Evidence map›Paper›PMID 21978001›Full record

ArticleImmunology2011

NOD-like receptors and RIG-I-like receptors in human eosinophils: activation by NOD1 and NOD2 agonists.

Anne Månsson Kvarnhammar, Terese Petterson, Lars-Olaf Cardell

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Exploring Asthma as a Protective Factor in COVID-19 Outcomes.International journal of molecular sciences · 2025
    Review
  7. NOD2-NLRP3 Axis and Asthma.Journal of asthma and allergy · 2025
    Review
  8. Review
  9. Review
  10. Vaccine adjuvants: mechanisms and platforms.Signal transduction and targeted therapy · 2023
    Review
  11. Review
  12. Article
  13. NOD-like receptors in asthma.Frontiers in immunology · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. Activity of Tracheal Cytotoxin ofFrontiers in cellular and infection microbiology · 2020
    Article
  18. Eosinophils: Nemeses of Pulmonary Pathogens?Current allergy and asthma reports · 2019
    Review
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

Anne Månsson KvarnhammarDivision of ENT Diseases, CLINTEC, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden. anne.mansson@ki.se
Terese Petterson
Lars-Olaf Cardell
Karolinska Institutet · SEKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NOD-like receptors (NLRs) and RIG-I-like receptors (RLRs) are newly discovered pattern-recognition receptors. They detect substructures of bacterial peptidoglycan and viral RNA, respectively, thereby initiating an immune response. However, their role in eosinophil activation remains to be explored. The aim of this study was to characterize the expression of a range of NLRs and RLRs in purified human eosinophils and assess their functional importance. Expression of NOD1, NOD2, NLRP3, RIG-I and MDA-5 was investigated using real-time reverse transcription PCR, flow cytometry and immunohistochemistry. The effects of the corresponding agonists iE-DAP (NOD1), MDP (NOD2), alum (NLRP3) and poly(I:C)/LyoVec (RIG-I/MDA-5) were studied in terms of cytokine secretion, degranulation, survival, expression of adhesion molecules and activation markers, and chemotactic migration. Eosinophils expressed NOD1 and NOD2 mRNA and protein. Low levels of RIG-I and MDA-5 were found, whereas expression of NLRP3 was completely absent. In accordance, stimulation with iE-DAP and MDP was found to induce secretion of interleukin-8, up-regulate expression of CD11b, conversely down-regulate CD62 ligand, increase expression of CD69 and induce migration. The MDP also promoted release of eosinophil-derived neurotoxin, whereas iE-DAP failed to do so. No effects were seen upon stimulation with alum or poly(I:C)/LyoVec. Moreover, the NOD1-induced and NOD2-induced activation was mediated via the nuclear factor-κB signalling pathway and augmented by interleukin-5 and granulocyte-macrophage colony-stimulating factor, but not interferon-γ. Taken together, the NLR system represents a novel pathway for eosinophil activation. The responses are enhanced in the presence of cytokines that regulate T helper type 2 immunity, suggesting that the NLRs constitute a link between respiratory infections and exacerbations of allergic disease.

Indexed as

Acetylmuramyl-Alanyl-IsoglutamineAntigens, CDAntigens, Differentiation, T-LymphocyteCarrier ProteinsCD11b AntigenCD69 AntigensCell MovementCells, CulturedDEAD Box Protein 58DEAD-box RNA HelicasesDiaminopimelic AcidEosinophil-Derived NeurotoxinEosinophilsFlow CytometryGene ExpressionHumansAcetylmuramyl-Alanyl-IsoglutamineAntigens, CDAntigens, Differentiation, T-LymphocyteCarrier ProteinsCD11b AntigenCD69 AntigensDEAD Box Protein 58DEAD-box RNA HelicasesDiaminopimelic AcidEosinophil-Derived NeurotoxinIFIH1 protein, humanInterferon-Induced Helicase, IFIH1Interleukin-8Lectins, C-TypeL-SelectinN(2)-(gamma-D-glutamyl)-meso-2,2'-diaminopimelic acidNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanNOD1 protein, humanNod1 Signaling Adaptor ProteinNOD2 protein, humanNod2 Signaling Adaptor ProteinReceptors, ImmunologicRIGI protein, human

Identifiers

PMID21978001
PMCPMC3209571
OpenAlexW1511555415

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.