4.6 Article

Induced CAR-Macrophages as a Novel Therapeutic Cell Type for Cancer Immune Cell Therapies

期刊

CELLS
卷 11, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/cells11101652

关键词

chimeric antigen receptor (CAR); human primary macrophage cells; induced pluripotent stem cells (iPSC)-derived macrophage cells (iMac); anticancer cell functions

资金

  1. Natural Science Foundation projects of China [91857116, 31871453]
  2. National Key Research and Development Program of China [2018YFA0107100, 2018YFA0107103, 2018YFC1005002]
  3. Zhejiang Innovation Team grant [2019R01004]
  4. Zhejiang Natural Science Foundation projects of China [LR19C120001]
  5. Zhejiang Natural Science Foundation of China [LQ22H160001]
  6. China Postdoctoral Science Foundation [2019M662035]

向作者/读者索取更多资源

CAR-T cell therapy has achieved progress in treating hematological malignancies, but faces multiple challenges in treating solid tumors. CAR-Ms and CAR-iMacs are considered as efficient and inexpensive alternatives for tumor immune cell therapy. This review outlines the current development of human CAR-macrophages and highlights their crucial functions in the field of tumor immune cell therapy.
The Chimeric antigen receptor (CAR)-T cell therapy has made inroads in treating hematological malignancies. Nonetheless, there are still multiple hurdles in CAR-T cell therapy for solid tumors. Primary CAR-expressing macrophage cells (CAR-Ms) and induced pluripotent stem cells (iPSCs)-derived CAR-expressing macrophage cells (CAR-iMacs) have emerged as attractive alternatives in our quest for an efficient and inexpensive approach for tumor immune cell therapy. In this review, we list the current state of development of human CAR-macrophages and provide an overview of the crucial functions of human CAR-macrophages in the field of tumor immune cell therapy.

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