Evidence map›Paper›PMID 37853762›Full record

ArticleGut microbes2023

Industrialized human gut microbiota increases CD8+ T cells and mucus thickness in humanized mouse gut.

Pajau Vangay, Tonya Ward, Sarah Lucas, Lalit K Beura, Dominique Sabas, Max Abramson, Lisa Till, Susan L Hoops, Purna Kashyap, Ryan C Hunter and 2 more

Open access · goldAbstract read
In one paragraph

Article in Gut microbes, 2023. 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
0.9field-weighted citation impact, top 24% 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, 6 citations in OpenAlex.

  1. Article
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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

12 authors at 6 institutions in 1 country.

Pajau VangayBioinformatics and Computational Biology Program, University of Minnesota, Minneapolis, MN, USA.
Tonya WardBioTechnology Institute, University of Minnesota, Minneapolis, MN, USA.
Sarah LucasDepartment of Biology, Syracuse University, Syracuse, NY, USA.
Lalit K BeuraDepartment of Molecular Microbiology and Immunology, Brown University, Providence, RI, USA.
Dominique SabasDepartment of Food Science and Nutrition, University of Minnesota, Minneapolis, MN, USA.
Max AbramsonDepartment of Neuroscience, Macalester College, St. Paul, MN, USA.
Lisa TillDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Susan L HoopsDepartment of Computer Science and Engineering, University of Minnesota, Minneapolis, MN, USA.
Purna KashyapDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Mayo Clinic, Rochester, MN, USA.
Ryan C HunterDepartment of Biology, Syracuse University, Syracuse, NY, USA.
David MasopustDepartment of Biology, Syracuse University, Syracuse, NY, USA.
Dan KnightsBioinformatics and Computational Biology Program, University of Minnesota, Minneapolis, MN, USA.
University of Minnesota · USSyracuse University · USMayo Clinic in Arizona · USBiotechnology Institute · USBrown University · USMacalester College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immigration to a highly industrialized nation has been associated with metabolic disease and simultaneous shifts in microbiota composition, but the underlying mechanisms are challenging to test in human studies. Here, we conducted a pilot study to assess the differential effects of human gut microbiota collected from the United States (US) and rural Thailand on the murine gut mucosa and immune system. Colonization of germ-free mice with microbiota from US individuals resulted in an increased accumulation of innate-like CD8 T cells in the small intestine lamina propria and intra-epithelial compartments when compared to colonization with microbiota from Thai individuals. Both TCRγδ and CD8αα T cells showed a marked increase in mice receiving Western microbiota and, interestingly, this phenotype was also associated with an increase in intestinal mucus thickness. Serendipitously, an accidentally infected group of mice corroborated this association between elevated inflammatory response and increased mucus thickness. These results suggest that Western-associated human gut microbes contribute to a pro-inflammatory immune response.

Indexed as

Gastrointestinal MicrobiomeAnimalsCD8-Positive T-LymphocytesHumansInflammationIntestinal MucosaMiceMucusPilot ProjectsdietimmigrationinfectioninflammationMicrobiomemicrobiotamucosal barrier

Identifiers

PMID37853762
PMCPMC10588527
OpenAlexW4387765691

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.