Evidence map›Paper›PMID 32687575›Full record

ArticleThe Journal of experimental medicine2020

Intestinal CD8αα IELs derived from two distinct thymic precursors have staggered ontogeny.

Roland Ruscher, S Thera Lee, Oscar C Salgado, Elise R Breed, Sara H Osum, Kristin A Hogquist

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Intraepithelial Lymphocytes of the Intestine.Annual review of immunology · 2024
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Innate and Innate-like Effector Lymphocytes in Health and Disease.Journal of immunology (Baltimore, Md. : 1950) · 2022
    Review
  15. Article
  16. Article
  17. Bcl-2 Is Necessary to Counteract Bim and Promote Survival of TCRαβJournal of immunology (Baltimore, Md. : 1950) · 2022
    Article
  18. Article
  19. Article
  20. Human Thymic CD10International journal of molecular sciences · 2020
    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

6 authors at 1 institution in 1 country.

Roland RuscherCenter for Immunology and Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN.
S Thera LeeCenter for Immunology and Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN.
Oscar C SalgadoCenter for Immunology and Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN.
Elise R BreedCenter for Immunology and Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN.
Sara H OsumCenter for Immunology and Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN.
Kristin A HogquistCenter for Immunology and Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN.
University of Minnesota Medical Center · US

Funding

Type I interferons in tolerance in the steady stateP01AI035296 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HOGQUIST, KRISTIN A. · 1993 to 2023
$31.1M
TCR signal strength in thymic selectionR37AI039560 · NIAID · UNIVERSITY OF MINNESOTA · PI HOGQUIST, KRISTIN A. · 2012 to 2021
$3.7M
Stem Cell Biology Training ProgramT32GM113846 · NIGMS · UNIVERSITY OF MINNESOTA · PI PERLINGEIRO, RITA C. R. · 2015 to 2019
$712k
NIAID NIH HHS P01 AI035296NIAID NIH HHS R37 AI039560NIGMS NIH HHS T32 GM113846
6 · The paper itself

Abstract

CD8αα intraepithelial lymphocytes (IELs) are abundant T cells that protect the gut epithelium. Their thymic precursors (IELps) include PD-1+ type A and Tbet+ type B populations, which differ in their antigen-receptor specificities. To better understand CD8αα IEL ontogeny, we performed "time-stamp" fate mapping experiments and observed that it seeds the intestine predominantly during a narrow time window in early life. Adoptively transferred IELps parked better in the intestines of young mice than in adults. In young mice, both type A and type B IELps had an S1PR1+ and α4β7+ emigration- and mucosal-homing competent phenotype, while this was restricted to type A IELps in adults. Only CD8αα IELs established in early life were enriched in cells bearing type B IELp TCR usage. Together, our results suggest that the young intestine facilitates CD8αα IEL establishment and that early IELs are distinct from IELs established after this initial wave. These data provide novel insight into the ontogeny of CD8αα IELs.

Indexed as

Immunity, MucosalAnimalsCD8 AntigensCell MovementIntestinal MucosaIntraepithelial LymphocytesMiceMice, TransgenicThymocytesCD8 antigen, alpha chainCD8 Antigens

Identifiers

PMID32687575
PMCPMC7398160
OpenAlexW3044545971

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.