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Review
. 2020 Dec;19(12):102686.
doi: 10.1016/j.autrev.2020.102686. Epub 2020 Oct 22.

The NZB/W F1 mouse model for Sjögren's syndrome: A historical perspective and lessons learned

Affiliations
Review

The NZB/W F1 mouse model for Sjögren's syndrome: A historical perspective and lessons learned

Harini Bagavant et al. Autoimmun Rev. 2020 Dec.

Abstract

Sjögren's syndrome (SS) is a chronic rheumatic autoimmune disorder affecting multiple organ systems. The clinical findings in SS patients show considerable heterogeneity and overlap with other autoimmune diseases. In addition, the autoimmune response in SS initiates several years before the appearance of clinical symptoms. Thus, understanding the pathogenic mechanisms involved in the disease process have been a challenge. Several animal model systems of SS-like disease have been developed to overcome these issues. The New Zealand Black (NZB) x New Zealand White (NZW) F1 (NZB/W F1) mouse represents the first spontaneous mouse model of SS. In this review, we provide a historical perspective and detailed description of this mouse model focusing on exocrine gland histopathology, autoantibody populations, and glandular dysfunction. Considering that NZB/W F1 mice also develop a systemic lupus erythematosus (SLE)-like disease, this mouse model mimics the clinical presentation of polyautoimmunity seen in a sizable subset of SS patients. It is plausible that such patients will require distinct therapeutic interventions necessary to treat both SLE and SS. Therefore, the NZB/W F1 mouse is a powerful tool to decipher pathogenic mechanisms involved in SS related polyautoimmunity and develop appropriate therapeutic strategies.

Keywords: Lupus; Mouse; NZB/W F1; Polyautoimmunity; Salivary gland; Sjögren's syndrome.

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Figures

Figure 1.
Figure 1.. Salivary gland inflammation in NZB/W F1 female mice at 6–7 months of age.
(A) Representative image of a hematoxylin and eosin-stained submandibular salivary gland showing a large peri-ductal and peri-vascular lymphocytic focus, extending into the gland parenchyma (arrows). Magnification 10×. (B) Immunostaining of the submandibular salivary gland showing the presence of B cells (anti-B220, green) and T cells (anti-CD4, red) within a lymphocytic focus. Magnification 20×.

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