Evidence map›Paper›PMID 30867143›Full record

ArticleBlood advances2019

Modulation of TAP-dependent antigen compartmentalization during human monocyte-to-DC differentiation.

Marius Döring, Hanna Blees, Nicole Koller, Sabine Tischer-Zimmermann, Mathias Müsken, Frederik Henrich, Jennifer Becker, Elena Grabski, Junxi Wang, Hans Janssen and 6 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2019. 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 32% 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. Quantitative nanoscale imaging shows peptide-MHC I complexes are monomeric and spatially regulated in human dendritic cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Key immune regulators in retinal ischemia-reperfusion injuryInternational journal of ophthalmology · 2025
    Article
  3. Review
  4. Dynamic interactome of the MHC I peptide loading complex in human dendritic cells.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

16 authors at 6 institutions in 2 countries.

Marius DöringInstitute for Experimental Infection Research, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Helmholtz Centre for Infection Research and Hannover Medical School, Hannover, Germany.ORCID 0000-0002-5278-8376
Hanna BleesInstitute of Biochemistry, Biocenter, Goethe University Frankfurt, Frankfurt, Germany.
Nicole KollerInstitute of Biochemistry, Biocenter, Goethe University Frankfurt, Frankfurt, Germany.
Sabine Tischer-ZimmermannInstitute for Transfusion Medicine, Hannover Medical School, Hannover, Germany.ORCID 0000-0003-2326-0342
Mathias MüskenInstitute of Molecular Bacteriology, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Helmholtz Centre for Infection Research and Hannover Medical School, Hannover, Germany.ORCID 0000-0002-5624-1378
Frederik HenrichInstitute for Experimental Infection Research, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Helmholtz Centre for Infection Research and Hannover Medical School, Hannover, Germany.
Jennifer BeckerInstitute for Experimental Infection Research, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Helmholtz Centre for Infection Research and Hannover Medical School, Hannover, Germany.
Elena GrabskiInstitute for Experimental Infection Research, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Helmholtz Centre for Infection Research and Hannover Medical School, Hannover, Germany.
Junxi WangBiostatistics, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Hans JanssenDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
Werner ZuschratterLeibniz Institute for Neurobiology, Magdeburg, Germany.
Jacques NeefjesDivision of Cell Biology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.ORCID 0000-0001-6763-2211
Frank KlawonnBiostatistics, Helmholtz Centre for Infection Research, Braunschweig, Germany.ORCID 0000-0001-9613-182X
Britta Eiz-VesperInstitute for Transfusion Medicine, Hannover Medical School, Hannover, Germany.
Robert TampéInstitute of Biochemistry, Biocenter, Goethe University Frankfurt, Frankfurt, Germany.ORCID 0000-0002-0403-2160
Ulrich KalinkeInstitute for Experimental Infection Research, TWINCORE, Centre for Experimental and Clinical Infection Research, a joint venture between the Helmholtz Centre for Infection Research and Hannover Medical School, Hannover, Germany.ORCID 0000-0003-0503-9564
Medizinische Hochschule Hannover · DEGoethe University Frankfurt · DEThe Netherlands Cancer Institute · NLHelmholtz Centre for Infection Research · DELeibniz Institute for Neurobiology · DEOstfalia University of Applied Sciences · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) take up antigen in the periphery, migrate to secondary lymphoid organs, and present processed antigen fragments to adaptive immune cells and thus prime antigen-specific immunity. During local inflammation, recirculating monocytes are recruited from blood to the inflamed tissue, where they differentiate to macrophages and DCs. In this study, we found that monocytes showed high transporter associated with antigen processing (TAP)-dependent peptide compartmentalization and that after antigen pulsing, they were not able to efficiently stimulate antigen-specific T lymphocytes. Nevertheless, upon in vitro differentiation to monocyte-derived DCs, TAP-dependent peptide compartmentalization as well as surface major histocompatibility complex I turnover decreased and the cells efficiently restimulated T lymphocytes. Although TAP-dependent peptide compartmentalization decreased during DC differentiation, TAP expression levels increased. Furthermore, TAP relocated from early endosomes in monocytes to the endoplasmic reticulum (ER) and lysosomal compartments in DCs. Collectively, these data are compatible with the model that during monocyte-to-DC differentiation, the subcellular relocation of TAP and the regulation of its activity assure spatiotemporal separation of local antigen uptake and processing by monocytes and efficient T-lymphocyte stimulation by DCs.

Indexed as

Cell CompartmentationAntigen PresentationATP-Binding Cassette TransportersCell DifferentiationCells, CulturedDendritic CellsHumansLysosomesMonocytesT-LymphocytesATP-Binding Cassette Transporterstransporter associated with antigen processing (TAP)

Identifiers

PMID30867143
PMCPMC6436010
OpenAlexW2921290751

What OpenQuestion holds

Textmetadata
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.