题名 | IL-12 nanochaperone-engineered CAR T cell for robust tumor-immunotherapy |
作者 | |
通讯作者 | Cai,Lintao |
发表日期 | 2022-02-01
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DOI | |
发表期刊 | |
ISSN | 0142-9612
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EISSN | 1878-5905
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卷号 | 281 |
摘要 | Although chimeric antigen receptor T (CAR T) cell immunotherapy has demonstrated remarkable success in clinical, therapeutic effects are still limited in solid tumor due to lack of activated T cell infiltration in immunosuppression of tumor microenvironment. Herein, we develop IL-12 nanostimulant-engineered CAR T cell (INS-CAR T) biohybrids for boosting antitumor immunity of CAR T cells via immunofeedback. As stimulating nanochaperone, IL-12-loaded human serum albumin (HSA) nanoparticles are effectively conjugated onto CAR T cells via bioorthogonal chemistry without influencing their antitumor capabilities. IL-12 is responsively released from INS-CAR T biohybrids in presence of the increased thiol groups on cell-surface triggered by tumor antigens. In return, released IL-12 obviously promotes the secretion of CCL5, CCL2 and CXCL10, which further selectively recruits and expands CD8 CAR T cells in tumors. Ultimately, the immune-enhancing effects of IL-12 nanochaperone significantly boost CAR T cell antitumor capabilities, dramatically eliminated solid tumor and minimized unwanted side effects. Hence, immunofeedback INS-CAR T biohybrids, which include INS that serves as an intelligent ‘nanochaperone’, could provide a powerful tool for efficient and safe antitumor immunotherapy. |
关键词 | |
相关链接 | [Scopus记录] |
收录类别 | |
语种 | 英语
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学校署名 | 其他
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EI入藏号 | 20220211443963
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EI主题词 | Antigens
; Cell membranes
; Cytology
; Tumors
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EI分类号 | Biological Materials and Tissue Engineering:461.2
; Biology:461.9
; Immunology:461.9.1
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ESI学科分类 | MATERIALS SCIENCE
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Scopus记录号 | 2-s2.0-85122388927
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来源库 | Scopus
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引用统计 |
被引频次[WOS]:51
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成果类型 | 期刊论文 |
条目标识符 | http://sustech.caswiz.com/handle/2SGJ60CL/274016 |
专题 | 南方科技大学第二附属医院 |
作者单位 | 1.Guangdong Key Laboratory of Nanomedicine,CAS Key Laboratory of Health Informatics,CAS-HK Joint Lab of Biomaterials,Shenzhen Institutes of Advanced Technology (SIAT),Chinese Academy of Sciences,Shenzhen,518055,China 2.National Clinical Research Center for Infectious Disease,Shenzhen Third People's Hospital,The Second Affiliated Hospital,Southern University of Science and Technology Shenzhen,518112,China 3.Key Laboratory for Nanomedicine,Department of Histology and Embryology and School of Pharmacy,Guangdong Medical University,Dongguan,523808,China 4.Zhuhai Institute of Advanced Technology Chinese Academy of Sciences,Zhuhai,519000,China 5.School of Information Science and Engineering,Harbin Institute of Technology,Weihai,264209,China |
推荐引用方式 GB/T 7714 |
Luo,Yingmei,Chen,Ze,Sun,Mingjian,et al. IL-12 nanochaperone-engineered CAR T cell for robust tumor-immunotherapy[J]. BIOMATERIALS,2022,281.
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APA |
Luo,Yingmei.,Chen,Ze.,Sun,Mingjian.,Li,Baohong.,Pan,Fan.,...&Cai,Lintao.(2022).IL-12 nanochaperone-engineered CAR T cell for robust tumor-immunotherapy.BIOMATERIALS,281.
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MLA |
Luo,Yingmei,et al."IL-12 nanochaperone-engineered CAR T cell for robust tumor-immunotherapy".BIOMATERIALS 281(2022).
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条目包含的文件 | 条目无相关文件。 |
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