Evidence map›Paper›PMID 30258726›Full record

ArticlePeerJ2018

Interleukin 35 induced Th2 and Tregs bias under normal conditions in mice.

Xiaoning Zhang, Zhiqiang Zhang, Zhiqiang He, Mingyan Ju, Jiaci Li, Jinghua Yuan, Yaqing Jing, Keqiu Li, Yi Liu, Guang Li

Abstract read
In one paragraph

Article in PeerJ, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Clinical characteristics and decreased CD4Frontiers in immunology · 2026
    Article
  2. Article
  3. Immunomodulatory cytokine interleukin-35 and immune thrombocytopaenia.The Journal of international medical research · 2020
    Review
  4. IL-35 inhibits CD8Translational cancer research · 2019
    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

10 authors.

Xiaoning Zhang *Department of Genetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Zhiqiang Zhang *Department of Pathology, Tianjin Hospital of ITCWM, Nankai Hospital, Tianjin, China.
Zhiqiang HeDepartment of Genetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Mingyan JuDepartment of Genetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Jiaci LiDepartment of Genetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Jinghua YuanDepartment of Genetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Yaqing JingDepartment of Genetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Keqiu LiDepartment of Genetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Yi LiuDepartment of Genetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.
Guang LiDepartment of Genetics, School of Basic Medical Sciences, Tianjin Medical University, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe benefits of IL-35 treatment have been verified in multiple animal models of diseases, while its influence on T cells immunity under normal condition still needs to be elucidated. The present study was designed to investigate the effects modulating IL-35 levels

methodsA plasmid pMSCV-IL-35-GFP carrying mouse linear IL-35 fragment with two subunits joint together was constructed and the heterodimer expression was confirmed. Normal mice were randomly divided into three groups and received an intravenous injection of PBS, pMSCV-GFP and pMSCV-IL-35-GFP respectively. After 72 h, spleen tissues and peripheral blood were harvested for following analysis. Meanwhile, splenic T cells were isolated and incubated with 10, 30, or 50 ng/mL recombinant IL-35 factor for 24 h with the addition of anti-CD3/CD28

resultsWestern blotting confirmed a 52 kDa band in the cell lysate of HEK 293T transducted with pMSCV-IL-35-GFP plasmid, indicating a successful expression of IL-35. Ebi3 and IL-12A, two subunits of IL-35, could be identified 72 h post DNA injection. IL-35 upregulation

conclusionThe results indicated Th1 and CD8

Indexed as

CytokinesHelper T cellsInterleukin 35Regulatory T cellsT-cell subsets

Identifiers

PMID30258726
PMCPMC6152461

What OpenQuestion holds

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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.