METHODS OF GENERATING ANTIGEN-SPECIFIC T CELLS FOR ADOPTIVE IMMUNOTHERAPY
    4.
    发明申请
    METHODS OF GENERATING ANTIGEN-SPECIFIC T CELLS FOR ADOPTIVE IMMUNOTHERAPY 审中-公开
    产生抗原特异性T细胞用于采集免疫疗法的方法

    公开(公告)号:WO2017156365A1

    公开(公告)日:2017-09-14

    申请号:PCT/US2017/021730

    申请日:2017-03-10

    发明人: KOEHNE, Quenther

    IPC分类号: C12N5/0783

    CPC分类号: C12N5/0638 C12N2501/22

    摘要: Provided herein are methods of generating antigen-specific T cells for therapeutic administration to a human patient having or suspected of having a pathogen or cancer using a CD34 fraction of an apheresis collection from G-CSF mobilized donors. Also disclosed are methods of treating a human patient using antigen-specific T cells generated by such methods, and methods of assessing antigen-specific T cells for suitability for therapeutic administration to a human patient.

    摘要翻译: 本文提供产生抗原特异性T细胞的方法,所述抗原特异性T细胞用于使用来自G-CSF动员供体的单采血液成分采集的CD34级分对患有或怀疑患有病原体或癌症的人患者进行治疗性施用。 还公开了使用通过这些方法产生的抗原特异性T细胞治疗人类患者的方法,以及评估抗原特异性T细胞适用于对患者进行治疗施用的方法。

    MODIFIED T CELLS AND METHODS OF MAKING AND USING THE SAME
    10.
    发明申请
    MODIFIED T CELLS AND METHODS OF MAKING AND USING THE SAME 审中-公开
    改良的T细胞及其制备和使用方法

    公开(公告)号:WO2016160721A1

    公开(公告)日:2016-10-06

    申请号:PCT/US2016/024554

    申请日:2016-03-28

    IPC分类号: A61K35/12 A61K35/17 C12N15/85

    摘要: Disclosed herein are modified primary human T cells and populations thereof comprising a genome in which the CTLA4, PD1, TCRA, TCRB, and/or B2M genes have been edited to generate an off-the-shelf universal CAR T cell from allogeneic healthy donors that can be administered to any patient while reducing or eliminating the risk of immune rejection or graft versus host disease, and which are not prone to T cell inhibition, and methods for allogeneic administration of such cells to reduce the likelihood that the cells will trigger a host immune response when the cells are administered to a subject in need of such cells.

    摘要翻译: 本文公开了修饰的原代人T细胞及其群体,其包含其中已编辑CTLA4,PD1,TCRA,TCRB和/或B2M基因以从同种异体健康供体产生现成的通用CAR T细胞的基因组, 可以对任何患者施用,同时减少或消除免疫排斥或移植物抗宿主病的风险,并且其不容易受到T细胞的抑制,以及用于同种异体施用此类细胞以降低细胞将触发宿主的可能性的方法 当将细胞施用于需要这种细胞的受试者时的免疫应答。