Evidence map›Paper›PMID 23907435›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2013

Helminth-excreted/secreted products are recognized by multiple receptors on DCs to block the TLR response and bias Th2 polarization in a cRAF dependent pathway.

César A Terrazas, Marcela Alcántara-Hernández, Laura Bonifaz, Luis I Terrazas, Abhay R Satoskar

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

35 citing papers in PubMed, 59 citations in OpenAlex.

  1. Infection and immunity · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Macrophage Gal/GalNAc lectin 2 (MGL2)Scientific reports · 2022
    Article
  9. Review
  10. Pathogens (Basel, Switzerland) · 2021
    Article
  11. Article
  12. Article
  13. Cells · 2019
    Article
  14. Article
  15. Bioscience reports · 2019
    Article
  16. Journal of immunology research · 2019
    Article
  17. Review
  18. Review
  19. Article
  20. Frontiers in immunology · 2017
    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 4 institutions in 2 countries.

César A Terrazas1A.S., Department of Pathology, The Ohio State University, Columbus, OH 43210, USA. abhay.satoskar@osumc.edu.
Marcela Alcántara-Hernández
Laura Bonifaz
Luis I Terrazas
Abhay R Satoskar
Centro Medico Nacional Siglo XXI · MXThe Ohio State University · USThe Ohio State University Wexner Medical Center · USUniversidad Nacional Autónoma de México · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs) recognize pathogens and initiate the T-cell response. The DC-helminth interaction induces an immature phenotype in DCs; as a result, these DCs display impaired responses to TLR stimulation and prime Th2-type responses. However, the DC receptors and intracellular pathways targeted by helminth molecules and their importance in the initiation of the Th2 response are poorly understood. In this report, we found that products excreted/secreted by Taenia crassiceps (TcES) triggered cRAF phosphorylation through MGL, MR, and TLR2. TcES interfered with the LPS-induced NFκB p65 and p38 MAPK signaling pathways. In addition, TcES-induced cRAF signaling pathway was critical for down-regulation of the TLR-mediated DC maturation and secretion of IL-12 and TNF-α. Finally, we show for the first time that blocking cRAF in DCs abolishes their ability to induce Th2 polarization in vitro after TcES exposure. Our data demonstrate a new mechanism by which helminths target intracellular pathways to block DC maturation and efficiently program Th2 polarization.

Indexed as

AnimalsAsialoglycoproteinsDendritic CellsDown-RegulationImmunomodulationInterleukin-12Lectins, C-TypeMannose-Binding LectinsMannose ReceptorMAP Kinase Signaling SystemMembrane ProteinsMiceMice, Inbred BALB CMice, Inbred C57BLp38 Mitogen-Activated Protein KinasesPhosphorylationAsialoglycoproteinsClec10a protein, mouseInterleukin-12Lectins, C-TypeMannose-Binding LectinsMannose ReceptorMembrane Proteinsp38 Mitogen-Activated Protein KinasesProto-Oncogene Proteins c-rafReceptors, Cell SurfaceToll-Like Receptor 2Transcription Factor RelATumor Necrosis Factor-alphaCLRsdendritic cellimmunomodulationmannose receptorMGL

Identifiers

PMID23907435
PMCPMC3804751
OpenAlexW2165049240

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.