Evidence map›Paper›PMID 30949175›Full record

ReviewFrontiers in immunology2019

Pleiotropic Effects of IL-33 on CD4

Fernando Alvarez, Jörg H Fritz, Ciriaco A Piccirillo

Open access · goldAbstract 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 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 77 citations in OpenAlex.

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  16. The role of IL-33/ST2 signaling in the tumor microenvironment and Treg immunotherapy.Experimental biology and medicine (Maywood, N.J.) · 2022
    Review
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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

3 authors at 1 institution in 1 country.

Fernando AlvarezDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Jörg H FritzDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
Ciriaco A PiccirilloDepartment of Microbiology and Immunology, McGill University, Montréal, QC, Canada.
McGill University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IL-33, a member of the IL-1 family of cytokines, was originally described in 2005 as a promoter of type 2 immune responses. However, recent evidence reveals a more complex picture. This cytokine is released locally as an alarmin upon cellular damage where innate cell types respond to IL-33 by modulating their differentiation and influencing the polarizing signals they provide to T cells at the time of antigen presentation. Moreover, the prominent expression of the IL-33 receptor, ST2, on GATA3

Indexed as

Lymphocyte ActivationCell DifferentiationGene Expression RegulationHumansInterleukin-33Organic Cation Transport ProteinsT-Lymphocytes, Helper-InducerIL33 protein, humanInterleukin-33Organic Cation Transport ProteinsSLC22A16 protein, humanIL-33immunoregulationinfectionST2T cell differentiationTh17 and Tregs cellsth1/th2 balance

Identifiers

PMID30949175
PMCPMC6435597
OpenAlexW2923908603

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.