TGFβ를 코딩하는 뉴클레오티드 서열이 도입된 간엽줄기세포 및 그의 용도
    2.
    发明公开
    TGFβ를 코딩하는 뉴클레오티드 서열이 도입된 간엽줄기세포 및 그의 용도 有权
    引入编码TGFβ的核苷酸序列的MESENCHYMAL STEM CELL及其用途

    公开(公告)号:KR1020110044490A

    公开(公告)日:2011-04-29

    申请号:KR1020090101194

    申请日:2009-10-23

    Abstract: PURPOSE: A mesenchymsal stem cells and a composition containing the same for treating autoimmune diseases are provided to enhance autoantigen-specific CD4+ CD25+ Foxp3+ regulatory T cells and to treat autoimmune diseases. CONSTITUTION: A composition for treating autoimmune diseases contains mesenchymal stem cells in which TFG-beta-encoding nucleotide sequence is introduced and pharmaceutically acceptable carrier. The TGF-beta-encoding nucleotide sequence is sequence number 2. The TGF-beta-encoding nucleotide sequence is introduced by adenovirus-associated vector. The mesenchymal stem cell is derived from bone marrow-derived mesenchymal stem cells or adipose-derived mesenchymal stem cells.

    Abstract translation: 目的:提供间充质干细胞和含有其的用于治疗自身免疫性疾病的组合物,以增强自身抗原特异性CD4 + CD25 + Foxp3 +调节性T细胞并治疗自身免疫性疾病。 构成:用于治疗自身免疫性疾病的组合物含有引入TFG-β编码核苷酸序列的间充质干细胞和药学上可接受的载体。 TGF-β编码核苷酸序列是序列号2.由腺病毒相关载体引入TGF-β编码的核苷酸序列。 间充质干细胞衍生自骨髓间充质干细胞或脂肪来源的间充质干细胞。

    간엽줄기세포 및 면역조절 T 세포를 유효성분으로 포함하는 이식편대숙주질환 예방 또는 치료용 세포치료제 조성물
    5.
    发明公开
    간엽줄기세포 및 면역조절 T 세포를 유효성분으로 포함하는 이식편대숙주질환 예방 또는 치료용 세포치료제 조성물 无效
    用于预防或治疗包含MESENCHYMAL STEM细胞和调节性T细胞的GRAFT-VERSUS-HOST疾病的细胞治疗组合物

    公开(公告)号:KR1020120095022A

    公开(公告)日:2012-08-28

    申请号:KR1020110014398

    申请日:2011-02-18

    Abstract: PURPOSE: A cell therapy composition for preventing or treating graft-versus-host diseases including immune-modulating T cells and mesenchymal stem cells is provided to control rejection against the host after transplanted marrow is engrafted, thereby reducing the generation of the graft-versus-host diseases. CONSTITUTION: A cell therapy composition for preventing or treating graft-versus-host diseases includes immune-modulating T cells and mesenchymal stem cells. The mesenchymal stem cell is a human derivative mesenchymal stem cell. The immune-modulating T cell is an immune-modulating T cell which is induced by retinal. The immune-modulated T cell is CD4+CD25+ immune-modulated T cell which is induced by processing retinal, anti-CD3, TGF-b, and anti-CD28 on the CD4+ T cell. The composition includes 1×10^4 cell/kg-1×10^8 cell/kg of the Cell Therapy Products.

    Abstract translation: 目的:提供用于预防或治疗移植物抗宿主病,包括免疫调节性T细胞和间充质干细胞的细胞治疗组合物,用于在移植骨髓后控制对宿主的排斥反应,从而减少移植物抗宿主病的产生, 宿主病。 构成:用于预防或治疗移植物抗宿主病的细胞治疗组合物包括免疫调节T细胞和间充质干细胞。 间充质干细胞是人类衍生的间充质干细胞。 免疫调节性T细胞是由视网膜诱导的免疫调节性T细胞。 免疫调节的T细胞是通过在CD4 + T细胞上处理视网膜,抗CD3,TGF-b和抗CD28诱导的CD4 + CD25 +免疫调节的T细胞。 该组合物包括1×10 ^ 4细胞/ kg-1×10 ^ 8细胞/ kg的细胞治疗产品。

    간엽줄기세포 및 면역조절 T 세포를 유효성분으로 포함하는 면역질환의 예방 또는 치료용 세포치료제 조성물
    6.
    发明公开
    간엽줄기세포 및 면역조절 T 세포를 유효성분으로 포함하는 면역질환의 예방 또는 치료용 세포치료제 조성물 有权
    用于预防或治疗包含MESENCHYMAL STEM细胞和调节性T细胞的免疫疾病的细胞治疗组合物

    公开(公告)号:KR1020140040696A

    公开(公告)日:2014-04-03

    申请号:KR1020137021403

    申请日:2012-02-17

    Abstract: The present invention relates to a cell therapy composition for preventing or treating immune diseases comprising mesenchymal stem cells and immunoregulatory T-cells as active ingredients. By infusing the mesenchymal stem cells and the immunoregulatory T-cells, which are cellular therapeutic agents of the present invention, into bone marrow transplanted animals, rejection to a host is suppressed after an engraftment of the transplanted bone marrow, thereby obtaining an effect of reducing immune diseases, such as graft-versus-host disease (GVHD). Moreover, the effect of such GVHD reduction is significantly greater than that of a reduction level obtained from a sole infusion of mesenchymal stem cells. Accordingly, the cell therapy composition of the present invention having such effects can be useful in the prevention or treatment of immune diseases. [Reference numerals] (AA) First experimental group; (BB) Second experimental group; (CC) Control group

    Abstract translation: 本发明涉及用于预防或治疗包含间充质干细胞和免疫调节性T细胞作为活性成分的免疫疾病的细胞治疗组合物。 通过将作为本发明的细胞治疗剂的间充质干细胞和免疫调节性T细胞注入骨髓移植动物中,移植移植的骨髓被移植后抑制宿主的排斥,从而获得降低 免疫疾病,如移植物抗宿主病(GVHD)。 此外,这种GVHD降低的效果显着大于从单次输注间充质干细胞获得的还原水平的效果。 因此,具有这种效果的本发明的细胞治疗组合物可用于预防或治疗免疫疾病。 (附图标记)(AA)第一实验组; (BB)第二实验组; (CC)对照组

    IL-27을 유효성분으로 포함하는 면역거부질환의 예방 또는 치료용 조성물
    8.
    发明公开
    IL-27을 유효성분으로 포함하는 면역거부질환의 예방 또는 치료용 조성물 有权
    用于预防或治疗包含IL-27作为有效成分的免疫抑制剂的组合物

    公开(公告)号:KR1020120095046A

    公开(公告)日:2012-08-28

    申请号:KR1020110014438

    申请日:2011-02-18

    CPC classification number: A61K38/20 A61K48/005 Y10S424/81

    Abstract: PURPOSE: A composition for preventing or treating immunological rejection diseases including IL-27 is provided to alleviate the immunological rejection disease by suppressing rejection towards the host after the transplanted cell or organ is engrafted. CONSTITUTION: A composition for preventing or treating immunological rejection diseases includes IL-27 as an active component. The IL-27 has amino acid sequence described in the sequence number 1(SEQ ID NO:1). The composition for preventing or treating immunological rejection diseases includes a vector containing polynucleotide which codes the IL-27 as an active ingredient. The polynucleotide has the base sequence described in the sequence number 2. The immunological rejection disease is graft-versus-host disease.

    Abstract translation: 目的:提供一种用于预防或治疗免疫排斥疾病(包括IL-27)的组合物,用于通过在移植的细胞或器官移植后抑制对宿主的排斥来减轻免疫排斥疾病。 构成:用于预防或治疗免疫排斥疾病的组合物包括IL-27作为活性成分。 IL-27具有序列号1(SEQ ID NO:1)中描述的氨基酸序列。 用于预防或治疗免疫排斥疾病的组合物包括编码IL-27作为活性成分的含有多核苷酸的载体。 多核苷酸具有序列号2中描述的碱基序列。免疫排斥疾病是移植物抗宿主病。

Patent Agency Ranking