Evidence map›Paper›PMID 38066380›Full record

ArticleImmunologic research2024

Long non-coding RNA ENSMUST00000197208 promotes a shift in the Th17/Treg ratio via the P2X7R-NLRP3 inflammasome axis in collagen-induced arthritis.

Yuting Pan, Yan Wu, Yingying Liu, Panpan Wang, Hui Huang, Jing Jin, Yuying Fang, Shuoyin Huang, Zhidan Fan, Haiguo Yu

Abstract read
PubMed Publisher
In one paragraph

Article in Immunologic research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  3. An anti-complement homogeneous polysaccharide fromActa pharmaceutica Sinica. B · 2025
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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

10 authors at 2 institutions in 1 country.

Yuting PanDepartment of Rheumatology and Immunology, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China.
Yan WuDepartment of Child Health Care, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China.
Yingying LiuDepartment of Rheumatology and Immunology, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China.
Panpan WangDepartment of Rheumatology and Immunology, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China.
Hui HuangDepartment of Rheumatology and Immunology, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China.
Jing JinDepartment of Rheumatology and Immunology, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China.
Yuying FangDepartment of Rheumatology and Immunology, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China.
Shuoyin HuangDepartment of Rheumatology and Immunology, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China.
Zhidan Fan *Department of Rheumatology and Immunology, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China. zhidan1728@163.com.
Haiguo Yu *Department of Rheumatology and Immunology, Children's Hospital of Nanjing Medical University, Nanjing, 210008, China. haiguo_yu@njmu.edu.cn.ORCID 0000-0002-6836-421X
Second Affiliated Hospital of Nanjing Medical University · CNNanjing Children's Hospital · CN

Funding

National Key R&D Program of China 2021YFC2702003National Natural Science Foundation of China 81202345National Natural Science Foundation of China 81771762Project of the Jiangsu Provincial Health Commission M2021080Project of the Nanjing Municipal Health Commission YKK21144
6 · The paper itself

Abstract

Recently, long non‑coding RNAs (lncRNAs) have been implicated in several human diseases, including arthritis. However, the role of lncRNAs in regulating the Th17/Treg ratio during the progression of collagen-induced arthritis (CIA) is poorly understood. Therefore, the aim of this study was to determine the role of the lncRNA ENSMUST00000197208 and the P2X7R-NLRP3 inflammasome axis in changes in the Th17/Treg ratio in CIA. To achieve this, the distribution of T cell subgroups in the spleen cells of a CIA mouse model and control mice was examined. Additionally, we examined the expression profile of ENSMUST00000197208 in a CIA mouse model and healthy mice. The results showed that ENSMUST00000197208 expression was significantly upregulated in the CIA models compared with the control group. Additionally, the P2X7R-NLRP3 inflammasome axis participated in the pathogenesis of CIA and knockdown of ENSMUST00000197208 inhibited CD4

Indexed as

Arthritis, ExperimentalMicroRNAsRNA, Long NoncodingAnimalsDisease Models, AnimalHumansInflammasomesMiceNLR Family, Pyrin Domain-Containing 3 ProteinTh17 CellsT-Lymphocytes, RegulatoryInflammasomesMicroRNAsNLR Family, Pyrin Domain-Containing 3 ProteinRNA, Long NoncodingCD4+ T-cell differentiationCollagen-induced arthritislncRNANLRP3P2X7R

Identifiers

PMID38066380
OpenAlexW4389473646

What OpenQuestion holds

Textmetadata
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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.