Evidence map›Paper›PMID 36428462›Full record

ArticleBiomedicines2022

The Immunological Epigenetic Landscape of the Human Life Trajectory.

Iva Juříčková, Michael Hudec, Felix Votava, Jan Vosáhlo, Saak Victor Ovsepian, Marie Černá, Valerie Bríd O'Leary

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 88% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 2 institutions in 2 countries.

Iva JuříčkováDepartment of Medical Genetics, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic.
Michael HudecDepartment of Medical Genetics, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic.ORCID 0000-0002-6593-9911
Felix VotavaDepartment of Children and Adolescents, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic.
Jan VosáhloDepartment of Children and Adolescents, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic.
Saak Victor OvsepianFaculty of Engineering and Science, University of Greenwich London, Chatham Maritime, Kent ME4 4TB, UK.
Marie ČernáDepartment of Medical Genetics, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic.ORCID 0000-0002-1208-5588
Valerie Bríd O'LearyDepartment of Medical Genetics, Third Faculty of Medicine, Charles University, Vinohrady, 10000 Prague, Czech Republic.ORCID 0000-0003-1171-9830
Charles University · CZUniversity of Greenwich · GB

Funding

Charles University 260531/SVV/2020-2022COOPERATIO: the scientific project 'Medical Diagnostics and Basic Medical Sciences' (the field 'Medical Genetics') 207036
6 · The paper itself

Abstract

Adaptive immunity changes over an individual’s lifetime, maturing by adulthood and diminishing with old age. Epigenetic mechanisms involving DNA and histone methylation form the molecular basis of immunological memory during lymphocyte development. Monocytes alter their function to convey immune tolerance, yet the epigenetic influences at play remain to be fully understood in the context of lifespan. This study of a healthy genetically homogenous cohort of children, adults and seniors sought to decipher the epigenetic dynamics in B-lymphocytes and monocytes. Variable global cytosine methylation within retro-transposable LINE-1 repeats was noted in monocytes compared to B-lymphocytes across age groups. The expression of the human leukocyte antigen (HLA)-DQ alpha chain gene HLA-DQA1*01 revealed significantly reduced levels in monocytes in all ages relative to B-lymphocytes, as well as between lifespan groups. High melting point analysis and bisulfite sequencing of the HLA-DQA1*01 promoter in monocytes highlighted variable cytosine methylation in children and seniors but greater stability at this locus in adults. Further epigenetic evaluation revealed higher histone lysine 27 trimethylation in monocytes from this adult group. Chromatin immunoprecipitation and RNA pulldown demonstrated association with a novel lncRNA TINA with structurally conserved similarities to the previously recognized epigenetic modifier PARTICLE. Seeking to interpret the epigenetic immunological landscape across three representative age groups, this study focused on HLA-DQA1*01 to expose cytosine and histone methylation alterations and their association with the non-coding transcriptome. Such insights unveil previously unknown complex epigenetic layers, orchestrating the strength and weakening of adaptive immunity with the progression of life.

Indexed as

ChIPhistoneHLAlong non-coding RNAmethylationPARTICLETINA

Identifiers

PMID36428462
PMCPMC9687906
OpenAlexW4308970093

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.