Evidence map›Paper›PMID 26669617›Full record

ArticleGut2017

Interaction between tumour-infiltrating B cells and T cells controls the progression of hepatocellular carcinoma.

Marta Garnelo, Alex Tan, Zhisheng Her, Joe Yeong, Chun Jye Lim, Jinmiao Chen, Kiat Hon Lim, Achim Weber, Pierce Chow, Alexander Chung and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 310 papers.

0numbers the graph read from it
0cells of the map it votes in
310citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

310 citing papers in PubMed, 459 citations in OpenAlex.

  1. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
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  18. Tissue-resident memory CD8Nature reviews. Gastroenterology & hepatology · 2025
    Review
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  20. Review

250 more citing papers are in PubMed but not listed here.

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

18 authors at 11 institutions in 10 countries.

Marta GarneloSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Biopolis, Singapore.
Alex TanSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Biopolis, Singapore.
Zhisheng HerInstitute of Molecular and Cell Biology (IMCB), A*STAR, Biopolis, Singapore.
Joe YeongSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Biopolis, Singapore.
Chun Jye LimSingHealth Translational Immunology and Inflammation Centre (STIIC), Singapore Health Services Pte Ltd, Singapore, Singapore.
Jinmiao ChenSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Biopolis, Singapore.
Kiat Hon LimDepartment of Pathology, Singapore General Hospital, Singapore, Singapore.
Achim WeberInstitute of Surgical Pathology, University Hospital of Zurich, Zurich, Switzerland.
Pierce ChowNational Cancer Centre, Singapore, Singapore.
Alexander ChungNational Cancer Centre, Singapore, Singapore.
London Lucien Pj OoiNational Cancer Centre, Singapore, Singapore.
Han Chong TohNational Cancer Centre, Singapore, Singapore.
Mathias HeikenwalderDivision of Chronic Inflammation and Cancer, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Irene O L NgDepartment of Pathology, The University of Hong Kong, Queen Mary Hospital, Hong Kong, Hong Kong.
Alessandra NardinSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Biopolis, Singapore.
Qingfeng ChenInstitute of Molecular and Cell Biology (IMCB), A*STAR, Biopolis, Singapore.
Jean-Pierre AbastadoSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Biopolis, Singapore.
Valerie ChewSingapore Immunology Network (SIgN), Agency for Science, Technology and Research (A*STAR), Biopolis, Singapore.
National Cancer Centre Singapore · SGSingapore General Hospital · SGAgency for Science, Technology and Research · SGSingapore Immunology Network · SGStar Technology and Research (United States) · USDuke-NUS Medical School · SGHeidelberg University · DENational Cancer Centre Japan · JPQueen Mary Hospital · CNSingHealth · SGUniversity Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe nature of the tumour-infiltrating leucocytes (TILs) is known to impact clinical outcome in carcinomas, including hepatocellular carcinoma (HCC). However, the role of tumour-infiltrating B cells (TIBs) remains controversial. Here, we investigate the impact of TIBs and their interaction with T cells on HCC patient prognosis.

designTissue samples were obtained from 112 patients with HCC from Singapore, Hong Kong and Zurich and analysed using immunohistochemistry and immunofluorescence. RNA expression of CD19, CD8A, IFNG was analysed using quantitative PCR. The phenotype of freshly isolated TILs was analysed using flow cytometry. A mouse model depleted of mature B cells was used for functional study.

resultsTumour-infiltrating T cells and B cells were observed in close contact with each other and their densities are correlated with superior survival in patients with HCC. Furthermore, the density of TIBs was correlated with an enhanced expression of granzyme B and IFN-γ, as well as with reduced tumour viability defined by low expression of Ki-67, and an enhanced expression of activated caspase-3 on tumour cells. CD27 and CD40 costimulatory molecules and TILs expressing activation marker CD38 in the tumour were also correlated with patient survival. Mice depleted of mature B cells and transplanted with murine hepatoma cells showed reduced tumour control and decreased local T cell activation, further indicating the important role of B cells.

conclusionsThe close proximity of tumour-infiltrating T cells and B cells indicates a functional interaction between them that is linked to an enhanced local immune activation and contributes to better prognosis for patients with HCC.

Indexed as

Lymphocytes, Tumor-InfiltratingADP-ribosyl Cyclase 1AdultAgedAged, 80 and overAnimalsAntigens, CDAntigens, CD19Antigens, CD20B-LymphocytesCarcinoma, HepatocellularCaspase 3CD3 ComplexCD40 AntigensCD8 AntigensDisease ProgressionADP-ribosyl Cyclase 1Antigens, CDAntigens, CD19Antigens, CD20Caspase 3CD3 ComplexCD40 AntigensCD8 antigen, alpha chainCD8 AntigensGranzymesInterferon-gammaKi-67 AntigenTumor Necrosis Factor Receptor Superfamily, Member 7B CELLCANCER IMMUNOBIOLOGYHEPATOCELLULAR CARCINOMAIMMUNOREGULATIONT LYMPHOCYTES

Identifiers

PMID26669617
PMCPMC5284473
OpenAlexW2204209053

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.