Evidence map›Paper›PMID 37915574›Full record

ReviewFrontiers in immunology2023

Tolerogenic dendritic cells and TLR4/IRAK4/NF-κB signaling pathway in allergic rhinitis.

Chenglin Kang, Xiaomei Li, Peng Liu, Yue Liu, Yuan Niu, Xianhai Zeng, Hailiang Zhao, Jiangqi Liu, Shuqi Qiu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

32 citing papers in PubMed, 38 citations in OpenAlex.

  1. Pharmaceutics · 2026
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  7. Article
  8. Molecules (Basel, Switzerland) · 2026
    Article
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  11. Article
  12. Review
  13. Review
  14. Review
  15. Exploring Siglecs: Potential Modulators of Immune Cells in Food Allergy and Therapeutic Applications.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2025
    Review
  16. Article
  17. Article
  18. Article
  19. Mechanisms and Therapeutic Implications of EZH2 in Nasal Diseases.Clinical reviews in allergy & immunology · 2025
    Review
  20. Review
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

9 authors at 4 institutions in 1 country.

Chenglin KangDepartment of Graduate and Scientific Research, Zunyi Medical University Zhuhai Campus, Zhuhai, China.
Xiaomei LiDepartment of Otolaryngology, Second People's Hospital of Gansu Province, Lanzhou, China.
Peng LiuDepartment of Graduate and Scientific Research, Zunyi Medical University Zhuhai Campus, Zhuhai, China.
Yue LiuDepartment of Graduate and Scientific Research, Zunyi Medical University Zhuhai Campus, Zhuhai, China.
Yuan NiuDepartment of Neurology, Second People's Hospital of Gansu Province, Lanzhou, China.
Xianhai ZengDepartment of Graduate and Scientific Research, Zunyi Medical University Zhuhai Campus, Zhuhai, China.
Hailiang ZhaoDepartment of Graduate and Scientific Research, Zunyi Medical University Zhuhai Campus, Zhuhai, China.
Jiangqi LiuDepartment of Graduate and Scientific Research, Zunyi Medical University Zhuhai Campus, Zhuhai, China.
Shuqi QiuDepartment of Graduate and Scientific Research, Zunyi Medical University Zhuhai Campus, Zhuhai, China.
Zunyi Medical University · CNNantong University · CNLonggang Central Hospital · CNSecond People's Hospital of NanTong · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dendritic cells (DCs), central participants in the allergic immune response, can capture and present allergens leading to allergic inflammation in the immunopathogenesis of allergic rhinitis (AR). In addition to initiating antigen-specific immune responses, DCs induce tolerance and modulate immune homeostasis. As a special type of DCs, tolerogenic DCs (tolDCs) achieve immune tolerance mainly by suppressing effector T cell responses and inducing regulatory T cells (Tregs). TolDCs suppress allergic inflammation by modulating immune tolerance, thereby reducing symptoms of AR. Activation of the TLR4/IRAK4/NF-κB signaling pathway contributes to the release of inflammatory cytokines, and inhibitors of this signaling pathway induce the production of tolDCs to alleviate allergic inflammatory responses. This review focuses on the relationship between tolDCs and TLR4/IRAK4/NF-κB signaling pathway with AR.

Indexed as

NF-kappa BRhinitis, AllergicDendritic CellsHumansInflammationInterleukin-1 Receptor-Associated KinasesSignal TransductionToll-Like Receptor 4Interleukin-1 Receptor-Associated KinasesIRAK4 protein, humanNF-kappa BTLR4 protein, humanToll-Like Receptor 4allergic rhinitisimmune responseimmune toleranceTLR4/IRAK4/NF-κB signaling pathwaytolerogenic dendritic cells

Identifiers

PMID37915574
PMCPMC10616250
OpenAlexW4387704105

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.