Evidence map›Paper›PMID 36329504›Full record

ArticleJournal of translational medicine2022

Single-cell RNA sequencing reveals rebalancing of immunological response in patients with periodontitis after non-surgical periodontal therapy.

Hansong Lee, Ji-Young Joo, Dong Hyun Sohn, Junho Kang, Yeuni Yu, Hae Ryoun Park, Yun Hak Kim

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Journal of dental anesthesia and pain medicine · 2026
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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

7 authors at 2 institutions in 1 country.

Hansong Lee *Convergence Medical Sciences, Pusan National University, 50612, Yangsan, Republic of Korea.
Ji-Young Joo *Department of Periodontology, School of Dentistry, Pusan National University, 50612, Yangsan, Republic of Korea.
Dong Hyun SohnDepartment of Microbiology and Immunology, School of Medicine, Pusan National University, 50612, Yangsan, Republic of Korea.
Junho KangMedical Research Institute, Pusan National University, 50612, Yangsan, Republic of Korea.
Yeuni YuMedical Research Institute, Pusan National University, 50612, Yangsan, Republic of Korea.
Hae Ryoun ParkDepartment of Oral Pathology, School of Dentistry, Pusan National University, 49 Busandaehak- ro, 50612, Yangsan, Republic of Korea. parkhr@pusan.ac.kr.
Yun Hak KimConvergence Medical Sciences, Pusan National University, 50612, Yangsan, Republic of Korea. yunhak10510@pusan.ac.kr.ORCID 0000-0002-9796-8266
Pusan National University · KRPusan National University Yangsan Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeriodontitis is a major inflammatory disease of the oral mucosa that is not limited to the oral cavity but also has systemic consequences. Although the importance of chronic periodontitis has been emphasized, the systemic immune response induced by periodontitis and its therapeutic effects remain elusive. Here, we report the transcriptomes of peripheral blood mononuclear cells (PBMCs) from patients with periodontitis.

methodsUsing single-cell RNA sequencing, we profiled PBMCs from healthy controls and paired pre- and post-treatment patients with periodontitis. We extracted differentially expressed genes and biological pathways for each cell type and calculated activity scores reflecting cellular characteristics. Intercellular crosstalk was classified into therapy-responsive and -nonresponsive pathways.

resultsWe analyzed pan-cellular differentially expressed genes caused by periodontitis and found that most cell types showed a significant increase in CRIP1, which was further supported by the increased levels of plasma CRIP1 observed in patients with periodontitis. In addition, activated cell type-specific ligand-receptor interactions, including the BTLA, IFN-γ, and RESISTIN pathways, were prominent in patients with periodontitis. Both the BTLA and IFN-γ pathways returned to similar levels in healthy controls after periodontal therapy, whereas the RESISTIN pathway was still activated even after therapy.

conclusionThese data collectively provide insights into the transcriptome changes and molecular interactions that are responsive to periodontal treatment. We identified periodontitis-specific systemic inflammatory indicators and suggest unresolved signals of non-surgical therapy as future therapeutic targets.

Indexed as

Chronic PeriodontitisResistinHumansLeukocytes, MononuclearSequence Analysis, RNAResistinChronic periodontitisCRIP1Immune responseRESISTINSingle-cell RNA sequencingTherapeutic target

Identifiers

PMID36329504
PMCPMC9635198
OpenAlexW4308425552

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LicenceCC BY
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Registered trials

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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.