Evidence map›Paper›PMID 32380150›Full record

ArticleAntiviral research2020

BX795 demonstrates potent antiviral benefits against herpes simplex Virus-1 infection of human cell lines.

Aqsa Iqbal, Rahul Suryawanshi, Tejabhiram Yadavalli, Ipsita Volety, Deepak Shukla

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Antiviral research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. HerpDock: A GUI-based gateway to HSV-1 molecular docking insights.Computational and structural biotechnology journal · 2024
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Aqsa IqbalDepartment of Ophthalmology and Visual Sciences, University of Illinois Medical Center, Chicago, IL 60612, USA. Electronic address: aiqbal20@uic.edu.
Rahul SuryawanshiDepartment of Ophthalmology and Visual Sciences, University of Illinois Medical Center, Chicago, IL 60612, USA. Electronic address: rahuls@uic.edu.
Tejabhiram YadavalliDepartment of Ophthalmology and Visual Sciences, University of Illinois Medical Center, Chicago, IL 60612, USA. Electronic address: yteja@uic.edu.
Ipsita VoletyDepartment of Ophthalmology and Visual Sciences, University of Illinois Medical Center, Chicago, IL 60612, USA. Electronic address: ivolet2@uic.edu.
Deepak ShuklaDepartment of Ophthalmology and Visual Sciences, University of Illinois Medical Center, Chicago, IL 60612, USA; Department of Bioengineering, University of Illinois, Chicago, IL 60607, USA. Electronic address: dshukla@uic.edu.
University of Illinois Chicago · US

Funding

Translational Core for Therapeutic and Diagnostic DevelopmentP30EY001792 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHUKLA, DEEPAK · 1985 to 2025
$14.8M
A new molecular therapy against ocular herpesR01EY024710 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DEEPAK SHUKLA · 2015 to 2026
$5.2M
NEI NIH HHS P30 EY001792NEI NIH HHS R01 EY024710
6 · The paper itself

Abstract

Herpes simplex virus-1 (HSV-1) infection is known to cause skin blisters, keratitis as well as deadly cases of encephalitis in some situations. Only a few therapeutic modalities are available for this globally prevalent infection. Very recently, a small molecule BX795 was identified as an inhibitor of HSV-1 protein synthesis in an ocular model of infection. In order to demonstrate its broader antiviral benefits, this study was aimed at evaluating the antiviral efficacy, mode-of-action, and toxicity of BX795 against HSV-1 infection of three human cell lines: HeLa, HEK, and HCE. Several different assays, including cell survival analysis, imaging, plaque analysis, Immunoblotting, and qRT-PCR, were performed. In all cases, BX795 demonstrated low toxicity at therapeutic concentration and showed strong antiviral benefits. Quite interestingly, cell line-dependent differences in the mechanism of antiviral action and cytokine response to infection were seen upon BX795 treatment. Taken together, our results suggest that BX795 may exert its antiviral benefits via cell-line specific mechanisms.

Indexed as

Antiviral AgentsCell LineCytokinesHEK293 CellsHeLa CellsHerpes SimplexHerpesvirus 1, HumanHumansPyrimidinesThiophenesAntiviral AgentsBX795CytokinesPyrimidinesThiophenesAntiviral drugBX795HCEHEKHeLaHerpes simplex virus-1

Identifiers

PMID32380150
PMCPMC7387215
OpenAlexW3020839541

What Socratic holds

Textmetadata
LicenceTDM
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.