Evidence map›Paper›PMID 39127869›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2024

IL-35 promotes IL-35

Fatemeh Saheb Sharif-Askari, Adel M Zakri, Maha Fahad Alenazy, Mohammed S El-Wetidy, Baraa Khalid Salah Al-Sheakly, Narjes Saheb Sharif-Askari, Roua M ALKufeidy, Mohammed A Omair, Saleh Al-Muhsen, Rabih Halwani

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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2024. 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
–field-weighted citation impact
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.

  1. Review
  2. IL-27-DependentInternational journal of molecular sciences · 2026
    Article
  3. The role and mechanism of IL‑35 in myasthenia gravis (Review).International journal of molecular medicine · 2026
    Review
  4. Article
  5. Review
  6. T Regulatory Mechanisms in Airway and Interstitial Lung Disease.Seminars in respiratory and critical care medicine · 2025
    Review
  7. Review
  8. Review
  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.

Fatemeh Saheb Sharif-Askari *Sharjah Institute for Medical Research, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Adel M Zakri *Department of Plant Production, Faculty of Agriculture and Food Sciences, King Saud University, Riyadh, Saudi Arabia.
Maha Fahad AlenazyImmunology Research Lab, Department of Pediatrics, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Mohammed S El-WetidyCollege of Medicine Research Center, King Saud University, Riyadh, Saudi Arabia.
Baraa Khalid Salah Al-SheaklySharjah Institute for Medical Research, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Narjes Saheb Sharif-AskariSharjah Institute for Medical Research, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Roua M ALKufeidyPrince Naif Center for Immunology Research and Asthma Research Chair, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Mohammed A OmairRheumatology Unit, Department of Medicine, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Saleh Al-MuhsenImmunology Research Laboratory, Department of Pediatrics, College of Medicine and King Saud University Medical City , King Saud University, Riyadh, Saudi Arabia.
Rabih HalwaniSharjah Institute for Medical Research, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates. rhalwani@sharjah.ac.ae.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThis study aimed to investigate the effect of interleukin-35 (IL-35) on inflamed lung tissue in a murine model of asthma. IL-35 was examined for its potential to induce regulatory lymphocytes during ovalbumin (OVA)-induced acute lung injury.

methodsFemale BALB/c mice sensitized with OVA and were treated with recombinant IL-35 (rIL-35) via intranasal or intraperitoneal routes and were administered 4 h before OVA challenge. The effects of rIL-35 treatment on the lung and blood levels of regulatory B cells (Bregs) and regulatory T cells (Tregs), as well as their production of immunosuppressive cytokines, were determined using flow cytometry and enzyme-linked immunosorbent assay (ELISA), respectively.

resultsTreatment of OVA-sensitized asthmatic mice with rIL-35, whether administered intranasally or intraperitoneally, resulted in reduced lung inflammation and injury. This reduction was accompanied by an increase in the frequency of IL-35 producing Bregs, IL-35 and IL-10 producing Bregs, and conventional LAG3

conclusionsThe results of this study suggest that IL-35, through its ability to increase Bregs and Tregs, is effective in reversing lung inflammation in the context of asthma. Since the increase was more pronounced with intranasal administration, this highlights the therapeutic potential of its local intrapulmonary application in managing asthma-related inflammation.

Indexed as

AsthmaB-Lymphocytes, RegulatoryInterleukin-10InterleukinsLungMice, Inbred BALB COvalbuminT-Lymphocytes, RegulatoryAnimalsAntigens, CDFemaleLymphocyte Activation Gene 3 ProteinMiceAntigens, CDIL10 protein, mouseInterleukin-10interleukin-35, mouseInterleukinsLymphocyte Activation Gene 3 ProteinOvalbuminAsthmaIL-17IL-35IL-35+ IL-10+ BregLAG3+ Treg

Identifiers

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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.