Evidence map›Paper›PMID 32477365›Full record

ArticleFrontiers in immunology2020

KLRG1 and CD103 Expressions Define Distinct Intestinal Tissue-Resident Memory CD8 T Cell Subsets Modulated in Crohn's Disease.

Hugo Bottois, Marjolaine Ngollo, Nassim Hammoudi, Tristan Courau, Julie Bonnereau, Victor Chardiny, Céline Grand, Brice Gergaud, Matthieu Allez, Lionel Le Bourhis

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

47 citing papers in PubMed, 66 citations in OpenAlex.

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  7. Evolving role of CD8Frontiers in immunology · 2026
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  10. GZMK-expressing CD8Nature · 2025
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  14. DAMP-ing IBD: Extinguish the Fire and Prevent Smoldering.Digestive diseases and sciences · 2025
    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 4 institutions in 1 country.

Hugo BottoisUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Marjolaine NgolloUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Nassim HammoudiUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Tristan CourauUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Julie BonnereauUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Victor ChardinyUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Céline GrandUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Brice GergaudUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Matthieu AllezUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Lionel Le BourhisUniversité de Paris, INSERM U1160, EMiLy, Institut de Recherche Saint-Louis, Paris, France.
Inserm · FRUniversité Paris Cité · FRUniversity of London Institute in Paris · FRHôpital Saint-Louis · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intestinal tissue-resident memory CD8 T cells (Trm) are non-recirculating effector cells ideally positioned to detect and react to microbial infections in the gut mucosa. There is an emerging understanding of Trm cell differentiation and functions, but their implication in inflammatory bowel diseases, such as Crohn's disease (CD), is still unknown. Here, we describe CD8 cells in the human intestine expressing KLRG1 or CD103, two receptors of E-cadherin. While CD103 CD8 T cells are present in high numbers in the mucosa of CD patients and controls, KLRG1 CD8 T cells are increased in inflammatory conditions. Mucosal CD103 CD8 T cells are more responsive to TCR restimulation, but KLRG1 CD8 T cells show increased cytotoxic and proliferative potential. CD103 CD8 T cells originate mostly from KLRG1 negative cells after TCR triggering and TGFβ stimulation. Interestingly, mucosal CD103 CD8 T cells from CD patients display major changes in their transcriptomic landscape compared to controls. They express Th17 related genes including CCL20, IL22, and IL26, which could contribute to the pathogenesis of CD. Overall, these findings suggest that CD103 CD8 T cells in CD induce a tissue-wide alert increasing innate immune responses and recruitment of effector cells such as KLRG1 CD8 T cells.

Indexed as

Immunologic MemoryAntigens, CDCD8-Positive T-LymphocytesClinical Trials as TopicCrohn DiseaseGene Expression ProfilingHumansImmunity, InnateInflammationIntegrin alpha ChainsInterleukinsIntestinal MucosaLectins, C-TypeReceptors, ImmunologicT-Lymphocyte Subsetsalpha E integrinsAntigens, CDIntegrin alpha ChainsInterleukinsKLRG1 protein, humanLectins, C-TypeReceptors, ImmunologicCD103Crohn's diseaseIBD – inflammatory bowel diseasesKLRG1T cellsTRM cells

Identifiers

PMID32477365
PMCPMC7235448
OpenAlexW3024934015

What OpenQuestion holds

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LicenceCC BY
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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.