Evidence map›Paper›PMID 37998374›Full record

ArticleCells2023

A High-Throughput, High-Containment Human Primary Epithelial Airway Organ-on-Chip Platform for SARS-CoV-2 Therapeutic Screening.

Christine R Fisher, Felix Mba Medie, Rebeccah J Luu, Robert B Gaibler, Thomas J Mulhern, Caitlin R Miller, Chelsea J Zhang, Logan D Rubio, Elizabeth E Marr, Vidhya Vijayakumar and 9 more

Abstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Bridging the Gap Between Static Histology and Dynamic Organ-on-a-Chip Models.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. 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

19 authors.

Christine R FisherBioengineering Division, Draper, Cambridge, MA 02139, USA.
Felix Mba MedieBioengineering Division, Draper, Cambridge, MA 02139, USA.
Rebeccah J LuuBioengineering Division, Draper, Cambridge, MA 02139, USA.
Robert B GaiblerBioengineering Division, Draper, Cambridge, MA 02139, USA.ORCID 0000-0002-7492-683X
Thomas J MulhernBioengineering Division, Draper, Cambridge, MA 02139, USA.
Caitlin R MillerBioengineering Division, Draper, Cambridge, MA 02139, USA.
Chelsea J ZhangBioengineering Division, Draper, Cambridge, MA 02139, USA.
Logan D RubioBioengineering Division, Draper, Cambridge, MA 02139, USA.
Elizabeth E MarrBioengineering Division, Draper, Cambridge, MA 02139, USA.
Vidhya VijayakumarBioengineering Division, Draper, Cambridge, MA 02139, USA.
Elizabeth P GabrielBioengineering Division, Draper, Cambridge, MA 02139, USA.ORCID 0000-0003-4287-7006
Landys Lopez QuezadaBioengineering Division, Draper, Cambridge, MA 02139, USA.ORCID 0000-0002-8789-4283
Chun-Hui ZhangDepartment of Chemistry, Yale University, New Haven, CT 06520, USA.
Karen S AndersonDepartment of Pharmacology, Yale University, New Haven, CT 06520, USA.
William L JorgensenDepartment of Chemistry, Yale University, New Haven, CT 06520, USA.
Jehan W AlladinaDivision of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID 0000-0003-0136-6859
Benjamin D MedoffDivision of Pulmonary and Critical Care Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.ORCID 0000-0002-2558-0449
Jeffrey T BorensteinBioengineering Division, Draper, Cambridge, MA 02139, USA.ORCID 0000-0002-4482-3274
Ashley L GardBioengineering Division, Draper, Cambridge, MA 02139, USA.ORCID 0000-0001-7436-469X

Funding

POTENTIAL FUNCTIONS FOR WATER PROTEIN INTERACTIONSR01GM032136 · NIGMS · YALE UNIVERSITY · PI JORGENSEN, WILLIAM L. · 1985 to 2023
$8.2M
NIGMS NIH HHS R01 GM032136
6 · The paper itself

Abstract

COVID-19 emerged as a worldwide pandemic in early 2020, and while the rapid development of safe and efficacious vaccines stands as an extraordinary achievement, the identification of effective therapeutics has been less successful. This process has been limited in part by a lack of human-relevant preclinical models compatible with therapeutic screening on the native virus, which requires a high-containment environment. Here, we report SARS-CoV-2 infection and robust viral replication in PREDICT96-ALI, a high-throughput, human primary cell-based organ-on-chip platform. We evaluate unique infection kinetic profiles across lung tissue from three human donors by immunofluorescence, RT-qPCR, and plaque assays over a 6-day infection period. Enabled by the 96 devices/plate throughput of PREDICT96-ALI, we also investigate the efficacy of Remdesivir and MPro61 in a proof-of-concept antiviral study. Both compounds exhibit an antiviral effect against SARS-CoV-2 in the platform. This demonstration of SARS-CoV-2 infection and antiviral dosing in a high-throughput organ-on-chip platform presents a critical capability for disease modeling and therapeutic screening applications in a human physiology-relevant in vitro system.

Indexed as

COVID-19SARS-CoV-2Antiviral AgentsHumansLungVirus ReplicationAntiviral AgentsantiviralcoronavirusCOVID-19epithelial cellsmicrofluidicsorgan modelpandemicrespiratorySARS-CoV-2throughput

Identifiers

PMID37998374
PMCPMC10669988

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.