Evidence map›Paper›PMID 37925159›Full record

ArticleSLAS discovery : advancing life sciences R & D2024

High-Throughput cell-based immunofluorescence assays against influenza.

Yohanka Martinez-Gzegozewska, Lynn Rasmussen, Sara McKellip, Anna Manuvakhova, N Miranda Nebane, Andrew J Reece, Pedro Ruiz, Melinda Sosa, Robert Bostwick, Paige Vinson

Open access · diamondAbstract read
In one paragraph

Article in SLAS discovery : advancing life sciences R & D, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. A high-throughput response to the SARS-CoV-2 pandemic.SLAS discovery : advancing life sciences R & D · 2024
    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

10 authors at 1 institution in 1 country.

Yohanka Martinez-GzegozewskaScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States. Electronic address: ymartinez@southernresearch.org.
Lynn RasmussenScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States.
Sara McKellipScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States.
Anna ManuvakhovaScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States.
N Miranda NebaneScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States.
Andrew J ReeceScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States.
Pedro RuizScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States.
Melinda SosaScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States.
Robert BostwickScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States.
Paige VinsonScientific Platforms Division, Southern Research, High-Throughput Screening Center, Birmingham, Alabama, United States.
Southern Research Institute · US

Funding

Project 4 - Influenza - UABU19AI142759 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WHITLEY, RICHARD J. · 2019 to 2023
$37.5M
NIAID NIH HHS U19 AI142759
6 · The paper itself

Abstract

A rapid drug discovery response to influenza outbreaks with the potential to reach pandemic status could help minimize the virus's impact by reducing the time to identify anti-influenza drugs. Although several anti-influenza strategies have been considered in the search for new drugs, only a few therapeutic agents are approved for clinical use. The cytopathic effect induced by the influenza virus in Madin Darby canine kidney (MDCK) cells has been widely used for high-throughput anti-influenza drug screening, but the fact that the MDCK cells are not human cells constitutes a disadvantage when searching for new therapeutic agents for human use. We have developed a highly sensitive cell-based imaging assay for the identification of inhibitors of influenza A and B virus that is high-throughput compatible using the A549 human cell line. The assay has also been optimized for the assessment of the neutralizing effect of anti-influenza antibodies in the absence of trypsin, which allows testing of purified antibodies and serum samples. This assay platform can be applied to full high-throughput screening campaigns or later stages requiring quantitative potency determinations for structure-activity relationships.

Indexed as

Influenza, HumanAnimalsCell LineDogsFluorescent Antibody TechniqueHigh-Throughput Screening AssaysHumansMadin Darby Canine Kidney Cells

Identifiers

PMID37925159
PMCPMC10859970
OpenAlexW4388249253

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.