Evidence map›Paper›PMID 26589811›Full record

ArticleJournal of endodontics2016

Characterization of the Protective Role of Regulatory T Cells in Experimental Periapical Lesion Development and Their Chemoattraction Manipulation as a Therapeutic Tool.

Carolina Favaro Francisconi, Andreia Espindola Vieira, Claudia Cristina Biguetti, Andrew J Glowacki, Ana Paula Favaro Trombone, Ariadne Letra, Renato Menezes Silva, Charles S Sfeir, Steven R Little, Gustavo Pompermaier Garlet

Open access · greenAbstract read
In one paragraph

Article in Journal of endodontics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Immune Tolerance in the Oral Mucosa.International journal of molecular sciences · 2021
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Engineering Immune Tolerance with Biomaterials.Advanced healthcare materials · 2019
    Review
  15. Review
  16. CD8Inflammation · 2018
    Article
  17. Article
  18. CD8Frontiers in immunology · 2017
    Article
  19. Review
  20. 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 5 institutions in 2 countries.

Carolina Favaro FrancisconiDepartment of Biological Sciences, School of Dentistry of Bauru, University of São Paulo, Bauru, São Paulo, Brazil.
Andreia Espindola VieiraDepartment of Biological Sciences, School of Dentistry of Bauru, University of São Paulo, Bauru, São Paulo, Brazil.
Claudia Cristina BiguettiDepartment of Biological Sciences, School of Dentistry of Bauru, University of São Paulo, Bauru, São Paulo, Brazil.
Andrew J GlowackiDepartments of Chemical and Petroleum Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Center for Craniofacial Regeneration, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Ana Paula Favaro TromboneUniversidade do Sagrado Coração (USC); Bauru, São Paulo, Brazil.
Ariadne LetraDepartment of Endodontics, School of Dentistry, University of Texas Health Science Center at Houston, Houston, Texas.
Renato Menezes SilvaDepartment of Endodontics, School of Dentistry, University of Texas Health Science Center at Houston, Houston, Texas.
Charles S SfeirDepartment of Center for Craniofacial Regeneration, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Oral Biology, University of Pittsburgh, Pittsburgh, Pennsylvania.
Steven R LittleDepartments of Chemical and Petroleum Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Center for Craniofacial Regeneration, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Immunology, University of Pittsburgh, Pittsburgh, Pennsylvania; Department of Bioengineering, University of Pittsburgh, Pittsburgh, Pennsylvania.
Gustavo Pompermaier GarletDepartment of Biological Sciences, School of Dentistry of Bauru, University of São Paulo, Bauru, São Paulo, Brazil. Electronic address: garletgp@usp.br.
Universidade de São Paulo · BRMcGowan Institute for Regenerative Medicine · USThe University of Texas Health Science Center at Houston · USUniversidade Sagrado Coração · BRUniversity of Pittsburgh · US

Funding

Treatment of Periodontitis via Recruitment of Regulatory LymphocytesR01DE021058 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LITTLE, STEVEN R · 2011 to 2015
$1.8M
Resolution and Regeneration in Periodontitis via Recruitment of Regulatory LymphoR56DE021058 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LITTLE, STEVEN R · 2010 to 2010
$294k
NIDCR NIH HHS 1R01DE021058-01 A1NIDCR NIH HHS 1R56DE021058-01NIDCR NIH HHS R01 DE021058NIDCR NIH HHS R56 DE021058
6 · The paper itself

Abstract

introductionThe pathogenesis of periapical lesions is determined by the balance between host proinflammatory immune response and counteracting anti-inflammatory and reparative responses, which include regulatory T cells (Tregs) as potential immunoregulatory agents. In this study, we investigated (in a cause-and-effect manner) the involvement of CCL22-CCR4 axis in Treg migration to the periapical area and the role of Tregs in the determination of outcomes in periapical lesions.

methodsPeriapical lesions were induced in C57Bl/6 (wild-type) and CCR4KO mice (pulp exposure and bacterial inoculation) and treated with anti-glucocorticoid-induced TNF receptor family regulated gene to inhibit Treg function or alternatively with CCL22-releasing, polylactic-glycolic acid particles to induce site-specific migration of Tregs. After treatment, lesions were analyzed for Treg influx and phenotype, overall periapical bone loss, and inflammatory/immunologic and wound healing marker expression (analyzed by real-time polymerase chain reaction array).

resultsTreg inhibition by anti-glucocorticoid-induced TNF receptor family regulated gene or CCR4 depletion results in a significant increase in periapical lesion severity, associated with upregulation of proinflammatory, T-helper 1, T-helper 17, and tissue destruction markers in parallel with decreased Treg and healing marker expression. The local release of CCL22 in the root canal system resulted in the promotion of Treg migration in a CCR4-dependent manner, leading to the arrest of periapical lesion progression, associated with downregulation of proinflammatory, T-helper 1, T-helper 17, and tissue destruction markers in parallel with increased Treg and healing marker expression.

conclusionsBecause the natural and CCL22-induced Treg migration switches active lesion into inactivity phenotype, Treg chemoattractant may be a promising strategy for the clinical management of periapical lesions.

Indexed as

Chemotaxis, LeukocyteAnimalsChemokine CCL22HumansMiceMice, Inbred C57BLPeriapical DiseasesReceptors, CCR4T-Lymphocytes, RegulatoryCcl22 protein, mouseCcr4 protein, mouseChemokine CCL22Receptors, CCR4Apical lesionscytokinesregulatory T cellsT helperwound healing

Identifiers

PMID26589811
PMCPMC4690748
OpenAlexW2211122879

What OpenQuestion holds

Textmetadata
LicenceTDM
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.