Evidence map›Paper›PMID 40537863›Full record

ArticleClinical epigenetics2025

Changes of methylation at enhancers appear to be essential for HIV infection progression.

Olga Taryma-Leśniak, Jan Bińkowski, Kaja Mielczak, Bogusz Aksak-Wąs, Malwina Karasińska-Cieślak, Marta Sobalska-Kwapis, Dominik Strapagiel, Miłosz Parczewski, Tomasz Kazimierz Wojdacz

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Article in Clinical epigenetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Olga Taryma-Leśniak *Independent Clinical Epigenetics Laboratory, Pomeranian Medical University in Szczecin, Szczecin, Poland.
Jan Bińkowski *Independent Clinical Epigenetics Laboratory, Pomeranian Medical University in Szczecin, Szczecin, Poland.
Kaja MielczakDepartment of Infectious, Tropical Diseases and Immune Deficiency, Pomeranian Medical University in Szczecin, Szczecin, Poland.
Bogusz Aksak-WąsDepartment of Infectious, Tropical Diseases and Immune Deficiency, Pomeranian Medical University in Szczecin, Szczecin, Poland.
Malwina Karasińska-CieślakDepartment of Infectious, Tropical Diseases and Immune Deficiency, Pomeranian Medical University in Szczecin, Szczecin, Poland.
Marta Sobalska-KwapisCentre for Digital Biology and Biomedical Science - Biobank Lodz, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
Dominik StrapagielCentre for Digital Biology and Biomedical Science - Biobank Lodz, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.
Miłosz ParczewskiRegional Centre for Digital Medicine, Pomeranian Medical University in Szczecin, Szczecin, Poland.
Tomasz Kazimierz WojdaczIndependent Clinical Epigenetics Laboratory, Pomeranian Medical University in Szczecin, Szczecin, Poland. tomasz.wojdacz@pum.edu.pl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe studied the influence of the European HIV-1 subtype B (most common in the Western and Central Europe) and subtype A6 (prevalent in Eastern Europe including Ukraine and Russia) on host methylome during infection progression and in virus-subtype-specific manner.

resultsOur results show that regardless of virus subtype, in the initial phase of the infection, HIV-related methylation changes more frequently affect parts of the genome with low expression activity including heterochromatin and quiescent regions. But, at stage four of the infection regions of the genome harboring HIV-related methylation changes are enhancers. We further showed that the effect of each of the virus subtypes on host methylome is to a large extent similar. And both virus subtypes appear to induce hypomethylation of loci associated with key pathways involved in viral infection such as 'type I interferon signaling pathway,' 'innate immune response' or 'negative regulation of viral genome replication.' Nevertheless, our results also indicate that each of the virus subtypes at least to some extent affects host methylome in virus-subtype-specific manner. Lastly, we showed that infection progression-related methylation changes that we identified are reversed with antiretroviral therapy.

conclusionsWe have shown that progression of HIV infection is associated with hypomethylation of enhancers regardless of virus subtype. This suggests that methylation changes at the enhancers may be key for infection progression. However, we also identified methylation changes indicating that, each of the virus subtypes affects host methylome in specific manner, but these findings need to be confirmed in studies that include larger number of participants.

Indexed as

DNA MethylationEnhancer Elements, GeneticHIV-1HIV InfectionsAdultDisease ProgressionFemaleHumansMaleEpigeneticsHIVMethylationProgression

Identifiers

PMID40537863
PMCPMC12178028

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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.