Evidence map›Paper›PMID 26331349›Full record

ArticleImmunology2015

CD73-mediated adenosine production promotes stem cell-like properties in mouse Tc17 cells.

Felipe Flores-Santibáñez, Dominique Fernández, Daniel Meza, Gabriela Tejón, Leonardo Vargas, Lorena Varela-Nallar, Sebastián Arredondo, Victoria Guixé, Mario Rosemblatt, María Rosa Bono and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

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  7. Crosstalk Between ATP-PFrontiers in cellular neuroscience · 2021
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  17. Frontiers in immunology · 2018
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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

11 authors at 2 institutions in 1 country.

Felipe Flores-SantibáñezDepartamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Dominique FernándezDepartamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Daniel MezaDepartamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Gabriela TejónDepartamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Leonardo VargasDepartamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Lorena Varela-NallarCentro de Investigaciones Biomedicas, Facultad de Ciencias Biológicas y Facultad de Medicina, Universidad Andres Bello, Santiago, Chile.
Sebastián ArredondoCentro de Investigaciones Biomedicas, Facultad de Ciencias Biológicas y Facultad de Medicina, Universidad Andres Bello, Santiago, Chile.
Victoria GuixéDepartamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Mario RosemblattDepartamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
María Rosa BonoDepartamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
Daniela SaumaDepartamento de Biologia, Facultad de Ciencias, Universidad de Chile, Santiago, Chile.
University of Chile · CLUniversidad Andrés Bello · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CD73 ectonucleotidase catalyses the hydrolysis of AMP to adenosine, an immunosuppressive molecule. Recent evidence has demonstrated that this ectonucleotidase is up-regulated in T helper type 17 cells when generated in the presence of transforming growth factor-β (TGF-β), and hence CD73 expression is related to the acquisition of immunosuppressive potential by these cells. TGF-β is also able to induce CD73 expression in CD8(+) T cells but the function of this ectonucleotidase in CD8(+) T cells is still unknown. Here, we show that Tc17 cells present high levels of the CD73 ectonucleotidase and produce adenosine; however, they do not suppress the proliferation of CD4(+) T cells. Interestingly, we report that adenosine signalling through A2A receptor favours interleukin-17 production and the expression of stem cell-associated transcription factors such as tcf-7 and lef-1 but restrains the acquisition of Tc1-related effector molecules such as interferon-γ and Granzyme B by Tc17 cells. Within the tumour microenvironment, CD73 is highly expressed in CD62L(+) CD127(+) CD8(+) T cells (memory T cells) and is down-regulated in GZMB(+) KLRG1(+) CD8(+) T cells (terminally differentiated T cells), demonstrating that CD73 is expressed in memory/naive cells and is down-regulated during differentiation. These data reveal a novel function of CD73 ectonucleotidase in arresting CD8(+) T-cell differentiation and support the idea that CD73-driven adenosine production by Tc17 cells may promote stem cell-like properties in Tc17 cells.

Indexed as

5'-NucleotidaseAdenosineAdenosine MonophosphateAdoptive TransferAnimalsCD8-Positive T-LymphocytesCell DifferentiationCytokinesDown-RegulationImmunologic MemoryImmunophenotypingLymphocytes, Tumor-InfiltratingMelanoma, ExperimentalMiceMice, TransgenicPhenotype5'-NucleotidaseAdenosineAdenosine MonophosphateCytokinesadenosineCD73cell differentiationstem cellTc17tumour immunology

Identifiers

PMID26331349
PMCPMC4693903
OpenAlexW2153403185

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.