Evidence map›Paper›PMID 25862391›Full record

ArticleClinical immunology (Orlando, Fla.)2015

Estrogen receptor alpha signaling promotes Sle1-induced loss of tolerance and immune cell activation and is responsible for sex bias in B6.Sle1 congenic mice.

Shayla D Yoachim, Jenny S Nuxoll, Kimberly K Bynoté, Karen A Gould

Open access · greenAbstract read
In one paragraph

Article in Clinical immunology (Orlando, Fla.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 9 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

4 authors at 3 institutions in 1 country.

Shayla D YoachimDepartment of Genetics, Cell Biology & Anatomy, University of Nebraska Medical Center, 985805 Nebraska Medical Center, Omaha, NE 68198-5805, USA.
Jenny S NuxollDepartment of Genetics, Cell Biology & Anatomy, University of Nebraska Medical Center, 985805 Nebraska Medical Center, Omaha, NE 68198-5805, USA.
Kimberly K BynotéDepartment of Genetics, Cell Biology & Anatomy, University of Nebraska Medical Center, 985805 Nebraska Medical Center, Omaha, NE 68198-5805, USA.
Karen A GouldDepartment of Genetics, Cell Biology & Anatomy, University of Nebraska Medical Center, 985805 Nebraska Medical Center, Omaha, NE 68198-5805, USA. Electronic address: kagould@unmc.edu.
University of Nebraska Medical Center · USNebraska Medical Center · USPediatrics and Genetics · US

Funding

Estrogen Receptor a Regulation of Lupus Development and PathogenesisR01AI075167 · NIAID · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI GOULD, KAREN A. · 2010 to 2014
$1.9M
Estrogen Receptor a Regulation of Lupus Development & PathogenesisR56AI075167 · NIAID · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI GOULD, KAREN A. · 2009 to 2009
$417k
NIAID NIH HHS R01 AI075167NIAID NIH HHS R01AI075167NIAID NIH HHS R56 AI075167
6 · The paper itself

Abstract

Sex bias in lupus incidence is thought to be due, in part, to the ability of estrogens to promote loss of tolerance. Previously, we showed that estrogens promote lupus via estrogen receptor α (ERα). C57BL/6 (B6) mice carrying the Sle1 lupus susceptibility locus (B6.Sle1) display loss of tolerance and develop anti-nuclear antibodies and immune cell hyperactivation. The incidence of loss of tolerance in B6.Sle1 females is greater than in males. Here, we show that a deficiency of either estrogens or ERα attenuates loss of tolerance and autoantibody development in B6.Sle1 females. Furthermore, we demonstrate that immune cell activation in B6.Sle1 mice shows sex bias and that ERα deficiency diminishes this phenotype in B6.Sle1 females. Thus, estrogens, acting via ERα, control sex bias in the Sle1 phenotype. Furthermore, we show that ERα may impact the Sle1 phenotype by modulating the expression of Pbx1, one of genes that underlies the Sle1 locus.

Indexed as

AnimalsEpitopesEstrogen Receptor alphaEstrogensFemaleGene Expression RegulationGenetic Predisposition to DiseaseLupus Erythematosus, SystemicMaleMiceMice, KnockoutSex FactorsSignal TransductionEpitopesEstrogen Receptor alphaEstrogensEstrogen receptor alphaImmune cell activationImmunologic toleranceLupusSex bias

Identifiers

PMID25862391
PMCPMC4465054
OpenAlexW1988353904

What OpenQuestion holds

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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.