Abstract:
The present invention relates to pharmaceutical uses of IL-2 and IL-2 antibody which are used for preventing or treating immune diseases caused by abnormality of immune responses and, more specifically, to a composition for preventing or treating immune diseases for elderly which includes IL-2 and IL-2 antibody. The IL-2 and IL-2 antibody according to the present invention can be effectively used as a pharmaceutical composition which can prevent or treat immune diseases in elderly such as autoimmune disease, inflammatory disease, and transplant rejection diseases which are caused by abnormal control of various immune responses by suppressing immune cells which are abnormally activated, suppressing activation of immune regulatory T cells (Treg) which controls inflammation responses, increasing expression of Foxp3 and STAT5, suppressing expression of Cebpb or IL-20, and having enhanced effects when IL-2 and IL-2 antibody are treated in elderly. Also the IL-2 and IL-2 antibody have no toxicity and side effects for medicine so that IL-2 and IL-2 antibody cab be used for inflammation diseases for long time, and have stable effects in vivo.
Abstract:
PURPOSE: A composition for preventing and treating immunization diseases including nutlin-3a compound is provided to suppress the expression of IL-17 through overexpression of p53. CONSTITUTION: A composition for preventing and treating immunization diseases includes nutlin-3a compound. The nutlin-3a compound suppresses the IL-17 production. The IL-17 production suppression is completed by the overexpression of p53. The immunization disease is autoimmune disease, inflammation disease, transplantation rejection disease of cell, tissue or organ. The autoimmune disease or inflammation disease is rheumatoid arthritis, asthma], dermatitis, psoriasis, cystic fibrosis, multiple sclerosis, systemic lupus erythematosus, sjogren syndrome, hashimoto thyroiditis, polymyositis, scleroderma, Addison disease, vitiligo, pernicious anemia, glomerulonephritis, pulmonary fibrosis, inflammatory Bowel dieseses, autoimmune diabetes, diabetic retinopathy, rhinitis, ischemia-reperfusion injury, post-angioplasty restenosis, chronic obstructive pulmonary diseases(COPD), Graves disease, gastrointestinal allergies, conjunctivitis, and atherosclerosis. [Reference numerals] (AA) Producing amount of IL-17(pg/ml)
Abstract:
PURPOSE: A TNFR2-IL21R fusion protein as a double antagonist to TNF-alpha and IL-21 is provided to reduce inflammatory cytokine secretion and to increase anti-inflammatory cytokine secretion. CONSTITUTION: A composition for preventing and treating autoimmune disease contains a fusion protein having a fragment with extracellular region of TNFR2(Tumor necrosis factor receptor type 2) or TNFR2 and a fragment with extracellular region of IL21R(Interleukin-21 receptor) protein or IL21R as an active ingredient. The fusion protein has an amino acid sequence of sequence number 1.
Abstract:
PURPOSE: A pharmaceutical composition containing Vitis vinifera seed extract is provided to suppress osteoclast differentiation and to prevent and treat osteoporosis. CONSTITUTION: A pharmaceutical composition for preventing or treating osteoporosis contains Vitis vinifera seed extract and pharmaceutically acceptable carrier. The Vitis vinifera seed extract has 80-130 of procyanidolic value(PCV), 30% or less (+) catechin and (-) epicatechin, and 95-105% of proanthocyanine. A method for manufacturing the Vitis vinifera seed extract comprises: a step of adding mixture solvent of water and acetone to pulverized Vitis vinifera seed and extracting at room temperature; a step of removing acetone and suturing sodium chloride and filtering; a step of extracting the extract with acetate and concentrating; and a step of adding chloroform to the concentrate and filtering.
Abstract:
PURPOSE: A composition containing epigallocatechin gallate (EGCG) as one of green tea polyphenols as an effective ingredient is provided. The EGCG controls an inflammatory reaction in the lesion area of rheumatoid arthritis and a cell-mediated immune reaction which specifically reacts with an antigen and thus has a therapeutic effect on rheumatoid arthritis. CONSTITUTION: The agent for the treatment of rheumatoid arthritis contains (-)-epigallocatechin gallate and a pharmaceutically acceptable carrier such as physiological saline. The dosage of EGCG is 1 to 100mg/kg. The EGCG is administered in the form of an EGCG-PLGA complex by impregnating into a PLGA(poly/lactide/glycolide) polymer.