Evidence map›Paper›PMID 24628276›Full record

ArticleMolecular pharmaceutics2014

Immunocompetent 3D model of human upper airway for disease modeling and in vitro drug evaluation.

Helen Harrington, Paul Cato, Fabian Salazar, Malcolm Wilkinson, Alan Knox, John W Haycock, Felicity Rose, Jon W Aylott, Amir M Ghaemmaghami

Abstract read
In one paragraph

Article in Molecular pharmaceutics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 2 pooled it
–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

38 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Modeling Immunity In Vitro: Slices, Chips, and Engineered Tissues.Annual review of biomedical engineering · 2021
    Pooled it
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  19. The Fabrication andFrontiers in bioengineering and biotechnology · 2020
    Article
  20. Nanofibrous Scaffolds Support a 3DFrontiers in pharmacology · 2019
    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

9 authors.

Helen HarringtonDivision of Immunology, School of Life Sciences, Faculty of Medicine & Health Sciences, University of Nottingham , Nottingham NG7 2UH, United Kingdom.
Paul Cato
Fabian Salazar
Malcolm Wilkinson
Alan Knox
John W Haycock
Felicity Rose
Jon W Aylott
Amir M Ghaemmaghami

Funding

Biotechnology and Biological Sciences Research Council BB/H010971/1Biotechnology and Biological Sciences Research Council BB/H011293/1National Centre for the Replacement, Refinement and Reduction of Animals in Research G1001804/1
6 · The paper itself

Abstract

The development of more complex in vitro models for the assessment of novel drugs and chemicals is needed because of the limited biological relevance of animal models to humans as well as ethical considerations. Although some human-cell-based assays exist, they are usually 2D, consist of single cell type, and have limited cellular and functional representation of the native tissue. In this study, we have used biomimetic porous electrospun scaffolds to develop an immunocompetent 3D model of the human respiratory tract comprised of three key cell types present in upper airway epithelium. The three cell types, namely, epithelial cells (providing a physical barrier), fibroblasts (extracellular matrix production), and dendritic cells (immune sensing), were initially grown on individual scaffolds and then assembled into the 3D multicell tissue model. The epithelial layer was cultured at the air-liquid interface for up to four weeks, leading to formation of a functional barrier as evidenced by an increase in transepithelial electrical resistance (TEER) and tight junction formation. The response of epithelial cells to allergen exposure was monitored by quantifying changes in TEER readings and by assessment of cellular tight junctions using immunostaining. It was found that epithelial cells cocultured with fibroblasts formed a functional epithelial barrier at a quicker rate than single cultures of epithelial cells and that the recovery from allergen exposure was also more rapid. Also, our data show that dendritic cells within this model remain viable and responsive to external stimulation as evidenced by their migration within the 3D construct in response to allergen challenge. This model provides an easy to assemble and physiologically relevant 3D model of human airway epithelium that can be used for studies aiming at better understanding lung biology, the cross-talk between immune cells, and airborne allergens and pathogens as well as drug delivery.

Indexed as

AllergensBiomimeticsCell LineCoculture TechniquesDendritic CellsDrug EvaluationEpithelial CellsFibroblastsHumansPharmaceutical PreparationsRespiratory MucosaRespiratory SystemTight JunctionsTissue ScaffoldsAllergensPharmaceutical Preparations

Identifiers

PMID24628276
PMCPMC4086737

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.