Evidence map›Paper›PMID 32053234›Full record

ArticleImmunology2020

HIV infection suppresses TLR3 activation-mediated antiviral immunity in microglia and macrophages.

Hang Liu, Run-Hong Zhou, Yu Liu, Le Guo, Xu Wang, Wen-Hui Hu, Wen-Zhe Ho

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

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  6. Human Brain Organoids: Development and Applications.Journal of microbiology and biotechnology · 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

7 authors at 2 institutions in 2 countries.

Hang LiuSchool of Basic Medical Sciences, Wuhan University, Wuhan, China.ORCID 0000-0001-8511-6018
Run-Hong ZhouDepartment of Pathology and Laboratory Medicine, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Yu LiuDepartment of Pathology and Laboratory Medicine, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Le GuoDepartment of Pathology and Laboratory Medicine, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Xu WangDepartment of Pathology and Laboratory Medicine, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Wen-Hui HuDepartment of Pathology and Laboratory Medicine, Temple University Lewis Katz School of Medicine, Philadelphia, PA, USA.
Wen-Zhe HoSchool of Basic Medical Sciences, Wuhan University, Wuhan, China.ORCID 0000-0001-6571-3878
Temple University · USWuhan University · CN

Funding

Virus & Reservoirs CoreP30AI045008 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI DAVID S METZGER · 1999 to 2026
$78.6M
Role of miRNAs in Methamphetamine/HIV-mediated Immune ActivationR01DA045568 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI HO, WENZHE · 2018 to 2022
$2.0M
Methamphetamine, Innate Immunity and HIVR01DA041302 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI HO, WENZHE · 2016 to 2020
$1.8M
Effect of Methamphetamine and/or HIV on Human iPSCs-derived microglia and NeuronR21DA051396 · NIDA · TEMPLE UNIV OF THE COMMONWEALTH · PI HO, WENZHE · 2020 to 2021
$436k
NIAID NIH HHS P30 AI045008NIDA NIH HHS R01 DA041302NIDA NIH HHS R01 DA045568NIDA NIH HHS R21 DA051396
6 · The paper itself

Abstract

Monocytic-lineage cells in the central nervous system (CNS), including microglia and brain resident macrophages, are the key players in the CNS innate immunity against viral infections, including human immunodeficiency virus (HIV). However, these cells also serve as the major targets and reservoirs for HIV in the CNS. To address the question of how HIV can establish persistent infection in the target cells in the CNS, we examined whether HIV has the ability to counteract Toll-like receptor 3 (TLR3) activation-mediated antiviral immunity in microglia and macrophages. We observed that HIV latently infected microglial cells (HC69·5) expressed reduced levels of TLR3 and TLR3 activation-mediated interferons (IFN-α/β and IFN-λ) as compared with the uninfected control cells (C20). In addition, HIV infection of primary human macrophages suppressed the expression of TLR3 and the IFNs. HIV infection also inhibited the expression of the antiviral IFN-stimulated genes (ISGs) and the HIV-restriction miRNAs. Mechanistically, HIV infection inhibited the phosphorylation of IFN regulatory factors (IRF3 and IRF7) and signal transducer and activator of transcription proteins (STAT1 and STAT3) in both HIV latently infected microglia and acutely infected macrophages. These findings provide previously unrecognized and sound mechanisms for HIV infection and persistence in the primary target and reservoir cells in the brain.

Indexed as

Cell LineGene Expression RegulationHIV-1HIV InfectionsHumansImmune ToleranceImmunity, InnateInterferon Regulatory Factor-3Interferon Regulatory Factor-7InterferonsMacrophagesMicrogliaOrgan SpecificitySTAT1 Transcription FactorSTAT3 Transcription FactorToll-Like Receptor 3Interferon Regulatory Factor-3Interferon Regulatory Factor-7InterferonsIRF3 protein, humanIRF7 protein, humanSTAT1 Transcription FactorSTAT3 Transcription FactorTLR3 protein, humanToll-Like Receptor 3HIVmacrophagemicrogliaToll-like receptor 3

Identifiers

PMID32053234
PMCPMC7341545
OpenAlexW3005782880

What OpenQuestion holds

Textmetadata
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.