Evidence map›Paper›PMID 31824482›Full record

ArticleFrontiers in immunology2019

T Regulatory Cells From Non-obese Diabetic Mice Show Low Responsiveness to IL-2 Stimulation and Exhibit Differential Expression of Anergy-Related and Ubiquitination Factors.

Gloria J Godoy, Carolina Olivera, Daniela A Paira, Florencia C Salazar, Yamile Ana, Cinthia C Stempin, Ruben D Motrich, Virginia E Rivero

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

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  11. Activation pathways that drive CD4Immunological reviews · 2022
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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

8 authors at 3 institutions in 1 country.

Gloria J GodoyCentro de Investigaciones en Bioquímica Clínica e Inmunología, CONICET, Córdoba, Argentina.
Carolina OliveraCentro de Investigaciones en Bioquímica Clínica e Inmunología, CONICET, Córdoba, Argentina.
Daniela A PairaCentro de Investigaciones en Bioquímica Clínica e Inmunología, CONICET, Córdoba, Argentina.
Florencia C SalazarCentro de Investigaciones en Bioquímica Clínica e Inmunología, CONICET, Córdoba, Argentina.
Yamile AnaCentro de Investigaciones en Bioquímica Clínica e Inmunología, CONICET, Córdoba, Argentina.
Cinthia C StempinCentro de Investigaciones en Bioquímica Clínica e Inmunología, CONICET, Córdoba, Argentina.
Ruben D MotrichCentro de Investigaciones en Bioquímica Clínica e Inmunología, CONICET, Córdoba, Argentina.
Virginia E RiveroCentro de Investigaciones en Bioquímica Clínica e Inmunología, CONICET, Córdoba, Argentina.
Research Centre in Biological Chemistry of Córdoba · ARConsejo Nacional de Investigaciones Científicas y Técnicas · ARUniversidad Nacional de Córdoba · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Foxp3+ Regulatory T cells (Tregs) are pivotal for the maintenance of tolerance. Alterations in their number and/or function have been proposed to occur in the autoimmune-prone non-obese diabetic (NOD) mouse. Comparing the frequencies and absolute numbers of CD4+Foxp3+CD25+ Tregs among 4 to 6-week old NOD, B6, and BALB/c mice, we observed differences in counts and Foxp3 expression in Tregs from secondary lymphoid organs, but not in the thymus. Upon TCR and IL-2 stimulation, NOD Tregs showed lower responses than Tregs from B6 and BALB/c mice. Indeed, NOD Tregs responded with less proliferation and with smaller increments in the expression of CD25, LAP-1, CD39, PD-1, PD-L1, and LAG-3, when

Indexed as

AnimalsClonal AnergyFemaleInterleukin-2Lymphocyte ActivationMiceMice, Inbred NODSelf ToleranceT-Lymphocytes, RegulatoryUbiquitinationInterleukin-2GRAILIL-2 signalingNOD miceregulatory T cellsSTUB1USP7

Identifiers

PMID31824482
PMCPMC6886461
OpenAlexW2989603947

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.