Evidence map›Paper›PMID 28361884›Full record

ArticleScientific reports2017

AT-RvD1 Promotes Resolution of Inflammation in NOD/ShiLtJ mice.

Ching-Shuen Wang, Christina L Maruyama, Justin T Easley, Bryan G Trump, Olga J Baker

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Lipid Metabolism: An Emerging Player in Sjögren's Syndrome.Clinical reviews in allergy & immunology · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Ruscogenin Ameliorated Sjögren's Syndrome by Inhibiting NLRP3 Inflammasome Activation.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  12. Article
  13. Review
  14. SPM Receptor Expression and Localization in Irradiated Salivary Glands.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2021
    Article
  15. Article
  16. Review
  17. Formyl peptide receptors in the mucosal immune system.Experimental & molecular medicine · 2020
    Review
  18. Sex-mediated elevation of the specialized pro-resolving lipid mediator levels in a Sjögren's syndrome mouse model.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Ching-Shuen WangSchool of Dentistry, University of Utah, Salt Lake City, UT, USA.
Christina L MaruyamaSchool of Dentistry, University of Utah, Salt Lake City, UT, USA.
Justin T EasleySchool of Dentistry, University of Utah, Salt Lake City, UT, USA.
Bryan G TrumpSchool of Dentistry, University of Utah, Salt Lake City, UT, USA.
Olga J BakerSchool of Dentistry, University of Utah, Salt Lake City, UT, USA.
University of Utah · US

Funding

THE USE OF FIBRIN HYDROGELS TO PROMOTE SALIVARY GLAND REGENERATIONR01DE022971 · NIDCR · UNIVERSITY OF UTAH · PI ANDREADIS, STELIOS T., BAKER, OLGA JULIANA · 2012 to 2025
$7.2M
Resolution of Cytokine-Mediated Salivary Gland InflammationR01DE021697 · NIDCR · UNIVERSITY OF UTAH · PI BAKER, OLGA JULIANA · 2012 to 2016
$2.3M
NIDCR NIH HHS R01 DE021697NIDCR NIH HHS R01 DE022971
6 · The paper itself

Abstract

Sjögren's syndrome (SS) is a chronic inflammatory autoimmune disease characterized by diminished secretory function of the exocrine glands. Treatments for hyposalivation are limited to the use of saliva substitutes and medications that provide only temporary relief. In light of the high degree of need and the limitations of current therapies, development of alternative treatments to restore functioning is essential. Resolvins (Rv), which are highly potent lipid mediators, offer a viable alternative for better treating inflammatory diseases such as SS. The goal of this study was to determine whether systemic preventive treatment with Aspirin-triggered RvD1 (AT-RvD1) reduces inflammation and preserves secretory functioning in NOD/ShiLtJ SS-like mice. Our results indicate that systemic treatment with AT-RvD1 diminishes the progression of the disease in salivary epithelium from female mice as follows: (a) improves secretory function, (b) reduces pro-inflammatory molecule gene expression, (c) increases anti-inflammatory molecule gene expression and (d) induces M2 macrophage polarization. Finally, AT-RvD1 decreases lymphocytic infiltration into the salivary glands when used with small doses of the steroid, dexamethasone, and promotes the tissue healing process.

Indexed as

AnimalsAspirinDexamethasoneDocosahexaenoic AcidsEpitheliumFemaleInflammationMaleMiceMice, Inbred C57BLMice, Inbred NODMice, KnockoutSalivary GlandsSjogren's SyndromeXerostomiaAspirinDexamethasoneDocosahexaenoic Acidsresolvin D1

Identifiers

PMID28361884
PMCPMC5374540
OpenAlexW2598930830

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.