Evidence map›Paper›PMID 31701299›Full record

ArticleOdontology2020

IL-10 secreting B cells regulate periodontal immune response during periodontitis.

Tie Shi, Ying Jin, Yibin Miao, Ye Wang, Yong Zhou, Xiaoping Lin

Abstract read
PubMed Publisher
In one paragraph

Article in Odontology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 52 citations in OpenAlex.

  1. Pooled it
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  10. Role of regulatory immune cells in pathogenesis and therapy of periodontitis.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  11. Impact of LiveMicroorganisms · 2025
    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

6 authors at 1 institution in 1 country.

Tie ShiDepartment of Stomatology, Shengjing Hospital of China Medical University, San Hao St. No. 36, Shenyang, 110004, Liaoning, China.
Ying JinDepartment of Stomatology, Shengjing Hospital of China Medical University, San Hao St. No. 36, Shenyang, 110004, Liaoning, China.
Yibin MiaoDepartment of Stomatology, Shengjing Hospital of China Medical University, San Hao St. No. 36, Shenyang, 110004, Liaoning, China.
Ye WangDepartment of Stomatology, Shengjing Hospital of China Medical University, San Hao St. No. 36, Shenyang, 110004, Liaoning, China.
Yong ZhouDepartment of Stomatology, Shengjing Hospital of China Medical University, San Hao St. No. 36, Shenyang, 110004, Liaoning, China.
Xiaoping LinDepartment of Stomatology, Shengjing Hospital of China Medical University, San Hao St. No. 36, Shenyang, 110004, Liaoning, China. xiaoping_ba@126.com.ORCID http://orcid.org/0000-0003-0892-7348
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Periodontitis is a disease caused by periodontopathogens and is characterized by periodontal inflammation and alveolar bone resorption. As has been proven, host immune responses incite the development and progression of periodontitis. The present study sought to establish B10 cell functions and mechanisms in regulating host immunity during periodontitis. Periodontopathogen-specific B10 cells were purified and then injected into recipients to create the adoptive transfer models. We compared inflammatory cytokines and regulatory T (Treg)/Th17 cell expression in a healthy, normal model, an experimental periodontitis model, and experimental periodontitis model adoptively transferred with B10 cells. Compared with experimental periodontitis animals, our results showed that transfer of B10 cells alleviated alveolar bone resorption (P < 0.05) by reducing periodontal osteoclastogenesis (P < 0.05). Additionally, we found that B10 cell transfer into the experimental periodontitis ones resulted in increased IL-10 (P < 0.05), but decreased IL-17 (P < 0.05) and receptor activator for nuclear factor κB ligand (RANKL) (P < 0.05) gene and protein expression in local lesions. Moreover, adoptive transfer of B10 cells reduced the proportion of Th17 cells (P < 0.05) in the gingiva. The results of our study confirmed that B10 cells can modulate local host immune responses and prevent inflammatory damage of alveolar bone by reducing pro-inflammatory cytokine expression and decreasing local proliferation of Th17 cells.

Indexed as

Alveolar Bone LossPeriodontitisAdoptive TransferAnimalsB-LymphocytesInterleukin-10RANK LigandInterleukin-10RANK LigandB cellsIL-10ImmunomodulationPeriodontitisTreg/Th17

Identifiers

PMID31701299
OpenAlexW2985190173

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.