Evidence map›Paper›PMID 37753092›Full record

ReviewFrontiers in immunology2023

Reprogramming of Treg cells in the inflammatory microenvironment during immunotherapy: a literature review.

Xinyan Wu, Zhigang Zhou, Qiang Cao, Yuquan Chen, Junling Gong, Qi Zhang, Yi Qiang, Yanfeng Lu, Guangzhu Cao

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. Article
  2. Review
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  5. Review
  6. Review
  7. Article
  8. A laminin α4-CD8Oncoimmunology · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
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  19. Autophagy: regulating the seesaw of bone-fat balance.Frontiers in cell and developmental biology · 2025
    Review
  20. Article
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

9 authors.

Xinyan WuDepartment of Earth Sciences, Kunming University of Science and Technology, Kunming, China.
Zhigang ZhouDepartment of Oncology, Changde Hospital, Xiangya School of Medicine, Central South University, Changde, China.
Qiang CaoDepartment of Earth Sciences, Kunming University of Science and Technology, Kunming, China.
Yuquan ChenInstitute of Medical Information/Library, Chinese Academy of Medical Sciences, Beijing, China.
Junling GongSchool of Public Health, Nanchang University, Qianhu, Nanchang, China.
Qi ZhangUndergraduate Department, Taishan University, Taian, China.
Yi QiangDepartment of Earth Sciences, Kunming University of Science and Technology, Kunming, China.
Yanfeng LuDepartment of Earth Sciences, Kunming University of Science and Technology, Kunming, China.
Guangzhu CaoDepartment of Earth Sciences, Kunming University of Science and Technology, Kunming, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cells (Treg), as members of CD4+ T cells, have garnered extensive attention in the research of tumor progression. Treg cells have the function of inhibiting the immune effector cells, preventing tissue damage, and suppressing inflammation. Under the stimulation of the tumor inflammatory microenvironment (IM), the reprogramming of Treg cells enhances their suppression of immune responses, ultimately promoting tumor immune escape or tumor progression. Reducing the number of Treg cells in the IM or lowering the activity of Treg cells while preventing their reprogramming, can help promote the body's anti-tumor immune responses. This review introduces a reprogramming mechanism of Treg cells in the IM; and discusses the regulation of Treg cells on tumor progression. The control of Treg cells and the response to Treg inflammatory reprogramming in tumor immunotherapy are analyzed and countermeasures are proposed. This work will provide a foundation for downregulating the immunosuppressive role of Treg in the inflammatory environment in future tumor immunotherapy.

Indexed as

CD4-Positive T-LymphocytesT-Lymphocytes, RegulatoryHumansImmunosuppressive AgentsImmunotherapyInflammationImmunosuppressive Agentscancer progressionFoxp3immune evasionimmunotherapyinflammatory microenvironmentTregs

Identifiers

PMID37753092
PMCPMC10518452

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.