Evidence map›Paper›PMID 21253584›Full record

ReviewJournal of biomedicine & biotechnology2011

Current concepts: mouse models of Sjögren's syndrome.

Tegan N Lavoie, Byung Ha Lee, Cuong Q Nguyen

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of biomedicine & biotechnology, 2011. 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
1.5field-weighted citation impact, top 18% 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, 67 citations in OpenAlex.

  1. Article
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  4. Organoid-based modeling and regenerative strategies for salivary gland dysfunction.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2025
    Review
  5. Review
  6. Article
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  8. Article
  9. Early Dry Eye Disease Onset in a NOD.H-2h4 Mouse Model of Sjögren's Syndrome.Investigative ophthalmology & visual science · 2022
    Article
  10. Plasmacytoid dendritic cells promote the pathogenesis of Sjögren's syndrome.Biochimica et biophysica acta. Molecular basis of disease · 2022
    Article
  11. Blocking IAgLife sciences · 2022
    Article
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  14. Review
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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

3 authors at 2 institutions in 1 country.

Tegan N LavoieDepartment of Oral Biology, College of Dentistry, University of Florida, P.O. Box 100424, 1600 SW Archer Road, Gainesville, FL 32610, USA.
Byung Ha Lee
Cuong Q Nguyen
University of Florida · USMassachusetts Institute of Technology · US

Funding

Immuno-pathophysiology of Lymphocytic Foci in Sjogren?s SyndromeR00DE018958 · NIDCR · UNIVERSITY OF FLORIDA · PI NGUYEN, CUONG Q · 2011 to 2013
$717k
Gene therapy targeting the Th17 / IL-27 system in autoimmune exocrinopathyR21AI081952 · NIAID · UNIVERSITY OF FLORIDA · PI PECK, AMMON B · 2009 to 2010
$403k
Immune-pathophysiology of lymphocytic foci in Sjogren's syndromeK99DE018958 · NIDCR · UNIVERSITY OF FLORIDA · PI NGUYEN, CUONG Q · 2009 to 2010
$216k
NIAID NIH HHS R21 AI081952NIAID NIH HHS R21AI081952NIDCR NIH HHS K99 DE018958NIDCR NIH HHS K99DE018958NIDCR NIH HHS R00 DE018958
6 · The paper itself

Abstract

Sjögren's syndrome (SjS) is a complex chronic autoimmune disease of unknown etiology which primarily targets the exocrine glands, resulting in eventual loss of secretory function. The disease can present as either primary SjS or secondary SjS, the latter of which occurs concomitantly with another autoimmune disease such as rheumatoid arthritis, systemic lupus erythematosus, scleroderma, or primary biliary cirrhosis. Current advancements in therapeutic prevention and treatment for SjS are impeded by lack of understanding in the pathophysiological and clinical progression of the disease. Development of appropriate mouse models for both primary and secondary SjS is needed in order to advance knowledge of this disease. This paper details important features, advantages, and pitfalls of current animal models of SjS, including spontaneous, transgenic, knockout, immunization, and transplantation chimera mouse models, and emphasizes the need for a better model in representing the human SjS phenotype.

Indexed as

Disease Models, AnimalAnimalsChimeraHumansImmunizationMiceMice, TransgenicSjogren's SyndromeTransplantation

Identifiers

PMID21253584
PMCPMC3018660
OpenAlexW2136589687

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.