首页> 外国专利> COMPOSITION FOR STABILIZING SURVIVAL OF TRANSPLANTED HEMATOPOIETIC STEM CELL, KIT FOR OBTAINING THE COMPOSITION, METHOD OF STABILIZING SURVIVIAL OF TRANSPLANTED HEMATOPOIETIC STEMCELL, HUMAN MONOCLONAL ANTIBODY OR HUMAN POLYCLONAL ANTIBODY AND METHOD OF PRODUCING THE SAME, GENE ENCODING HUMAN MONOCLONAL ANTIBODY AND TRANSFORMATION INTRODUCING THE GENE

COMPOSITION FOR STABILIZING SURVIVAL OF TRANSPLANTED HEMATOPOIETIC STEM CELL, KIT FOR OBTAINING THE COMPOSITION, METHOD OF STABILIZING SURVIVIAL OF TRANSPLANTED HEMATOPOIETIC STEMCELL, HUMAN MONOCLONAL ANTIBODY OR HUMAN POLYCLONAL ANTIBODY AND METHOD OF PRODUCING THE SAME, GENE ENCODING HUMAN MONOCLONAL ANTIBODY AND TRANSFORMATION INTRODUCING THE GENE

机译:用于稳定移植的造血干细胞存活的组合物,用于获得该组合物的试剂盒,用于稳定移植的造血干细胞存活的方法,人类单克隆抗体或人类多聚体胶体的胶体和胶体的方法

摘要

[PROBLEMS] To stabilize the survival of transplanted hematopoietic stem cellsby using HLA-matched activated lymphocytes. [MEANS FOR SOLVING PROBLEMS] HLA-matched activated lymphocytes in mononuclear cells separated from peripheralblood or umbilical cord blood are proliferated and activated. After separatingand collecting, the HLA-matched activated lymphocytes are employed as the maincomponent of a composition for stabilizing the survival of transplantedhematopoietic stem cells. The obtained composition is widely usable in, forexample, prevention of insufficient survival of transplanted hematopoieticstem cells and therapy for promoting the survival thereof. Although the doseof the composition varies depending on the age, conditions, etc. of a patient,a humanized antibody is administered in a dose of from 0.2 to 20 mg/kg/day tomammals including humans. The composition is administered by intravenousinjection either once a day (single administration or continuousadministration) or intermittently 1 to 3 times in a week or once in 2 or 3weeks.
机译:[问题]稳定移植造血干细胞的存活通过使用HLA匹配的活化淋巴细胞。 [解决问题的方法] HLA-与外周血分离的单核细胞中匹配的活化淋巴细胞血液或脐带血被增殖并活化。分离后收集HLA匹配的活化淋巴细胞作为主要稳定移植物存活的组合物成分造血干细胞。所获得的组合物可广泛用于例如,预防移植造血细胞存活不足干细胞及其促进生存的疗法。虽然剂量成分的变化取决于患者的年龄,状况等,人源化抗体的给药剂量为0.2至20 mg / kg /天,哺乳动物,包括人类。该组合物通过静脉内给药每天一次(单次或连续注射)一次)或每周1到3次或2或3次一次周。

著录项

  • 公开/公告号CA2531569A1

    专利类型

  • 公开/公告日2004-12-16

    原文格式PDF

  • 申请/专利权人 LYMPHOTEC INC.;

    申请/专利号CA20042531569

  • 申请日2004-05-26

  • 分类号C12N5/078;C12N5/0789;A61K35/14;C07K16;C12N5/10;C12N15/13;C12P21/08;

  • 国家 CA

  • 入库时间 2022-08-21 22:14:02

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