Evidence map›Paper›PMID 40170606›Full record

ArticleAIDS (London, England)2025

Dolutegravir plus lamivudine downregulates cellular stress responses vs. three-drug HIV regimens.

Victoria Rios-Vazquez, Wilhelm A J W Vos, Marc J T Blaauw, Louise E Van Eekeren, Albert L Groenendijk, Adriana Navas, Nadira Vadaq, Leo A B Joosten, Mihai G Netea, Willem L Blok and 4 more

Abstract readComparative Study
In one paragraph

Article in AIDS (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

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

14 authors.

Victoria Rios-VazquezDepartment of Internal Medicine and Radboud Center of Infectious Diseases.
Wilhelm A J W VosDepartment of Internal Medicine and Radboud Center of Infectious Diseases.
Marc J T BlaauwDepartment of Internal Medicine and Radboud Center of Infectious Diseases.
Louise E Van EekerenDepartment of Internal Medicine and Radboud Center of Infectious Diseases.
Albert L GroenendijkDepartment of Internal Medicine and Department of Medical Microbiology and Infectious Diseases, ErasmusMC, Erasmus University, Rotterdam, The Netherlands.
Adriana NavasDepartment of Internal Medicine and Radboud Center of Infectious Diseases.
Nadira VadaqDepartment of Internal Medicine and Radboud Center of Infectious Diseases.
Leo A B JoostenDepartment of Internal Medicine and Radboud Center of Infectious Diseases.
Mihai G NeteaDepartment of Internal Medicine and Radboud Center of Infectious Diseases.
Willem L BlokDepartment of Internal Medicine and Infectious Diseases, OLVG, Amsterdam.
Janneke E StalenhoefDepartment of Internal Medicine and Infectious Diseases, OLVG, Amsterdam.
Lambert Van Den HeuvelDepartment of Genetics and Pediatrics, Radboudumc, Radboud University, Nijmegen.
Andre J A M Van Der VenDepartment of Internal Medicine and Radboud Center of Infectious Diseases.
Jan Van LunzenDepartment of Internal Medicine and Radboud Center of Infectious Diseases.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo compare the systemic and immune effects of two-drug regimens (2DR) and three-drug regimens (3DR) in people with HIV (PWH).

designIn a cross-sectional study, multiomics data were analyzed in dolutegravir (DTG) plus lamivudine (3TC) 2DR and 3DR comprising DTG with two nucleoside reverse transcriptase inhibitors (NRTIs).

methodsData from the 2000HIV cohort of virally suppressed PWH on combination antiretroviral treatment (cART) regimens were analyzed. Groups included DTG + 3TC ( n  = 191), DTG + 3TC + abacavir (ABC) ( n  = 188), and DTG + tenofovir disoproxil fumarate or tenofovir alafenamide (TDF/TAF) + emtricitabine (FTC) ( n  = 115). Systemic functions were assessed via plasma protein profiling (Olink Explore, 2367 proteins), while peripheral blood mononuclear cells (PBMCs) were used to evaluate immune effects by analyzing Bulk RNA-Seq and ex-vivo cytokine production capacity.

resultsPlasma protein analysis revealed that 2DR associated to lower protein expression and pathways related to metabolism, stress responses, chemokine signaling, and immune responses compared to 3DR. Four proteins - CXCL8, DDC, PMM2, and EPS8L2 - were consistently downregulated in 2DR. Differential gene expression analysis identified 17 overlapping downregulated genes across all 3DR vs. 2DR comparisons, linked to chromatin structure, cellular senescence, stress response, and cytokine activity. Cytokine production was similar across 2DR and 3DR groups, except for enhanced interleukin (IL)-17 production in DTG + TDF + FTC users.

conclusionsReducing NRTIs in DTG-based 2DR, particularly by omitting ABC or TAF/TDF, suggests decreased activation of stress response and immune-related pathways. Importantly, the functional capacity of circulating immune cells remains largely unchanged between 2DR and 3DR.

Indexed as

Anti-HIV AgentsHeterocyclic Compounds, 3-RingHIV InfectionsLamivudineStress, PhysiologicalAdultAntiretroviral Therapy, Highly ActiveCross-Sectional StudiesCytokinesDolutegravirDown-RegulationFemaleHumansLeukocytes, MononuclearMaleMiddle AgedAnti-HIV AgentsCytokinesDolutegravirHeterocyclic Compounds, 3-RingLamivudineOxazinesPiperazinesPyridonesantiretroviral therapydolutegravirHIVmultiomicsreverse transcriptase inhibitors

Identifiers

PMID40170606
PMCPMC12237123

What Socratic holds

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Registered trials

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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 Socratic graph.