Decreased expression of thymic stromal lymphopoietin in salivary glands of patients with primary Sjögren's syndrome is associated with increased disease activity

Objectives: Thymic Stromal Lymphopoietin (TSLP) is a potent immunomodulatory cytokine involved in Th2- and Th17-mediated immune responses in different autoimmune diseases. TSLP expression in relation to disease activity was studied in salivary glands of primary Sjögren's syndrome (pSS) patients...

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Veröffentlicht in:Modern rheumatology 2016-01, Vol.26 (1), p.105-109
Hauptverfasser: Hillen, Maarten R., Kruize, Aike A., Bikker, Angela, Wenting-van Wijk, Marion, Radstake, Timothy R. D. J., Hack, Cornelis E., Lafeber, Floris P. J. G., van Roon, Joel A. G.
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container_end_page 109
container_issue 1
container_start_page 105
container_title Modern rheumatology
container_volume 26
creator Hillen, Maarten R.
Kruize, Aike A.
Bikker, Angela
Wenting-van Wijk, Marion
Radstake, Timothy R. D. J.
Hack, Cornelis E.
Lafeber, Floris P. J. G.
van Roon, Joel A. G.
description Objectives: Thymic Stromal Lymphopoietin (TSLP) is a potent immunomodulatory cytokine involved in Th2- and Th17-mediated immune responses in different autoimmune diseases. TSLP expression in relation to disease activity was studied in salivary glands of primary Sjögren's syndrome (pSS) patients as compared to non-SS sicca (nSS) controls. Methods: Tissue sections of minor salivary glands from pSS and nSS patients were stained with monoclonal antibodies against human TSLP, CD3, CD19 and cytokeratin high molecular weight (CK HMW) or stained for Alcian blue to detect mucus production. The number of TSLP-expressing cells was quantified and expression was correlated to local and systemic disease parameters. Results: The number of TSLP-expressing cells was significantly lower in pSS patients than in nSS controls and correlated with a range of disease markers. In pSS patients, TSLP was expressed outside of lymphocytic infiltrates at sections that also encompassed high numbers of intact acinar cells. This difference was independent of tissue destruction. Conclusions: Reduced TSLP expression in pSS patients is associated with increased local and systemic inflammatory markers. Loss of TSLP expression may contribute to Th1/Th17-associated immunopathology in pSS, in line with previous studies demonstrating that TSLP promotes a protective Th2 milieu at mucosal sites.
doi_str_mv 10.3109/14397595.2015.1054089
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D. J. ; Hack, Cornelis E. ; Lafeber, Floris P. J. G. ; van Roon, Joel A. G.</creator><creatorcontrib>Hillen, Maarten R. ; Kruize, Aike A. ; Bikker, Angela ; Wenting-van Wijk, Marion ; Radstake, Timothy R. D. J. ; Hack, Cornelis E. ; Lafeber, Floris P. J. G. ; van Roon, Joel A. G.</creatorcontrib><description>Objectives: Thymic Stromal Lymphopoietin (TSLP) is a potent immunomodulatory cytokine involved in Th2- and Th17-mediated immune responses in different autoimmune diseases. TSLP expression in relation to disease activity was studied in salivary glands of primary Sjögren's syndrome (pSS) patients as compared to non-SS sicca (nSS) controls. Methods: Tissue sections of minor salivary glands from pSS and nSS patients were stained with monoclonal antibodies against human TSLP, CD3, CD19 and cytokeratin high molecular weight (CK HMW) or stained for Alcian blue to detect mucus production. The number of TSLP-expressing cells was quantified and expression was correlated to local and systemic disease parameters. Results: The number of TSLP-expressing cells was significantly lower in pSS patients than in nSS controls and correlated with a range of disease markers. In pSS patients, TSLP was expressed outside of lymphocytic infiltrates at sections that also encompassed high numbers of intact acinar cells. This difference was independent of tissue destruction. Conclusions: Reduced TSLP expression in pSS patients is associated with increased local and systemic inflammatory markers. Loss of TSLP expression may contribute to Th1/Th17-associated immunopathology in pSS, in line with previous studies demonstrating that TSLP promotes a protective Th2 milieu at mucosal sites.</description><identifier>ISSN: 1439-7595</identifier><identifier>EISSN: 1439-7609</identifier><identifier>DOI: 10.3109/14397595.2015.1054089</identifier><identifier>PMID: 25995032</identifier><language>eng</language><publisher>United States: Taylor &amp; Francis</publisher><subject>Adult ; Aged ; Autoimmune diseases ; Biomarkers - metabolism ; Cells ; Correlation analysis ; Cytokines ; Cytokines - metabolism ; Epithelial cells ; Female ; Humans ; Immunopathology ; Inflammation - immunology ; Inflammation - metabolism ; Inflammation - pathology ; Lymphocytes ; Male ; Middle Aged ; Monoclonal antibodies ; Salivary Glands - immunology ; Salivary Glands - metabolism ; Salivary Glands - pathology ; Severity of Illness Index ; Sjogren's Syndrome - diagnosis ; Sjogren's Syndrome - immunology ; Sjogren's Syndrome - metabolism ; Sjögren's syndrome ; Th17 Cells - immunology ; Th17 Cells - metabolism ; Thymic stromal lymphopoietin ; Tissues</subject><ispartof>Modern rheumatology, 2016-01, Vol.26 (1), p.105-109</ispartof><rights>2015 Japan College of Rheumatology 2015</rights><rights>Copyright Informa Healthcare 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-5455879a2aba7e71f8396280d1205cd64ec28c22a4678f659fca305bdb6d2a103</citedby><cites>FETCH-LOGICAL-c464t-5455879a2aba7e71f8396280d1205cd64ec28c22a4678f659fca305bdb6d2a103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25995032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hillen, Maarten R.</creatorcontrib><creatorcontrib>Kruize, Aike A.</creatorcontrib><creatorcontrib>Bikker, Angela</creatorcontrib><creatorcontrib>Wenting-van Wijk, Marion</creatorcontrib><creatorcontrib>Radstake, Timothy R. D. J.</creatorcontrib><creatorcontrib>Hack, Cornelis E.</creatorcontrib><creatorcontrib>Lafeber, Floris P. J. G.</creatorcontrib><creatorcontrib>van Roon, Joel A. G.</creatorcontrib><title>Decreased expression of thymic stromal lymphopoietin in salivary glands of patients with primary Sjögren's syndrome is associated with increased disease activity</title><title>Modern rheumatology</title><addtitle>Mod Rheumatol</addtitle><description>Objectives: Thymic Stromal Lymphopoietin (TSLP) is a potent immunomodulatory cytokine involved in Th2- and Th17-mediated immune responses in different autoimmune diseases. TSLP expression in relation to disease activity was studied in salivary glands of primary Sjögren's syndrome (pSS) patients as compared to non-SS sicca (nSS) controls. Methods: Tissue sections of minor salivary glands from pSS and nSS patients were stained with monoclonal antibodies against human TSLP, CD3, CD19 and cytokeratin high molecular weight (CK HMW) or stained for Alcian blue to detect mucus production. The number of TSLP-expressing cells was quantified and expression was correlated to local and systemic disease parameters. Results: The number of TSLP-expressing cells was significantly lower in pSS patients than in nSS controls and correlated with a range of disease markers. In pSS patients, TSLP was expressed outside of lymphocytic infiltrates at sections that also encompassed high numbers of intact acinar cells. This difference was independent of tissue destruction. Conclusions: Reduced TSLP expression in pSS patients is associated with increased local and systemic inflammatory markers. Loss of TSLP expression may contribute to Th1/Th17-associated immunopathology in pSS, in line with previous studies demonstrating that TSLP promotes a protective Th2 milieu at mucosal sites.</description><subject>Adult</subject><subject>Aged</subject><subject>Autoimmune diseases</subject><subject>Biomarkers - metabolism</subject><subject>Cells</subject><subject>Correlation analysis</subject><subject>Cytokines</subject><subject>Cytokines - metabolism</subject><subject>Epithelial cells</subject><subject>Female</subject><subject>Humans</subject><subject>Immunopathology</subject><subject>Inflammation - immunology</subject><subject>Inflammation - metabolism</subject><subject>Inflammation - pathology</subject><subject>Lymphocytes</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Monoclonal antibodies</subject><subject>Salivary Glands - immunology</subject><subject>Salivary Glands - metabolism</subject><subject>Salivary Glands - pathology</subject><subject>Severity of Illness Index</subject><subject>Sjogren's Syndrome - diagnosis</subject><subject>Sjogren's Syndrome - immunology</subject><subject>Sjogren's Syndrome - metabolism</subject><subject>Sjögren's syndrome</subject><subject>Th17 Cells - immunology</subject><subject>Th17 Cells - metabolism</subject><subject>Thymic stromal lymphopoietin</subject><subject>Tissues</subject><issn>1439-7595</issn><issn>1439-7609</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU2O1DAQhSMEYoaBI4AssYBNN_6Jk3jHaPiVRmIBrK1q25l2K7GDyz1DrsMhuAAXw6G7WbBAsuSS_b1XZb-qesroWjCqXrFaqFYqueaUyTWjsqaduledL-ertqHq_qku0Fn1CHFHqZCqUw-rMy6VklTw8-rHG2eSA3SWuO9Tcog-BhJ7krfz6A3BnOIIAxnmcdrGKXqXfSBlIQz-FtJMbgYIFhfJBNm7kJHc-bwlU_Ljcv959-vnTXLhBRKcgy12jngkgBiNh1wa_8F9OM1hPS4FAZP9rc_z4-pBDwO6J8f9ovr67u2Xqw-r60_vP15dXq9M3dR5JWspu1YBhw20rmV9J1TDO2oZp9LYpnaGd4ZzqJu26xupegOCyo3dNJYDo-KiennwnVL8tneY9ejRuKG8z8U9atZKLiRVoi3o83_QXdynUKYrlGJCdg1rCiUPlEkRMbleH_9EM6qXEPUpRL2EqI8hFt2zo_t-Mzr7V3VKrQCvD4APfUwj3MU0WJ1hHmLqEwTjcfH_X4_fZBmv6A</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Hillen, Maarten R.</creator><creator>Kruize, Aike A.</creator><creator>Bikker, Angela</creator><creator>Wenting-van Wijk, Marion</creator><creator>Radstake, Timothy R. 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D. J.</creatorcontrib><creatorcontrib>Hack, Cornelis E.</creatorcontrib><creatorcontrib>Lafeber, Floris P. J. G.</creatorcontrib><creatorcontrib>van Roon, Joel A. G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Modern rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hillen, Maarten R.</au><au>Kruize, Aike A.</au><au>Bikker, Angela</au><au>Wenting-van Wijk, Marion</au><au>Radstake, Timothy R. D. J.</au><au>Hack, Cornelis E.</au><au>Lafeber, Floris P. J. G.</au><au>van Roon, Joel A. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased expression of thymic stromal lymphopoietin in salivary glands of patients with primary Sjögren's syndrome is associated with increased disease activity</atitle><jtitle>Modern rheumatology</jtitle><addtitle>Mod Rheumatol</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>26</volume><issue>1</issue><spage>105</spage><epage>109</epage><pages>105-109</pages><issn>1439-7595</issn><eissn>1439-7609</eissn><abstract>Objectives: Thymic Stromal Lymphopoietin (TSLP) is a potent immunomodulatory cytokine involved in Th2- and Th17-mediated immune responses in different autoimmune diseases. TSLP expression in relation to disease activity was studied in salivary glands of primary Sjögren's syndrome (pSS) patients as compared to non-SS sicca (nSS) controls. Methods: Tissue sections of minor salivary glands from pSS and nSS patients were stained with monoclonal antibodies against human TSLP, CD3, CD19 and cytokeratin high molecular weight (CK HMW) or stained for Alcian blue to detect mucus production. The number of TSLP-expressing cells was quantified and expression was correlated to local and systemic disease parameters. Results: The number of TSLP-expressing cells was significantly lower in pSS patients than in nSS controls and correlated with a range of disease markers. In pSS patients, TSLP was expressed outside of lymphocytic infiltrates at sections that also encompassed high numbers of intact acinar cells. This difference was independent of tissue destruction. Conclusions: Reduced TSLP expression in pSS patients is associated with increased local and systemic inflammatory markers. Loss of TSLP expression may contribute to Th1/Th17-associated immunopathology in pSS, in line with previous studies demonstrating that TSLP promotes a protective Th2 milieu at mucosal sites.</abstract><cop>United States</cop><pub>Taylor &amp; Francis</pub><pmid>25995032</pmid><doi>10.3109/14397595.2015.1054089</doi><tpages>5</tpages></addata></record>
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source MEDLINE; Oxford University Press Journals All Titles (1996-Current)
subjects Adult
Aged
Autoimmune diseases
Biomarkers - metabolism
Cells
Correlation analysis
Cytokines
Cytokines - metabolism
Epithelial cells
Female
Humans
Immunopathology
Inflammation - immunology
Inflammation - metabolism
Inflammation - pathology
Lymphocytes
Male
Middle Aged
Monoclonal antibodies
Salivary Glands - immunology
Salivary Glands - metabolism
Salivary Glands - pathology
Severity of Illness Index
Sjogren's Syndrome - diagnosis
Sjogren's Syndrome - immunology
Sjogren's Syndrome - metabolism
Sjögren's syndrome
Th17 Cells - immunology
Th17 Cells - metabolism
Thymic stromal lymphopoietin
Tissues
title Decreased expression of thymic stromal lymphopoietin in salivary glands of patients with primary Sjögren's syndrome is associated with increased disease activity
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