Evidence map›Paper›PMID 19770268›Full record

ArticleThe Journal of experimental medicine2009

A murine DC-SIGN homologue contributes to early host defense against Mycobacterium tuberculosis.

Antoine Tanne, Bo Ma, Frédéric Boudou, Ludovic Tailleux, Hélène Botella, Edgar Badell, Florence Levillain, Maureen E Taylor, Kurt Drickamer, Jérome Nigou and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

55 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Pooled it
  2. Antiviral Role of Surface Layer Protein A (SlpA) ofPathogens (Basel, Switzerland) · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. From structure to function - Ligand recognition by myeloid C-type lectin receptors.Computational and structural biotechnology journal · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. TheThe Biochemical journal · 2019
    Review
  17. Article
  18. Article
  19. Review
  20. Identification of genes required forProceedings of the National Academy of Sciences of the United States of America · 2018
    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

20 authors at 9 institutions in 5 countries.

Antoine TanneCentre National de la Recherche Scientifique, Université de Toulouse, Toulouse, France.
Bo Ma
Frédéric Boudou
Ludovic Tailleux
Hélène Botella
Edgar Badell
Florence Levillain
Maureen E Taylor
Kurt Drickamer
Jérome Nigou
Karen M Dobos
Germain Puzo
Dietmar Vestweber
Martin K Wild
Marie Marcinko
Peter Sobieszczuk
Lauren Stewart
Daniel Lebus
Brigitte Gicquel
Olivier Neyrolles
Scripps Research Institute · USInstitut Pasteur · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FRImperial College London · GBMax Planck Institute for Molecular Biomedicine · DECentre National pour la Recherche Scientifique et Technique (CNRST) · MAColorado State University · USInstitut de Pharmacologie et de Biologie Structurale · FRUniversité Toulouse III - Paul Sabatier · FR

Funding

Wellcome Trust
6 · The paper itself

Abstract

The C-type lectin dendritic cell-specific intercellular adhesion molecule-3 grabbing nonintegrin (DC-SIGN) mediates the innate immune recognition of microbial carbohydrates. We investigated the function of this molecule in the host response to pathogens in vivo, by generating mouse lines lacking the DC-SIGN homologues SIGNR1, SIGNR3, and SIGNR5. Resistance to Mycobacterium tuberculosis was impaired only in SIGNR3-deficient animals. SIGNR3 was expressed in lung phagocytes during infection, and interacted with M. tuberculosis bacilli and mycobacterial surface glycoconjugates to induce secretion of critical host defense inflammatory cytokines, including tumor necrosis factor (TNF). SIGNR3 signaling was dependent on an intracellular tyrosine-based motif and the tyrosine kinase Syk. Thus, the mouse DC-SIGN homologue SIGNR3 makes a unique contribution to protection of the host against a pulmonary bacterial pathogen.

Indexed as

AnimalsAntigens, CDCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinExtracellular Signal-Regulated MAP KinasesFemaleGlycoconjugatesInterleukin-6Lectins, C-TypeLipopolysaccharidesLungMaleMiceMice, Inbred C57BLMice, KnockoutNF-kappa BAntigens, CDCell Adhesion MoleculesDC-Specific ICAM-3 Grabbing NonintegrinExtracellular Signal-Regulated MAP KinasesGlycoconjugatesInterleukin-6Lectins, C-TypelipoarabinomannanLipopolysaccharidesNF-kappa BProto-Oncogene Proteins c-rafReceptors, Cell SurfaceSIGNR3 protein, mouseTlr2 protein, mouseToll-Like Receptor 2Tumor Necrosis Factor-alpha

Identifiers

PMID19770268
PMCPMC2757888
OpenAlexW2141206527

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.