Evidence map›Paper›PMID 33777849›Full record

ArticleFrontiers in cellular and infection microbiology2021

Harnessing Colon Chip Technology to Identify Commensal Bacteria That Promote Host Tolerance to Infection.

Francesca S Gazzaniga, Diogo M Camacho, Meng Wu, Matheus F Silva Palazzo, Alexandre L M Dinis, Francis N Grafton, Mark J Cartwright, Michael Super, Dennis L Kasper, Donald E Ingber

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 41 citations in OpenAlex.

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  12. In Vitro Models for Investigating Intestinal Host-Pathogen Interactions.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  13. Human organ chips for regenerative pharmacology.Pharmacology research & perspectives · 2024
    Review
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  15. Article
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  19. ExploringFrontiers in cellular and infection microbiology · 2023
    Review
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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 3 institutions in 2 countries.

Francesca S GazzanigaWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
Diogo M CamachoWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
Meng WuDepartment of Immunology, Harvard Medical School, Boston, MA, United States.
Matheus F Silva PalazzoBiophysics Institute Carlos Chagas Filho, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.
Alexandre L M DinisWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
Francis N GraftonWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
Mark J CartwrightWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
Michael SuperWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
Dennis L KasperDepartment of Immunology, Harvard Medical School, Boston, MA, United States.
Donald E IngberWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, United States.
Harvard University · USBoston Children's Hospital · USUniversidade Federal do Rio de Janeiro · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Commensal bacteria within the gut microbiome contribute to development of host tolerance to infection, however, identifying specific microbes responsible for this response is difficult. Here we describe methods for developing microfluidic organ-on-a-chip models of small and large intestine lined with epithelial cells isolated from duodenal, jejunal, ileal, or colon organoids derived from wild type or transgenic mice. To focus on host-microbiome interactions, we carried out studies with the mouse Colon Chip and demonstrated that it can support co-culture with living gut microbiome and enable assessment of effects on epithelial adhesion, tight junctions, barrier function, mucus production, and cytokine release. Moreover, infection of the Colon Chips with the pathogenic bacterium,

Indexed as

ColonSymbiosisAnimalsBacteriaIntestinal MucosaMiceTechnologygutinfectionintestinemicrobiomemicrofluidictolerance

Identifiers

PMID33777849
PMCPMC7996096
OpenAlexW3136395746

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.