Evidence map›Paper›PMID 35840529›Full record

ReviewTrends in immunology2022

The potential role of HIV-1 latency in promoting neuroinflammation and HIV-1-associated neurocognitive disorder.

Sheetal Sreeram, Fengchun Ye, Yoelvis Garcia-Mesa, Kien Nguyen, Ahmed El Sayed, Konstantin Leskov, Jonathan Karn

Open access · bronzeAbstract readReview
In one paragraph

Review in Trends in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 3% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

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4 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Sheetal SreeramDepartment of Molecular Biology and Microbiology. Case Western Reserve University, Cleveland, OH, USA.
Fengchun YeDepartment of Molecular Biology and Microbiology. Case Western Reserve University, Cleveland, OH, USA.
Yoelvis Garcia-MesaDepartment of Molecular Biology and Microbiology. Case Western Reserve University, Cleveland, OH, USA.
Kien NguyenDepartment of Molecular Biology and Microbiology. Case Western Reserve University, Cleveland, OH, USA.
Ahmed El SayedDepartment of Molecular Biology and Microbiology. Case Western Reserve University, Cleveland, OH, USA.
Konstantin LeskovDepartment of Molecular Biology and Microbiology. Case Western Reserve University, Cleveland, OH, USA.
Jonathan KarnDepartment of Molecular Biology and Microbiology. Case Western Reserve University, Cleveland, OH, USA. Electronic address: jxk153@case.edu.
Case Western Reserve University · US

Funding

WG3: HIV, Co-infections and Co-morbiditiesP30AI036219 · NIAID · CASE WESTERN RESERVE UNIVERSITY · PI Immaculate Lillian Nankya · 1994 to 2026
$50.0M
Regulation of HIV latency by microglial-neuronal interactionsR01DA049481 · NIDA · CASE WESTERN RESERVE UNIVERSITY · PI KARN, JONATHAN · 2019 to 2023
$4.0M
Targeted inactivation of HIV in CNS reservoirsR01MH113457 · NIMH · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CANNON, PAULA M · 2017 to 2021
$3.7M
Reversal of HIV latency by METH and InflammationR01DA043159 · NIDA · CASE WESTERN RESERVE UNIVERSITY · PI KARN, JONATHAN · 2016 to 2020
$3.7M
Drugs of abuse and the epigenetic and signaling pathways controlling HIV latencyR01DA036171 · NIDA · CASE WESTERN RESERVE UNIVERSITY · PI GOLDSTEIN, HARRIS, HARVEY, BRANDON K · 2013 to 2017
$3.6M
NIAID NIH HHS P30 AI036219NIDA NIH HHS R01 DA036171NIDA NIH HHS R01 DA043159NIDA NIH HHS R01 DA049481NIMH NIH HHS R01 MH113457
6 · The paper itself

Abstract

Despite potent suppression of HIV-1 viral replication in the central nervous system (CNS) by antiretroviral therapy (ART), between 15% and 60% of HIV-1-infected patients receiving ART exhibit neuroinflammation and symptoms of HIV-1-associated neurocognitive disorder (HAND) - a significant unmet challenge. We propose that the emergence of HIV-1 from latency in microglia underlies both neuroinflammation in the CNS and the progression of HAND. Recent molecular studies of cellular silencing mechanisms of HIV-1 in microglia show that HIV-1 latency can be reversed both by proinflammatory cytokines and by signals from damaged neurons, potentially creating intermittent cycles of HIV-1 reactivation and silencing in the brain. We posit that anti-inflammatory agents that also block HIV-1 reactivation, such as nuclear receptor agonists, might provide new putative therapeutic avenues for the treatment of HAND.

Indexed as

HIV-1HIV InfectionsHumansMicrogliaNeurocognitive DisordersNeuroinflammatory DiseasesVirus Latencyanti-inflammatory strategiesantiretroviral therapyHIV-1-associated neurocognitive disorderHIV-1 latencymicroglial cell activation

Identifiers

PMID35840529
PMCPMC9339484
OpenAlexW4285097503

What OpenQuestion holds

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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.