Evidence map›Paper›PMID 25385798›Full record

ArticleInfection and immunity2015

Role of dendritic cells in the pathogenesis of Whipple's disease.

Katina Schinnerling, Anika Geelhaar-Karsch, Kristina Allers, Julian Friebel, Kristina Conrad, Christoph Loddenkemper, Anja A Kühl, Ulrike Erben, Ralf Ignatius, Verena Moos and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 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
1.5field-weighted citation impact, top 19% 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, 20 citations in OpenAlex.

  1. Deciphering whipple's disease complexity.Clinical and experimental medicine · 2026
    Review
  2. Uptake ofInternational journal of molecular sciences · 2023
    Article
  3. Intestinal Barrier in Post-Biomolecules · 2023
    Article
  4. Review
  5. Article
  6. Article
  7. Whipple's disease: a fatal mimic.Autopsy & case reports · 2021
    Article
  8. Article
  9. [The rich diversity of Whipple's disease].Zeitschrift fur Rheumatologie · 2019
    Review
  10. Article
  11. Article
  12. Article
  13. 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

11 authors at 2 institutions in 1 country.

Katina SchinnerlingMedizinische Klinik I, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany.
Anika Geelhaar-KarschMedizinische Klinik I, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany.
Kristina AllersMedizinische Klinik I, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany.
Julian FriebelMedizinische Klinik I, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany.
Kristina ConradMedizinische Klinik I, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany.
Christoph LoddenkemperInstitut für Pathologie, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany.
Anja A KühlMedizinische Klinik I, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany.
Ulrike ErbenMedizinische Klinik I, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany.
Ralf IgnatiusInstitut für Tropenmedizin und Internationale Gesundheit, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Verena MoosMedizinische Klinik I, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany verena.moos@charite.de.
Thomas SchneiderMedizinische Klinik I, Charité-Universitätsmedizin Berlin, CBF, Berlin, Germany.
Charité - Universitätsmedizin Berlin · DEBerlin Institute of Health at Charité - Universitätsmedizin Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulation of Tropheryma whipplei-stuffed macrophages in the duodenum, impaired T. whipplei-specific Th1 responses, and weak secretion of interleukin-12 (IL-12) are hallmarks of classical Whipple's disease (CWD). This study addresses dendritic cell (DC) functionality during CWD. We documented composition, distribution, and functionality of DC ex vivo or after in vitro maturation by fluorescence-activated cell sorting (FACS) and by immunohistochemistry in situ. A decrease in peripheral DC of untreated CWD patients compared to healthy donors was due to reduced CD11c(high) myeloid DC (M-DC). Decreased maturation markers CD83, CD86, and CCR7, as well as low IL-12 production in response to stimulation, disclosed an immature M-DC phenotype. In vitro-generated monocyte-derived DC from CWD patients showed normal maturation and T cell-stimulatory capacity under proinflammatory conditions but produced less IL-12 and failed to activate T. whipplei-specific Th1 cells. In duodenal and lymphoid tissues, T. whipplei was found within immature DC-SIGN(+) DC. DC and proliferating lymphocytes were reduced in lymph nodes of CWD patients compared to levels in controls. Our results indicate that dysfunctional IL-12 production by DC provides suboptimal conditions for priming of T. whipplei-specific T cells during CWD and that immature DC carrying T. whipplei contribute to the dissemination of the bacterium.

Indexed as

AdultAgedAged, 80 and overAntigens, CDB7-2 AntigenCD11c AntigenCD83 AntigenCell Adhesion MoleculesCell ProliferationDC-Specific ICAM-3 Grabbing NonintegrinDendritic CellsDuodenumFemaleFlow CytometryHumansImmunoglobulinsAntigens, CDB7-2 AntigenCCR7 protein, humanCD11c AntigenCD83 AntigenCD86 protein, humanCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinIL12A protein, humanImmunoglobulinsInterleukin-12 Subunit p35Lectins, C-TypeMembrane GlycoproteinsReceptors, CCR7Receptors, Cell Surface

Identifiers

PMID25385798
PMCPMC4294246
OpenAlexW2021124965

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.