Evidence map›Paper›PMID 32010147›Full record

ArticleFrontiers in immunology2019

Lineage Tracking the Generation of T Regulatory Cells From Microbial Activated T Effector Cells in Naïve Mice.

Kun Zhu, Chenfeng He, Si-Qi Liu, Mingjuan Qu, Tao Xie, Xiaofeng Yang, Lei Lei, Xiaobo Zhou, Lin Shi, Dan Zhang and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. 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

17 authors at 4 institutions in 2 countries.

Kun ZhuDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Chenfeng HeDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, United States.
Si-Qi LiuDepartment of Immunology, Duke University Medical Center, Durham, NC, United States.
Mingjuan QuDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, United States.
Tao XieDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Xiaofeng YangDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Lei LeiDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Xiaobo ZhouDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Lin ShiDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Dan ZhangDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Yanbin ChengDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Yae SunDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Huiqiang ZhengDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Xiaonan ShenDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Qijing LiDepartment of Immunology, Duke University Medical Center, Durham, NC, United States.
Ning JiangDepartment of Biomedical Engineering, The University of Texas at Austin, Austin, TX, United States.
Baojun ZhangDepartment of Pathogenic Microbiology and Immunology, School of Basic Medical Sciences, Xi'an Jiaotong University, Xi'an, China.
Xi'an Jiaotong University · CNThe University of Texas at Austin · USDuke Medical Center · USDuke University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cells (Tregs) are essential for the maintenance of gut homeostasis by suppressing conventional CD4

Indexed as

Cell TrackingAnimalsCell LineageHomologous RecombinationHost-Pathogen InteractionsImmune ToleranceImmunophenotypingLymphocyte ActivationMiceMicrobiotaPeyer's PatchesReceptors, Antigen, T-CellT-Lymphocytes, RegulatoryToll-Like ReceptorsReceptors, Antigen, T-CellToll-Like Receptorsgutinducible TregsmicrobiotaTCR repertoiretolerance

Identifiers

PMID32010147
PMCPMC6978744
OpenAlexW2999250399

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.