Indicators of salivary gland inflammation in primary Sjögren's syndrome

The aim of this study was to establish additional indicators in saliva and plasma which are associated with salivary gland inflammation in patients with primary Sjögren's syndrome (SS). ELISA assays were used to determine the concentrations of sICAM‐1, sVCAM‐1, sIL‐2Rz, IgA, IgG, calprotectin a...

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Bibliographic Details
Published inEuropean journal of oral sciences Vol. 105; no. 3; pp. 228 - 233
Main Authors Cuida, Mihaela, Halse, Anne-Kristine, Johannessen, Anne Christine, Tynning, Turid, Jonsson, Roland
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.06.1997
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Summary:The aim of this study was to establish additional indicators in saliva and plasma which are associated with salivary gland inflammation in patients with primary Sjögren's syndrome (SS). ELISA assays were used to determine the concentrations of sICAM‐1, sVCAM‐1, sIL‐2Rz, IgA, IgG, calprotectin and albumin in parotid saliva, whole saliva and plasma samples. Soluble ICAM‐1 was present in whole and parotid saliva samples from primary SS patients. Soluble VCAM‐1 and sIL‐IRx could not be detected in salivary samples from either primary SS or control subjects. IgA, IgG, calprotectin and albumin concentrations were higher in both whole and parotid saliva in the patient group compared with the control group. The results showed increased levels of calprotectin in all saliva samples compared to plasma, suggesting that calprotectin may be locally produced. Increased plasma values of sICAM‐1. sVCAM‐1, SIL‐2Rα, IgA, IgG and calprotectin were detected in primary SS patients when compared to controls. The output/min of IgA. IgG, calprotectin and albumin was decreased in SS patients. Plasma levels of various proteins could offer information concerning glandular and extraglandular inflammatory processes. However, salivary levels of these proteins (particularly sICAM‐1) tend to reflect more the local inflammatory activity, providing a convenient and non‐invasive tool for diagnosis.
Bibliography:ark:/67375/WNG-T5ZJ5W45-5
ArticleID:EOS228
istex:2F67D69D11A3459FC572AEF393253FE1B30A1B46
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0909-8836
1600-0722
DOI:10.1111/j.1600-0722.1997.tb00205.x