Evidence map›Paper›PMID 30235890›Full record

ReviewVaccines2018

BDCA1+CD14+ Immunosuppressive Cells in Cancer, a Potential Target?

Thomas J van Ee, Heleen H Van Acker, Tom G van Oorschot, Viggo F Van Tendeloo, Evelien L Smits, Ghaith Bakdash, Gerty Schreibelt, I Jolanda M de Vries

Open access · goldAbstract readReview
In one paragraph

Review in Vaccines, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Tolerogenic Dendritic Cell-Based Approaches in Autoimmunity.International journal of molecular sciences · 2021
    Review
  6. Article
  7. Review
  8. Article
  9. Subsets of CD1cFrontiers in immunology · 2020
    Review
  10. 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

8 authors at 3 institutions in 3 countries.

Thomas J van EeDepartment of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboudumc, Nijmegen 6525 GA, The Netherlands. Thomas.vanEe@radboudumc.nl.
Heleen H Van AckerLaboratory of Experimental Hematology, University of Antwerp, Antwerp 2000, Belgium. Heleen.VanAcker@uantwerpen.be.
Tom G van OorschotDepartment of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboudumc, Nijmegen 6525 GA, The Netherlands. Tom.vanOorschot@radboudumc.nl.ORCID 0000-0003-3890-7137
Viggo F Van TendelooLaboratory of Experimental Hematology, University of Antwerp, Antwerp 2000, Belgium. viggovantendeloo@gmail.com.ORCID 0000-0003-3217-9917
Evelien L SmitsLaboratory of Experimental Hematology, University of Antwerp, Antwerp 2000, Belgium. Evelien.Smits@uza.be.
Ghaith BakdashAllergic Inflammation Discovery Performance Unit, Respiratory Therapy Area, GlaxoSmithKline, Stevenage SG1 2NY, UK. ghaith.x.bakdash@gsk.com.ORCID 0000-0002-0156-8365
Gerty SchreibeltDepartment of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboudumc, Nijmegen 6525 GA, The Netherlands. gerty.schreibelt@radboudumc.nl.ORCID 0000-0002-0156-8365
I Jolanda M de VriesDepartment of Tumor Immunology, Radboud Institute for Molecular Life Sciences, Radboudumc, Nijmegen 6525 GA, The Netherlands. Jolanda.devries@radboudumc.nl.
Radboud University Nijmegen · NLUniversity of Antwerp · BEGlaxoSmithKline (United Kingdom) · GB

Funding

Fonds Wetenschappelijk Onderzoek PhD fellowshipNederlandse Organisatie voor Wetenschappelijk Onderzoek 918.14.655
6 · The paper itself

Abstract

Dendritic cell (DC) vaccines show promising effects in cancer immunotherapy. However, their efficacy is affected by a number of factors, including (1) the quality of the DC vaccine and (2) tumor immune evasion. The recently characterized BDCA1+CD14+ immunosuppressive cells combine both aspects; their presence in DC vaccines may directly hamper vaccine efficacy, whereas, in patients, BDCA1+CD14+ cells may suppress the induced immune response in an antigen-specific manner systemically and at the tumor site. We hypothesize that BDCA1+CD14+ cells are present in a broad spectrum of cancers and demand further investigation to reveal treatment opportunities and/or improvement for DC vaccines. In this review, we summarize the findings on BDCA1+CD14+ cells in solid cancers. In addition, we evaluate the presence of BDCA1+CD14+ cells in leukemic cancers. Preliminary results suggest that the presence of BDCA1+CD14+ cells correlates with clinical features of acute and chronic myeloid leukemia. Future research focusing on the differentiation from monocytes towards BDCA1+CD14+ cells could reveal more about their cell biology and clinical significance. Targeting these cells in cancer patients may improve the outcome of cancer immunotherapy.

Indexed as

BDCA1+CD14+ cellscancercancer immunotherapydendritic cellsimmune suppressiontumor microenvironment

Identifiers

PMID30235890
PMCPMC6161086
OpenAlexW2889912233

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.