Evidence map›Paper›PMID 36036450›Full record

ReviewAmerican journal of physiology. Cell physiology2022

The multifunctional nature of CD103 (αEβ7 integrin) signaling in tissue-resident lymphocytes.

Weili Xu, Tessa Bergsbaken, Karen L Edelblum

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Cell physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Increased CD103Cancer immunology, immunotherapy : CII · 2025
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Tissue-Resident Memory T Cells Are Implicated in the Pathogenesis of Hypersensitivity Pneumonitis.American journal of respiratory and critical care medicine · 2023
    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

3 authors at 1 institution in 1 country.

Weili XuDepartment of Pathology, Immunology and Laboratory Medicine, Center for Immunity and Inflammation, Rutgers New Jersey Medical School, Newark, New Jersey.
Tessa BergsbakenDepartment of Pathology, Immunology and Laboratory Medicine, Center for Immunity and Inflammation, Rutgers New Jersey Medical School, Newark, New Jersey.
Karen L EdelblumDepartment of Pathology, Immunology and Laboratory Medicine, Center for Immunity and Inflammation, Rutgers New Jersey Medical School, Newark, New Jersey.ORCID 0000-0001-8288-4898
Rutgers, The State University of New Jersey · US

Funding

Differentiation and function of intestinal tissue-resident memory T cellsR01AI153096 · NIAID · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI BERGSBAKEN, TESSA · 2020 to 2024
$1.9M
Interferon regulation of gamma delta intraepithelial lymphocyte activationR01DK119349 · NIDDK · RBHS-NEW JERSEY MEDICAL SCHOOL · PI EDELBLUM, KAREN LEIGH · 2019 to 2023
$1.8M
Microbiota-gamma delta IEL-Paneth cell axis in host antimicrobial responseR21AI171959 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI EDELBLUM, KAREN LEIGH · 2022 to 2023
$439k
Profiling intraepithelial lymphocyte populations in health and Crohn’s diseaseR21DK123488 · NIDDK · RBHS-NEW JERSEY MEDICAL SCHOOL · PI EDELBLUM, KAREN LEIGH · 2019 to 2020
$437k
Mobilization of tissue-resident lymphocytes during secondary infectionR21AI148900 · NIAID · RBHS-NEW JERSEY MEDICAL SCHOOL · PI BERGSBAKEN, TESSA · 2020 to 2021
$420k
NIAID NIH HHS R01 AI153096NIAID NIH HHS R21 AI148900NIAID NIH HHS R21 AI171959NIDDK NIH HHS R01 DK119349NIDDK NIH HHS R21 DK123488
6 · The paper itself

Abstract

Intestinal tissue-resident lymphocytes are critical for maintenance of the mucosal barrier and to prevent enteric infections. The activation of these lymphocytes must be tightly regulated to prevent aberrant inflammation and epithelial damage observed in autoimmune diseases, yet also ensure that antimicrobial host defense remains uncompromised. Tissue-resident lymphocytes express CD103, or αE integrin, which dimerizes with the β7 subunit to bind to E-cadherin expressed on epithelial cells. Although the role of CD103 in homing and retention of lymphocytes to and within peripheral tissues has been well characterized, the molecular signals activated following CD103 engagement remain understudied. Here, we highlight recent studies that elucidate the functional contribution of CD103 in various lymphocyte subpopulations, either as an independent signaling molecule or in the context of TCR co-stimulation. Finally, we will discuss the gaps in our understanding of CD103 biology and the therapeutic potential of targeting CD103 on tissue-resident lymphocytes.

Indexed as

CadherinsIntegrinsAntigens, CDCD8-Positive T-LymphocytesHumansIntegrin alpha ChainsLymphocytesReceptors, Antigen, T-Cellalpha E integrinsAntigens, CDCadherinsIntegrin alpha ChainsIntegrinsReceptors, Antigen, T-Celladhesionintegrinintracellular signalinglymphocytemigration

Identifiers

PMID36036450
PMCPMC9576162
OpenAlexW4293433423

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.