Evidence map›Paper›PMID 37228757›Full record

ArticleCell genomics2023

Transposable elements are associated with the variable response to influenza infection.

Xun Chen, Alain Pacis, Katherine A Aracena, Saideep Gona, Tony Kwan, Cristian Groza, Yen Lung Lin, Renata Sindeaux, Vania Yotova, Albena Pramatarova and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  3. PervasivebioRxiv : the preprint server for biology · 2025
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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

14 authors at 5 institutions in 3 countries.

Xun ChenInstitute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto University, Kyoto 606-8501, Japan.
Alain PacisCanadian Center for Computational Genomics, McGill University, Montréal, QC H3A 0G1, Canada.
Katherine A AracenaDepartment of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
Saideep GonaDepartment of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
Tony KwanVictor Phillip Dahdaleh Institute of Genomic Medicine at McGill University, Montréal, QC H3A 0G1, Canada.
Cristian GrozaQuantitative Life Science, McGill University, Montréal, QC H3A 1E3, Canada.
Yen Lung LinDepartment of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
Renata SindeauxCentre de Recherche, CHU Sainte-Justine, Université de Montréal, Montréal, QC H3T 1C5, Canada.
Vania YotovaCentre de Recherche, CHU Sainte-Justine, Université de Montréal, Montréal, QC H3T 1C5, Canada.
Albena PramatarovaVictor Phillip Dahdaleh Institute of Genomic Medicine at McGill University, Montréal, QC H3A 0G1, Canada.
Marie-Michelle SimonVictor Phillip Dahdaleh Institute of Genomic Medicine at McGill University, Montréal, QC H3A 0G1, Canada.
Tomi PastinenGenomic Medicine Center, Children's Mercy Hospital and Research Institute, Kansas City, MO 64108, USA.
Luis B BarreiroDepartment of Human Genetics, University of Chicago, Chicago, IL 60637, USA.
Guillaume BourqueInstitute for the Advanced Study of Human Biology (WPI-ASHBi), Kyoto University, Kyoto 606-8501, Japan.
McGill University · CAUniversity of Chicago · USCentre Hospitalier Universitaire Sainte-Justine · CAKyoto University · JPChildren's Mercy Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Influenza A virus (IAV) infections are frequent every year and result in a range of disease severity. Here, we wanted to explore the potential contribution of transposable elements (TEs) to the variable human immune response. Transcriptome profiling in monocyte-derived macrophages from 39 individuals following IAV infection revealed significant inter-individual variation in viral load post-infection. Using transposase-accessible chromatin using sequencing (ATAC-seq), we identified a set of TE families with either enhanced or reduced accessibility upon infection. Of the enhanced families, 15 showed high variability between individuals and had distinct epigenetic profiles. Motif analysis showed an association with known immune regulators (e.g., BATFs, FOSs/JUNs, IRFs, STATs, NFkBs, NFYs, and RELs) in stably enriched families and with other factors in variable families, including KRAB-ZNFs. We showed that TEs and host factors regulating TEs were predictive of viral load post-infection. Our findings shed light on the role TEs and KRAB-ZNFs may play in inter-individual variation in immunity.

Indexed as

epigeneticsgene regulationinfluenza infectionKruppel-associated box zinc finger proteins (KRAB-ZNFs)transposable elementsvariable response

Identifiers

PMID37228757
PMCPMC10203045
OpenAlexW4362696984

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.