| Literature DB >> 28526333 |
Jeremy Kiripolsky1, Long Shen2, Yichen Liang3, Alisa Li3, Lakshmanan Suresh4, Yun Lian5, Quan-Zhen Li5, Daniel P Gaile6, Jill M Kramer7.
Abstract
Animal models that recapitulate human disease are crucial for the study of Sjögren's Syndrome (SS). While several SS mouse models exist, there are few primary SS (pSS) models that mimic systemic disease manifestations seen in humans. Similar to pSS patients, NOD.B10Sn-H2b/J (NOD.B10) mice develop exocrine gland disease and anti-nuclear autoantibodies. However, the disease kinetics and spectrum of extra-glandular disease remain poorly characterized in this model. Our objective was to characterize local and systemic SS manifestations in depth in NOD.B10 female mice at early and late disease time points. To this end, sera, exocrine tissue, lung, and kidney were analyzed. NOD.B10 mice have robust lymphocytic infiltration of salivary and lacrimal tissue. In addition, they exhibit significant renal and pulmonary inflammation. We identified numerous autoantibodies, including those directed against salivary proteins. In conclusion, the NOD.B10 model recapitulates both local and systemic pSS disease and represents an excellent model for translational studies.Entities:
Keywords: Autoantibodies; Extra-glandular disease; NOD.B10; Sjögren's syndrome
Mesh:
Substances:
Year: 2017 PMID: 28526333 PMCID: PMC6082154 DOI: 10.1016/j.clim.2017.04.009
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969