Evidence map›Paper›PMID 40493320›Full record

ArticleClinical rheumatology2025

LncRNA PVT1 regulates CD4 + T cell dysregulation in systemic lupus erythematosus: insights from human patients and MRL/lpr mouse.

Jiali Zhang, Ying Yuan, Shuangying Ni, Siqi Mu, Wanrong Wang, Feiyang Sun, Bo Liang, Peng Lu, Yue Qiu, Wenhui Du and 10 more

Abstract read
In one paragraph

Article in Clinical rheumatology, 2025. 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
–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

5 citing papers in PubMed.

  1. 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

20 authors.

Jiali Zhang *Institute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0003-3110-0541
Ying Yuan *Institute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0009-0006-0397-2130
Shuangying Ni *Institute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0001-9649-6749
Siqi MuFirst Clinical Medical College, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0009-0002-3991-8137
Wanrong WangFirst Clinical Medical College, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0009-0003-4157-9653
Feiyang SunFirst Clinical Medical College, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0009-0004-3389-6752
Bo LiangInstitute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0003-0267-8184
Peng LuInstitute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0009-0005-3289-3338
Yue QiuInstitute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0009-0007-6938-6326
Wenhui DuInstitute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0001-6474-703X
Chenjun WangDepartment of Dermatology, Shannan People's Hospital, Shannan, China.ORCID http://orcid.org/0009-0001-0363-2762
Huijie DuanDepartment of Dermatology, Shannan People's Hospital, Shannan, China.ORCID http://orcid.org/0009-0009-9519-2239
Zejuan HuDepartment of Dermatology, Shannan People's Hospital, Shannan, China.ORCID http://orcid.org/0009-0003-5055-436X
Leilei WenInstitute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0002-8943-1549
Xiaodong ZhengInstitute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0002-6658-6492
Yujun ShengDepartment of Dermatology, Friendship Hospital, Beijing, China.ORCID http://orcid.org/0000-0002-6022-3359
Shengquan ZhangDepartment of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0001-6098-1208
Shanyu ChenDepartment of Rheumatology and Immunology, The First Affiliated Hospital of Anhui Medical University, Hefei, China.ORCID http://orcid.org/0009-0004-0889-4202
Xueli YinFunctional Experiment Center, School of Basic Medical Sciences, Anhui Medical University, Hefei, China.ORCID http://orcid.org/0000-0002-9869-8288
Zhengwei ZhuInstitute of Dermatology and Department of Dermatology, the First Affiliated Hospital, Anhui Medical University, Hefei, China. ahmuzzw@163.com.ORCID http://orcid.org/0000-0001-9343-8287

Funding

Anhui Provincial Institute of Translational Medicine 2021zhyx-C41Female Center for Scientific and Medical Colleges, King Saud University 2021xkjT048Grants for Scientific Research of BSKY from Anhui Medical University XJ201939Key Laboratory of Dermatology, Anhui Medical University, Ministry of Education, China AYPYS-2023-6National Key R&D Program of China 2022YFC3602000National Natural Science Foundation of China 81803117National Natural Science Foundation of China 82003330National Outstanding Youth Science Fund Project of National Natural Science Foundation of China 2208085Y25Natural Science Foundation of Xizang Autonomous Region XZ2024ZR-ZY064(Z)Science Fund for Distinguished Young Scholars of Anhui Province 1808085QH284The College Students' Innovative Entrepreneurial Training Plan Program 202210366017The key Project of Natural Science Research Projects of Anhui Higher Education Institutions 2022AH050737The Youth Science Foundation of the First Affiliated Hospital of Anhui Medical University 2017kj17
6 · The paper itself

Abstract

objectivesTo investigate the role of lncRNA PVT1 in modulating CD4

methodsMeasured PVT1 and miR-30e-5p expression in SLE patients (n = 65) and healthy controls (HCs) using qRT-PCR. Analyzed Th1/Th2/Th17/Treg cell frequencies by flow cytometry and cytokine levels (IL-2, IL-4, IL-6, IL-17, TGF-β) via ELISA. Constructed lentiviral vectors to silence (SLE + si-Pvt1) or overexpress Pvt1 (SLE + lenti-Pvt1) in MRL/lpr mice (n = 40).

resultsPVT1 was upregulated (p = 0.0488) and miR-30e-5p downregulated (p = 0.0095) in SLE patients. Th2 (p = 0.0165) and Th17 (p = 0.0017) cells exhibited a significant increase, while Th1 and Treg cells decreased. Pvt1 silencing reversed SLE phenotypes, increasing Th1 and Treg cells, reducing Th2 and Th17 cells, restoring IL-2 and TGF-β levels and reducing levels of IL-6 and IL-17. Overexpression of Pvt1 exacerbated disease severity. Pvt1 acted as a ceRNA to sponge miR-30e-5p, modulating T-bet/GATA3/RORγt/Foxp3 expression.

conclusionsPVT1 dysregulation disrupts CD4

Indexed as

CD4-Positive T-LymphocytesLupus Erythematosus, SystemicRNA, Long NoncodingAdultAnimalsCase-Control StudiesCytokinesDisease Models, AnimalFemaleHumansMaleMiceMice, Inbred MRL lprMicroRNAsMiddle AgedT-Lymphocytes, RegulatoryCytokinesMicroRNAsPVT1 long-non-coding RNA, humanPVT1 long-non-coding RNA, mouseRNA, Long NoncodingCD4+T cellsLncRNA PVT1MiRNA-30e-5pMRL/lpr miceSystemic lupus erythematosus (SLE)

Identifiers

PMID40493320
PMCPMC12234576

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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.