Evidence map›Paper›PMID 22551352›Full record

ArticleArthritis research & therapy2012

PAD4 is not essential for disease in the K/BxN murine autoantibody-mediated model of arthritis.

Amanda S Rohrbach, Saskia Hemmers, Sanja Arandjelovic, Maripat Corr, Kerri A Mowen

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

49 citing papers in PubMed, 83 citations in OpenAlex.

  1. Article
  2. Review
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  4. Review
  5. Sepsis-induced NET formation requires MYD88 but is independent of GSDMD and PAD4.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. The Role of the Neutrophilic Network in the Pathogenesis of Psoriasis.International journal of molecular sciences · 2022
    Review
  15. Article
  16. Neutrophils in the Pathogenesis of Rheumatic Diseases: Fueling the Fire.Clinical reviews in allergy & immunology · 2021
    Review
  17. Review
  18. Review
  19. Atherosclerosis in Rheumatoid Arthritis: Promoters and Opponents.Clinical reviews in allergy & immunology · 2020
    Review
  20. Review
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

5 authors at 2 institutions in 1 country.

Amanda S RohrbachDepartment of Chemical Physiology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
Saskia Hemmers
Sanja Arandjelovic
Maripat Corr
Kerri A Mowen
Scripps Research Institute · USUniversity of California, San Diego · US

Funding

Cytokine Gene Regulation by Modification of Arginine ResiduesR01AI067460 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI MOWEN, KERRI A · 2006 to 2010
$2.3M
The Role of Arginine Methyltransferases in Interferon SignalingR01GM085117 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI MOWEN, KERRI A · 2008 to 2011
$1.5M
NIAID NIH HHS AI067460NIGMS NIH HHS GM085117-01
6 · The paper itself

Abstract

introductionBoth murine and human genome-wide association studies have implicated peptidyl arginine deiminase (PAD4) as a susceptibility gene in rheumatoid arthritis (RA). In addition, patients with RA commonly have autoantibodies which recognize PAD4 or and/or citrullinated peptides. This study aims to evaluate the role of PAD4 in the effector phase of arthritis.

methodsPAD4 knock out (KO) and wild type (WT) C57BL/6J mice were injected with K/BxN sera to induce disease. Progression of disease was monitored by measuring paw and ankle swelling and clinical indexes of disease, and pathogenesis was assessed by indexing of clinical progression on paws collected from WT and PAD4 KO mice injected with K/BxN serum. PAD4 activity was determined by visualization of neutrophil extracellular traps (NETs) and immunohistological analysis of histone citrullination.

resultsPAD4 activity is readily detectable in the inflamed synovium of WT but not PAD4 deficient animals, as demonstrated by histone citrullination and NET formation. However, PAD4 WT and KO animals develop K/BxN serum transfer disease with comparable severity and kinetics, with no statistically significant differences noted in clinical scores, swelling, joint erosion or joint invasion.

conclusionsPAD4 WT and KO mice develop disease in the K/BxN serum transfer model of arthritis with similar severity and kinetics, indicating that PAD4 is dispensable in this effector phase model of disease.

Indexed as

AnimalsArthritis, RheumatoidAutoantibodiesDisease Models, AnimalHydrolasesImmunohistochemistryJointsMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicNeutrophilsProtein-Arginine Deiminase Type 4AutoantibodiesHydrolasespeptidylarginine deiminase 4, mouseProtein-Arginine Deiminase Type 4

Identifiers

PMID22551352
PMCPMC3446481
OpenAlexW2004118660

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Registered trials

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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.