Evidence map›Paper›PMID 19273556›Full record

ArticleInfection and immunity2009

Anthrax edema toxin induces maturation of dendritic cells and enhances chemotaxis towards macrophage inflammatory protein 3beta.

Francisco J Maldonado-Arocho, Kenneth A Bradley

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2019
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Cellular and physiological effects of anthrax exotoxin and its relevance to disease.Frontiers in cellular and infection microbiology · 2012
    Review
  9. Article
  10. Modeling the host response to inhalation anthrax.Journal of theoretical biology · 2011
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. 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

2 authors at 1 institution in 1 country.

Francisco J Maldonado-ArochoDepartment of Microbiology, Immunology, & Molecular Genetics, University of California at Los Angeles, 609 Charles E. Young Dr. East, Los Angeles, CA 90095, USA.
Kenneth A Bradley
University of California, Los Angeles · US

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Virology CoreP30AI028697 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI JAMIESON-KARAVODIN, BETH DEIRDRE · 1991 to 2018
$39.9M
CHARACTERIZATION OF ANTHRAX TOXIN RECEPTOR INTERACTIONSR01AI057870 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BRADLEY, KENNETH ALAN · 2004 to 2008
$1.7M
Regulation and Function of Anthrax Toxin Receptor 1F31AI061837 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MALDONADO-AROCHO, FRANCISCO J · 2006 to 2008
$92k
NCI NIH HHS CA-16042NCI NIH HHS P30 CA016042NIAID NIH HHS 5F31AI061837-03NIAID NIH HHS AI057870NIAID NIH HHS AI-28697NIAID NIH HHS F31 AI061837NIAID NIH HHS P30 AI028697NIAID NIH HHS R01 AI057870
6 · The paper itself

Abstract

Bacillus anthracis secretes two bipartite toxins, edema toxin (ET) and lethal toxin (LT), which impair immune responses and contribute directly to the pathology associated with the disease anthrax. Edema factor, the catalytic subunit of ET, is an adenylate cyclase that impairs host defenses by raising cellular cyclic AMP (cAMP) levels. Synthetic cAMP analogues and compounds that raise intracellular cAMP levels lead to phenotypic and functional changes in dendritic cells (DCs). Here, we demonstrate that ET induces a maturation state in human monocyte-derived DCs (MDDCs) similar to that induced by lipopolysaccharide (LPS). ET treatment results in downregulation of DC-SIGN, a marker of immature DCs, and upregulation of DC maturation markers CD83 and CD86. Maturation of DCs by ET is accompanied by an increased ability to migrate toward the lymph node-homing chemokine macrophage inflammatory protein 3beta, like LPS-matured DCs. Interestingly, cotreating with LT differentially affects the ET-induced maturation of MDDCs while not inhibiting ET-induced migration. These findings reveal a mechanism by which ET impairs normal innate immune function and may explain the reported adjuvant effect of ET.

Indexed as

ChemotaxisAntigens, BacterialAntigens, CDB7-2 AntigenBacterial ToxinsCD83 AntigenCell Adhesion MoleculesChemokine CCL19DC-Specific ICAM-3 Grabbing NonintegrinDendritic CellsHumansImmunoglobulinsLectins, C-TypeMembrane GlycoproteinsReceptors, Cell Surfaceanthrax toxinAntigens, BacterialAntigens, CDB7-2 AntigenBacterial ToxinsCD83 AntigenCD86 protein, humanCell Adhesion MoleculesChemokine CCL19DC-Specific ICAM-3 Grabbing NonintegrinImmunoglobulinsLectins, C-TypeMembrane GlycoproteinsReceptors, Cell Surface

Identifiers

PMID19273556
PMCPMC2681763
OpenAlexW2129194923

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.