Evidence map›Paper›PMID 27872476›Full record

ReviewNature reviews. Rheumatology2016

New insights into the immunopathogenesis of systemic lupus erythematosus.

George C Tsokos, Mindy S Lo, Patricia Costa Reis, Kathleen E Sullivan

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Rheumatology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 663 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
663citing papers in PubMed, 3 pooled it
76.6field-weighted citation impact, top 1% 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

663 citing papers in PubMed, 3 syntheses or guidelines pooled it, 1,212 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. Review
  9. NINJ1: implications for plasma membrane rupture and disease.Biochemical Society transactions · 2026
    Review
  10. The SLC15A4-TASL complex is essential for lupus development in mice.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Observational
  19. Review
  20. Review

603 more citing papers are in PubMed but not listed here.

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 4 institutions in 2 countries.

George C TsokosDivision of Rheumatology, Beth Israel Deaconess Medical Center, Harvard Medical School, 110 Francis Street, Boston, Massachusetts 02215, USA.
Mindy S LoDivision of Immunology, Boston Children's Hospital, Harvard Medical School, 300 Longwood Avenue, Boston, Massachusetts 02115, USA.
Patricia Costa ReisDepartment of Pediatrics, Lisbon Medical School, Lisbon University, Santa Maria Hospital, Avenida Professor Egas Moniz, 1649-035 Lisbon, Portugal.
Kathleen E SullivanDivision of Allergy and Immunology, The Children's Hospital of Philadelphia, The University of Pennsylvania Perelman School of Medicine, 3615 Civic Center Boulevard, Philadelphia, Pennsylvania 19104, USA.
Beth Israel Deaconess Medical Center · USBoston Children's Hospital · USChildren's Hospital of Philadelphia · USHospital de Santa Maria · PT

Funding

Epigenomics of SLER01AR058547 · NIAMS · CHILDREN'S HOSP OF PHILADELPHIA · PI SULLIVAN, KATHLEEN E · 2009 to 2013
$1.8M
NIAMS NIH HHS R01 AR058547
6 · The paper itself

Abstract

The aetiology of systemic lupus erythematosus (SLE) is multifactorial, and includes contributions from the environment, stochastic factors, and genetic susceptibility. Great gains have been made in understanding SLE through the use of genetic variant identification, mouse models, gene expression studies, and epigenetic analyses. Collectively, these studies support the concept that defective clearance of immune complexes and biological waste (such as apoptotic cells), neutrophil extracellular traps, nucleic acid sensing, lymphocyte signalling, and interferon production pathways are all central to loss of tolerance and tissue damage. Increased understanding of the pathogenesis of SLE is driving a renewed interest in targeted therapy, and researchers are now on the verge of developing targeted immunotherapy directed at treating either specific organ system involvement or specific subsets of patients with SLE. Accordingly, this Review places these insights within the context of our current understanding of the pathogenesis of SLE and highlights pathways that are ripe for therapeutic targeting.

Indexed as

AnimalsAntigen-Antibody ComplexApoptosisAutoantibodiesB-LymphocytesDendritic CellsDisease Models, AnimalEpigenesis, GeneticExtracellular TrapsGenetic Predisposition to DiseaseHumansImmune ToleranceImmunotherapyInterferonsLupus Erythematosus, CutaneousLupus Erythematosus, SystemicAntigen-Antibody ComplexAutoantibodiesInterferonsMicroRNAsToll-Like Receptors

Identifiers

PMID27872476
OpenAlexW2551404503

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.