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1.
公开(公告)号:EP3898983A1
公开(公告)日:2021-10-27
申请号:EP19898348.8
申请日:2019-12-20
发明人: WEI, Wensheng , ZHU, Shiyou , CAO, Zhongzheng , LIU, Zhiheng , HE, Yuan , YUAN, Pengfei
IPC分类号: C12N15/66 , C12N15/113 , C40B40/06 , C12N9/22 , C12N15/10
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公开(公告)号:EP3775205A1
公开(公告)日:2021-02-17
申请号:EP18913494.3
申请日:2018-04-02
发明人: WEI, Wensheng , LIU, Ying , CAO, Zhongzheng , WANG, Yinan , GUO, Yu , YUAN, Pengfei
IPC分类号: C12N15/113 , C12N15/86
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公开(公告)号:EP4086341A1
公开(公告)日:2022-11-09
申请号:EP20911101.2
申请日:2020-12-30
发明人: YUAN, Pengfei , WANG, Fei , NIU, Lichao , FU, Jianqiang , GU, Feng
IPC分类号: C12N5/10 , C12N15/113 , C07K16/28 , A61K35/17
摘要: A method for purifying a universal human CAR-T cell, comprising: (i) destroying, by using gene editing technology, a TRAC gene region from position 23016448 to position 23016490 of chromosome 14 and a B2M gene region from position 45003745 to position 4500378 of chromosome 15 in the human CAR-T cell; (ii) then introducing a mRNA targeting TCRα/β into the gene-edited CAR-T cell; and (iii) in vitro culturing the CAR-T cell population after the described treatment.
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4.
公开(公告)号:EP4086340A1
公开(公告)日:2022-11-09
申请号:EP20910719.2
申请日:2020-12-28
发明人: WANG, Fei , YUAN, Pengfei , NIU, Lichao , FU, Jianqiang , WU, Lanlan
IPC分类号: C12N5/10 , C12N15/113
摘要: A novel preparation method for a universal CAR-T cell targeting a T-cell lymphoma cell, the universal CAR-T cell prepared by means of the method and a biological product comprising the universal CAR-T cell. The preparation method for the universal CAR-T cell targeting a T-cell lymphoma cell comprises: obtaining a T cell from a human donor having a healthy lymphatic system, and then disrupting a TRAC genome region and a B2M genome region in the T cell by means of a gene editing technology, so that CAR molecules targeting the T-cell lymphoma cell TCRα/β are stably expressed in the T cell. The universal CAR-T cell targeting a T-cell lymphoma cell prepared by means of the preparation method eliminates the natural TCR expression of a T cell, greatly reduces the graft-versus-host reaction, and meanwhile, also greatly reduces the immunogenicity thereof, and can continuously and efficiently kill the T-cell lymphoma cell.
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公开(公告)号:EP3536796A1
公开(公告)日:2019-09-11
申请号:EP17812759.3
申请日:2017-06-16
发明人: WEI, Wensheng , ZHOU, Yuexin , ZHANG, Hongmin
摘要: Provided are a donor construct, a gene knockout method, and a system and a kit for gene knockout. In the gene knockout method, a marker gene contained in the donor construct is inserted into a double-strand break position in the cell genome by non-homologous end joining, thus improving the production efficiency of gene knockout by a sequence-specific nuclease through enrichment of gene knockout cells via the expressed marker.
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