Evidence map›Paper›PMID 23799083›Full record

ArticlePloS one2013

Uptake and intracellular trafficking of superantigens in dendritic cells.

María B Ganem, Mauricio C De Marzi, María J Fernández-Lynch, Carolina Jancic, Mónica Vermeulen, Jorge Geffner, Roy A Mariuzza, Marisa M Fernández, Emilio L Malchiodi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Group AInfection and immunity · 2024
    Article
  5. Review
  6. Review
  7. Article
  8. CD8αImmunology · 2020
    Article
  9. Article
  10. Article
  11. Article
  12. Frontiers in immunology · 2019
    Article
  13. Article
  14. The retrovirus/superantigen hypothesis of multiple sclerosis.Cellular and molecular neurobiology · 2014
    Review
  15. 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

9 authors at 4 institutions in 1 country.

María B GanemInstituto de Estudios de la Inmunidad Humoral (IDEHU), CONICET-UBA, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Buenos Aires, Argentina.
Mauricio C De Marzi
María J Fernández-Lynch
Carolina Jancic
Mónica Vermeulen
Jorge Geffner
Roy A Mariuzza
Marisa M Fernández
Emilio L Malchiodi
Institute of Astronomy and Space Physics · ARAcademia Nacional de Medicina · ARInstitute for Bioscience and Biotechnology ResearchUniversidad de Buenos Aires · AR

Funding

Structure and Function of Natural Killer Cell ReceptorsR03TW007972 · FIC · UNIVERSITY OF MD BIOTECHNOLOGY INSTITUTE · PI MARIUZZA, ROY A · 2007 to 2008
$77k
FIC NIH HHS R03 TW007972FIC NIH HHS TW007972
6 · The paper itself

Abstract

Bacterial superantigens (SAgs) are exotoxins produced mainly by Staphylococcus aureus and Streptococcus pyogenes that can cause toxic shock syndrome (TSS). According to current paradigm, SAgs interact directly and simultaneously with T cell receptor (TCR) on the T cell and MHC class II (MHC-II) on the antigen-presenting cell (APC), thereby circumventing intracellular processing to trigger T cell activation. Dendritic cells (DCs) are professional APCs that coat nearly all body surfaces and are the most probable candidate to interact with SAgs. We demonstrate that SAgs are taken up by mouse DCs without triggering DC maturation. SAgs were found in intracellular acidic compartment of DCs as biologically active molecules. Moreover, SAgs co-localized with EEA1, RAB-7 and LAMP-2, at different times, and were then recycled to the cell membrane. DCs loaded with SAgs are capable of triggering in vitro lymphocyte proliferation and, injected into mice, stimulate T cells bearing the proper TCR in draining lymph nodes. Transportation and trafficking of SAgs in DCs might increase the local concentration of these exotoxins where they will produce the highest effect by promoting their encounter with both MHC-II and TCR in lymph nodes, and may explain how just a few SAg molecules can induce the severe pathology associated with TSS.

Indexed as

AnimalsAntigens, BacterialCells, CulturedCoculture TechniquesDendritic CellsEndocytosisEndosomesEnterotoxinsLymphocyte ActivationLymphocytesLysosomal-Associated Membrane Protein 2MaleMiceMice, Inbred BALB CPeptide FragmentsPhenotypeAntigens, Bacterialearly endosome antigen 1enterotoxin G, staphylococcalenterotoxin I, staphylococcalEnterotoxinsLysosomal-Associated Membrane Protein 2Peptide Fragmentsrab7 GTP-Binding Proteinsrab GTP-Binding ProteinsReceptors, Antigen, T-Cell, alpha-betastreptococcal superantigen SSASuperantigensT-cell receptor Vbeta 8.2Vesicular Transport Proteins

Identifiers

PMID23799083
PMCPMC3682983
OpenAlexW2045223917

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.