Evidence map›Paper›PMID 25973005›Full record

ArticleInternational journal of clinical and experimental pathology2015

Relationship of TLR2, TLR4 and tissue remodeling in chronic rhinosinusitis.

Xin Wang, Chunyuan Zhao, Wenjun Ji, Yuan Xu, Huamin Guo

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Immunological Aspects of Chronic Rhinosinusitis.Diagnostics (Basel, Switzerland) · 2022
    Review
  6. Article
  7. Inflammation-driven vascular dysregulation in chronic rhinosinusitis.International forum of allergy & rhinology · 2021
    Observational
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Observational
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 2 institutions in 1 country.

Xin WangDepartment of Otorhinolaryngology & Head and Neck Surgery, Second Hospital Affiliated to Harbin Medical University Harbin, China.
Chunyuan ZhaoDepartment of Otorhinolaryngology & Head and Neck Surgery, Second Hospital Affiliated to Harbin Medical University Harbin, China.
Wenjun JiDepartment of Otorhinolaryngology & Head and Neck Surgery, Second Hospital Affiliated to Harbin Medical University Harbin, China.
Yuan XuDepartment of ENT, People Hospital of Hailin City Hailin, China.
Huamin GuoDepartment of Otorhinolaryngology & Head and Neck Surgery, Second Hospital Affiliated to Harbin Medical University Harbin, China.
Harbin Medical University · CNHaikou City People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In order to explore the role of innate immunity in the remodeling of CRS (chronic rhinosinusitis), we investigated the correlation between TLR2, TLR4 and remodeling involved cytokines and histopathological features. Immunohistochemical staining was applied to detect the expression of TLR2, TLR4 and TGF-β1. Masson staining was used for observing the collagen deposition. The other histopathologic features of remodeling were observed by hemotoxylin and eosin (HE) staining. Nasal epithelial cell culture was used to elucidate the effect of TLR2, TLR4 agonists and inhibitors on the expression of TGF-β1 and MMP-9. The association study showed that the significantly higher expression of TLR2, TLR4, TGF-β1 and collagen appeared in CRSsNP (chronic rhinosinusitis without nasal polyps) patients compared with CRSwNP (chronic rhinosinusitis with nasal polyps) patients. In CRSsNP, patients with a severe epithelial damage (score 3) had a significantly higher expression of TLR2 than patients with mild epithelial damage (score ≤ 2) (P < 0.05). Moreover the expression of TLR2 correlated negatively with squamous hyperplasia in CRSsNP, and positively with gland hyperplasia in CRSwNP. The expression of TLR2 and TLR4 was closely related to neutrophil infiltration in CRSsNP (P < 0.01). TGF-β1 was downregulated by TLR2 agonist in CRSwNP and upregulated by TLR4 agonist in CRSsNP (P < 0.05). MMP-9 was upregulated by TLR4 agonist in CRSwNP (P < 0.05). TLR2 and TLR4 had close relationship with TGF-β1 and the histologic features of remodeling, especially collagen deposition and neutrophil infiltration in CRSsNP. The innate immunity could influence the histologic characteristics and involved cytokines through TLR2 and TLR4 in the remodeling of CRS.

Indexed as

AdolescentAdultAgedChildChronic DiseaseCollagenFemaleHumansImmunity, InnateInflammationMaleMiddle AgedNasal MucosaNasal PolypsNeutrophil InfiltrationRhinitisCollagenToll-Like Receptor 2Toll-Like Receptor 4Transforming Growth Factor beta1chronic rhinosinusitisTGF-β1tissue remodelingTLR2TLR4

Identifiers

PMID25973005
PMCPMC4396292
OpenAlexW2427062493

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.