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NOD-Aec1Aec2 mice, followed by lymphocytic infiltration at approximately 16–20 weeks of age in male and female B6.

NOD-Aec1Aec2 mice, preceded by the loss of secretory function in both sexes mice than the male counterpart during the adaptive phase with progressive severity during the clinical-disease phase.

Our data indicate that IL-17 is a potent inflammatory molecule in the induction of chemoattractants, cytokines, and glandular apoptosis in males and females. Il17 mice showed no significant loss of saliva from 4–28 weeks of age. NOD-Aec1Aec2 mice exhibited significant loss of SFR over similar age span.

Analysis of the B cell response revealed that IL-17 is highly involved in modulating Th2 cytokines and altering autoantibody profiles while changing plasma cell and germinal center B cell populations in female and male Sj S. The decrease in SFR with advanced age (28 weeks) was more than 80% of normal baseline at 4 weeks of age in male and female B6.

While Sj S can be diagnosed as an independent disease, referred to as primary Sj S (p Sj S), it is often seen in association with other connective tissue disease, referred to as secondary Sj S.

The underlying pathogenesis of Sj S is still elusive, but it is thought to involve abnormal salivary gland homeostasis, neural circuitry malfunction from the presence of autoantibodies, and progressive tissue destruction mediated by infiltrating lymphocytes.

There is evidence to suggest that secretion of IL-17 by salivary gland epithelial cells leads to sequestration of neutrophils and monocytes in the glands.

Enumerating the focus score, the results indicated that male and female diseased B6. NOD-Aec1Aec2 displayed higher numbers of neutrophils and macrophages than their male counterparts whereas minimal numbers of neutrophils and macrophages were detected in both sexes of B6 and B6.

NOD-Aec1Aec2 mice exhibited higher focus scores (1.250 ± 0.313, 1.619 ± 0.381, respectively) in comparison to male and female B6 (0.400 ± 0.163, 0.385 ± 0.140) or B6. Il17 mice showed smaller aggregates of inflammatory cells and an absence of neutrophils and macrophages (Supplementary Fig. The results suggest that IL-17 plays an important role in influencing the numbers of inflammatory cells as well as the cell type in inflammatory infiltrate organization.

Involvement of the musculature often leads to fibromyalgia-like symptoms and chronic fatigue.

Between 4% and 10% of patients with Sj S will develop non-Hodgkin’s B cell lymphomas, some of which become high-grade malignancies patients had significantly increased levels of IL-1RA, IL-15, IL-17A (IL-17) and IFN-α, and of chemokines including macrophage inflammatory proteins (MIPs)-1α, MIP-1β, eotaxin and MCP-1, with higher levels of autoantibodies against Ro-52, Ro-60 and La-48 compared with GC.

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This coincided with a higher composition of infiltrating B and T cells in the salivary glands, which exhibited stronger proliferative potential in females.

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