Evidence map›Paper›PMID 28069953›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

C-type lectin receptor DCIR modulates immunity to tuberculosis by sustaining type I interferon signaling in dendritic cells.

Anthony Troegeler, Ingrid Mercier, Céline Cougoule, Danilo Pietretti, André Colom, Carine Duval, Thien-Phong Vu Manh, Florence Capilla, Renaud Poincloux, Karine Pingris and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. The Role of Glycans in Human Immunity-A Sweet Code.Molecules (Basel, Switzerland) · 2025
    Review
  5. Review
  6. The C-type lectin receptor Dcir (Frontiers in immunology · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Transcriptional profiling of a fungal granuloma reveals a low metabolic activity ofFrontiers in cellular and infection microbiology · 2023
    Article
  16. Review
  17. Review
  18. Article
  19. Article
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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

19 authors at 7 institutions in 3 countries.

Anthony TroegelerInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Ingrid MercierInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Céline CougouleInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Danilo PietrettiInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
André ColomInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Carine DuvalInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Thien-Phong Vu ManhCentre d'Immunologie de Marseille-Luminy, INSERM U1104, CNRS UMR7280, Aix Marseille Université, F-13288 Marseille Cedex 09, France.
Florence CapillaService d'Histopathologie, INSERM/UPS-Unité de service 006/Centre Régional d'Exploration fonctionnelle et Ressources Expérimentales, Centre Hospitalier Universitaire Purpan, 31300 Toulouse, France.
Renaud PoinclouxInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Karine PingrisInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Jérôme NigouInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Jörg RademannPharmaceutical and Medicinal Chemistry, Freie Universität Berlin, 14195 Berlin, Germany.
Marc DalodCentre d'Immunologie de Marseille-Luminy, INSERM U1104, CNRS UMR7280, Aix Marseille Université, F-13288 Marseille Cedex 09, France.
Frank A W VerreckDepartment of Parasitology, Biomedical Primate Research Centre, 2288 GJ, Rijswijk, The Netherlands.
Talal Al SaatiService d'Histopathologie, INSERM/UPS-Unité de service 006/Centre Régional d'Exploration fonctionnelle et Ressources Expérimentales, Centre Hospitalier Universitaire Purpan, 31300 Toulouse, France.
Geanncarlo Lugo-VillarinoInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Bernd LepeniesImmunology Unit, University of Veterinary Medicine Hannover, 30559 Hannover, Germany.
Denis HudrisierInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France.
Olivier NeyrollesInstitut de Pharmacologie et de Biologie Structurale (IPBS), CNRS, 31000 Toulouse, France; olivier.neyrolles@ipbs.fr.
Institut de Pharmacologie et de Biologie Structurale · FRUniversité Toulouse III - Paul Sabatier · FRCentre National de la Recherche Scientifique · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FRBiomedical Primate Research Centre · NLFreie Universität Berlin · DEUniversity of Veterinary Medicine Hannover, Foundation · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune response against pathogens is a tightly regulated process that must ensure microbial control while preserving integrity of the infected organs. Tuberculosis (TB) is a paramount example of a chronic infection in which antimicrobial immunity is protective in the vast majority of infected individuals but can become detrimental if not finely tuned. Here, we report that C-type lectin dendritic cell (DC) immunoreceptor (DCIR), a key component in DC homeostasis, is required to modulate lung inflammation and bacterial burden in TB. DCIR is abundantly expressed in pulmonary lesions in Mycobacterium tuberculosis-infected nonhuman primates during both latent and active disease. In mice, we found that DCIR deficiency impairs STAT1-mediated type I IFN signaling in DCs, leading to increased production of IL-12 and increased differentiation of T lymphocytes toward Th1 during infection. As a consequence, DCIR-deficient mice control M. tuberculosis better than WT animals but also develop more inflammation characterized by an increased production of TNF and inducible NOS (iNOS) in the lungs. Altogether, our results reveal a pathway by which a C-type lectin modulates the equilibrium between infection-driven inflammation and pathogen's control through sustaining type I IFN signaling in DCs.

Indexed as

AnimalsDendritic CellsFemaleInterferon Type ILectins, C-TypeMacaca mulattaMice, Inbred C57BLMice, KnockoutPhosphorylationSignal TransductionSTAT1 Transcription FactorTuberculosisDcir protein, mouseInterferon Type ILectins, C-TypeStat1 protein, mouseSTAT1 Transcription FactorC-type lectininflammationtuberculosis

Identifiers

PMID28069953
PMCPMC5278472
OpenAlexW2568695491

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.