Evidence map›Paper›PMID 34962663›Full record

ArticleImmunology and cell biology2022

The ICOS-ICOSL pathway tunes thymic selection.

Mengqi Dong, Jinsam Chang, Marie-Ève Lebel, Noémie Gervais, Marilaine Fournier, Ève Mallet Gauthier, Woong-Kyung Suh, Heather J Melichar

Open access · hybridAbstract read
In one paragraph

Article in Immunology and cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. ICOSL: more than a trigger of ICOS function.Cell communication and signaling : CCS · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Stabilization of β-Catenin Directs HEB to Limit Thymic Selection.Journal of immunology (Baltimore, Md. : 1950) · 2024
    Article
  8. Review
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

8 authors at 2 institutions in 1 country.

Mengqi DongDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montréal, QC, Canada.
Jinsam ChangInstitut de Recherches Cliniques de Montréal, Montréal, QC, Canada.
Marie-Ève LebelImmunology-Oncology Unit, Maisonneuve-Rosemont Hospital Research Center, Montréal, QC, Canada.
Noémie GervaisImmunology-Oncology Unit, Maisonneuve-Rosemont Hospital Research Center, Montréal, QC, Canada.
Marilaine FournierImmunology-Oncology Unit, Maisonneuve-Rosemont Hospital Research Center, Montréal, QC, Canada.
Ève Mallet GauthierDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montréal, QC, Canada.
Woong-Kyung SuhDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montréal, QC, Canada.
Heather J MelicharImmunology-Oncology Unit, Maisonneuve-Rosemont Hospital Research Center, Montréal, QC, Canada.ORCID 0000-0003-0951-334X
Hôpital Maisonneuve-Rosemont · CAMontreal Clinical Research Institute · CA

Funding

CIHR PJT-159526CIHR PJT-168862
6 · The paper itself

Abstract

Negative selection of developing T cells plays a significant role in T-cell tolerance to self-antigen. This process relies on thymic antigen-presenting cells which express both self-antigens and cosignaling molecules. Inducible T-cell costimulator (ICOS) belongs to the CD28 family of cosignaling molecules and binds to ICOS ligand (ICOSL). The ICOS signaling pathway plays important roles in shaping the immune response to infections, but its role in central tolerance is less well understood. Here we show that ICOSL is expressed by subsets of thymic dendritic cells and medullary thymic epithelial cells as well as thymic B cells. ICOS expression is upregulated as T cells mature in the thymus and correlates with T-cell receptor signal strength during thymic selection. We also provide evidence of a role for ICOS signaling in mediating negative selection. Our findings suggest that ICOS may fine-tune T-cell receptor signals during thymic selection contributing to the generation of a tolerant T-cell population.

Indexed as

Antigen-Presenting CellsT-LymphocytesB-LymphocytesCD28 AntigensInducible T-Cell Co-Stimulator LigandCD28 AntigensInducible T-Cell Co-Stimulator LigandICOSICOSLnegative selectionthymic antigen-presenting cellsthymocytes

Identifiers

PMID34962663
PMCPMC9304562
OpenAlexW4200371566

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.