Evidence map›Paper›PMID 37696984›Full record

ArticleNature biomedical engineering2023

Suppression of cytokine release syndrome during CAR-T-cell therapy via a subcutaneously injected interleukin-6-adsorbing hydrogel.

Xianlei Li, Ningqiang Gong, Falin Tian, Shangkun Zhang, Yuxuan Zhang, Yufei Wang, Guangchao Qing, Yongchao Wang, Fangzhou Li, Yihui Xu and 11 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature biomedical engineering, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
13.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  8. Platelet-engineered CAR-T cells as adjuvant therapy after cancer surgery.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
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  13. Article
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  15. Article
  16. Emerging Strategies of Cell and Gene Therapy Targeting Tumor Immune Microenvironment.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Review
  17. Review
  18. Review
  19. Novel strategies to manage CAR-T cell toxicity.Nature reviews. Drug discovery · 2025
    Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors at 4 institutions in 1 country.

Xianlei Li *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, P. R. China.ORCID http://orcid.org/0000-0001-5837-5073
Ningqiang Gong *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, P. R. China. gongnq@nanoctr.cn.
Falin TianUniversity of Chinese Academy of Sciences, Beijing, P. R. China.
Shangkun ZhangInstitute of Biology and Medicine, Wuhan University of Science and Technology, Wuhan, Hubei, P. R. China.ORCID http://orcid.org/0000-0002-1337-5341
Yuxuan ZhangLaboratory 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, P. R. China.ORCID http://orcid.org/0000-0002-1247-6319
Yufei WangLaboratory 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, P. R. China.
Guangchao QingLaboratory 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, P. R. China.
Yongchao WangLaboratory 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, P. R. China.
Fangzhou LiLaboratory 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, P. R. China.
Yihui XuCenter for Transformative Science, ShanghaiTech University, Shanghai, P. R. China.
Linlin ZhangSchool of Life Science and Technology, ShanghaiTech University, Shanghai, P. R. China.
Jinjin WangLaboratory 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, P. R. China.
Qiankun NiLaboratory 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, P. R. China.
Yaling GanLaboratory 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, P. R. China.
Chaojiang GuInstitute of Biology and Medicine, Wuhan University of Science and Technology, Wuhan, Hubei, P. R. China.
Huaidong JiangCenter for Transformative Science, ShanghaiTech University, Shanghai, P. R. China.
Xingxu HuangSchool of Life Science and Technology, ShanghaiTech University, Shanghai, P. R. China.ORCID http://orcid.org/0000-0001-8934-1247
Xinghua ShiUniversity of Chinese Academy of Sciences, Beijing, P. R. China.
Tongcun ZhangInstitute of Biology and Medicine, Wuhan University of Science and Technology, Wuhan, Hubei, P. R. China.
Yan WuLaboratory 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, P. R. China. wuy@nanoctr.cn.ORCID http://orcid.org/0000-0001-8508-7077
Xing-Jie LiangLaboratory 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, P. R. China. liangxj@nanoctr.cn.ORCID http://orcid.org/0000-0002-4793-1705
Chinese Academy of Sciences · CNNational Center for Nanoscience and Technology · CNShanghaiTech University · CNWuhan University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Interleukin-6Receptors, Chimeric AntigenAnimalsAntibodies, NeutralizingCell- and Tissue-Based TherapyCytokine Release SyndromeCytokinesHumansHydrogelsMiceSalicylatesAntibodies, NeutralizingCytokinesHydrogelsInterleukin-6methyl salicylateReceptors, Chimeric AntigenSalicylates

Identifiers

PMID37696984
OpenAlexW4386609992

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.