Abstract:
본발명은메트포민및 스타틴의복합제를이용한자가면역질환의예방또는치료용조성물에관한것이다. 본발명에따른메트포민및 스타틴을유효성분으로포함하는복합제인자가면역질환의예방또는치료용약학적조성물은염증성사이토카인의생성을효과적으로억제시킬수 있고, 항체생산 B 세포의생성을저해또는활성을감소시킬수 있으며, 파골세포의분화를억제하고관절파괴를억제하는효과를가지며동맥경화반(Artherosclerotic plaque) 전구세포를형성하는거품세포(Foam cell)의생성억제효과가뛰어나메트포민및 스타틴을유효성분으로하는복합제는자가면역질환의치료제로서매우유용하게활용될수 있다.
Abstract:
The present invention relates to a composition for preventing or treating inflammatory diseases or immunological rejection diseases containing coenzyme Q10 as an active ingredient. In particular, coenzyme Q10 of the present invention: inhibits or reduces activity of Th17; has excellent effects of promoting or increasing activity of a regulatory T cell (Treg); and thus can be used for a composition capable of preventing or treating inflammatory diseases or immunological rejection diseases such as transplant rejection diseases. Moreover, the composition of the present invention does not have cytotoxicity, toxicity with respect to medicines, and side effects and thus can be safely taken by a person for a long period of time. In addition, the composition is safe to a human body.
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:
본 발명은 STA-21을 유효성분으로 포함하는 암 또는 면역질환의 예방 및 치료용 조성물에 관한 것으로서, 보다 구체적으로 본 발명은 STA-21을 화합물 또는 그의 약학적으로 허용 가능한 염을 유효성분으로 함유하는 암 또는 면역질환의 예방 및 치료용 조성물, 면역억제용 조성물, STA-21을 이용한 미분화 T 세포의 Th17 세포로의 분화를 감소 또는 억제하는 방법 및 조절 T 세포를 활성화시키는 방법에 관한 것이다. 본 발명에 따른 STA-21 화합물은 염증성 사이토카인을 생성 및 분비하는 세포 독성 Th17 세포의 분화를 억제하는 효과가 우수하고, 비정상적으로 활성화된 면역세포의 기능을 억제하고 염증 반응을 제어하는 특성을 갖는 면역조절 T 세포(Treg)를 활성화 시키는 효과가 우수하므로 면역반응의 조절 이상으로 유발되는 자가면역질환, 염증성질환 및 이식거부질환과 같은 면역질환을 예방 및 치료할 수 있는 약학적 조성물 또는 면역 억제제로 유용하게 사용될 수 있는 효과가 있다.
Abstract:
PURPOSE: A cell therapeutic composition containing a natural killer cell inhibitor and mesenchymal stem cells is provided to effectively suppress immune rejection responses, and to enhance a treatment effect. CONSTITUTION: A cell therapeutic composition for preventing or treating graft-versus-host diseases contains 2.5mg/kg-250mg/kg of a natural killer cell inhibitor and 2x10^5-2x10^7 mesenchymal stem cells as active ingredients. The mesenchymal stem cells are derived from human. The inhibitor is anti-asialo GM1. The composition contains is administered by intravenous or intradural injection.
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 composition containing AG490 compounds is provided to enhance regulatory T cell(Treg) activity and to prevent or treat immune diseases. CONSTITUTION: A composition for preventing or treating immune diseases contains AG490 compounds of chemical formula 1 or pharmaceutically acceptable salt thereof as an active ingredient. The immune diseases are autoimmune diseases, inflammatory diseases, and transplantation rejection. A method for reducing or suppressing differentiation of undifferentiated T cells in vitro into Th17 cells comprises a step of treating AG490 compounds or pharmaceutically acceptable salt thereof to the undifferentiated T cells.
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.