Evidence map›Paper›PMID 31445190›Full record

ArticleCellular and molecular gastroenterology and hepatology2020

Unique T-Cell Populations Define Immune-Inflamed Hepatocellular Carcinoma.

Daniela Di Blasi, Tujana Boldanova, Lucia Mori, Luigi Terracciano, Markus H Heim, Gennaro De Libero

Open access · goldAbstract read
In one paragraph

Article in Cellular and molecular gastroenterology and hepatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

46 citing papers in PubMed, 58 citations in OpenAlex.

  1. γδ T cells in colorectal and liver cancer.Nature reviews. Gastroenterology & hepatology · 2026
    Review
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  6. ICOSL: more than a trigger of ICOS function.Cell communication and signaling : CCS · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Daniela Di BlasiExperimental Immunology, Department of Biomedicine, University of Basel, Switzerland; Hepatology Laboratory, Department of Biomedicine, University of Basel, Switzerland.
Tujana BoldanovaHepatology Laboratory, Department of Biomedicine, University of Basel, Switzerland; Division of Gastroenterology and Hepatology, University Hospital Basel, Basel, Switzerland.
Lucia MoriExperimental Immunology, Department of Biomedicine, University of Basel, Switzerland.
Luigi TerraccianoInstitute of Pathology, Division of Molecular Pathology, University Hospital Basel, Basel, Switzerland.
Markus H HeimHepatology Laboratory, Department of Biomedicine, University of Basel, Switzerland; Division of Gastroenterology and Hepatology, University Hospital Basel, Basel, Switzerland. Electronic address: markus.heim@unibas.ch.
Gennaro De LiberoExperimental Immunology, Department of Biomedicine, University of Basel, Switzerland. Electronic address: gennaro.delibero@unibas.ch.
University of Basel · CHUniversity Hospital of Basel · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsThe characterization of T cells infiltrating hepatocellular carcinoma (HCC) provides information on cancer immunity and also on selection of patients with precise indication of immunotherapy. The aim of the study was to characterize T-cell populations within tumor tissue and compare them with non-neoplastic liver tissue as well as circulating cells of the same patients.

methodsThe presence of unique cell populations was investigated in 36 HCC patients by multidimensional flow cytometry followed by t-distributed stochastic neighbor embedding analysis. Functional activity of tumor-infiltrating T cells was determined after activation by phorbol 12-myristate 13-acetate and ionomycin.

resultsWithin the tumor there were more cells expressing CD137 and ICOS than in non-neoplastic liver tissue, possibly after recent antigenic activation. These cells contained several populations, including the following: (1) functionally impaired, proliferating CD4

conclusionsUnique populations of activated T cells are present in HCC tissue, whose antigen specificity remains to be investigated. Some of these cell populations are functionally impaired and nivolumab treatment restores their responsiveness. The finding of ongoing immune response within the tumor shows which lymphocyte populations are impaired within the HCC and identifies the patients who might take benefit from immunotherapy.

Indexed as

AgedAged, 80 and overBiopsyCarcinoma, HepatocellularCohort StudiesFemaleHumansImmune Checkpoint InhibitorsInducible T-Cell Co-Stimulator ProteinLiverLiver NeoplasmsLymphocyte ActivationLymphocytes, Tumor-InfiltratingMaleMiddle AgedNivolumabICOS protein, humanImmune Checkpoint InhibitorsInducible T-Cell Co-Stimulator ProteinNivolumabPDCD1 protein, humanProgrammed Cell Death 1 ReceptorTNFRSF9 protein, humanTumor Necrosis Factor Receptor Superfamily, Member 9Cancer ImmunityImmunotherapytSNE Analysis

Identifiers

PMID31445190
PMCPMC6957799
OpenAlexW2969843242

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.