Evidence map›Paper›PMID 16418399›Full record

ArticleThe Journal of experimental medicine2006

Uptake of Leishmania major by dendritic cells is mediated by Fcgamma receptors and facilitates acquisition of protective immunity.

Florian Woelbing, Susanna Lopez Kostka, Katharina Moelle, Yasmine Belkaid, Cord Sunderkoetter, Sjef Verbeek, Ari Waisman, Axel P Nigg, Juergen Knop, Mark C Udey and 1 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
19.0field-weighted citation impact, top 1% 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

101 citing papers in PubMed, 204 citations in OpenAlex.

  1. Review
  2. Unleashing the immune modulatory potential ofFrontiers in molecular biosciences · 2025
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  4. ExploitingCells · 2024
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  9. Impact ofCells · 2022
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  10. Article
  11. Article
  12. Immune Responses in Leishmaniasis: An Overview.Tropical medicine and infectious disease · 2022
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Visualizing theFrontiers in immunology · 2021
    Review
  18. Microorganisms · 2020
    Review
  19. Frontiers in immunology · 2020
    Article
  20. Article

41 more citing papers are in PubMed but not listed here.

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 5 institutions in 3 countries.

Florian WoelbingDepartment of Dermatology and 2Section for Pathophysiology, First Department of Internal Medicine, Johannes Gutenberg-University, Mainz 55131, Germany.
Susanna Lopez Kostka
Katharina Moelle
Yasmine Belkaid
Cord Sunderkoetter
Sjef Verbeek
Ari Waisman
Axel P Nigg
Juergen Knop
Mark C Udey
Esther von Stebut
Johannes Gutenberg University Mainz · DELeiden University Medical Center · NLNational Institute of Allergy and Infectious Diseases · USNational Institutes of Health · USUniversity of Münster · DE

Funding

Regulation of Cutaneous Accessory Cell Activity in Health and DiseaseZIASC003669 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI UDEY, MARK · 2009 to 2017
$2.2M
REGULATION OF CUTANEOUS ACCESSORY CELL ACTIVITY IN HEALTH AND DISEASEZ01SC003669 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI UDEY, MARK · 1996 to 2008
$1.7M
Intramural NIH HHS
6 · The paper itself

Abstract

Uptake of Leishmania major by dendritic cells (DCs) results in activation and interleukin (IL)-12 release. Infected DCs efficiently stimulate CD4- and CD8- T cells and vaccinate against leishmaniasis. In contrast, complement receptor 3-dependent phagocytosis of L. major by macrophages (MPhi) leads exclusively to MHC class II-restricted antigen presentation to primed, but not naive, T cells, and no IL-12 production. Herein, we demonstrate that uptake of L. major by DCs required parasite-reactive immunoglobulin (Ig)G and involved FcgammaRI and FcgammaRIII. In vivo, DC infiltration of L. major-infected skin lesions coincided with the appearance of antibodies in sera. Skin of infected B cell-deficient mice and Fcgamma-/- mice contained fewer parasite-infected DCs in vivo. Infected B cell-deficient mice as well as Fcgamma-/- mice (all on the C57BL/6 background) showed similarly increased disease susceptibility as assessed by lesion volumes and parasite burdens. The B cell-deficient mice displayed impaired T cell priming and dramatically reduced IFN-gamma production, and these deficits were normalized by infection with IgG-opsonized parasites. These data demonstrate that DC and MPhi use different receptors to recognize and ingest L. major with different outcomes, and indicate that B cell-derived, parasite-reactive IgG and DC FcgammaRI and FcgammaRIII are essential for optimal development of protective immunity.

Indexed as

AnimalsB-LymphocytesCells, CulturedDendritic CellsImmunoglobulin GLeishmania majorLeishmaniasis, CutaneousMacrophage-1 AntigenMacrophagesMiceMice, Inbred BALB CMice, Inbred C57BLMice, KnockoutPhagocytosisReceptors, IgGImmunoglobulin GMacrophage-1 AntigenReceptors, IgG

Identifiers

PMID16418399
PMCPMC2118064
OpenAlexW2109529611

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.