Evidence map›Paper›PMID 32763436›Full record

ArticleJournal of endodontics2020

Immunomodulation Mediated by Azithromycin in Experimental Periapical Inflammation.

Ana Cristina Andrada, Mariane Maffei Azuma, Hisako Furusho, Kimito Hirai, Shuang Xu, Robert R White, Hajime Sasaki

Open access · greenAbstract read
In one paragraph

Article in Journal of endodontics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

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  11. Next-generation biomaterials for dental pulp tissue immunomodulation.Dental materials : official publication of the Academy of Dental Materials · 2023
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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 6 institutions in 2 countries.

Ana Cristina AndradaDivision of Endodontics, Department of Essentials and Simulation, University of Detroit Mercy School of Dentistry, Detroit, Michigan; Division of Endodontics, Department of Restorative Dentistry and Biomaterials Sciences, Harvard School of Dental Medicine, Boston, Massachusetts.
Mariane Maffei AzumaDepartment of Cariology, Restorative Sciences and Endodontics, University of Michigan School of Dentistry, Ann Arbor, Michigan 48109.
Hisako FurushoDepartment of Oral and Maxillofacial Pathobiology, Hiroshima University, Hiroshima, Japan.
Kimito HiraiDepartment of Cariology, Restorative Sciences and Endodontics, University of Michigan School of Dentistry, Ann Arbor, Michigan 48109; Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, Massachusetts; Department of Periodontics and Endodontics, Okayama University School of Dentistry, Kitaku, Okayama, Japan.
Shuang XuDepartment of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, Massachusetts; Functional Genomics Laboratory, Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Robert R WhiteDivision of Endodontics, Department of Restorative Dentistry and Biomaterials Sciences, Harvard School of Dental Medicine, Boston, Massachusetts.
Hajime SasakiDepartment of Cariology, Restorative Sciences and Endodontics, University of Michigan School of Dentistry, Ann Arbor, Michigan 48109; Department of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, Massachusetts; Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, Boston, Massachusetts. Electronic address: hajimes@umich.edu.
Brigham and Women's Hospital · USHarvard University · USHiroshima University · JPOkayama University · JPUniversity of Detroit Mercy · USUniversity of Michigan · US

Funding

Functional role of Serum Amyloid A in periapical inflammationR01DE024796 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SASAKI, HAJIME · 2015 to 2020
$2.1M
HIF-1alpha Mediated Wound Healing in Periapical LesionR21DE023178 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI SASAKI, HAJIME · 2013 to 2014
$542k
MicroCT Core Facility in the Forsyth InstituteS10RR027553 · NCRR · ADA FORSYTH INSTITUTE, INC. · PI SASAKI, HAJIME · 2010 to 2010
$295k
NCRR NIH HHS S10 RR027553NIDCR NIH HHS R01 DE024796NIDCR NIH HHS R21 DE023178
6 · The paper itself

Abstract

introductionThe purpose of the present study was to compare the immunomodulatory effect of azithromycin (AZM), ampicillin (AMP), amoxicillin (AMX), and clindamycin (CLI) in vitro and AZM on preexisting periapical lesions compared with AMP.

methodsThe susceptibility of 4 common human endodontic pathogens (Parvimonas micra, Streptococcus intermedius, Prevotella intermedia, and Fusobacterium nucleatum) to AZM, AMP, AMX, and CLI was confirmed by agar disk diffusion assay. Preexisting periapical lesions in C57BL/6J mice were treated with AZM, AMP, or phosphate-buffered saline (PBS). Periapical bone healing and the pattern of inflammatory cell infiltration were evaluated after a 10-day treatment by micro-computed tomographic and histology, respectively. Besides, the effect of antibiotics in pathogen-stimulated nuclear factor kappa B activation and the production of interleukin 1 alpha and tumor necrosis factor alpha was assessed in vitro by luciferase assay and enzyme-linked immunosorbent assay.

resultsAll examined endodontic pathogens were susceptible to AZM, AMP, AMX, and CLI. AZM significantly attenuated periapical bone loss versus PBS. PBS resulted in widely diffused infiltration of mixed inflammatory cells. By contrast, AZM brought about localized infiltration of neutrophils and M2 macrophages and advanced fibrosis. Although the effect of AMP on bone was uncertain, inflammatory cell infiltration was considerably milder than PBS. However, most macrophages observed seemed to be M1 macrophages. AZM suppressed pathogen-stimulated nuclear factor kappa B activation and cytokine production, whereas AMP, AMX, and CLI reduced only cytokine production moderately.

conclusionsThis study showed that AZM led to the resolution of preexisting experimental periapical inflammation. Our data provide a perspective on host response in antibiotic selection for endodontic treatment. However, well-designed clinical trials are necessary to better elucidate the benefits of AZM as an adjunctive therapy for endodontic treatment when antibiotic therapy is recommended. Although both AZM and AMP were effective on preexisting periapical lesions, AZM led to advanced wound healing, probably depending on its immunomodulatory effect.

Indexed as

Anti-Bacterial AgentsAzithromycinAnimalsBacillotaImmunomodulationInflammationMiceMice, Inbred C57BLAnti-Bacterial AgentsAzithromycinAmpicillinazithromycinendodontic infectionimmunomodulationperiapical periodontitis

Identifiers

PMID32763436
PMCPMC7862415
OpenAlexW3047442873

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.