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Article: Humanized Mouse Models of Sjögren's Disease

TitleHumanized Mouse Models of Sjögren's Disease
Authors
Keywordshumanized
immunization
mouse model
Sjögren's disease
Issue Date1-Jul-2025
PublisherWiley
Citation
Current Protocols in Neuroscience, 2025, v. 5, n. 7 How to Cite?
Abstract

Sjögren's disease (SjD), or Sjögren's syndrome, is a chronic autoimmune condition that targets exocrine glands, leading to dryness symptoms. With the treatment plan for SjD having remained unchanged for the past decade, there is a critical need for innovative therapeutic strategies. To bridge the gap between mouse models and human patients, we have established a mouse model of experimental Sjögren's syndrome with a human immune system (HIS-ESS). Immunizing mice with antigens derived from human salivary epithelial cells results in HIS-ESS mice that display clinical features of SjD that include salivary dysfunction, increased serum autoantibodies, and dysregulated immune responses. Effector T cell subsets such as Th1, Th17, and T follicular helper (Tfh) cells are also elevated in HIS-ESS mice. Thus, this humanized model can effectively recapitulate SjD outcomes and immunopathogenesis, offering a promising platform for drug screening and preclinical research. © 2025 Wiley Periodicals LLC. Basic Protocol: Establishment of humanized mouse models of primary Sjögren's syndrome. Support Protocol 1: Irradiation of neonatal mice. Support Protocol 2: Preparation of proteins from A-253 human salivary epithelial cells. Support Protocol 3: Determination of mouse saliva flow rate.


Persistent Identifierhttp://hdl.handle.net/10722/358787
ISSN
2023 SCImago Journal Rankings: 0.928

 

DC FieldValueLanguage
dc.contributor.authorYu, Sulan-
dc.contributor.authorLin, Xiang-
dc.date.accessioned2025-08-13T07:48:02Z-
dc.date.available2025-08-13T07:48:02Z-
dc.date.issued2025-07-01-
dc.identifier.citationCurrent Protocols in Neuroscience, 2025, v. 5, n. 7-
dc.identifier.issn1934-8576-
dc.identifier.urihttp://hdl.handle.net/10722/358787-
dc.description.abstract<p>Sjögren's disease (SjD), or Sjögren's syndrome, is a chronic autoimmune condition that targets exocrine glands, leading to dryness symptoms. With the treatment plan for SjD having remained unchanged for the past decade, there is a critical need for innovative therapeutic strategies. To bridge the gap between mouse models and human patients, we have established a mouse model of experimental Sjögren's syndrome with a human immune system (HIS-ESS). Immunizing mice with antigens derived from human salivary epithelial cells results in HIS-ESS mice that display clinical features of SjD that include salivary dysfunction, increased serum autoantibodies, and dysregulated immune responses. Effector T cell subsets such as Th1, Th17, and T follicular helper (Tfh) cells are also elevated in HIS-ESS mice. Thus, this humanized model can effectively recapitulate SjD outcomes and immunopathogenesis, offering a promising platform for drug screening and preclinical research. © 2025 Wiley Periodicals LLC. Basic Protocol: Establishment of humanized mouse models of primary Sjögren's syndrome. Support Protocol 1: Irradiation of neonatal mice. Support Protocol 2: Preparation of proteins from A-253 human salivary epithelial cells. Support Protocol 3: Determination of mouse saliva flow rate.</p>-
dc.languageeng-
dc.publisherWiley-
dc.relation.ispartofCurrent Protocols in Neuroscience-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjecthumanized-
dc.subjectimmunization-
dc.subjectmouse model-
dc.subjectSjögren's disease-
dc.titleHumanized Mouse Models of Sjögren's Disease-
dc.typeArticle-
dc.identifier.doi10.1002/cpz1.70178-
dc.identifier.pmid40657698-
dc.identifier.scopuseid_2-s2.0-105010697949-
dc.identifier.volume5-
dc.identifier.issue7-
dc.identifier.eissn2691-1299-
dc.identifier.issnl1934-8576-

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