Evidence map›Paper›PMID 38592427›Full record

ReviewCancer metastasis reviews2024

In vivo manufacture and manipulation of CAR-T cells for better druggability.

Rui Hou, Xiaoxue Zhang, Xu Wang, Xuan Zhao, Sijin Li, Zhangchun Guan, Jiang Cao, Dan Liu, Junnian Zheng, Ming Shi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cancer metastasis reviews, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Oncology research · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Strategies for Altering Delivery Technologies to Optimize CAR Therapy.International journal of molecular sciences · 2025
    Review
  10. Review
  11. Review
  12. 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

10 authors.

Rui Hou *College of Pharmacy, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xiaoxue Zhang *Department of Hematology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xu WangCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xuan ZhaoCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Sijin LiCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Zhangchun GuanCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Jiang CaoDepartment of Hematology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Dan LiuCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China. 100002017003@xzhmu.edu.cn.
Junnian ZhengCenter of Clinical Oncology, The Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China. jnzheng@xzhmu.edu.cn.
Ming ShiCancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China. mingshi@xzhmu.edu.cn.

Funding

National Natural Science Foundation of China 81972719National Natural Science Foundation of China 82204541National science research in Universities of Jiangsu Province 21KJA320008National science research in Universities of Jiangsu Province 22KJB320009Natural Science Foundation of Jiangsu Province BK20201012Natural Science Foundation of Jiangsu Province BK20210910Natural Science Foundation of Jiangsu Province BK20210913Natural Science Foundation of Jiangsu Province BK20220671
6 · The paper itself

Abstract

The current CAR-T cell therapy products have been hampered in their druggability due to the personalized preparation required, unclear pharmacokinetic characteristics, and unpredictable adverse reactions. Enabling standardized manufacturing and having clear efficacy and pharmacokinetic characteristics are prerequisites for ensuring the effective practicality of CAR-T cell therapy drugs. This review provides a broad overview of the different approaches for controlling behaviors of CAR-T cells in vivo. The utilization of genetically modified vectors enables in vivo production of CAR-T cells, thereby abbreviating or skipping the lengthy in vitro expansion process. By equipping CAR-T cells with intricately designed control elements, using molecule switches or small-molecule inhibitors, the control of CAR-T cell activity can be achieved. Moreover, the on-off control of CAR-T cell activity would yield potential gains in phenotypic remodeling. These methods provide beneficial references for the future development of safe, controllable, convenient, and suitable for standardized production of CAR-T cell therapy products.

Indexed as

Immunotherapy, AdoptiveNeoplasmsReceptors, Chimeric AntigenAnimalsHumansT-LymphocytesReceptors, Chimeric AntigenCAR-T cellDruggabilityIn situ manipulationIn vivo manufacture

Identifiers

What OpenQuestion holds

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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.