Evidence map›Paper›PMID 34804062›Full record

ArticleFrontiers in immunology2021

Hsa-miR-31 Governs T-Cell Homeostasis in HIV Protection

Lingyan Zhu, Chao Qiu, Lili Dai, Linxia Zhang, Meiqi Feng, Yu Yang, Chenli Qiu, Anli Zhang, Jun Huang, Ying Wang and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 52% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. 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

16 authors at 6 institutions in 1 country.

Lingyan ZhuShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Chao QiuShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Lili DaiBeijing You'an Hospital, Capital Medical University, Beijing, China.
Linxia ZhangShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Meiqi FengShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Yu YangShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Chenli QiuShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Anli ZhangShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Jun HuangShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Ying WangDepartment of AIDS/STD, Shanghai Municipal Center for Disease Control and Prevention, Shanghai, China.
Ying WanBiomedical Analysis Center, Army Medical University, Chongqing, China.
Chen ZhaoShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Hao WuBeijing You'an Hospital, Capital Medical University, Beijing, China.
Jianxin LyuSchool of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, China.
Xiaoyan ZhangShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Jianqing XuShanghai Public Health Clinical Center and Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Shanghai Public Health Clinical Center · CNArmy Medical University · CNBeijing YouAn Hospital · CNCapital Medical University · CNShanghai Municipal Center For Disease Control Prevention · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It remains poorly defined whether any human miRNAs play protective roles during HIV infection. Here, focusing on a unique cohort of HIV-infected former blood donors, we identified miR-31 (hsa-miR-31) by comparative miRNA profiling as the only miRNA inversely correlating with disease progression. We further validated this association in two prospective cohort studies. Despite conservation during evolution, hsa-miR-31, unlike its mouse counterpart (mmu-miR-31), was downregulated in human T cell upon activation. Our

Indexed as

AdultBiomarkersDisease ProgressionFemaleGenetic Predisposition to DiseaseHEK293 CellsHIV InfectionsHomeostasisHumansInterferon-gammaMaleMicroRNAsMiddle AgedSTAT1 Transcription FactorT-bet Transcription FactorT-Box Domain ProteinsBiomarkersInterferon-gammaMicroRNAsMIRN31 microRNA, humanSTAT1 protein, humanSTAT1 Transcription FactorT-bet Transcription FactorT-Box Domain ProteinsCD4+ T celldisease progressionHIV-1miR-31STAT1T-bet

Identifiers

PMID34804062
PMCPMC8602903
OpenAlexW3212816982

What OpenQuestion 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 OpenQuestion graph.