Evidence map›Paper›PMID 26488300›Full record

ArticlePloS one2015

CD8+ T Cells Mediate Female-Dominant IL-4 Production and Airway Inflammation in Allergic Asthma.

Chihiro Ito, Kaori Okuyama-Dobashi, Tomomitsu Miyasaka, Chiaki Masuda, Miki Sato, Tasuku Kawano, Yuichi Ohkawara, Toshiaki Kikuchi, Motoaki Takayanagi, Isao Ohno

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. T-cell responses in asthma exacerbations.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2022
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Herbal MedicineEvidence-based complementary and alternative medicine : eCAM · 2016
    Article
  9. 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

10 authors at 2 institutions in 1 country.

Chihiro ItoDepartment of Pathophysiology, Tohoku Pharmaceutical University, Miyagi, Japan.
Kaori Okuyama-DobashiDepartment of Pathophysiology, Tohoku Pharmaceutical University, Miyagi, Japan.
Tomomitsu MiyasakaDepartment of Pathophysiology, Tohoku Pharmaceutical University, Miyagi, Japan.
Chiaki MasudaDepartment of Pathophysiology, Tohoku Pharmaceutical University, Miyagi, Japan.
Miki SatoDepartment of Pathophysiology, Tohoku Pharmaceutical University, Miyagi, Japan.
Tasuku KawanoDepartment of Pathophysiology, Tohoku Pharmaceutical University, Miyagi, Japan.
Yuichi OhkawaraDepartment of Pathophysiology, Tohoku Pharmaceutical University, Miyagi, Japan.
Toshiaki KikuchiDepartment of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Motoaki TakayanagiDepartment of Pathophysiology, Tohoku Pharmaceutical University, Miyagi, Japan.
Isao OhnoDepartment of Pathophysiology, Tohoku Pharmaceutical University, Miyagi, Japan.
Tohoku Medical and Pharmaceutical University · JPNiigata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prevalence and severity of bronchial asthma are higher in females than in males after puberty. Although antigen-specific CD8+ T cells play an important role in the development of asthma through their suppressive effect on cytokine production, the contribution of CD8+ T cells to sex differences in asthmatic responses remains unclear. In the present study, we investigated the sex-specific effect of CD8+ T cells in the suppression of asthma using an ovalbumin mouse model of asthma. The number of inflammatory cells in bronchoalveolar lavage (BAL) fluid, lung type 2 T-helper cytokine levels, and interleukin-4 (IL-4) production by bronchial lymph node cells were significantly higher in female wild-type (WT) mice compared with male mice, whereas no such sex differences were observed between male and female cd8α-disrupted mice. The adaptive transfer of male, but not female, CD8+ T cells reduced the number of inflammatory cells in the recovered BAL fluid of male recipient mice, while no such sex difference in the suppressive activity of CD8+ T cells was observed in female recipient mice. Male CD8+ T cells produced higher levels of IFN-γ than female CD8+ T cells did, and this trend was associated with reduced IL-4 production by male, but not female, CD4+ T cells. Interestingly, IFN-γ receptor expression on CD4+ T cells was significantly lower in female mice than in male mice. These results suggest that female-dominant asthmatic responses are orchestrated by the reduced production of IFN-γ by CD8+ T cells and the lower expression of IFN-γ receptor on CD4+ T cells in females compared with males.

Indexed as

Adoptive TransferAnimalsAsthmaBronchoalveolar Lavage FluidCD4-Positive T-LymphocytesCD8 AntigensCD8-Positive T-LymphocytesFemaleInterferon-gammaInterferon gamma ReceptorInterleukin-4LungLymph NodesMaleMiceMice, Inbred C57BLCD8alpha antigenCD8 AntigensInterferon-gammaInterferon gamma ReceptorInterleukin-4OvalbuminReceptors, Interferon

Identifiers

PMID26488300
PMCPMC4619475
OpenAlexW2168049552

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.