Search

Objective. To investigate the expression and source of chemokines in minor salivary gland biopsies (MSGs) in patients with Sjogren's syndrome (SS).Methods. Immunohistochemical analysis was used to determine the pattern of chemokine expression in MSGs from patients with (n = 6) and without (n = 5) SS, as well as to examine the phenotype of both resident and infiltrating cells expressing chemokines.Results. Significant differences in the number of infiltrating mononuclear (MN) cells in patients with and without SS were noted. Ductal epithelial cells of SS biopsies expressed significantly increased levels of macrophage inflammatory protein (MIP)-1α, MIP-1β, interleukin-8 (IL-8) and RANTES (Regulated upon Activation, Normal T cell Expressed and Secreted). Biopsies from patients with SS showed that MIP-1β was expressed by 51% of infiltrating cells, while 51% expressed MIP-1α, whereas 22 and 7% expressed RANTES and IL-8, respectively.Conclusion. Chemokines expressed by ductal epithelial cells may attract circulating leucocytes, in particular CD4+ T cells, towards the site of inflammation, thereby orchestrating the influx of MN cells characteristically seen in MSGs in SS. Chemokines may be induced directly by a putative triggering agent for SS, or secondary to the release of pro-inflammatory cytokines produced by epithelial cells. These findings further implicate epithelial cells as playing a major role in the pathogenesis of SS and implicate chemokines in the leucocyte recruitment in this setting.Keywords: Pathology, T cells, Sjogren's syndrome, Chemokines, Ductular epithelium.

Objective. To investigate the expression and source of chemokines in minor salivary gland biopsies (MSGs) in patients with Sjogren's syndrome (SS).
Methods. Immunohistochemical analysis was used to determine the pattern of chemokine expression in MSGs from patients with (n = 6) and without (n = 5) SS, as well as to examine the phenotype of both resident and infiltrating cells expressing chemokines.
Results. Significant differences in the number of infiltrating mononuclear (MN) cells in patients with and without SS were noted. Ductal epithelial cells of SS biopsies expressed significantly increased levels of macrophage inflammatory protein (MIP)-1α, MIP-1β, interleukin-8 (IL-8) and RANTES (Regulated upon Activation, Normal T cell Expressed and Secreted). Biopsies from patients with SS showed that MIP-1β was expressed by 51% of infiltrating cells, while 51% expressed MIP-1α, whereas 22 and 7% expressed RANTES and IL-8, respectively.
Conclusion. Chemokines expressed by ductal epithelial cells may attract circulating leucocytes, in particular CD4⁺ T cells, towards the site of inflammation, thereby orchestrating the influx of MN cells characteristically seen in MSGs in SS. Chemokines may be induced directly by a putative triggering agent for SS, or secondary to the release of pro-inflammatory cytokines produced by epithelial cells. These findings further implicate epithelial cells as playing a major role in the pathogenesis of SS and implicate chemokines in the leucocyte recruitment in this setting.