Evidence map›Paper›PMID 31736959›Full record

ReviewFrontiers in immunology2019

Biology of IL-36 Signaling and Its Role in Systemic Inflammatory Diseases.

Zhi-Chao Yuan, Wang-Dong Xu, Xiao-Yan Liu, Xing-You Liu, An-Fang Huang, Lin-Chong Su

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing 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

75 citing papers in PubMed.

  1. Review
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  11. Review
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  16. Article
  17. IL-36/IL-36R signaling promotes CD4Frontiers in immunology · 2025
    Article
  18. Review
  19. Article
  20. Review

15 more citing papers are in PubMed but not listed here.

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

6 authors.

Zhi-Chao YuanDepartment of Evidence-Based Medicine, School of Public Health, Southwest Medical University, Luzhou, China.
Wang-Dong XuDepartment of Evidence-Based Medicine, School of Public Health, Southwest Medical University, Luzhou, China.
Xiao-Yan LiuDepartment of Nutrition and Food Hygiene, School of Public Health, Southwest Medical University, Luzhou, China.
Xing-You LiuSchool of Traditional Chinese Medicine, Southwest Medical University, Luzhou, China.
An-Fang HuangDepartment of Rheumatology and Immunology, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Lin-Chong SuDepartment of Rheumatology and Immunology, Minda Hospital of Hubei Minzu University, Enshi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin (IL)-36 is a member of the IL-1 superfamily and includes three agonists (IL-36α, IL-36β, and IL-36γ) and an antagonist (IL-36Ra). IL-36 agonists bind to heterodimeric receptor complexes. Then, the heterotrimer complexes signal via intracellular functional domains, binding to downstream signaling proteins and inducing inflammatory responses. In this review, we summarized the current knowledge about the biological role of IL-36 and its correlation with systemic inflammatory diseases. The information collected will help to increase the understanding of the potential of IL-36 and may give clues for developing novel therapeutic strategies.

Indexed as

AnimalsHumansInterleukin-1Signal TransductionSystemic Inflammatory Response SyndromeIL36A protein, humanIL36B protein, humanIL36G protein, humanInterleukin-1autoimmunitycytokineIL-36immune cellinflammation

Identifiers

PMID31736959
PMCPMC6839525

What OpenQuestion holds

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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.