Evidence map›Paper›PMID 26482613›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Ovarian carcinoma-infiltrating regulatory T cells were more potent suppressors of CD8(+) T cell inflammation than their peripheral counterparts, a function dependent on TIM3 expression.

Meimei Bu, Yizhen Shen, William L Seeger, Shizhi An, Rongqin Qi, Joanna A Sanderson, Yan Cai

Abstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 63 citations in OpenAlex.

  1. Oncoimmunology · 2025
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Immune pathway through endometriosis to ovarian cancer.World journal of clinical oncology · 2024
    Review
  7. Review
  8. Article
  9. Review
  10. Immune Tumor Microenvironment in Ovarian Cancer Ascites.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Immune checkpoint inhibitors in ovarian cancer: where do we stand?Therapeutic advances in medical oncology · 2021
    Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. 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

7 authors at 3 institutions in 2 countries.

Meimei BuDepartment of Anesthesiology, The Maternal and Child Health Hospital of Jinan City, Jinan, Shandong, 250001, China.
Yizhen ShenDepartment of Urology, General Hospital of Jinan Military Command, Jinan, Shandong, 250031, China.
William L SeegerResearch Center, Lingbin Biotechnology, Surrey, BC, Canada.
Shizhi AnDepartment of Anesthesiology, The Maternal and Child Health Hospital of Jinan City, Jinan, Shandong, 250001, China.
Rongqin QiDepartment of Anesthesiology, The Maternal and Child Health Hospital of Jinan City, Jinan, Shandong, 250001, China.
Joanna A SandersonResearch Center, Lingbin Biotechnology, Surrey, BC, Canada.
Yan CaiDepartment of Prenatal Diagnosis, The Maternal and Child Health Hospital of Jinan City, No.2 Jian Guo Xiao Jing San Road, Jinan, Shandong, 250001, China. yancai_jn@sina.com.
Shandong Maternal and Child Health Hospital · CNSurrey Memorial Hospital · CAGeneral Hospital of Jinan Military Command · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian carcinoma is one of the most severe cancers in women, with a high relapse rate and limited secondary treatment options. To assist research in novel treatment technologies, including CD8(+) T cell-base immunotherapy, we examined the effect of tumor-infiltrating regulatory T cells (Tregs) in inhibiting CD8(+) T cell inflammation. We found that compared to their peripheral blood counterparts, tumor-infiltrating Tregs exhibited more potent inhibitory function, which was associated with higher interleukin 10 (IL-10) production in tumor-infiltrating Tregs. Blockade of T cell immunoglobulin mucin 3 (TIM3), a regulatory molecule overrepresented on tumor-infiltrating Tregs, had significantly reverted Treg-mediated suppression. Moreover, expression of TIM3 on tumor-infiltrating Tregs was directly correlated with tumor size. Together, our results demonstrated that ovarian tumor-infiltrating Treg cells were more immunosuppressive than their peripheral blood counterparts in a TIM3-dependent fashion.

Indexed as

AdultAgedCD8-Positive T-LymphocytesFemaleHepatitis A Virus Cellular Receptor 2HumansImmunosuppression TherapyInterleukin-10Lymphocyte CountLymphocytes, Tumor-InfiltratingMiddle AgedNeoplasms, Glandular and EpithelialOvarian NeoplasmsT-Lymphocytes, RegulatoryTumor BurdenHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2IL10 protein, humanInterleukin-10Ovarian cancerRegulatory T cellTIM3Tumor-infiltrating lymphocyte

Identifiers

PMID26482613
OpenAlexW2126268734

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.