Evidence map›Paper›PMID 35860254›Full record

ArticleFrontiers in immunology2022

Increased Development of Th1, Th17, and Th1.17 Cells Under T1 Polarizing Conditions in Juvenile Idiopathic Arthritis.

Anna E Patrick, Kayla Shoaff, Tashawna Esmond, David M Patrick, David K Flaherty, T Brent Graham, Philip S Crooke, Susan Thompson, Thomas M Aune

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. 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
2.9field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Anna E PatrickDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, United States.
Kayla ShoaffDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, United States.
Tashawna EsmondDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
David M PatrickDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
David K FlahertyOffice of Research (OOR) Shared Resources Department, Vanderbilt University Medical Center, Nashville, TN, United States.
T Brent GrahamDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, United States.
Philip S CrookeDepartment of Mathematics, Vanderbilt University, Nashville, TN, United States.
Susan ThompsonDepartment of Pediatrics, Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, United States.
Thomas M AuneDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, United States.
Vanderbilt University Medical Center · USUniversity of Cincinnati · USVanderbilt University · US

Funding

Pediatric Rheumatology Tissue RepostoryP01AR048929 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI GROM, ALEXEI A · 2003 to 2015
$13.6M
Tissue Repository CoreP30AR070549 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI Grant Sanford Schulert · 2016 to 2026
$7.7M
IFN GAMMA GENE REGULATION IN T CELLS AND NK CELLSR01AI044924 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI AUNE, THOMAS M. · 2000 to 2019
$5.8M
Pathogenesis, Targeted Therapeutics, and New Vaccines for Childhood DiseaseK12HD087023 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Michael R. DeBaun, Juan C Salazar · 2016 to 2026
$4.1M
A Role of Isolevuglandin Adducts in Essential Hypertension and Systemic Lupus ErythematosusK08HL153789 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PATRICK, DAVID · 2020 to 2021
$317k
NHLBI NIH HHS K08 HL153789NIAID NIH HHS R01 AI044924NIAMS NIH HHS P01 AR048929NIAMS NIH HHS P30 AR070549NICHD NIH HHS K12 HD087023
6 · The paper itself

Abstract

In juvenile idiopathic arthritis (JIA) inflammatory T cells and their produced cytokines are drug targets and play a role in disease pathogenesis. Despite their clinical importance, the sources and types of inflammatory T cells involved remain unclear. T cells respond to polarizing factors to initiate types of immunity to fight infections, which include immunity types 1 (T1), 2 (T2), and 3 (T17). Polarizing factors drive CD4

Indexed as

Arthritis, JuvenileInterleukin-17CD8-Positive T-LymphocytesChildCytokinesHumansLeukocytes, MononuclearNuclear Receptor Subfamily 1, Group F, Member 3Th1 CellsCytokinesInterleukin-17Nuclear Receptor Subfamily 1, Group F, Member 3interferon gamma (IFNγ)interleukin 17 (IL-17)juvenile idiopathic arthritis (JIA)T cellTh1.17Th17Th1 polarizationT helper cell (Th)

Identifiers

PMID35860254
PMCPMC9290377
OpenAlexW4283803161

What OpenQuestion holds

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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 OpenQuestion graph.