Evidence map›Paper›PMID 26553466›Full record

ArticleInfection and immunity2016

Accumulation of Regulatory T Cells and Chronic Inflammation in the Middle Ear in a Mouse Model of Chronic Otitis Media with Effusion Induced by Combined Eustachian Tube Blockage and Nontypeable Haemophilus influenzae Infection.

Takashi Hirano, Satoru Kodama, Toshiaki Kawano, Masashi Suzuki

Open access · hybridAbstract read
In one paragraph

Article in Infection and immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Frontiers in bioengineering and biotechnology · 2022
    Article
  4. Article
  5. Panel 7 - Pathogenesis of otitis media - a review of the literature between 2015 and 2019.International journal of pediatric otorhinolaryngology · 2020
    Review
  6. Panel 1: Biotechnology, biomedical engineering and new models of otitis media.International journal of pediatric otorhinolaryngology · 2020
    Review
  7. Cellular Immune Response against NontypeableInfection and immunity · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. The Role of Regulatory T Cell in NontypeableMediators of inflammation · 2018
    Article
  12. Review
  13. Review
  14. Article
  15. 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

4 authors at 1 institution in 1 country.

Takashi HiranoDepartment of Otolaryngology, Faculty of Medicine, Oita University, Oita, Japan thirano@oita-u.ac.jp suzukim@oita-u.ac.jp.
Satoru KodamaDepartment of Otolaryngology, Faculty of Medicine, Oita University, Oita, Japan.
Toshiaki KawanoDepartment of Otolaryngology, Faculty of Medicine, Oita University, Oita, Japan.
Masashi SuzukiDepartment of Otolaryngology, Faculty of Medicine, Oita University, Oita, Japan thirano@oita-u.ac.jp suzukim@oita-u.ac.jp.
Oita University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nontypeable Haemophilus influenzae (NTHi) is associated with chronic otitis media (COM). In this study, we generated a murine model of COM by using eustachian tube (ET) obstruction and NTHi (10(7) CFU) inoculation into the tympanic bulla, and we investigated the relationship between regulatory T cells (Treg) and chronic inflammation in the middle ear. Middle ear effusions (MEEs) and middle ear mucosae (MEM) were collected at days 3 and 14 and at 1 and 2 months after inoculation. Untreated mice served as controls. MEEs were used for bacterial counts and to measure the concentrations of cytokines. MEM were collected for histological evaluation and flow cytometric analysis. Inflammation of the MEM was prolonged throughout this study, and the incidence of NTHi culture-positive MEE was 38% at 2 months after inoculation. The levels of interleukin-1β (IL-β), tumor necrosis factor alpha, IL-10, and transforming growth factor β were increased in the middle ear for up to 2 months after inoculation. CD4(+) CD25(+) FoxP3(+) Treg accumulated in the middle ear, and the percentage of Treg in the MEM increased for up to 2 months after inoculation. Treg depletion induced a 99.9% reduction of bacterial counts in MEEs and also significantly reduced the ratio of NTHi culture-positive MEE. The levels of these cytokines were also reduced in MEEs. In summary, we developed a murine model of COM, and our findings indicate that Treg confer infectious tolerance to NTHi in the middle ear.

Indexed as

AnimalsChronic DiseaseDisease Models, AnimalEar, MiddleEustachian TubeHaemophilus InfectionsHaemophilus influenzaeInflammationInterleukin-10Interleukin-1betaLymphocyte CountMiceMice, Inbred BALB CMucous MembraneOtitis Media with EffusionT-Lymphocytes, RegulatoryIL10 protein, mouseIL1B protein, mouseInterleukin-10Interleukin-1betaTransforming Growth Factor betaTumor Necrosis Factor-alpha

Identifiers

PMID26553466
PMCPMC4694021
OpenAlexW2284230430

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.