Evidence map›Paper›PMID 12379672›Full record

ArticleInfection and immunity2002

Primary dendritic cells phagocytose Cryptococcus neoformans via mannose receptors and Fcgamma receptor II for presentation to T lymphocytes.

Rachel M Syme, Jason C L Spurrell, Ernest K Amankwah, Francis H Y Green, Christopher H Mody

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

60 citing papers in PubMed, 133 citations in OpenAlex.

  1. Cell surface (Amsterdam, Netherlands) · 2026
    Article
  2. Article
  3. Dendritic Cells: Multifunctional Roles in Host Defenses toJournal of fungi (Basel, Switzerland) · 2023
    Review
  4. Innate Pulmonary Phagocytes and Their Interactions with PathogenicJournal of fungi (Basel, Switzerland) · 2023
    Review
  5. Review
  6. Article
  7. Influence of Pathogen Carbon Metabolism on Interactions With Host Immunity.Frontiers in cellular and infection microbiology · 2022
    Review
  8. Observational
  9. Review
  10. Monocytes and the Host Response to Fungal Pathogens.Frontiers in cellular and infection microbiology · 2020
    Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Innate Immune Responses toJournal of fungi (Basel, Switzerland) · 2017
    Article
  18. Immune Recognition of Fungal Polysaccharides.Journal of fungi (Basel, Switzerland) · 2017
    Review
  19. Article
  20. Innate host defenses against Cryptococcus neoformans.Journal of microbiology (Seoul, Korea) · 2016
    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

5 authors at 1 institution in 1 country.

Rachel M SymeDepartment of Microbiology and Infectious Diseases, University of Calgary, Calgary, Alberta, Canada.
Jason C L Spurrell
Ernest K Amankwah
Francis H Y Green
Christopher H Mody
University of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Different "professional" antigen-presenting cells (APC) have unique characteristics that favor or restrict presentation of microbial antigens to T cells, depending on the organism. Cryptococcus neoformans is a pathogenic yeast that presents unique challenges to APC, including its large size, its rigid cell wall, and its ability to stimulate T cells as a mitogen. T-cell proliferation in response to the C. neoformans mitogen (CnM) requires phagocytosis and processing of the organisms by accessory cells prior to presentation of CnM to T cells. Because of the requirement for uptake of the organism and more limited costimulatory requirements of mitogens, macrophages might be the most likely cellular source for the accessory cell. However, the present study demonstrates that a transiently adherent cell that was CD3(-), CD14(-), CD19(-), CD56(-), HLA-DR(+), and CD83(+) with a dendritic morphology, rather than monocyte-derived or tissue (alveolar) macrophages, was the most efficient APC for presentation of CnM. A large number of these cells bound and internalized the organism, and only a small number of dendritic cells were required for presentation of the mitogen to T cells. Further, the mannose receptor and Fcgamma receptor II were required for presentation of C. neoformans, as blocking either of these receptors abrogated both uptake of C. neoformans and lymphocyte proliferation in response to CnM. These studies demonstrate the surprising fact that dendritic cells are the most efficient accessory cells for CnM.

Indexed as

Antigen PresentationLectins, C-TypeMannose-Binding LectinsPhagocytosisAdultAntigen-Presenting CellsAntigens, CDCD83 AntigenCell AdhesionCryptococcus neoformansDendritic CellsHLA-DR AntigensHumansImmunoglobulinsLymphocyte ActivationMacrophages, AlveolarAntigens, CDCD83 AntigenHLA-DR AntigensImmunoglobulinsLectins, C-TypeMannose-Binding LectinsMannose ReceptorMembrane GlycoproteinsReceptors, Cell SurfaceReceptors, IgG

Identifiers

PMID12379672
PMCPMC130340
OpenAlexW2134936774

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.