Evidence map›Paper›PMID 27760209›Full record

ArticlePloS one2016

Pristane-Accelerated Autoimmune Disease in (SWR X NZB) F1 Mice Leads to Prominent Tubulointerstitial Inflammation and Human Lupus Nephritis-Like Fibrosis.

Agnes Gardet, Wei C Chou, Taylor L Reynolds, Diana B Velez, Kai Fu, Julia M Czerkowicz, Jeffrey Bajko, Ann M Ranger, Normand Allaire, Hannah M Kerns and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
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

18 authors at 3 institutions in 1 country.

Agnes GardetBiogen, Cambridge, Massachusetts, United States of America.
Wei C ChouBiogen, Cambridge, Massachusetts, United States of America.
Taylor L ReynoldsBiogen, Cambridge, Massachusetts, United States of America.
Diana B VelezBiogen, Cambridge, Massachusetts, United States of America.
Kai FuBiogen, Cambridge, Massachusetts, United States of America.
Julia M CzerkowiczBiogen, Cambridge, Massachusetts, United States of America.
Jeffrey BajkoBiogen, Cambridge, Massachusetts, United States of America.
Ann M RangerBiogen, Cambridge, Massachusetts, United States of America.
Normand AllaireBiogen, Cambridge, Massachusetts, United States of America.
Hannah M KernsBiogen, Cambridge, Massachusetts, United States of America.
Sarah RyanBiogen, Cambridge, Massachusetts, United States of America.
Holly M LegaultBiogen, Cambridge, Massachusetts, United States of America.
Robert W DunstanBiogen, Cambridge, Massachusetts, United States of America.
Robert LafyatisDivision of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, United States of America.
Matvey LukashevBiogen, Cambridge, Massachusetts, United States of America.
Joanne L VineyBiogen, Cambridge, Massachusetts, United States of America.
Jeffrey L BrowningBoston University School of Medicine, Department of Microbiology, Boston, United States of America.
Dania RabahBiogen, Cambridge, Massachusetts, United States of America.
Biogen (United States) · USBoston University · USUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mouse models lupus nephritis (LN) have provided important insights into disease pathogenesis, although none have been able to recapitulate all features of the human disease. Using comprehensive longitudinal analyses, we characterized a novel accelerated mouse model of lupus using pristane treatment in SNF1 (SWR X NZB F1) lupus prone mice (pristane-SNF1 mice). Pristane treatment in SNF1 mice accelerated the onset and progression of proteinuria, autoantibody production, immune complex deposition and development of renal lesions. At week 14, the pristane-SNF1 model recapitulated kidney disease parameters and molecular signatures seen in spontaneous disease in 36 week-old SNF1 mice and in a traditional IFNα-accelerated NZB X NZW F1 (BWF1) model. Blood transcriptome analysis revealed interferon, plasma cell, neutrophil, T-cell and protein synthesis signatures in the pristane-SNF1 model, all known to be present in the human disease. The pristane-SNF1 model appears to be particularly useful for preclinical research, robustly exhibiting many characteristics reminiscent of human disease. These include i) a stronger upregulation of the cytosolic nucleic acid sensing pathway, which is thought to be key component of the pathogenesis of the human disease, and ii) more prominent kidney interstitial inflammation and fibrosis, which have been both associated with poor prognosis in human LN. To our knowledge, this is the only accelerated model of LN that exhibits a robust tubulointerstitial inflammatory and fibrosis response. Taken together our data show that the pristane-SNF1 model is a novel accelerated model of LN with key features similar to human disease.

Indexed as

AnimalsAutoantibodiesDisease Models, AnimalDisease ProgressionDNA-Binding ProteinsFemaleFibrosisGlomerulonephritisHumansHypergammaglobulinemiaInflammationKidney TubulesLupus NephritisMembrane ProteinsMiceSTING ProteinAim2 protein, mouseAutoantibodiesDNA-Binding ProteinsMembrane ProteinspristaneSting1 protein, mouseSTING ProteinTerpenes

Identifiers

PMID27760209
PMCPMC5070861
OpenAlexW2534734215

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.