Evidence map›Paper›PMID 25753268›Full record

ArticleImmunology and cell biology2015

A discrete population of IFN λ-expressing BDCA3hi dendritic cells is present in human thymus.

Víctor G Martínez, Noelia M Canseco, Laura Hidalgo, Jaris Valencia, Ana Entrena, Lidia M Fernández-Sevilla, Carmen Hernández-López, Rosa Sacedón, Angeles Vicente, Alberto Varas

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Article in Immunology and cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Víctor G MartínezDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Noelia M CansecoDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Laura HidalgoDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Jaris ValenciaDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Ana EntrenaDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Lidia M Fernández-SevillaDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Carmen Hernández-LópezDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Rosa SacedónDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Angeles VicenteDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Alberto VarasDepartment of Cell Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
Universidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human thymus contains two major subpopulations of dendritic cells (DCs), conventional DCs (cDCs) and plasmacytoid DCs (pDCs), which are mainly involved in central tolerance and also in protecting the thymus against infections. In blood and peripheral organs cDCs include the subpopulation of BDCA3(hi) DCs, considered as equivalents to mouse CD8α(+) DCs. In this study we describe in human thymus the presence of a discrete population of BDCA3(hi) DCs that, like their peripheral counterparts, express CD13, low-intermediate levels of CD11c, CLEC9A, high levels of XCR1, IRF8 and TLR3, and mostly lack the expression of CD11b, CD14 and TLR7. Thymic BDCA3(hi) DCs display immature features with a low expression of costimulatory molecules and HLA-DR, and a low allostimulatory capacity. Also, BDCA3(hi) DCs exhibit a strong response to TLR3 stimulation, producing high levels of interferon (IFN)-λ1 and CXCL10, which indicates that, similarly to thymic pDCs, BDCA3(hi) DCs can have an important role in thymus protection against viral infections.

Indexed as

Antigens, DifferentiationAntigens, SurfaceApoptosisCells, CulturedChemokine CXCL10Child, PreschoolCoculture TechniquesDendritic CellsHLA-DR AntigensHumansInfantInfant, NewbornInterferon LambdaInterferonsInterleukinsLectins, C-TypeAntigens, DifferentiationAntigens, SurfaceChemokine CXCL10CLEC9a protein, humanCXCL10 protein, humanHLA-DR AntigensInterferon Lambdainterferon-lambda, humanInterferonsInterleukinsLectins, C-TypeReceptors, G-Protein-CoupledReceptors, MitogenRNA, MessengerTHBD protein, humanThrombomodulinTLR3 protein, humanToll-Like Receptor 3XCR1 protein, human

Identifiers

PMID25753268
OpenAlexW2041453401

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.