Evidence map›Paper›PMID 28475283›Full record

ReviewEuropean journal of immunology2017

CD69: from activation marker to metabolic gatekeeper.

Danay Cibrián, Francisco Sánchez-Madrid

Open access · bronzeAbstract readReview
In one paragraph

Review in European journal of immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 585 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
585citing papers in PubMed, 1 pooled it
17.2field-weighted citation impact, top 1% 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

585 citing papers in PubMed, 1 synthesis or guideline pooled it, 913 citations in OpenAlex.

  1. Pooled it
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  13. Lung Resident T Cells Across the Spectrum of TB Infection and Disease.bioRxiv : the preprint server for biology · 2026
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525 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Danay CibriánHospital Universitario de la Princesa, Instituto Investigación Sanitaria Princesa (IIS-IP), Universidad Autónoma de Madrid, Madrid, Spain.
Francisco Sánchez-MadridHospital Universitario de la Princesa, Instituto Investigación Sanitaria Princesa (IIS-IP), Universidad Autónoma de Madrid, Madrid, Spain.ORCID 0000-0001-5303-0762
Instituto de Salud Carlos III · ES

Funding

European Research Council 294340
6 · The paper itself

Abstract

CD69 is a membrane-bound, type II C-lectin receptor. It is a classical early marker of lymphocyte activation due to its rapid appearance on the surface of the plasma membrane after stimulation. CD69 is expressed by several subsets of tissue resident immune cells, including resident memory T (TRM) cells and gamma delta (γδ) T cells, and is therefore considered a marker of tissue retention. Recent evidence has revealed that CD69 regulates some specific functions of selected T-cell subsets, determining the migration-retention ratio as well as the acquisition of effector or regulatory phenotypes. Specifically, CD69 regulates the differentiation of regulatory T (Treg) cells as well as the secretion of IFN-γ, IL-17, and IL-22. The identification of putative CD69 ligands, such as Galectin-1 (Gal-1), suggests that CD69-induced signaling can be regulated not only during cognate contacts between T cells and antigen-presenting cells in lymphoid organs, but also in the periphery, where cytokines and other metabolites control the final outcome of the immune response. Here, we will discuss new aspects of the molecular signaling mediated by CD69 and its involvement in the metabolic reprogramming regulating TH-effector lineages.

Indexed as

Lymphocyte ActivationAnimalsAntigen-Presenting CellsAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCell DifferentiationCytokinesGalectinsGene Expression RegulationHumansInterleukin-17Lectins, C-TypeSignal TransductionT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsAntigens, CDAntigens, Differentiation, T-LymphocyteCD69 AntigensCytokinesGalectinsInterleukin-17Lectins, C-TypeCD69Galectin-1LAT1MetabolismmTORS1P1T cells

Identifiers

PMID28475283
PMCPMC6485631
OpenAlexW2610932550

What OpenQuestion holds

Textmetadata
LicenceTDM
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.