Evidence map›Paper›PMID 29567043›Full record

ArticleJournal of immunological methods2018

Intravital endoscopic technology for real-time monitoring of inflammation caused in experimental periodontitis.

Alexandru Movila, Mikihito Kajiya, Wichaya Wisitrasameewong, Philip Stashenko, Saynur Vardar-Sengul, Maria Hernandez, H Thomas Temple, Toshihisa Kawai

Abstract read
In one paragraph

Article in Journal of immunological methods, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

8 authors at 3 institutions in 2 countries.

Alexandru MovilaThe Forsyth Institute, Department of Immunology, Cambridge, MA, USA; Harvard University School of Dental Medicine, Department of Oral Medicine, Infection, and Immunity, Boston, MA, USA; Nova Southeastern University, College of Dental Medicine, Fort Lauderdale, FL, USA. Electronic address: amovila@nova.edu.
Mikihito KajiyaThe Forsyth Institute, Department of Immunology, Cambridge, MA, USA.
Wichaya WisitrasameewongChulalongkorn University, Faculty of Dentistry, Department of Periodontology, Bangkok, Thailand.
Philip StashenkoHarvard University School of Dental Medicine, Department of Oral Medicine, Infection, and Immunity, Boston, MA, USA.
Saynur Vardar-SengulNova Southeastern University, College of Dental Medicine, Fort Lauderdale, FL, USA.
Maria HernandezNova Southeastern University, College of Dental Medicine, Fort Lauderdale, FL, USA.
H Thomas TempleNova Southeastern University, College of Allopathic Medicine, Fort Lauderdale, FL, USA.
Toshihisa KawaiNova Southeastern University, College of Dental Medicine, Fort Lauderdale, FL, USA.
Nova Southeastern University · USHarvard University · USChulalongkorn University · TH

Funding

REGULATORY CELLS IN EXPERIMENTAL PERIODONTAL DISEASER01DE003420 · NIDCR · FORSYTH INSTITUTE · PI KAWAI, TOSHIHISA · 1985 to 2012
$4.3M
Programming dendritic cells in concert with morphagen delivery for periodontal reR01DE019917 · NIDCR · HARVARD UNIVERSITY · PI KAWAI, TOSHIHISA, MOONEY, DAVID J · 2009 to 2013
$3.5M
T-Regulatory Cells in PeriodontitisR01DE018499 · NIDCR · ADA FORSYTH INSTITUTE, INC. · PI KAWAI, TOSHIHISA · 2008 to 2011
$1.9M
Effects of aging on MIF-mediated migration of circulating osteoclast precursors to particle-induced osteolysis lesionsR03AG053615 · NIA · NOVA SOUTHEASTERN UNIVERSITY · PI MOVILA, ALEXANDRU · 2017 to 2018
$173k
REGULATORY CELLS IN EXPERIMENTAL PERIODONTAL DISEASER37DE003420 · NIDCR · FORSYTH INSTITUTE · PI TAUBMAN, MARTIN A · 1990 to 1999
–
NIA NIH HHS R03 AG053615NIDCR NIH HHS R01 DE003420NIDCR NIH HHS R01 DE018499NIDCR NIH HHS R01 DE019917NIDCR NIH HHS R37 DE003420
6 · The paper itself

Abstract

We report a novel method for in situ imaging of microvascular permeability in inflamed gingival tissue, using state-of-the-art Cellvizio™ intravital endoscopic technology and a mouse model of ligature-induced periodontitis. The silk ligature was first placed at the upper left second molar. Seven days later, the ligature was removed, and the animals were intravenously injected with Evans blue. Evans blue dye, which selectively binds to blood albumin, was used to monitor the level of inflammation by monitoring vascular permeability in control non-diseased and ligature-induced experimental periodontitis tissue. More specifically, leakage of Evans blue-bound albumin from the micro-capillary to connective tissue indicates the state of inflammation occurring in the specific site. Evans blue leakage from blood vessels was imaged in situ by directly attaching the endoscope (mini Z tip) of the Cellvizio™ system to the gingival tissue without any surgical incision. Evans blue emission intensity was significantly elevated in gingiva of periodontitis lesions, but not control non-ligature placed gingiva, indicating that this technology can be used as a potential minimally invasive diagnostic tool to monitor the level of inflammation at the periodontal disease site.

Indexed as

AnimalsDisease Models, AnimalEndoscopyEvans BlueGingivaIntravital MicroscopyLigationMaleMiceMice, Inbred C57BLPeriodontitisVasculitisEvans Blue

Identifiers

PMID29567043
PMCPMC5924649
OpenAlexW2790345580

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.