Evidence map›Paper›PMID 35293780›Full record

ArticleAntimicrobial agents and chemotherapy2022

Anti-HIV Drugs Cause Mitochondrial Dysfunction in Monocyte-Derived Macrophages.

Jennillee Wallace, Hemil Gonzalez, Reshma Rajan, Srinivas D Narasipura, Amber K Virdi, Arnold Z Olali, Ankur Naqib, Zarema Arbieva, Mark Maienschein-Cline, Lena Al-Harthi

Open access · hybridAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  4. Viruses and neurodegeneration: a growing concern.Journal of translational medicine · 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

10 authors at 2 institutions in 1 country.

Jennillee WallaceDepartment of Microbial Pathogens and Immunity, Rush University Medical Centergrid.240684.c, Chicago, Illinois, USA.
Hemil GonzalezDepartment of Microbial Pathogens and Immunity, Rush University Medical Centergrid.240684.c, Chicago, Illinois, USA.
Reshma RajanDepartment of Microbial Pathogens and Immunity, Rush University Medical Centergrid.240684.c, Chicago, Illinois, USA.
Srinivas D NarasipuraDepartment of Microbial Pathogens and Immunity, Rush University Medical Centergrid.240684.c, Chicago, Illinois, USA.
Amber K VirdiDepartment of Microbial Pathogens and Immunity, Rush University Medical Centergrid.240684.c, Chicago, Illinois, USA.
Arnold Z OlaliDepartment of Microbial Pathogens and Immunity, Rush University Medical Centergrid.240684.c, Chicago, Illinois, USA.
Ankur NaqibRush Research Informatics Core, Rush University Medical Centergrid.240684.c, Chicago, Illinois, USA.
Zarema ArbievaResearch Informatics Core, Research Resources Center, University of Illinois at Chicago, Chicago, Illinois, USA.
Mark Maienschein-ClineGenome Research Core, University of Illinois at Chicago, Chicago, Illinois, USA.
Lena Al-HarthiDepartment of Microbial Pathogens and Immunity, Rush University Medical Centergrid.240684.c, Chicago, Illinois, USA.ORCID 0000-0003-3915-3904
Rush University Medical Center · USUniversity of Illinois Chicago · US

Funding

cART effects on glial cellsR21MH122241 · NIMH · RUSH UNIVERSITY MEDICAL CENTER · PI AL-HARTHI, LENA · 2020 to 2021
$432k
NIMH NIH HHS R21 MH122241
6 · The paper itself

Abstract

Combination antiretroviral therapy (cART) dramatically changed the face of the HIV/AIDS pandemic, making it one of the most prominent medical breakthroughs of the past 3 decades. However, as the life span of persons living with HIV (PLWH) continues to approach that of the general population, the same cannot be said regarding their quality of life. PLWH are affected by comorbid conditions such as high blood pressure, diabetes, and neurocognitive impairment at a higher rate and increased severity than their age-matched counterparts. PLWH also have higher levels of inflammation, the drivers of which are not entirely clear. As cART treatment is lifelong, we assessed here the effects of cART, independent of HIV, on primary human monocyte-derived macrophages (MDMs). MDMs were unskewed or skewed to an alternative phenotype and treated with Atripla or Triumeq, two first-line cART treatments. We report that Triumeq skewed alternative MDMs toward an inflammatory nonsenescent phenotype. Both Atripla and Triumeq caused mitochondrial dysfunction, specifically efavirenz and abacavir. Additionally, transcriptome sequencing (RNA-seq) demonstrated that both Atripla and Triumeq caused differential regulation of genes involved in immune regulation and cell cycle and DNA repair. Collectively, our data demonstrate that cART, independent of HIV, alters the MDM phenotype. This suggests that cART may contribute to cell dysregulation in PLWH that subsequently results in increased susceptibility to comorbidities.

Indexed as

Anti-HIV AgentsHIV-1HIV InfectionsEfavirenz, Emtricitabine, Tenofovir Disoproxil Fumarate Drug CombinationHumansMacrophagesMitochondriaQuality of LifeAnti-HIV AgentsEfavirenz, Emtricitabine, Tenofovir Disoproxil Fumarate Drug Combinationantiretroviral agentshuman immunodeficiency virusmacrophagesmitochondriamonocyte-derived macrophage

Identifiers

PMID35293780
PMCPMC9017340
OpenAlexW4220998691

What OpenQuestion holds

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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.