Evidence map›Paper›PMID 27707583›Full record

ArticleAllergology international : official journal of the Japanese Society of Allergology2017

Intranasal administration of IL-35 inhibits allergic responses and symptoms in mice with allergic rhinitis.

Motohiko Suzuki, Makoto Yokota, Yoshihisa Nakamura, Shinya Ozaki, Shingo Murakami

Open access · goldAbstract read
In one paragraph

Article in Allergology international : official journal of the Japanese Society of Allergology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Taurine promotes the production of CD4Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2021
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Regulatory T Cells in Allergy and Asthma.Frontiers in pediatrics · 2017
    Review
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

5 authors at 1 institution in 1 country.

Motohiko SuzukiDepartment of Otorhinolaryngology, Nagoya City University, Aichi, Japan. Electronic address: suzu-mo@med.nagoya-cu.ac.jp.
Makoto YokotaDepartment of Otorhinolaryngology, Nagoya City University, Aichi, Japan.
Yoshihisa NakamuraDepartment of Otorhinolaryngology, Nagoya City University, Aichi, Japan.
Shinya OzakiDepartment of Otorhinolaryngology, Nagoya City University, Aichi, Japan.
Shingo MurakamiDepartment of Otorhinolaryngology, Nagoya City University, Aichi, Japan.
Nagoya City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIL-35 was recently identified as an anti-inflammatory cytokine. We previously reported that recombinant fusion protein of murine IL-35 and human IgG1 Fc fragment (rIL-35) reduced Th2 cytokines (IL-4 and IL-5) in vitro. However, it is unclear whether IL-35 can attenuate nasal allergic responses and symptoms of allergic rhinitis in vivo.

methodsTo investigate the in vivo effect of IL-35 on allergic rhinitis in mice, mice were sensitized with ovalbumin (OVA). Intranasal administration of rIL-35 and intranasal challenge of OVA were then performed. Nasal symptoms were estimated after the last nasal challenge. Nasal tissue and cervical lymph nodes (CLN) were collected. OVA-specific IgE in sera, OVA-specific T cell response, and the production of cytokines (IL-4, IL-5, and IL-10) stimulated by the OVA antigen were measured. The transcription level of Foxp3 and the frequency of CD4

resultsrIL-35 significantly inhibited the number of sneezes and nasal rubbing movements. It also reduced the number of eosinophils in the nasal mucosa and significantly decreased the level of OVA-specific IgE, the OVA-specific T cell proliferation, and the production of IL-4 and IL-5. Furthermore, rIL-35 significantly increased the production of IL-10, the transcription level of Foxp3, and the frequency of CD4

conclusionsThis study showed for the first time that rIL-35 inhibits nasal allergic responses and symptoms in mice, and that rIL-35 increases IL-10, Foxp3, and CD4

Indexed as

PhenotypeAdministration, IntranasalAnimalsCytokinesDisease Models, AnimalImmunoglobulin EImmunoglobulin GInterleukinsLymphocyte ActivationMaleMiceNasal MucosaRecombinant Fusion ProteinsRhinitis, AllergicT-Lymphocyte SubsetsTreatment OutcomeCytokinesImmunoglobulin EImmunoglobulin Ginterleukin-35, mouseInterleukinsRecombinant Fusion ProteinsAllergic rhinitisCervical lymph nodeIL-10IL-35Regulatory T cell

Identifiers

PMID27707583
PMCPMC7130026
OpenAlexW2529144892

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.