알파-갈락토실세라미드를 이용한 항원 특이적 자가유래 CD8 T 세포의 활성화 방법
    42.
    发明公开
    알파-갈락토실세라미드를 이용한 항원 특이적 자가유래 CD8 T 세포의 활성화 방법 无效
    使用α-GALACTOSYLCERAMIDE活化抗原特异性自体CD8 T细胞的方法

    公开(公告)号:KR1020100051036A

    公开(公告)日:2010-05-14

    申请号:KR1020090107145

    申请日:2009-11-06

    Abstract: PURPOSE: An activation method of an antigen-specific autologous CD8 T cell using alpha-galactosylceramide is provided to minimize side effects by processing the activation in vitro, and to use the activated CD8 T as an anti-tumor vaccine composition. CONSTITUTION: An activation method of an antigen-specific autologous CD8 T cell comprises the following steps: dividing CD8 T cells from a biological material; mixing the CD8 T cells with an antigen presenting cell(APC); processing the mixed cells with alpha-galactosylceramide or its derivative and cultivating; and separating the activated CD8 T cell from the cultivated cells. The antigen-specific autologous CD8 T cell is combined with the alpha-galactosylceramide or its derivative to transfer the alpha-galactosylceramide or its derivative into a human body.

    Abstract translation: 目的:提供使用α-半乳糖神经酰胺的抗原特异性自体CD8T细胞的活化方法,以通过在体外处理活化来最小化副作用,并使用活化的CD8T作为抗肿瘤疫苗组合物。 构成:抗原特异性自体CD8T细胞的活化方法包括以下步骤:从生物材料中分离CD8T细胞; 将CD8T细胞与抗原呈递细胞(APC)混合; 用α-半乳糖神经酰胺或其衍生物处理混合细胞并培养; 并将活化的CD8T细胞与培养细胞分离。 将抗原特异性自体CD8T细胞与α-半乳糖神经酰胺或其衍生物结合以将α-半乳糖神经酰胺或其衍生物转移到人体内。

    AIDS 예방 및 치료를 위한 AIDS DNA백신(GX-127) 또는 재조합 아데노바이러스
    43.
    发明公开
    AIDS 예방 및 치료를 위한 AIDS DNA백신(GX-127) 또는 재조합 아데노바이러스 无效
    艾滋病疫苗或重组腺病毒治疗或预防艾滋病

    公开(公告)号:KR1020090090953A

    公开(公告)日:2009-08-26

    申请号:KR1020080016534

    申请日:2008-02-22

    Abstract: A DNA vaccine composition for preventing and treating AIDS (acquired immunodeficiency syndrome) or a recombinant adenovirus are provided to induce broad immune response. A vaccine composition for treating or preventing HIV (Human immunodeficiency virus) comprises an expression vector containing Gag, Env, Pol antigen gene of HIV B type, and conjugated antigen of regulatory protein or recombinant virus vector. Each N terminal of Env, Pol antigen and Reg gene is conjugated with signal sequence of tissue plasminogen activator (tPA). The Pol antigen gene is substituted to phenyulalanine from tyrosine which is 183th amino acid of removing enzyme activation of reverse transcriptase.

    Abstract translation: 提供用于预防和治疗AIDS(获得性免疫缺陷综合征)或重组腺病毒的DNA疫苗组合物以诱导广泛的免疫应答。 用于治疗或预防HIV(人类免疫缺陷病毒)的疫苗组合物包含含有HIV B型的Gag,Env,Pol抗原基因和调节蛋白或重组病毒载体的共轭抗原的表达载体。 Env,Pol抗原和Reg基因的每个N末端与组织纤溶酶原激活物(tPA)的信号序列缀合。 将Pol抗原基因从去除逆转录酶的酶活化的第183位氨基酸的酪氨酸取代为苯丙氨酸。

    최적의 진핵 세포 발현 벡터의 개발
    44.
    发明公开
    최적의 진핵 세포 발현 벡터의 개발 有权
    最佳真核表达载体的开发

    公开(公告)号:KR1020090090924A

    公开(公告)日:2009-08-26

    申请号:KR1020080016489

    申请日:2008-02-22

    Abstract: An expression vector of eukaryote which has optimal condition in gene therapy and DNA vaccine is provided to highly induce the expression by inserting the interleukin-12 mutant gene. A recombinant vector pGX27 for expressing foreign gene comprises a CMV promoter (pCMV), intron (gIVS) of beta gloving gene of rabbit, nucleic acid cloning area (MCS) which encodes a target protein, polyadenylation signal(SV40 poly(A)) of SV40 virus, SV40 virus enhancer and antibiotics-resistant gene. The antibiotics-resistant gene is a kanamycin resistant gene (Kan). A composition for vaccine immunization or gene therapy comprises a recombinant vector pGX27 of expressing a foreign gene.

    Abstract translation: 提供在基因治疗和DNA疫苗中具有最佳条件的真核生物的表达载体,通过插入白细胞介素-12突变基因来高度诱导表达。 用于表达外源基因的重组载体pGX27包含兔的β-葡聚糖基因的CMV启动子(pCMV),内含子(gIVS),编码靶蛋白的核酸克隆区(MCS),聚腺苷酸化信号(SV40聚(A)) SV40病毒,SV40病毒增强子和抗生素抗性基因。 抗生素抗性基因是卡那霉素抗性基因(Kan)。 用于疫苗免疫或基因治疗的组合物包含表达外源基因的重组载体pGX27。

    인터루킨-27, 인터루킨-27-에프씨 융합단백질 및 그돌연변이들을 포함하는 자가면역 질환의 예방 및 치료용약학적 조성물
    45.
    发明公开
    인터루킨-27, 인터루킨-27-에프씨 융합단백질 및 그돌연변이들을 포함하는 자가면역 질환의 예방 및 치료용약학적 조성물 无效
    用于预防和治疗包含白细胞介素-27蛋白,IL-27-FC融合蛋白及其突变体的自身免疫性疾病的药物组合物

    公开(公告)号:KR1020090038336A

    公开(公告)日:2009-04-20

    申请号:KR1020070103779

    申请日:2007-10-15

    Abstract: A pharmaceutical composition containing Interleukin-27, Il-27-Fc fusion protein and mutant thereof is provided to efficiently inhibit production of IL-17 and increase production of IFN-gamma by promoting differentiation of Th-1 in order to treat and prevent autoimmune diseases. A pharmaceutical composition for treatment and prevention of autoimmune diseases comprises Interleukin-27, Il-27-Fc fusion protein and mutant thereof. The Interleukin-27 is human-derived proteins. The pharmaceutical composition contains Il-27-Fc fusion protein wherein carboxyl terminal of the Interleukin-27 is coupled with amino terminal of immunoglobulin Fc and peptide. The immunoglobulin Fc is derived from one selected from the group consisting of IgG, IgA, IgM, IgE and IgD. The immunoglobulin Fc has a hinge site which can has one or more cysteins. The autoimmune diseases represent systemic lupus erythematosus, Sjogren syndrome, Hashimoto thyroiditis, rheumatoid arthritis, polymyositis, scleroderma, Addison disease, vitiligo, pernicious anemia, glomerulonephritis or pulmonary fibrosis.

    Abstract translation: 提供了含有白细胞介素-27,II-27-Fc融合蛋白及其突变体的药物组合物,以有效抑制IL-17的产生并通过促进Th-1的分化来增加IFN-γ的产生,从而治疗和预防自身免疫疾病 。 用于治疗和预防自身免疫疾病的药物组合物包含白细胞介素-27,II-27-Fc融合蛋白及其突变体。 白细胞介素-27是人源性蛋白质。 药物组合物含有II-27-Fc融合蛋白,其中白细胞介素-27的羧基末端与免疫球蛋白Fc和肽的氨基末端偶联。 免疫球蛋白Fc来自选自IgG,IgA,IgM,IgE和IgD的一种。 免疫球蛋白Fc具有可以具有一个或多个半胱氨酸的铰链位点。 自身免疫性疾病代表系统性红斑狼疮,干燥综合征,桥本甲状腺炎,类风湿性关节炎,多发性肌炎,硬皮病,艾迪生病,白癜风,恶性贫血,肾小球性肾炎或肺纤维化。

    항암 조성물
    46.
    发明授权
    항암 조성물 有权
    抗癌成分

    公开(公告)号:KR100788930B1

    公开(公告)日:2007-12-27

    申请号:KR1020060035130

    申请日:2006-04-18

    CPC classification number: C07K14/5434 A61K38/00

    Abstract: 본 발명은 IL-12M을 코딩하는 유전자 컨스트럭트(genetic construct)를 포함하는 재조합 벡터 및 면역조절인자 유전자를 포함하는 재조합 벡터를 포함하거나 하나의 벡터에서 상기의 유전자 컨스트럭터 및 면역 조절 인자 유전자를 동시에 발현하는 재조합 벡터를 포함하는 항암 조성물 및 이를 항암 치료가 필요한 개체에 투여하고 각 유전자를 발현시켜 신체 면역 반응을 증진시키고 종양세포의 증식을 억제시키는 방법에 관한 것이다. 본 발명은 종래의 항암 조성물보다 우수한 항암 효과를 제공한다.
    재조합 벡터, 항암 면역 치료제, 항암 유전자 치료제, IL-12, 면역 조절 인자

    신규한 히알루론산 기반 하이드로겔 및 이의 용도
    47.
    发明授权
    신규한 히알루론산 기반 하이드로겔 및 이의 용도 有权
    基于透明质酸的新型水凝胶及其用途

    公开(公告)号:KR101605528B1

    公开(公告)日:2016-03-23

    申请号:KR1020120145758

    申请日:2012-12-13

    Abstract: 본발명은세포분화제또는세포활성유도물질을포함하고, 쿠커비투릴과폴리아민을이용하여제조된히알루론산기반하이드로겔, 상기하이드로겔을포함하는세포치료보조용조성물, 상기세포분화제또는세포활성유도물질을포함하는하이드로겔과중간엽줄기세포를포함하는세포치료용조성물, 쿠커비투릴과폴리아민을이용하여제조된히알루론산기반하이드로겔을포함하는세포치료보조용조성물및 본발명의또 다른목적은상기하이드로겔과중간엽줄기세포를포함하는세포치료용조성물에관한것이다. 본발명에서제공하는히알루론산기반하이드로겔은세포치료제로서사용되는치료물질을발현시키는줄기세포를지지하는보조제로서의역할을수행하여, 상기치료물질의분비를촉진시키고, 세포생존율을증가시켜서세포치료제의치료효과를극대화시킬수 있으므로, 보다향상된효능을나타내는세포치료제의개발에널리활용될수 있을것이다.

    나노 다공성 박막을 이용한 인간 성장 호르몬-Fc 융합 단백질의 서방형 약물 전달 시스템
    49.
    发明公开
    나노 다공성 박막을 이용한 인간 성장 호르몬-Fc 융합 단백질의 서방형 약물 전달 시스템 有权
    通过使用聚合物膜与人体抗体FC融合的人类生长激素受体释放的药物递送系统

    公开(公告)号:KR1020130079011A

    公开(公告)日:2013-07-10

    申请号:KR1020120000243

    申请日:2012-01-02

    CPC classification number: A61K47/32 A61K9/0002 A61K38/27 A61K39/395 B82Y5/00

    Abstract: PURPOSE: A nanoporous membrane with nanopores, which is a depot system capable of controlling the release of functional proteins in cosmetics is provided to be used as a nanoporous carrier based on a block copolymer. CONSTITUTION: A nanoporous membrane is prepared using PS-b-PMMA[polystyrene-block-poly (methyl methacrylate) polymers. The particle size of nanopores of the nanoporous membrane is 10-20 nm. The average of the particle size is 15 nm. A method for delivering antibody-based proteins constantly maintains release rate using the nanoporous membrane. The nanoporous membrane is used in a sustained release drug delivery system of the antibody-based proteins.

    Abstract translation: 目的:提供一种具有纳米孔的纳米多孔膜,其是能够控制化妆品中功能性蛋白质释放的贮库系统,用作基于嵌段共聚物的纳米多孔载体。 构成:使用PS-b-PMMA [聚苯乙烯嵌段聚(甲基丙烯酸甲酯))聚合物制备纳米多孔膜。 纳米多孔膜的纳米孔的粒度为10-20nm。 粒径的平均值为15nm。 使用纳米多孔膜,用于递送基于抗体的蛋白质的方法不断地保持释放速率。 纳米多孔膜用于基于抗体的蛋白质的持续释放药物递送系统中。

    항 KIAA1114 항체를 유효성분으로 함유하는 KIAA1114 과발현에 의해 야기되는 암의 예방 또는 치료용 약학적 조성물
    50.
    发明公开
    항 KIAA1114 항체를 유효성분으로 함유하는 KIAA1114 과발현에 의해 야기되는 암의 예방 또는 치료용 약학적 조성물 无效
    用于预防或治疗癌症导致癌症的药物组合物K I A A 1 1 1 4包含抗体K I A A 1 1 1 4抗体

    公开(公告)号:KR1020130058390A

    公开(公告)日:2013-06-04

    申请号:KR1020110124375

    申请日:2011-11-25

    Abstract: PURPOSE: A pharmaceutical composition containing anti-KIAA1114 antibody as an active ingredient for preventing or treating cancer caused by KIAA1114 overexpression is provided to suppress cancer cell metastasis in a lung metastasis animal model using a KIAA1114-overexpressing cancer cell line. CONSTITUTION: A pharmaceutical composition for preventing or treating cancer caused by KIAA1114 overexpression contains anti-KIAA1114 antibody as an active ingredient. The antibody reacts human KIAA1114 protein with an amino acid sequence of sequence number 1 as an antigen. The antibody specifically binds to extracellular domain of KIAA1114 protein encoded by a base sequence of sequence number 3. The antibody binds to an epitope corresponding to 200-214th amino acid sequences of human KIAA1114 protein. The antibody contains a heavy chain variable region with an amino acid sequence of sequence number 6, and a light chain variable region with an amino acid sequence of sequence number 7.

    Abstract translation: 目的:提供一种含有抗KIAA1114抗体作为预防或治疗由KIAA1114过表达引起的癌症的活性成分的药物组合物,用于抑制肺转移动物模型中使用KIAA1114过表达癌细胞系的癌细胞转移。 构成:用于预防或治疗由KIAA1114过表达引起的癌症的药物组合物含有抗KIAA1114抗体作为活性成分。 抗体将人KIAA1114蛋白与序列号1的氨基酸序列作为抗原反应。 抗体特异性结合由序列号3的碱基序列编码的KIAA1114蛋白的细胞外结构域。抗体结合对应于人KIAA1114蛋白质的第200-214位氨基酸序列的表位。 抗体含有具有序列号6的氨基酸序列的重链可变区和具有序列号7的氨基酸序列的轻链可变区。

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