Evidence map›Paper›PMID 30728066›Full record

ArticleJournal of translational medicine2019

Peripheral T cell receptor beta immune repertoire is promptly reconstituted after acute myocardial infarction.

Dan Li, Longgang Hu, Qing Liang, Cuijuan Zhang, Yunzhen Shi, Bin Wang, Kejia Wang

Abstract read
In one paragraph

Article in Journal of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

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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

7 authors.

Dan LiDepartment of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Longgang HuDepartment of Cardiovascular Medicine, The Affiliated Cardiovascular Hospital of Qingdao University, Qingdao, China.
Qing LiangCollege of Basic Medicine, Qingdao University, Qingdao, Shandong, China.
Cuijuan ZhangDepartment of Cardiology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Yunzhen ShiCenter of Patients, West China Second University Hospital, Sichuan University, Chengdu, China.
Bin WangCollege of Basic Medicine, Qingdao University, Qingdao, Shandong, China.
Kejia WangCollege of Basic Medicine, Qingdao University, Qingdao, Shandong, China. princewkj@qdu.edu.cn.

Funding

Natural Science Foundation of Shandong Province Project ZR2016HP17Postdoctoral Application Research of Qingdao Project 2016063
6 · The paper itself

Abstract

backgroundAcute myocardial infarction (AMI) is characterized by an inflammatory process in which T cell plays a key role. However, the profile of immune microenvironment in AMI is still uncertain. High-throughput sequencing of T cell receptor (TCR) provides deep insight into monitoring the immune microenvironment.

methods30 patients with AMI were enrolled and 30 healthy individuals were recruited as controls. Flow cytometer were used to analyze the distribution of αβ T cells and their CD69 expression from peripheral leukomonocytes. TCRβ repertoire library was amplified by two-round multiplex PCR and detected by next-generation sequencing (NGS).

resultsThe percentage of αβ T cells in AMI patients were significantly restricted than those in healthy controls, while the highly activated αβ T cells along with distinguishing usage of variable (V), diversity (D) and joining (J) gene segments were also found in AMI patients. In addition, AMI induced a significantly restricted CDR3 amino acid (AA) diversity and remarkably reconstituted TCR immune repertoires. Finally, we identified several AMI-associated tendency of CDR3 AAs expression after AMI.

conclusionsOur work suggests that the aberrant αβ T cells distribution and activation may associated with the pathogenesis of AMI and demonstrates a reconstitution of TCRβ immune repertoire after AMI.

Indexed as

Complementarity Determining RegionsFemaleHumansLymphocyte ActivationMaleMiddle AgedMyocardial InfarctionReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesV(D)J RecombinationComplementarity Determining RegionsReceptors, Antigen, T-Cell, alpha-betaAcute myocardial infarctionImmune repertoireNext-generation sequencingT cell receptor beta

Identifiers

PMID30728066
PMCPMC6366076

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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.