein, or a salt thereof,
wherein the protein, or a salt thereof, comprises a mutant galectin 9 protein having β-galactoside binding activity and having the structure (N-CRD)-Linker-(C-CRD),
wherein the N-CRD (N-terminal Carbohydrate Recognition Domain) is
(a) a polypeptide having the amino acid sequence of SEQ ID NO: 3,
(b) a variant thereof differing from the amino acid sequence of SEQ ID NO: 3 by a deletion, substitution or addition of 1 to 8 amino acid residues and maintaining a carbohydrate recognition activity of N-CRD of natural galectin 9, or
(c) a variant thereof having an amino acid sequence at least 70% homologous to SEQ ID NO: 3 and maintaining a carbohydrate recognition activity of N-CRD of natural galectin 9;
wherein the C-CRD (C-terminal Carbohydrate Recognition Domain) is
(a) a polypeptide having the amino acid sequence of SEQ ID NO: 4,
(b) a variant thereof differing from the amino acid sequence of SEQ ID: 4 by a deletion, substitution or addition of 1 to 21 amino acid residues and maintaining a carbohydrate recognition activity of C-CRD of natural galectin 9, or
(c) a variant thereof having an amino acid sequence at least 70% homologous to SEQ ID NO: 4, and maintaining a carbohydrate recognition activity of C-CRD of natural galectin 9; and
wherein the Linker is
(a) an amino acid sequence consisting of 2 arbitrary natural amino acid residues, or
(b) the amino acid sequence Arg Ile Pro, and
wherein the pharmaceutical drug is an immunoregulator or immunomodulator capable of treating refractory autoimmune disease, pain disorder, asthmatic disease, rheumatism, rheumatoid arthritis, allergic disease, inflammatory disease, or a disorder related to bone metabolism.
2. A pharmaceutical drug according to claim 1 , wherein
the refractory autoimmune disease is autoimmune hemolytic anemia,
the pain disorder is neuropathic pain, inflammatory pain, chronic pain or acute pain,
the allergic disease is allergic asthma or urticaria,
the inflammatory disease is pleurisy, dermatitis, arthritis, angiitis, acute respiratory distress syndrome (ARDS), interstitial pneumonia, chronic inflammatory disease or acute inflammatory disease, and
the disorder related to bone metabolism is osteoporosis, loss of bone mass or bone fracture.
3. A pharmaceutical drug comprising:
an effective amount of a protein, or a salt thereof,
wherein the protein, or a salt thereof, comprises a mutant galectin 9 protein having β-galactoside binding activity and having the structure (N-CRD)-Linker-(C-CRD),
wherein the N-CRD (N-terminal Carbohydrate Recognition Domain) is
(a) a polypeptide having the amino acid sequence of SEQ ID NO: 3,
(b) a variant thereof differing from the amino acid sequence of SEQ ID NO: 3 by a deletion, substitution or addition of 1 to 8 amino acid residues and maintaining a carbohydrate recognition activity of N-CRD of natural galectin 9, or
(c) a variant thereof having an amino acid sequence at least 70% homologous to SEQ ID NO: 3 and maintaining a carbohydrate recognition activity of N-CRD of natural galectin 9;
wherein the C-CRD (C-terminal Carbohydrate Recognition Domain) is
(a) a polypeptide having the amino acid sequence of SEQ ID NO: 4,
(b) a variant thereof differing from the amino acid sequence of SEQ ID: 4 by a deletion, substitution or addition of 1 to 21 amino acid residues and maintaining a carbohydrate recognition activity of C-CRD of natural galectin 9, or
(c) a variant thereof having an amino acid sequence at least 70% homologous to SEQ ID NO: 4, and maintaining a carbohydrate recognition activity of C-CRD of natural galectin 9; and
wherein the Linker is
(a) an amino acid sequence consisting of 2 arbitrary natural amino acid residues, or
(b) the amino acid sequence Arg Ile Pro, and
wherein the pharmaceutical drug is an antineoplastic or antitumor agent capable of treating a blood cell tumor, non-epithelial neoplasm or epithelial neoplasm.
4. A pharmaceutical drug according to claim 3 , wherein
the blood cell tumor is leukemia,
the non-epithelial neoplasm is malignant melanoma, malignant lymphoma, Hodgkin's disease, plasmacytoma, glioma, myelofibrosis associated with agnogenic myeloid metaplasia, or others or sarcoma, and
the epithelial neoplasm is brain tumor (glioblastoma multiforme, etc.), spinal tumor, maxillary sinus carcinoma, pancreatic ductal adenocarcinoma, gingival cancer, tongue cancer, lip cancer, nasopharyngeal cancer, oropharyngeal cancer, hypopharyngeal cancer, laryngeal cancer, thyroid cancer, parathyroid cancer, lung cancer, pleural tumor, carcinomatous peritonitis, carcinomatous pleurisy, esophageal cancer, stomach cancer, colon cancer, bile duct cancer, gall bladder cancer, pancreatic cancer, liver cancer, renal cancer, urinary bladder cancer, prostatic cancer, penile cancer, testicular tumor, adrenal cancer, cervical cancer, endometrial cancer, vaginal cancer, vulvar cancer, ovarian cancer, chorioepithelioma, malignant bone tumor, soft part sarcoma, breast cancer, skin cancer, or basal cell tumor.
5. A method for treating refractory autoimmune disease, rheumatoid arthritis, allergic disease, inflammatory disease, or a disorder related to bone metabolism, which comprises administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical drug according to claim 1 or 2 .
6. A method for treating blood cell tumor, non-epithelial neoplasm or epithelial neoplasm, which comprises administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical drug according to claim 3 or 4 .