Evidence map›Paper›PMID 10931159›Full record

ArticleClinical and experimental immunology2000

Widespread susceptibility among inbred mouse strains to the induction of lupus autoantibodies by pristane.

M Satoh, H B Richards, V M Shaheen, H Yoshida, M Shaw, J O Naim, P H Wooley, W H Reeves

Open access · greenAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Clinical and experimental immunology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

55 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
  2. Article
  3. The conneXion between sex and immune responses.Nature reviews. Immunology · 2024
    Review
  4. Review
  5. Article
  6. Analysis of Nanoparticles' Potential to Induce Autoimmunity.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Excessive CD11cProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  20. 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

8 authors at 3 institutions in 1 country.

M SatohDivision of Rheumatology and Clinical Immunology, University of Florida, Gainesville, FL, USA.
H B Richards
V M Shaheen
H Yoshida
M Shaw
J O Naim
P H Wooley
W H Reeves
University of Florida · USRochester General Hospital · USWayne State University · US

Funding

Pathogenesis on Autoantibodies in Pristane-Induced LupusR01AR044731 · NIAMS · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI REEVES, WESTLEY H · 1997 to 2021
$6.6M
ARTHRITIS AND IMMUNOLOGYT32AR007416 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JORDAN, JOANNE M. · 1986 to 2009
$2.5M
IMMUNE MECHANISMS IN PRISTANE INDUCED LUPUS NEPHRITISR01AI044074 · NIAID · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI REEVES, WESTLEY H · 1999 to 2003
$927k
NIAID NIH HHS AI44074NIAMS NIH HHS R01 AR044731NIAMS NIH HHS R01-AR44731NIAMS NIH HHS T32 AR007416NIAMS NIH HHS T32-AR7416
6 · The paper itself

Abstract

Unlike other agents associated with drug-induced lupus, the isoprenoid alkane pristane induces autoantibodies pathognomonic of lupus, including anti-Sm, anti-dsDNA, and anti-ribosomal P in BALB/c and SJL/J mice. The susceptibility of other strains of mice to pristane-induced lupus is unknown and is the focus of the present study. Anti-nRNP/Sm, anti-Su, and anti-ribosomal P autoantibodies were produced by most strains of mice surveyed within several months of pristane treatment, although there was marked interstrain variability in their frequencies, levels, and times of onset. In sharp contrast, the production of autoantibodies against the double-stranded RNA binding proteins NF45/NF90/p110 was restricted to B6 and B10.S mice. We conclude that pristane selectively induces lupus-specific autoantibodies in virtually any strain of mouse regardless of its genetic background. However, H-2-linked as well as non-H2 genes influenced the expression of individual autoantibody markers. The widespread susceptibility of pristane-treated mice to lupus autoantibody production and the relatively small effect of MHC are unique features of this chemically induced lupus syndrome, with potential implications for understanding the pathogenesis of autoantibodies in idiopathic human systemic lupus erythematosus.

Indexed as

AnimalsAntibodies, AntinuclearAutoantibodiesAutoantigensAutoimmune DiseasesFemaleGenetic Predisposition to DiseaseH-2 AntigensHaplotypesHousing, AnimalHumansImmunoglobulin GK562 CellsLupus Erythematosus, SystemicMiceMice, Inbred AAntibodies, AntinuclearAutoantibodiesAutoantigensH-2 AntigensImmunoglobulin GPeptide Fragmentsphosphoprotein P2, ribosomalPhosphoproteinspristaneribosomal phosphoprotein P1ribosomal protein P0Ribosomal ProteinsTerpenes

Identifiers

PMID10931159
PMCPMC1905709
OpenAlexW2079796469

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.