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Suppression of cytokine release syndrome during CAR-T-cell therapy via a subcutaneously injected interleukin-6-adsorbing hydrogel | |
Li, Xianlei1,2; Gong, Ningqiang1,2; Tian, Falin2,3; Zhang, Shangkun4; Zhang, Yuxuan1,2; Wang, Yufei1,2; Qing, Guangchao1; Wang, Yongchao1; Li, Fangzhou1; Xu, Yihui5 ![]() ![]() ![]() | |
2023-09 | |
发表期刊 | NATURE BIOMEDICAL ENGINEERING (IF:26.8[JCR-2023],29.2[5-Year]) |
ISSN | 2157-846X |
EISSN | 2157-846X |
卷号 | 7期号:9页码:1129-1141 |
发表状态 | 已发表 |
DOI | 10.1038/s41551-023-01084-4 |
摘要 | The infusion of chimaeric antigen receptor (CAR) T cells can trigger the release of life-threatening supraphysiological levels of pro-inflammatory cytokines. However, uncertainty regarding the timing and severity of such cytokine release syndrome (CRS) demands careful monitoring of the conditions required for the administration of neutralizing antibodies. Here we show that a temperature-sensitive hydrogel conjugated with antibodies for the pro-inflammatory cytokine interleukin-6 (IL-6) and subcutaneously injected before the infusion of CAR-T cells substantially reduces the levels of IL-6 during CRS while maintaining the therapy’s antitumour efficacy. In immunodeficient mice and in mice with transplanted human haematopoietic stem cells, the subcutaneous IL-6-adsorbing hydrogel largely suppressed CAR-T-cell-induced CRS, substantially improving the animals’ survival and alleviating their levels of fever, hypotension and weight loss relative to the administration of free IL-6 antibodies. The implanted hydrogel, which can be easily removed with a syringe following a cooling-induced gel–sol transition, may allow for a shift in the management of CRS, from monitoring to prevention. © 2023, The Author(s), under exclusive licence to Springer Nature Limited. |
关键词 | Antibodies Cytology Hydrogels Mammals Sols Stem cells Anti-tumor efficacy Antigen receptors Cell therapy Condition Cytokines Interleukin6 (IL6) Neutralizing antibodies Proinflammatory cytokines Temperature-sensitive hydrogels Uncertainty |
收录类别 | EI |
语种 | 英语 |
出版者 | Nature Research |
EI入藏号 | 20233814736640 |
EI主题词 | T-cells |
EI分类号 | 461.2 Biological Materials and Tissue Engineering ; 461.9 Biology ; 461.9.1 Immunology ; 801.3 Colloid Chemistry ; 804 Chemical Products Generally |
原始文献类型 | Journal article (JA) |
引用统计 | 正在获取...
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文献类型 | 期刊论文 |
条目标识符 | https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/335582 |
专题 | 生命科学与技术学院 生命科学与技术学院_PI研究组_黄行许组 大科学中心_PI研究组_江怀东组 大科学中心_公共科研平台_大科学装置建设部 |
通讯作者 | Gong, Ningqiang; Wu, Yan; Liang, Xing-Jie |
作者单位 | 1.Laboratory of Controllable Nanopharmaceuticals, Chinese Academy of Sciences (CAS) Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, China; 2.University of Chinese Academy of Sciences, Beijing, China; 3.CAS Key Laboratory for Nanosystem and Hierarchy Fabrication, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, China; 4.Institute of Biology and Medicine, Wuhan University of Science and Technology, Hubei, Wuhan, China; 5.Center for Transformative Science, ShanghaiTech University, Shanghai, China; 6.School of Life Science and Technology, ShanghaiTech University, Shanghai, China; 7.School of Biomedical Engineering, Guangzhou Medical University, Guangdong, Guangzhou, China |
推荐引用方式 GB/T 7714 | Li, Xianlei,Gong, Ningqiang,Tian, Falin,et al. Suppression of cytokine release syndrome during CAR-T-cell therapy via a subcutaneously injected interleukin-6-adsorbing hydrogel[J]. NATURE BIOMEDICAL ENGINEERING,2023,7(9):1129-1141. |
APA | Li, Xianlei.,Gong, Ningqiang.,Tian, Falin.,Zhang, Shangkun.,Zhang, Yuxuan.,...&Liang, Xing-Jie.(2023).Suppression of cytokine release syndrome during CAR-T-cell therapy via a subcutaneously injected interleukin-6-adsorbing hydrogel.NATURE BIOMEDICAL ENGINEERING,7(9),1129-1141. |
MLA | Li, Xianlei,et al."Suppression of cytokine release syndrome during CAR-T-cell therapy via a subcutaneously injected interleukin-6-adsorbing hydrogel".NATURE BIOMEDICAL ENGINEERING 7.9(2023):1129-1141. |
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