Evidence map›Paper›PMID 31511645›Full record

ArticleCellular & molecular immunology2020

The transcription factor Zfp281 sustains CD4

Jing Guo, Zhonghui Xue, Ruoyu Ma, Weiwei Yi, Zhaoyuan Hui, Yixin Guo, Yuxi Yao, Wenqiang Cao, Jianli Wang, Zhenyu Ju and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular & molecular immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Zfp281 and Zfp148 control CD4Science immunology · 2023
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Bioengineered · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. 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

12 authors at 4 institutions in 1 country.

Jing Guo *Institute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Zhonghui Xue *Institute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Ruoyu MaInstitute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Weiwei YiInstitute of Aging Research, Hangzhou Normal University School of Medicine, Hangzhou, China.
Zhaoyuan HuiInstitute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yixin GuoInstitute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yuxi YaoInstitute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Wenqiang CaoInstitute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.ORCID http://orcid.org/0000-0002-5024-0817
Jianli WangInstitute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Zhenyu JuKey Laboratory of Regenerative Medicine of Ministry of Education, Institute of Aging and Regenerative Medicine, Jinan University, Guangzhou, China.
Linrong LuInstitute of Immunology, Zhejiang University School of Medicine, Hangzhou, China.ORCID http://orcid.org/0000-0002-0171-4115
Lie WangInstitute of Immunology, and Bone Marrow Transplantation Center, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. wanglie@zju.edu.cn.
First Affiliated Hospital Zhejiang University · CNHangzhou Normal University · CNJinan University · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of coinhibitory receptors, such as CTLA-4, on effector T cells is a key mechanism for the negative regulation of T-cell activation. However, the transcriptional regulation of CTLA-4 is not well understood. Zfp281, a C2H2 zinc finger protein, is a negative regulator of pluripotency maintenance of embryonic stem cells. Nevertheless, the function of Zfp281 in differentiated cells has not been studied. We generated Zfp281 conditional knockout mice in which the function of the Zfp281 gene was conditionally disrupted by the Cd4

Indexed as

Transcription, GeneticAnimalsCD4-Positive T-LymphocytesCTLA-4 AntigenCytokinesGene Expression RegulationListeriaListeriosisLymphocyte ActivationMice, KnockoutPromoter Regions, GeneticProtein BindingReceptors, Antigen, T-CellSignal TransductionTranscription FactorsCTLA-4 AntigenCytokinesReceptors, Antigen, T-CellTranscription FactorsZfp281 protein, mouseCTLA-4T cell activationTCR signalingZfp281

Identifiers

PMID31511645
PMCPMC7784856
OpenAlexW2973106765

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.