Evidence map›Paper›PMID 32277125›Full record

ArticleScientific reports2020

Tumour grade significantly correlates with total dysfunction of tumour tissue-infiltrating lymphocytes in renal cell carcinoma.

Atsunari Kawashima, Takayuki Kanazawa, Yujiro Kidani, Tetsuya Yoshida, Michinari Hirata, Kentaro Nishida, Satoshi Nojima, Yoshiyuki Yamamoto, Taigo Kato, Koji Hatano and 12 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

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  15. Tissue-resident memory T cells in the kidney.Seminars in immunopathology · 2022
    Review
  16. Article
  17. Redistribution of CD8+ T cell subsets in metastatic renal cell carcinoma patients treated with anti-PD-1 therapy.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2022
    Article
  18. Review
  19. Tumor-infiltrating CD8Cancer immunology, immunotherapy : CII · 2022
    Article
  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

22 authors at 3 institutions in 1 country.

Atsunari Kawashima *Department of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan. kawashima@uro.med.osaka-u.ac.jp.ORCID http://orcid.org/0000-0001-9369-4264
Takayuki Kanazawa *Department of Clinical Research in Tumour Immunology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Yujiro KidaniDrug Discovery & Disease Research Laboratory, Shionogi & Co., Ltd., Toyonaka, Japan.
Tetsuya YoshidaDrug Discovery & Disease Research Laboratory, Shionogi & Co., Ltd., Toyonaka, Japan.
Michinari HirataDepartment of Clinical Research in Tumour Immunology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Kentaro NishidaDepartment of Clinical Research in Tumour Immunology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Satoshi NojimaDepartment of Pathology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Yoshiyuki YamamotoDepartment of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Taigo KatoDepartment of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Koji HatanoDepartment of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Takeshi UjikeDepartment of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Akira NagaharaDepartment of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Kazutoshi FujitaDepartment of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Akiko Morimoto-OkazawaDepartment of Clinical Research in Tumour Immunology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Kota IwahoriDepartment of Clinical Research in Tumour Immunology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Motohide UemuraDepartment of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Ryoichi ImamuraDepartment of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Naganari OhkuraDepartment of Basic Research in Tumour Immunology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Eiichi MoriiDepartment of Pathology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.ORCID http://orcid.org/0000-0001-8490-3650
Shimon SakaguchiDepartment of Experimental Immunology, Immunology Frontier Research Centre, Osaka University, Suita, Osaka, Japan.
Hisashi WadaDepartment of Clinical Research in Tumour Immunology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Norio NonomuraDepartment of Urology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
The University of Osaka · JPShionogi (Japan) · JPOsaka Gakuin University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is important to evaluate the clinical importance of both CD8 T cells and CD4 T cells expression simultaneously because they have crucial networks in tumour targeting immune responses. In 97 RCC patients, RNA sequencing and gene set enrichment analysis of both CD8 and CD4 T cells based on the expression levels of PD-1 and TIM-3 implied that the populations of PD-1+TIM-3+ CD8 T cells and PD-1lowTIM-3 + CD4 T cells were characterized as exhausted CD8 T cells and regulatory CD4 T cells, respectively. These populations of CD4 and CD8 T cells were significantly upregulated in the patients with RCC of higher WHO/ISUP grade (grades 3, 4) (P < 0.001). Moreover, the cytokine productivities of each population in both CD4 and CD8 T cells of the higher-grade patients were significantly lower than those of the lower-grade patients (P < 0.05). Multivariate analysis showed the prognosis of patients with metastatic RCC of higher WHO/ISUP grade treated by nivolumab to be significantly worse than that of patients with lower grade (P = 0.026). This study showed that tumour grade significantly correlated with dysfunction of both CD4+ and CD8+ TILs and the efficacy of nivolumab treatment.

Indexed as

AdultAgedAged, 80 and overAntineoplastic Agents, ImmunologicalCarcinoma, Renal CellCD8-Positive T-LymphocytesCytokinesFemaleFollow-Up StudiesHepatitis A Virus Cellular Receptor 2HumansKidneyKidney NeoplasmsLymphocytes, Tumor-InfiltratingMaleMiddle AgedAntineoplastic Agents, ImmunologicalCytokinesHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2NivolumabPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID32277125
PMCPMC7148296
OpenAlexW3016024597

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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.