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成功通过类器官介导产生 iPSC 来源的 CAR-T 细胞。

Successful organoid-mediated generation of iPSC-derived CAR-T cells.

机构信息

Laboratory of Regenerative Immunotherapy, Department of Cell Growth and Differentiation, Center for iPS cell Research, Kyoto University, Sakyo-ku, Kyoto, Japan; Laboratory of Cancer Immunotherapy and Immunology, Transborder Medical Research Center, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan; Thyas Co. Ltd., Sakyo-ku, Kyoto, Japan.

出版信息

Cell Stem Cell. 2022 Apr 7;29(4):493-495. doi: 10.1016/j.stem.2022.03.005.


DOI:10.1016/j.stem.2022.03.005
PMID:35395182
Abstract

Artificial thymic organoids (ATOs) allow the selective differentiation of chimeric antigen receptor (CAR)-transduced human iPSCs into CAR-T cells. In this issue of Cell Stem Cell, Wang et al. now use ATOs to produce human CD19 CAR-T cells that mimic conventional CAR-T cells and effectively control the progression of human CD19 leukemia in an animal model.

摘要

人工胸腺类器官(ATOs)可实现嵌合抗原受体(CAR)转导的人诱导多能干细胞(iPSCs)向 CAR-T 细胞的选择性分化。在本期《Cell Stem Cell》杂志上,Wang 等人现在使用 ATOs 生产出了模拟传统 CAR-T 细胞的人 CD19 CAR-T 细胞,并在动物模型中有效控制了人 CD19 白血病的进展。

相似文献

[1]
Successful organoid-mediated generation of iPSC-derived CAR-T cells.

Cell Stem Cell. 2022-4-7

[2]
3D-organoid culture supports differentiation of human CAR iPSCs into highly functional CAR T cells.

Cell Stem Cell. 2022-4-7

[3]
Induced Pluripotent Stem Cell-Derived Chimeric Antigen Receptor T Cells: The Intersection of Stem Cells and Immunotherapy.

Cell Reprogram. 2023-10

[4]
Induced Pluripotent Stem Cells (iPSCs) Provide a Potentially Unlimited T Cell Source for CAR-T Cell Development and Off-the-Shelf Products.

Pharm Res. 2021-6

[5]
Strength of CAR signaling determines T cell versus ILC differentiation from pluripotent stem cells.

Cell Rep. 2023-3-28

[6]
Scalable generation of functional human iPSC-derived CAR-macrophages that efficiently eradicate CD19-positive leukemia.

J Immunother Cancer. 2023-12-22

[7]
Revolutionizing Cancer Treatments through Stem Cell-Derived CAR T Cells for Immunotherapy: Opening New Horizons for the Future of Oncology.

Cells. 2024-9-10

[8]
In Vitro Differentiation of T Cell: From CAR-Modified T-iPSC.

Methods Mol Biol. 2019

[9]
Non-clinical efficacy, safety and stable clinical cell processing of induced pluripotent stem cell-derived anti-glypican-3 chimeric antigen receptor-expressing natural killer/innate lymphoid cells.

Cancer Sci. 2020-3-31

[10]
CD19 chimeric antigen receptor-redirected T cells combined with epidermal growth factor receptor pathway substrate 8 peptide-derived dendritic cell vaccine in leukemia.

Cytotherapy. 2019-4-25

引用本文的文献

[1]
From Multi-Omics to Visualization and Beyond: Bridging Micro and Macro Insights in CAR-T Cell Therapy.

Adv Sci (Weinh). 2025-5

[2]
Expression Profiles of Five Common Cancer Membrane Protein Antigens Collected for the Development of Cocktail CAR-T Cell Therapies Applicable to Most Solid Cancer Patients.

Int J Mol Sci. 2025-2-27

[3]
Organoid co-culture models of the tumor microenvironment promote precision medicine.

Cancer Innov. 2023-12-17

[4]
Study on the Extrapolability of Current Tumorgenicity Test With Mice by Comparing the Syngeneic or Allogeneic Mouse Transplantation Model.

Stem Cells Transl Med. 2024-6-14

[5]
Application Prospect of Induced Pluripotent Stem Cells in Organoids and Cell Therapy.

Int J Mol Sci. 2024-2-26

[6]
Exploring the promising potential of induced pluripotent stem cells in cancer research and therapy.

Mol Cancer. 2023-11-28

[7]
Application of Induced Pluripotent Stem Cells in Malignant Solid Tumors.

Stem Cell Rev Rep. 2023-11

[8]
Breakthrough in large-scale production of iPSCs-derived exosomes to promote clinical applications.

Front Bioeng Biotechnol. 2023-8-24

[9]
New cell sources for CAR-based immunotherapy.

Biomark Res. 2023-5-6

[10]
Current advances and challenges in CAR T-Cell therapy for solid tumors: tumor-associated antigens and the tumor microenvironment.

Exp Hematol Oncol. 2023-1-27

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