Evidence map›Paper›PMID 26682057›Full record

ArticleClinical & translational immunology2015

Profiling of primary peripheral blood- and monocyte-derived dendritic cells using monoclonal antibodies from the HLDA10 Workshop in Wollongong, Australia.

Stella E Autenrieth, Sabrina Grimm, Susanne Malaika Rittig, Frank Grünebach, Cécile Gouttefangeas, Hans-Jörg Bühring

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  3. Review
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  7. Article
  8. Bovine DerivedFrontiers in immunology · 2019
    Article
  9. Review
  10. Cytokines Produced by Dendritic Cells Administered Intratumorally Correlate with Clinical Outcome in Patients with Diverse Cancers.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  11. Tumor-Resident Dendritic Cells and Macrophages Modulate the Accumulation of TCR-Engineered T Cells in Melanoma.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    Article
  12. Review
  13. 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

6 authors at 1 institution in 1 country.

Stella E AutenriethEberhard Karls Universität Tübingen, University Clinic of Tübingen, Faculty for Medicine, Department of Internal Medicine II, Division of Haematology, Immunology, Oncology, Rheumatology and Pulmonology, Laboratory for Stem Cell Research and Laboratory for Dendritic Cells , Tübingen, Germany.
Sabrina GrimmEberhard Karls Universität Tübingen, University Clinic of Tübingen, Faculty for Medicine, Department of Internal Medicine II, Division of Haematology, Immunology, Oncology, Rheumatology and Pulmonology, Laboratory for Stem Cell Research and Laboratory for Dendritic Cells , Tübingen, Germany.
Susanne Malaika RittigEberhard Karls Universität Tübingen, University Clinic of Tübingen, Faculty for Medicine, Department of Internal Medicine II, Division of Haematology, Immunology, Oncology, Rheumatology and Pulmonology, Laboratory for Stem Cell Research and Laboratory for Dendritic Cells , Tübingen, Germany.
Frank GrünebachEberhard Karls Universität Tübingen, University Clinic of Tübingen, Faculty for Medicine, Department of Internal Medicine II, Division of Haematology, Immunology, Oncology, Rheumatology and Pulmonology, Laboratory for Stem Cell Research and Laboratory for Dendritic Cells , Tübingen, Germany.
Cécile GouttefangeasEberhard Karls Universität Tübingen, Interfaculty Institute for Cell Biology, Department of Immunology , Tübingen, Germany.
Hans-Jörg BühringEberhard Karls Universität Tübingen, University Clinic of Tübingen, Faculty for Medicine, Department of Internal Medicine II, Division of Haematology, Immunology, Oncology, Rheumatology and Pulmonology, Laboratory for Stem Cell Research and Laboratory for Dendritic Cells , Tübingen, Germany.
University of Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) arise from hematopoietic stem cells and develop into a discrete cellular lineage distinct from other leucocytes. Mainly three phenotypically and functionally distinct DC subsets are described in the human peripheral blood (PB): plasmacytoid DCs (pDCs), which express the key marker CD303 (BDCA-2), and two myeloid DC subsets (CD1c(+) DC (mDC1) and CD141(+) DC (mDC2)), which express the key markers CD1c (BDCA-1) and CD141 (BDCA-3), respectively. In addition to these primary cell subsets, DCs can also be generated in vitro from either CD34(+) stem/progenitor cells in the presence of Flt3 (Fms-related tyrosine kinase 3) ligand or from CD14(+) monocytes (monocyte-derived DCs (mo-DCs)) in the presence of granulocyte-macrophage colony-stimulating factor+interleukin-4 (GM-CSF+IL-4). Here we compare the reactivity patterns of HLDA10 antibodies (monoclonal antibody (mAb)) with pDCs, CD1c(+) DCs and CD141(+) DCs, as well as with CD14(+)-derived mo-DCs cultured for 7 days in the presence of 100 ng/ml GM-CSF plus 20 ng/ml IL-4. A detailed profiling of these DC subsets based on immunophenotyping and multicolour flow cytometry analysis is presented. Using the panel of HLDA10 Workshop mAb, we could verify known targets selectively expressed on discrete DC subsets including CD370 as a selective marker for CD141(+) DCs and CD366 as a marker for both myeloid subsets. In addition, vimentin and other markers are heterogeneously expressed on all three subsets, suggesting the existence of so far not identified DC subsets.

Identifiers

PMID26682057
PMCPMC4673437
OpenAlexW2216585353

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.