Evidence map›Paper›PMID 32518420›Full record

ArticleGenes and immunity2020

The contribution from interleukin-27 towards rheumatoid inflammation: insights from gene expression.

Melanie J Millier, Kira Lazaro, Lisa K Stamp, Paul A Hessian

Abstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Plasma interleukin-23 and circulating IL-17AArthritis research & therapy · 2022
    Article
  5. Article
  6. Review
  7. 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

4 authors at 1 institution in 1 country.

Melanie J MillierDepartment of Medicine, University of Otago Dunedin, Dunedin, New Zealand.
Kira LazaroDepartment of Medicine, University of Otago Dunedin, Dunedin, New Zealand.
Lisa K StampDepartment of Medicine, University of Otago Christchurch, Christchurch, New Zealand.
Paul A HessianDepartment of Medicine, University of Otago Dunedin, Dunedin, New Zealand. paul.hessian@otago.ac.nz.ORCID http://orcid.org/0000-0001-6972-1242
University of Otago · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to assess expression of genes encoding the heterodimeric IL-27 cytokine and constituent subunits of the Il-27 receptor in rheumatoid arthritis (RA), including in extra-articular, subcutaneous rheumatoid nodules. Comparing between nodules and joint synovia, significantly elevated expression of IL27A within nodules, and comparable IL27B expression, identified nodules as a significant source of IL-27 in RA. T-lymphocytes were the main source of IL27RA transcript, and IL27RA expression correlated with a number of plasma cytokines, as well as tissue TNF expression in both nodules and RA synovia. In synovia, correlations between IL27A, IL27RA IL17A and CD21L expression, and significantly elevated expression of the genes encoding IL-27, associated the presence of IL-27 with B cell-dominated synovial inflammation. Impact from nodule derived IL-27 on systemic or synovial inflammation in RA remains unknown and further study of these implications is required. Our study raises questions regarding the appropriate circumstances for the blockade or administration of IL-27 as a potential therapeutic adjunct in RA.

Indexed as

AgedArthritis, RheumatoidB-LymphocytesFemaleGene ExpressionHumansInflammationInterleukin-17InterleukinsMaleMiddle AgedReceptors, Complement 3dRheumatoid NoduleSynovial MembraneIL17A protein, humanInterleukin-17InterleukinsMYDGF protein, humanReceptors, Complement 3d

Identifiers

PMID32518420
OpenAlexW3034020222

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.