Evidence map›Paper›PMID 26280204›Full record

ArticleCancer immunology, immunotherapy : CII2015

Expression of TNFR2 by regulatory T cells in peripheral blood is correlated with clinical pathology of lung cancer patients.

Fan Yan, Ruijuan Du, Feng Wei, Hua Zhao, Jinpu Yu, Changli Wang, Zhongli Zhan, Tingting Ding, Xiubao Ren, Xin Chen and 1 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  5. Article
  6. Review
  7. Unraveling the Core Components and Critical Targets ofCurrent pharmaceutical design · 2025
    Article
  8. Review
  9. Review
  10. Article
  11. TNFR2 antagonistic antibody induces the death of tumor infiltrating CD4Cellular oncology (Dordrecht, Netherlands) · 2023
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
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  18. TNFR2 antagonist and agonist: a potential therapeutics in cancer immunotherapy.Medical oncology (Northwood, London, England) · 2022
    Review
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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

11 authors at 2 institutions in 2 countries.

Fan YanDepartment of Immunology, Tianjin Medical University Cancer Institute & Hospital, Rm 0601, Bldg C6, Huanhuxi Road, Tiyuanbei, Hexi District, Tianjin, 300202, People's Republic of China.
Ruijuan DuDepartment of Immunology, Tianjin Medical University Cancer Institute & Hospital, Rm 0601, Bldg C6, Huanhuxi Road, Tiyuanbei, Hexi District, Tianjin, 300202, People's Republic of China.
Feng WeiDepartment of Immunology, Tianjin Medical University Cancer Institute & Hospital, Rm 0601, Bldg C6, Huanhuxi Road, Tiyuanbei, Hexi District, Tianjin, 300202, People's Republic of China.
Hua ZhaoDepartment of Immunology, Tianjin Medical University Cancer Institute & Hospital, Rm 0601, Bldg C6, Huanhuxi Road, Tiyuanbei, Hexi District, Tianjin, 300202, People's Republic of China.
Jinpu YuDepartment of Immunology, Tianjin Medical University Cancer Institute & Hospital, Rm 0601, Bldg C6, Huanhuxi Road, Tiyuanbei, Hexi District, Tianjin, 300202, People's Republic of China.
Changli WangNational Clinical Research Center of Cancer, Tianjin, People's Republic of China.
Zhongli ZhanNational Clinical Research Center of Cancer, Tianjin, People's Republic of China.
Tingting DingDepartment of Immunology, Tianjin Medical University Cancer Institute & Hospital, Rm 0601, Bldg C6, Huanhuxi Road, Tiyuanbei, Hexi District, Tianjin, 300202, People's Republic of China.
Xiubao RenDepartment of Biotherapy, Tianjin Medical University Cancer Institute & Hospital, Tianjin, People's Republic of China.
Xin ChenState Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Rm 7032, Bldg N22 (Office), Flat 4C, Staff Quarters S22 (Home), Avenida da Universidade, Taipa, Macau, SAR, People's Republic of China. xchen@umac.mo.
Hui LiDepartment of Immunology, Tianjin Medical University Cancer Institute & Hospital, Rm 0601, Bldg C6, Huanhuxi Road, Tiyuanbei, Hexi District, Tianjin, 300202, People's Republic of China. lihui@tjmuch.com.
Tianjin Medical University Cancer Institute and Hospital · CNUniversity of Macau · MO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD4(+)FoxP3(+) regulatory T cells (Tregs) represent a major cellular mediator of cancer immune evasion. The expression of tumor necrosis factor receptor type II (TNFR2) on Tregs is reported to identify the maximally suppressive Treg population in both mice and human. We therefore investigated the phenotype and function of TNFR2(+) Tregs present in the peripheral blood (PB) of 43 lung cancer patients. Further, the association of TNFR2 expression on Tregs with clinicopathological factors was analyzed. The results showed that in the PB of lung cancer patients, Tregs expressed markedly higher levels of TNFR2 than conventional T cells (Tconvs). Expression of TNFR2 appeared to correlate better than CD25(+) and CD127(-) with FoxP3 expression. PB TNFR2(+) Tregs in lung cancer patients were more proliferative and expressed higher levels of the immunosuppressive molecule CTLA-4, and consequently more potently suppressed IFNγ production by cocultured CD8 CTLs. More importantly, higher TNFR2 expression levels on Tregs were associated with lymphatic invasion, distant metastasis and more advanced clinical stage of lung cancer patients. Therefore, our study suggests that TNFR2(+) Tregs play a role in promoting tumor progressive metastasis and expression of TNFR2 by PB Tregs may prove to be a useful prognostic marker in lung cancer patients.

Indexed as

AdultAgedCD8-Positive T-LymphocytesFemaleHumansImmunophenotypingInterferon-gammaLung NeoplasmsMaleMiddle AgedReceptors, Tumor Necrosis Factor, Type IIT-Lymphocytes, RegulatoryInterferon-gammaReceptors, Tumor Necrosis Factor, Type IICD4+FoxP3+ regulatory T cellsClinical pathologyImmunosuppressionLung cancerTumor necrosis factor receptor type II (TNFR2)

Identifiers

PMID26280204
PMCPMC11029166
OpenAlexW1883117256

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.