Evidence map›Paper›PMID 38686549›Full record

ArticleCancer science2024

In-depth immune profiling of peripheral blood mononuclear cells in patients with pancreatic ductal adenocarcinoma reveals discriminative immune subpopulations.

Ernesto Rodriguez, Eline S Zwart, Alsya A Affandi, Jan Verhoeff, Mike de Kok, Lenka N C Boyd, Laura L Meijer, Tessa Y S Le Large, Katarzyna Olesek, Elisa Giovannetti and 4 more

Abstract read
In one paragraph

Article in Cancer science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. 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

14 authors.

Ernesto RodriguezDepartment of Molecular Cell Biology and Immunology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.
Eline S ZwartDepartment of Molecular Cell Biology and Immunology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-2121-8039
Alsya A AffandiDepartment of Molecular Cell Biology and Immunology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0003-0859-2322
Jan VerhoeffDepartment of Molecular Cell Biology and Immunology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.
Mike de KokDepartment of Molecular Cell Biology and Immunology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.
Lenka N C BoydCancer Center Amsterdam, Cancer Biology and Immunology, Amsterdam, The Netherlands.
Laura L MeijerCancer Center Amsterdam, Cancer Biology and Immunology, Amsterdam, The Netherlands.
Tessa Y S Le LargeCancer Center Amsterdam, Cancer Biology and Immunology, Amsterdam, The Netherlands.
Katarzyna OlesekDepartment of Molecular Cell Biology and Immunology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.
Elisa GiovannettiDepartment of Medical Oncology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.
Juan J García-VallejoDepartment of Molecular Cell Biology and Immunology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.
Reina E MebiusDepartment of Molecular Cell Biology and Immunology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.
Yvette van KooykDepartment of Molecular Cell Biology and Immunology, Amsterdam UMC, VU University Amsterdam, Amsterdam, The Netherlands.
Geert KazemierCancer Center Amsterdam, Cancer Biology and Immunology, Amsterdam, The Netherlands.

Funding

Associazione Italiana per la Ricerca sul CancroBennink Foundation 2005619Cancer Center Amsterdam Foundation 2017-4-09European Research Council ERC-339977-GlycotreatImmunoshape MSCA-ITN-2014-ETN No 642870Nederlandse Organisatie voor Wetenschappelijk Onderzoek
6 · The paper itself

Abstract

Pancreatic ductal adenocarcinoma (PDAC) has a dismal prognosis with a 5-year survival of less than 10%. More knowledge of the immune response developed in patients with PDAC is pivotal to develop better combination immune therapies to improve clinical outcome. In this study, we used mass cytometry time-of-flight to undertake an in-depth characterization of PBMCs from patients with PDAC and examine the differences with healthy controls and patients with benign diseases of the biliary system or pancreas. Peripheral blood mononuclear cells from patients with PDAC or benign disease are characterized by the increase of pro-inflammatory cells, as CD86

Indexed as

Carcinoma, Pancreatic DuctalLeukocytes, MononuclearPancreatic NeoplasmsAgedFemaleHumansMaleMemory T CellsMiddle AgedReceptors, CCR6Receptors, CXCR3Th17 CellsTh1 CellsT-Lymphocytes, RegulatoryCCR6 protein, humanCXCR3 protein, humanReceptors, CCR6Receptors, CXCR3biomarkerimmunophenotypingmass cytometrypancreatic cancerPBMC

Identifiers

PMID38686549
PMCPMC11247553

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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.