Evidence map›Paper›PMID 31068929›Full record

ArticleFrontiers in immunology2019

Silica Particles Mediate Phenotypic and Functional Alteration of Dendritic Cells and Induce Th2 Cell Polarization.

Suna Liu, Changfu Hao, Lei Bao, Dehua Zhao, Hongyi Zhang, Jianyong Hou, Di Wang, Huiting Chen, Feifei Feng, Wu Yao

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. CD4Frontiers in immunology · 2025
    Review
  3. The role of inflammation in silicosis.Frontiers in pharmacology · 2024
    Review
  4. Toxicity evaluation of silica nanoparticles for delivery applications.Drug delivery and translational research · 2023
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. 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

10 authors at 3 institutions in 1 country.

Suna LiuDepartment of Henan Newborn Screening Center, Department of Pediatrics, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Changfu HaoDepartment of Public Health, Zhengzhou University, Zhengzhou, China.
Lei BaoDepartment of Public Health, Zhengzhou University, Zhengzhou, China.
Dehua ZhaoDepartment of Henan Newborn Screening Center, Department of Pediatrics, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Hongyi ZhangHospital Infection Management, The First Affiliated Hospital of Henan University, Kaifeng, China.
Jianyong HouDepartment of Public Health, Zhengzhou University, Zhengzhou, China.
Di WangDepartment of Public Health, Zhengzhou University, Zhengzhou, China.
Huiting ChenDepartment of Public Health, Zhengzhou University, Zhengzhou, China.
Feifei FengDepartment of Public Health, Zhengzhou University, Zhengzhou, China.
Wu YaoDepartment of Public Health, Zhengzhou University, Zhengzhou, China.
Zhengzhou University · CNThird Affiliated Hospital of Zhengzhou University · CNFirst Affiliated Hospital of Henan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During silicosis, immune cells, including macrophages, T cells, B cells, and NK cells, participate in fibrosis development through alteration of the immune status. Dendritic cells (DCs) are professional antigen-presenting cells (APCs) with a key role in initiating immune responses and sustaining immune tolerance to maintain homeostasis. The relative contribution of DCs to silicosis progression is not well-documented. In the current study, we investigated the phenotypic and functional alterations of peripheral blood mononuclear cell (PBMC)-derived DCs of Sprague-Dawley (SD) rat during immune responses to silica exposure. We established models for direct and indirect exposure of DCs to silica by either treating DCs with silica or coculturing them with alveolar macrophages (AMs) treated with silica, respectively. The functional activity of DCs was analyzed by measuring their expression of costimulatory molecules, fluorescent microparticle uptake, cytokine production, and ability to mediate T cell polarization

Indexed as

Particulate MatterSilicon DioxideAnimalsBiomarkersCytokinesDendritic CellsDisease Models, AnimalImmunophenotypingLeukocytes, MononuclearLymphocyte ActivationMaleOccupational ExposurePhagocytosisPhenotypeRatsSilicosisBiomarkersCytokinesParticulate MatterSilicon Dioxidealveolar macrophagesdendritic cellsphagocytosissilicasilicosisTh2 polarization

Identifiers

PMID31068929
PMCPMC6491578
OpenAlexW2941413473

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.