Evidence map›Paper›PMID 34367046›Full record

ArticleFrontiers in neurology2021

Alprazolam Prompts HIV-1 Transcriptional Reactivation and Enhances CTL Response Through RUNX1 Inhibition and STAT5 Activation.

Angel Lin, Weam Othman Elbezanti, Alexis Schirling, Adel Ahmed, Rachel Van Duyne, Simon Cocklin, Zachary Klase

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Current drug discovery technologies · 2025
    Article
  3. Article
  4. Review
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 3 institutions in 1 country.

Angel LinDepartment of Biological Sciences, University of the Sciences, Philadelphia, PA, United States.
Weam Othman ElbezantiDepartment of Biological Sciences, University of the Sciences, Philadelphia, PA, United States.
Alexis SchirlingDepartment of Biological Sciences, University of the Sciences, Philadelphia, PA, United States.
Adel AhmedDepartment of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA, United States.
Rachel Van DuyneDepartment of Pharmacology and Physiology, Drexel University College of Medicine, Philadelphia, PA, United States.
Simon CocklinDepartment of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA, United States.
Zachary KlaseDepartment of Pharmacology and Physiology, Drexel University College of Medicine, Philadelphia, PA, United States.
Drexel University · USNational Cancer Institute · USUniversity of Pennsylvania · US

Funding

Understanding the overlap of chromatin alteration in HIV-1 and drug abuseDP2DA044550 · NIDA · UNIVERSITY OF THE SCIENCES PHILADELPHIA · PI KLASE, ZACHARY ALAN · 2017 to 2017
$2.1M
Novel anti-HIV compounds targeting the HIV-1 matrix proteinR01AI150491 · NIAID · DREXEL UNIVERSITY · PI LOLL, PATRICK J · 2020 to 2022
$1.7M
NIAID NIH HHS R01 AI150491NIDA NIH HHS DP2 DA044550
6 · The paper itself

Abstract

The HIV-1 pandemic is a significant challenge to the field of medicine. Despite advancements in antiretroviral (ART) development, 38 million people worldwide still live with this disease without a cure. A significant barrier to the eradication of HIV-1 lies in the persistently latent pool that establishes early in the infection. The "shock and kill" strategy relies on the discovery of a latency-reversing agent (LRA) that can robustly reactivate the latent pool and not limit immune clearance. We have found that a benzodiazepine (BDZ), that is commonly prescribed for panic and anxiety disorder, to be an ideal candidate for latency reversal. The BDZ Alprazolam functions as an inhibitor of the transcription factor RUNX1, which negatively regulates HIV-1 transcription. In addition to the displacement of RUNX1 from the HIV-1 5'LTR, Alprazolam potentiates the activation of STAT5 and its recruitment to the viral promoter. The activation of STAT5 in cytotoxic T cells may enable immune activation which is independent of the IL-2 receptor. These findings have significance for the potential use of Alprazolam in a curative strategy and to addressing the neuroinflammation associated with neuroHIV-1.

Indexed as

alprazolamHIV-1latencylatency reversing agentrunx1stat5

Identifiers

PMID34367046
PMCPMC8339301
OpenAlexW3186229862

What Socratic 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 Socratic graph.