Evidence map›Paper›PMID 38045827›Full record

ReviewMedComm2023

Chimeric antigen receptor natural killer cells: a promising antitumor immunotherapy.

Yan Wang, Shengjie Jin, Qiqi Zhuang, Na Liu, Ruyi Chen, Sofia Abdulkadir Adam, Jie Jin, Jie Sun

Abstract readReview
In one paragraph

Review in MedComm, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Novel CD73 Inhibitors for Treating Cancer.ACS medicinal chemistry letters · 2024
    Article
  11. 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

8 authors.

Yan WangDepartment of Hematology The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou Zhejiang China.
Shengjie JinDepartment of Hematology The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou Zhejiang China.
Qiqi ZhuangDepartment of Hematology The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou Zhejiang China.
Na LiuDepartment of Hematology The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou Zhejiang China.
Ruyi ChenDepartment of Hematology The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou Zhejiang China.
Sofia Abdulkadir AdamKey Laboratory of Hematologic Malignancies Diagnosis, and Treatment Hangzhou Zhejiang China.
Jie JinDepartment of Hematology The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou Zhejiang China.
Jie SunDepartment of Hematology The First Affiliated Hospital Zhejiang University School of Medicine Hangzhou Zhejiang China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chimeric antigen receptor (CAR) T cells have been successfully used in adoptive cell therapy for malignancies. However, some obstacles, including side effects such as graft-versus-host disease and cytokine release syndrome, therapy resistance, limited sources, as well as high cost, limited the application of CAR T cells. Recently, CAR natural killer (NK) cells have been pursued as the effector cells for adoptive immunotherapy for their attractive merits of strong intrinsic antitumor activity and relatively mild side effects. Additionally, CAR NK cells can be available from various sources and do not require strict human leukocyte antigen matching, which suggests them as promising "off-the-shelf" products for clinical application. Although the use of CAR NK cells is restrained by the limited proliferation and impaired efficiency within the immunosuppressive tumor microenvironment, further investigation in optimizing CAR structure and combination therapies will overcome these challenges. This review will summarize the advancement of CAR NK cells, CAR NK cell manufacture, the clinical outcomes of CAR NK therapy, the challenges in the field, and prospective solutions. Besides, we will discuss the emerging application of other immune cells for CAR engineering. Collectively, this comprehensive review will provide a valuable and informative summary of current progress and evaluate challenges and future opportunities of CAR NK cells in tumor treatment.

Indexed as

cancerchimeric antigen receptorhematologic malignanciesimmunotherapyleukemiaNK celltumor microenvironment

Identifiers

PMID38045827
PMCPMC10691297

What OpenQuestion holds

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Registered trials

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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.