Evidence map›Paper›PMID 35138593›Full record

ReviewJournal of neurovirology2022

Human microglial models to study HIV infection and neuropathogenesis: a literature overview and comparative analyses.

Stephanie B H Gumbs, Raphael Kübler, Lavina Gharu, Pauline J Schipper, Anne L Borst, Gijsje J L J Snijders, Paul R Ormel, Amber Berdenis van Berlekom, Annemarie M J Wensing, Lot D de Witte and 1 more

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of neurovirology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

28 citing papers in PubMed, 30 citations in OpenAlex.

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  19. Review
  20. Frontiers in cellular neuroscience · 2023
    Article
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

11 authors at 2 institutions in 2 countries.

Stephanie B H GumbsTranslational Virology, Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID 0000-0003-0797-437X
Raphael KüblerTranslational Virology, Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Lavina GharuTranslational Virology, Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Pauline J SchipperTranslational Virology, Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Anne L BorstTranslational Virology, Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Gijsje J L J SnijdersDepartment of Psychiatry, Icahn School of Medicine, New York, NY, USA.
Paul R OrmelDepartment of Psychiatry, University Medical Center Utrecht, Brain Center, Utrecht University, Utrecht, The Netherlands.
Amber Berdenis van BerlekomDepartment of Psychiatry, University Medical Center Utrecht, Brain Center, Utrecht University, Utrecht, The Netherlands.
Annemarie M J WensingTranslational Virology, Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.
Lot D de Witte *Department of Psychiatry, Icahn School of Medicine, New York, NY, USA.
Monique Nijhuis *Translational Virology, Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands. m.nijhuis@umcutrecht.nl.
University Medical Center Utrecht · NLUtrecht University · NL

Funding

Investigating the impact of inflammation on brain development using human cerebral organoids.R21MH120581 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DE WITTE, LOTJE DOROTHEE · 2020 to 2020
$466k
NIMH NIH HHS R21 MH120581
6 · The paper itself

Abstract

HIV persistence in the CNS despite antiretroviral therapy may cause neurological disorders and poses a critical challenge for HIV cure. Understanding the pathobiology of HIV-infected microglia, the main viral CNS reservoir, is imperative. Here, we provide a comprehensive comparison of human microglial culture models: cultured primary microglia (pMG), microglial cell lines, monocyte-derived microglia (MDMi), stem cell-derived microglia (iPSC-MG), and microglia grown in 3D cerebral organoids (oMG) as potential model systems to advance HIV research on microglia. Functional characterization revealed phagocytic capabilities and responsiveness to LPS across all models. Microglial transcriptome profiles of uncultured pMG showed the highest similarity to cultured pMG and oMG, followed by iPSC-MG and then MDMi. Direct comparison of HIV infection showed a striking difference, with high levels of viral replication in cultured pMG and MDMi and relatively low levels in oMG resembling HIV infection observed in post-mortem biopsies, while the SV40 and HMC3 cell lines did not support HIV infection. Altogether, based on transcriptional similarities to uncultured pMG and susceptibility to HIV infection, MDMi may serve as a first screening tool, whereas oMG, cultured pMG, and iPSC-MG provide more representative microglial culture models for HIV research. The use of current human microglial cell lines (SV40, HMC3) is not recommended.

Indexed as

HIV-1HIV InfectionsCells, CulturedHumansMicrogliaMonocytesVirus ReplicationCentral nervous systemHIVHIV-associated neurocognitive disorderMicrogliaNeuropathogenesisOrganoid

Identifiers

PMID35138593
PMCPMC9076745
OpenAlexW4210860317

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.