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公开(公告)号:US10947502B2
公开(公告)日:2021-03-16
申请号:US15769386
申请日:2016-10-20
Applicant: FUJIFILM Cellular Dynamics, Inc.
Inventor: Maksym A. Vodyanyk , Xin Zhang , Andrew J. Brandl , Deepika Rajesh , Bradley Swanson , Christie Munn , Sarah A. Burton , Wen Bo Wang
IPC: C12N5/0783 , C12N5/0784 , C12N5/0789 , C12N5/0781 , C12N15/85 , C12N15/86
Abstract: Provided herein are methods for the efficient in vitro differentiation of somatic cell-derived pluripotent stem cells to hematopoietic precursor cells, and the further differentiation of the hematopoietic precursor cells into immune cells of various myeloid or lymphoid lineages, particularly T cells, NK cells, and dendritic cells. The pluripotent cells may be maintained and differentiated under defined conditions; thus, the use of mouse feeder cells or serum is not required in certain embodiments for the differentiation of the hematopoietic precursor cells.
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公开(公告)号:US12129486B2
公开(公告)日:2024-10-29
申请号:US17063204
申请日:2020-10-05
Applicant: FUJIFILM Cellular Dynamics, Inc.
Inventor: Maksym A. Vodyanyk , Xin Zhang , Andrew J. Brandl , Deepika Rajesh , Bradley Swanson , Christie Munn , Sarah A. Burton , Wen Bo Wang
IPC: C12N5/0783 , C12N5/0781 , C12N5/0784 , C12N5/0789 , C12N15/85 , C12N15/86
CPC classification number: C12N5/0636 , C12N5/0635 , C12N5/0637 , C12N5/0638 , C12N5/0639 , C12N5/0646 , C12N5/0647 , C12N15/85 , C12N15/86 , C12N2500/38 , C12N2500/90 , C12N2501/115 , C12N2501/125 , C12N2501/145 , C12N2501/155 , C12N2501/165 , C12N2501/22 , C12N2501/2303 , C12N2501/2306 , C12N2501/2307 , C12N2501/25 , C12N2501/26 , C12N2501/60 , C12N2501/602 , C12N2501/603 , C12N2501/604 , C12N2501/605 , C12N2501/606 , C12N2501/608 , C12N2501/727 , C12N2501/998 , C12N2501/999 , C12N2506/025 , C12N2506/03 , C12N2506/09 , C12N2506/11 , C12N2506/45 , C12N2510/00 , C12N2533/50 , C12N2840/20
Abstract: Provided herein are methods for the efficient in vitro differentiation of somatic cell-derived pluripotent stem cells to hematopoietic precursor cells, and the further differentiation of the hematopoietic precursor cells into immune cells of various myeloid or lymphoid lineages, particularly T cells, NK cells, and dendritic cells. The pluripotent cells may be maintained and differentiated under defined conditions; thus, the use of mouse feeder cells or serum is not required in certain embodiments for the differentiation of the hematopoietic precursor cells.
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公开(公告)号:US12163155B2
公开(公告)日:2024-12-10
申请号:US16606120
申请日:2018-04-18
Applicant: FUJIFILM Cellular Dynamics, Inc.
Inventor: Maksym A. Vodyanyk , Xin Zhang , Andrew J. Brandl , Deepika Rajesh , Bradley Swanson , Christie Munn , Sarah Burton , Wen Bo Wang , Ethan McLEOD
IPC: C12N5/0783 , A61K35/17 , A61K35/545 , C07K14/725
Abstract: Provided herein are methods for the production of antigen-specific effector T cells and NK cells from pluripotent stem cells which express a chimeric antigen receptor (CAR). Further provided herein are methods for the adoptive cell therapy by administering the effector T cells and/or NK cells provided herein.
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公开(公告)号:US10828335B2
公开(公告)日:2020-11-10
申请号:US15614755
申请日:2017-06-06
Applicant: FUJIFILM Cellular Dynamics, Inc.
Inventor: Matt George , Carrie Chavez , Chris McMahon , Wen Bo Wang , Lucas Chase , Brad Swanson
IPC: A61K35/30 , B65D25/20 , G01N33/50 , C12N9/02 , C12Q1/68 , A61J1/00 , C12N5/0793 , C12Q1/6876
Abstract: Methods are provided for efficient production of midbrain dopaminergic (DA) neurons. In some aspects, methods involve differentiation and selection of DA neurons for a transgenic pluripotent cell population (e.g., cells comprising a selectable marker gene). Cell populations produced by the instant methods and methods of their use are likewise provided.
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公开(公告)号:US10590383B2
公开(公告)日:2020-03-17
申请号:US15678432
申请日:2017-08-16
Applicant: FUJIFILM Cellular Dynamics, Inc.
Inventor: Christopher W. McMahon , Lauren E. Little , Wen Bo Wang , Nathaniel A. Elliott
IPC: C12N5/00 , C12N5/0793 , A61K38/18 , C12N5/0797 , C07C215/28 , C07C229/36 , G01N33/50
Abstract: Methods are provided, in some aspects, for differentiating pluripotent cells into midbrain dopaminergic (DA) neurons using a mono-SMAD inhibition or inhibition of SMAD signaling with only one SMAD inhibitor. In some embodiments, mono-SMAD inhibition utilizes a single inhibitor of bone morphogenic protein (BMP) for differentiating pluripotent cells into midbrain DA neurons.
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