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Title:
Pluripotent stem cell-derived CAR-macrophage cells with antigen-dependent anti-cancer cell functions | Journal of Hematology & Oncology
Description:
The Chimera antigen receptor (CAR)-T cell therapy has gained great success in the clinic. However, there are still major challenges for its wider applications in a variety of cancer types including lack of effectiveness due to the highly complex tumor microenvironment, and the forbiddingly high cost due to the personalized manufacturing procedures. In order to overcome these hurdles, numerous efforts have been spent focusing on optimizing Chimera antigen receptors, engineering and improving T cell capacity, exploiting features of subsets of T cell or NK cells, or making off-the-shelf universal cells. Here, we developed induced pluripotent stem cells (iPSCs)-derived, CAR-expressing macrophage cells (CAR-iMac). CAR expression confers antigen-dependent macrophage functions such as expression and secretion of cytokines, polarization toward the pro-inflammatory/anti-tumor state, enhanced phagocytosis of tumor cells, and in vivo anticancer cell activity. This technology platform for the first time provides an unlimited source of iPSC-derived engineered CAR-macrophage cells which could be utilized to eliminate cancer cells.
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Keywords {🔍}
cells, fig, article, cell, car, additional, macrophage, file, stem, analysis, carimac, data, google, scholar, zhang, macrophages, showing, cancer, human, zhejiang, pluripotent, antigen, differentiated, genes, cas, expression, phagocytosis, showed, imac, university, china, antigendependent, anticancer, functions, ipscs, gene, error, mesoimac, induced, vivo, compared, differentiation, day, cytokine, research, wang, zhu, tumor, activity, ipscderived,
Topics {✒️}
lps/ifn-γ-polarized m1 cells pro-inflammatory/anti-tumor state car-expressing ipsc-induced macrophage anti-cancer cell functions single-cell rna-seq data il-4/il-10-polarized m2 cells antigen-expressing cancer cells car-ipsc-differentiated car-expressing anti-cancer drug research anti-tumor cell activity found antigen-dependent increase untransduced ipsc-differentiated macrophages rna-seq data showing jiajia wang & qinjie weng car-expressing macrophage cells cell stem cell vivo anti-tumor effects bulk rna-seq data relevant regulatory standards antigen-dependent phagocytosis pbmc-derived primary macrophages chimeric antigen receptors myeloid cell-based immunotherapy rna-sequencing data analysis stem cell rep large-scale hematopoietic differentiation k562-cd19 cancer cells innate immunity-related functions differentiated cells showed �cytokine activity gene car-imac cells expanded polarize car-imac cells article download pdf anticancer cell functions ipsc-derived cells chimera antigen receptor derived macrophage cells differentiated single cells human cell atlas national key research ipsc-derived macrophages ten clustered c0–c9 car-imac cells cultured eliminate cancer cells combat cancer cells pro-inflammatory state human macrophage activation single-cell data stem cell m2 polarized macrophages
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headline:Pluripotent stem cell-derived CAR-macrophage cells with antigen-dependent anti-cancer cell functions
description:The Chimera antigen receptor (CAR)-T cell therapy has gained great success in the clinic. However, there are still major challenges for its wider applications in a variety of cancer types including lack of effectiveness due to the highly complex tumor microenvironment, and the forbiddingly high cost due to the personalized manufacturing procedures. In order to overcome these hurdles, numerous efforts have been spent focusing on optimizing Chimera antigen receptors, engineering and improving T cell capacity, exploiting features of subsets of T cell or NK cells, or making off-the-shelf universal cells. Here, we developed induced pluripotent stem cells (iPSCs)-derived, CAR-expressing macrophage cells (CAR-iMac). CAR expression confers antigen-dependent macrophage functions such as expression and secretion of cytokines, polarization toward the pro-inflammatory/anti-tumor state, enhanced phagocytosis of tumor cells, and in vivo anticancer cell activity. This technology platform for the first time provides an unlimited source of iPSC-derived engineered CAR-macrophage cells which could be utilized to eliminate cancer cells.
datePublished:2020-11-11T00:00:00Z
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Chimera antigen receptor (CAR)
Induced pluripotent stem cells (iPSC)-derived macrophage cells (iMac)
Antigen-dependent activation
Anti-cancer cell functions
Oncology
Hematology
Cancer Research
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headline:Pluripotent stem cell-derived CAR-macrophage cells with antigen-dependent anti-cancer cell functions
description:The Chimera antigen receptor (CAR)-T cell therapy has gained great success in the clinic. However, there are still major challenges for its wider applications in a variety of cancer types including lack of effectiveness due to the highly complex tumor microenvironment, and the forbiddingly high cost due to the personalized manufacturing procedures. In order to overcome these hurdles, numerous efforts have been spent focusing on optimizing Chimera antigen receptors, engineering and improving T cell capacity, exploiting features of subsets of T cell or NK cells, or making off-the-shelf universal cells. Here, we developed induced pluripotent stem cells (iPSCs)-derived, CAR-expressing macrophage cells (CAR-iMac). CAR expression confers antigen-dependent macrophage functions such as expression and secretion of cytokines, polarization toward the pro-inflammatory/anti-tumor state, enhanced phagocytosis of tumor cells, and in vivo anticancer cell activity. This technology platform for the first time provides an unlimited source of iPSC-derived engineered CAR-macrophage cells which could be utilized to eliminate cancer cells.
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Chimera antigen receptor (CAR)
Induced pluripotent stem cells (iPSC)-derived macrophage cells (iMac)
Antigen-dependent activation
Anti-cancer cell functions
Oncology
Hematology
Cancer Research
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