Evidence map›Paper›PMID 34332095›Full record

ArticleDrug discovery today2021

Harnessing the power of microphysiological systems for COVID-19 research.

Nicole Kleinstreuer, Anthony Holmes

Abstract read
In one paragraph

Article in Drug discovery today, 2021. 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
–field-weighted citation impact
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.

  1. Article
  2. Review
  3. Article
  4. Review
  5. 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

2 authors.

Nicole KleinstreuerNICEATM, National Toxicology Program Interagency Center for the Evaluation of Alternative Toxicological Methods, RTP, NC, USA.
Anthony HolmesNational Centre for the Replacement, Refinement and Reduction of Animals in Research, London, UK. Electronic address: anthony.holmes@nc3rs.org.uk.

Funding

Research Initiatives on COVID-19 in the Division of Translational ToxicologyZIAES103367 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI GERMOLEC, DORI R · 2021 to 2025
$4.5M
6 · The paper itself

Abstract

The pharmaceutical industry is constantly striving for innovative ways to bridge the translational gap between preclinical and clinical drug development to reduce attrition. Substantial effort has focused on the preclinical application of human-based microphysiological systems (MPS) to better identify compounds not likely to be safe or efficacious in the clinic. The Coronavirus 2019 (COVID-19) pandemic provides a clear opportunity for assessing the utility of MPS models of the lungs and other organ systems affected by the disease in understanding the pathophysiology of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and in the development of effective therapeutics. Here, we review progress and describe the establishment of a global working group to coordinate activities around MPS and COVID-19 and to maximize their scientific, human health, and animal welfare impacts.

Indexed as

Biomedical ResearchCell Culture TechniquesCOVID-19 Drug TreatmentDrug DevelopmentMicrochip Analytical ProceduresHumansIn Vitro TechniquesLab-On-A-Chip DevicesLungOrganoidsSARS-CoV-23RsCOVID-19Microphysiological systemsMPSSARS-CoV-2

Identifiers

PMID34332095
PMCPMC8317448

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.