Submandibular and lacrimal gland immunoglobulin in the c3h.mrl-faslpr autoimmune mouse model of sjögren’s syndrome

Dennis R. Trune, Daniel A. Leedy

Research output: Contribution to journalArticlepeer-review


To distinguish potential autoimmune and nonautoimmune mechanisms underlying the salivary gland inflammation seen in Sjögren’s syndrome and normal aging. Immunohistochemical studies were conducted on the lacrimal and salivary glands of 2- and 5-month-old C3H.MRL-Faslpr autoimmune strain mice and age-matched C3H/HeJ nonautoimmune controls. Glandular inflammatory foci, interstitial areas, and vasculature were stained for immunoglobulin G (IgG), immunoglobulin A (IgA), and complement to determine differences in their local immune parameter. Differences between the two strains were compared for immune changes attributable to autoimmune disease and between the two normal groups for normal aging changes. Greater staining of IgG, IgA, and complement occurred in the inflammatory foci and interstitial areas of 5-month-old C3H.MRL-Faslpr lacrimal and submandibular glands compared with 5-month-old controls. Normal mice showed some increased immunoglobulin staining with aging, but little or no complement in any glands. These differential findings suggest that the systemic autoimmune disease plays a more direct role in focal glandular inflammation in Sjgren’s syndrome, whereas less severe immune mechanisms are involved in the inflammation of normal glands.

Original languageEnglish (US)
Pages (from-to)1729-1732
Number of pages4
Issue number11
StatePublished - Nov 1998

ASJC Scopus subject areas

  • Otorhinolaryngology


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