Evidence map›Paper›PMID 32849634›Full record

ReviewFrontiers in immunology2020

Regulatory T Cells: An Emerging Player in Radiation-Induced Lung Injury.

Tiantian Guo, Liqing Zou, Jianjiao Ni, Yue Zhou, Luxi Ye, Xi Yang, Zhengfei Zhu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.6field-weighted citation impact, top 8% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

  1. Review
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  13. The Role of Regulatory T Cells in Cancer Treatment Resistance.International journal of molecular sciences · 2023
    Review
  14. Influence of the irradiated pulmonary microenvironment on macrophage and T cell dynamics.Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology · 2023
    Article
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  19. Uveitis-mediated immune cell invasion through the extracellular matrix of the lens capsule.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
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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

7 authors at 2 institutions in 1 country.

Tiantian GuoDepartment of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Liqing ZouDepartment of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Jianjiao NiDepartment of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Yue ZhouDepartment of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Luxi YeDepartment of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Xi YangDepartment of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Zhengfei ZhuDepartment of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Shanghai Medical College of Fudan University · CNFudan University Shanghai Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cells (Tregs), which have long been recognized as essential regulators of both inflammation and autoimmunity, also impede effective antitumor immune response due to their immunosuppressive properties. Combined radiotherapy and immunotherapeutic interventions focusing on the removal of Tregs have recently garnered interest as a promising strategy to reverse immunosuppression. Meanwhile, Tregs are emerging as a key player in the pathogenesis of radiation-induced lung injury (RILI), a frequent and potentially life-threatening complication of thoracic radiotherapy. Recognition of the critical role of Tregs in RILI raises the important question of whether radiotherapy combined with Treg-targeting immunotherapy offers any beneficial effects in the protection of normal lung tissue. This present review focuses on the contributions of Tregs to RILI, with particular emphasis on the suspected differential role of Tregs in the pneumonitic phase and fibrotic phase of RILI. We also introduce recent progress on the potential mechanisms by which Tregs modulate RILI and the crosstalk among Tregs, other infiltrating T cells, fibrocytes, and resident epithelial cells driving disease pathogenesis. Finally, we discuss whether Tregs also hold promise as a potential target for immunotherapeutic interventions for RILI.

Indexed as

AnimalsCytokinesEpithelial-Mesenchymal TransitionHumansLungLung InjuryPhenotypePulmonary FibrosisRadiation PneumonitisRadiotherapySignal TransductionTh17 CellsTh1 CellsTh1-Th2 BalanceTh2 CellsT-Lymphocytes, RegulatoryCytokinesfibrosislungpneumonitisradiotherapyTreg

Identifiers

PMID32849634
PMCPMC7417370
OpenAlexW3047129242

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.