Evidence map›Paper›PMID 17679697›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Immune complex-induced enhancement of bacterial antigen presentation requires Fcgamma receptor III expression on dendritic cells.

Andrés A Herrada, Francisco J Contreras, Jaime A Tobar, Rodrigo Pacheco, Alexis M Kalergis

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Engineering therapeutic monoclonal antibodies.The Journal of allergy and clinical immunology · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Recombinant immune complexes as versatile and potent vaccines.Human vaccines & immunotherapeutics · 2016
    Article
  10. Article
  11. The Role of FcRn in Antigen Presentation.Frontiers in immunology · 2014
    Review
  12. Cross-presentation of IgG-containing immune complexes.Cellular and molecular life sciences : CMLS · 2013
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Antibodies protect against intracellular bacteria by Fc receptor-mediated lysosomal targeting.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 2 countries.

Andrés A HerradaDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas and Departamento de Reumatología, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago E-8331010, Chile.
Francisco J Contreras
Jaime A Tobar
Rodrigo Pacheco
Alexis M Kalergis
Millennium Engineering and Integration (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) are capable of initiating adaptive immune responses against infectious agents by presenting pathogen-derived antigens on MHC molecules to naïve T cells. Because of their key role in priming adaptive immunity, it is expected that interfering with DC function would be advantageous to the pathogen. We have previously shown that Salmonella enterica serovar Typhimurium (ST), is able to survive inside DCs and interfere with their function by avoiding activation of bacteria-specific T cells. In contrast, when ST is targeted to Fcgamma receptors on the DC surface, bacteria are degraded and their antigens presented to T cells. However, the specific Fcgamma receptor responsible of restoring presentation of antigens remains unknown. Here, we show that IgG-coated ST was targeted to lysosomes and degraded and its antigens presented on MHC molecules only when the low-affinity activating FcgammaRIII was expressed on DCs. FcgammaRIII-mediated enhancement of Ag presentation led to a robust activation of T cells specific for bacteria-expressed antigens. Laser confocal and electron microscopy analyses revealed that IgG-coated ST was rerouted to the lysosomal pathway through an FcgammaRIII-dependent mechanism. PI-3K activity was required for this process, because specific inhibitors promoted the survival of IgG-coated ST inside DCs and prevented DCs from activating bacteria-specific T cells. Our data suggest that the DC capacity to efficiently activate T cells upon capturing IgG-coated virulent bacteria is mediated by FcgammaRIII and requires PI-3K activity.

Indexed as

Antigen-Antibody ComplexAntigens, BacterialDendritic CellsLysosomesPhosphatidylinositol 3-KinasesReceptors, IgGSalmonella typhimuriumVirulenceAntigen-Antibody ComplexAntigens, BacterialPhosphatidylinositol 3-KinasesReceptors, IgG

Identifiers

PMID17679697
PMCPMC1948949
OpenAlexW1968095476

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.