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Presence of B cells within aortic valves in patients with aortic stenosis: Relation to severity of the disease
Abstract Background Aortic stenosis (AS) shares several similarities with atherosclerosis. Recent reports showed that B cells are implicated in atherosclerosis progression through macrophage–B cells bidirectional interaction. We aimed to study the in loco presence of B cells within aortic valves and...
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Published in: | Journal of cardiology 2016-01, Vol.67 (1), p.80-85 |
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description | Abstract Background Aortic stenosis (AS) shares several similarities with atherosclerosis. Recent reports showed that B cells are implicated in atherosclerosis progression through macrophage–B cells bidirectional interaction. We aimed to study the in loco presence of B cells within aortic valves and to determine its modulators. Methods Thirty-seven patients with severe AS were studied. Immunohistochemistry was performed on valve leaflets using antibodies against CD20, B cell-activating factor of the tumor necrosis factor family receptor (BAFF-R) and CD68. Plasma inflammatory markers were also determined. Results The B cells were detected within aortic leaflets from 5 to 31/mm2 (17.9 ± 11.6/mm2 ). Double-staining showed that 27 ± 13.5% of B cells express BAFF-R. There were positive correlations between the number of B cells and macrophages ( r = 0.45, p = 0.018), and between macrophages and B cell-associated BAFF-R expression ( r = 0.66, p = 0.002). The number of B cells was associated with the valve calcification ( r = 0.41, p = 0.039), and with the maximum transvalvular gradient ( r = 0.63, p = 0.02). The BAFF-R expression was positively correlated with maximum transvalvular gradient ( r = 0.39, p = 0.031) and negatively with aortic valve area ( r = −0.41, p = 0.048). There were no correlations between the number of B cells and plasma markers. Conclusions It might be hypothesized that, like in atherosclerosis, increasing number of B cells within aortic valves may accelerate inflammation and thus potentiate the progression of AS. |
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Recent reports showed that B cells are implicated in atherosclerosis progression through macrophage–B cells bidirectional interaction. We aimed to study the in loco presence of B cells within aortic valves and to determine its modulators. Methods Thirty-seven patients with severe AS were studied. Immunohistochemistry was performed on valve leaflets using antibodies against CD20, B cell-activating factor of the tumor necrosis factor family receptor (BAFF-R) and CD68. Plasma inflammatory markers were also determined. Results The B cells were detected within aortic leaflets from 5 to 31/mm2 (17.9 ± 11.6/mm2 ). Double-staining showed that 27 ± 13.5% of B cells express BAFF-R. There were positive correlations between the number of B cells and macrophages ( r = 0.45, p = 0.018), and between macrophages and B cell-associated BAFF-R expression ( r = 0.66, p = 0.002). The number of B cells was associated with the valve calcification ( r = 0.41, p = 0.039), and with the maximum transvalvular gradient ( r = 0.63, p = 0.02). The BAFF-R expression was positively correlated with maximum transvalvular gradient ( r = 0.39, p = 0.031) and negatively with aortic valve area ( r = −0.41, p = 0.048). There were no correlations between the number of B cells and plasma markers. Conclusions It might be hypothesized that, like in atherosclerosis, increasing number of B cells within aortic valves may accelerate inflammation and thus potentiate the progression of AS.</description><identifier>ISSN: 0914-5087</identifier><identifier>EISSN: 1876-4738</identifier><identifier>DOI: 10.1016/j.jjcc.2015.05.002</identifier><identifier>PMID: 26068299</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Aortic stenosis ; Aortic Valve - metabolism ; Aortic Valve - pathology ; Aortic Valve Stenosis - pathology ; B cells ; B-Cell Activation Factor Receptor - metabolism ; B-Lymphocytes - pathology ; Calcification ; Calcinosis - pathology ; Cardiovascular ; Female ; Humans ; Immunohistochemistry ; Inflammation ; Macrophages - metabolism ; Male ; Middle Aged ; Severity of Illness Index</subject><ispartof>Journal of cardiology, 2016-01, Vol.67 (1), p.80-85</ispartof><rights>Japanese College of Cardiology</rights><rights>2015 Japanese College of Cardiology</rights><rights>Copyright © 2015 Japanese College of Cardiology. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c549t-e1a18af58aa290e4abfd160436ea2feabec84ff490757019a06bc506888763833</citedby><cites>FETCH-LOGICAL-c549t-e1a18af58aa290e4abfd160436ea2feabec84ff490757019a06bc506888763833</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26068299$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Natorska, Joanna, PhD</creatorcontrib><creatorcontrib>Marek, Grzegorz, MD, PhD</creatorcontrib><creatorcontrib>Sadowski, Jerzy, MD, PhD</creatorcontrib><creatorcontrib>Undas, Anetta, MD, PhD</creatorcontrib><title>Presence of B cells within aortic valves in patients with aortic stenosis: Relation to severity of the disease</title><title>Journal of cardiology</title><addtitle>J Cardiol</addtitle><description>Abstract Background Aortic stenosis (AS) shares several similarities with atherosclerosis. Recent reports showed that B cells are implicated in atherosclerosis progression through macrophage–B cells bidirectional interaction. We aimed to study the in loco presence of B cells within aortic valves and to determine its modulators. Methods Thirty-seven patients with severe AS were studied. Immunohistochemistry was performed on valve leaflets using antibodies against CD20, B cell-activating factor of the tumor necrosis factor family receptor (BAFF-R) and CD68. Plasma inflammatory markers were also determined. Results The B cells were detected within aortic leaflets from 5 to 31/mm2 (17.9 ± 11.6/mm2 ). Double-staining showed that 27 ± 13.5% of B cells express BAFF-R. There were positive correlations between the number of B cells and macrophages ( r = 0.45, p = 0.018), and between macrophages and B cell-associated BAFF-R expression ( r = 0.66, p = 0.002). The number of B cells was associated with the valve calcification ( r = 0.41, p = 0.039), and with the maximum transvalvular gradient ( r = 0.63, p = 0.02). The BAFF-R expression was positively correlated with maximum transvalvular gradient ( r = 0.39, p = 0.031) and negatively with aortic valve area ( r = −0.41, p = 0.048). There were no correlations between the number of B cells and plasma markers. Conclusions It might be hypothesized that, like in atherosclerosis, increasing number of B cells within aortic valves may accelerate inflammation and thus potentiate the progression of AS.</description><subject>Aortic stenosis</subject><subject>Aortic Valve - metabolism</subject><subject>Aortic Valve - pathology</subject><subject>Aortic Valve Stenosis - pathology</subject><subject>B cells</subject><subject>B-Cell Activation Factor Receptor - metabolism</subject><subject>B-Lymphocytes - pathology</subject><subject>Calcification</subject><subject>Calcinosis - pathology</subject><subject>Cardiovascular</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Severity of Illness Index</subject><issn>0914-5087</issn><issn>1876-4738</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp9kc2LFDEQxYMo7rj6D3iQHL30WEl30mkRQRe_YGEXP84hk65m0_Z0xlRmZP5708yuhz0sFARSv_fgvWLspYC1AKHfjOtx9H4tQag1lAH5iK2EaXXVtLV5zFbQiaZSYNoz9oxoBNDQGf2UnUkN2siuW7H5OiHh7JHHgX_kHqeJ-N-Qb8LMXUw5eH5w0wGJl4-dywHnfALu1pRxjhToLf-OUwHizHPkhAdMIR8X23yDvA-EjvA5ezK4ifDF7XvOfn3-9PPia3V59eXbxYfLyqumyxUKJ4wblHFOdoCN2wy90NDUGp0c0G3Qm2YYmg5a1YLoHOiNVyWTKelrU9fn7PXJd5finz1StttASzg3Y9yTFa2SyjR1pwsqT6hPkSjhYHcpbF06WgF26dmOdunZLj1bKAOyiF7d-u83W-z_S-6KLcC7E4Al5SFgsuTD0nMfEvps-xge9n9_T-6nMAfvpt94RBrjPs2lPyssSQv2x3Lp5dBCQXEBUf8DpCukUg</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Natorska, Joanna, PhD</creator><creator>Marek, Grzegorz, MD, PhD</creator><creator>Sadowski, Jerzy, MD, PhD</creator><creator>Undas, Anetta, MD, PhD</creator><general>Elsevier Ltd</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160101</creationdate><title>Presence of B cells within aortic valves in patients with aortic stenosis: Relation to severity of the disease</title><author>Natorska, Joanna, PhD ; Marek, Grzegorz, MD, PhD ; Sadowski, Jerzy, MD, PhD ; Undas, Anetta, MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-e1a18af58aa290e4abfd160436ea2feabec84ff490757019a06bc506888763833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aortic stenosis</topic><topic>Aortic Valve - metabolism</topic><topic>Aortic Valve - pathology</topic><topic>Aortic Valve Stenosis - pathology</topic><topic>B cells</topic><topic>B-Cell Activation Factor Receptor - metabolism</topic><topic>B-Lymphocytes - pathology</topic><topic>Calcification</topic><topic>Calcinosis - pathology</topic><topic>Cardiovascular</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Inflammation</topic><topic>Macrophages - metabolism</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Severity of Illness Index</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Natorska, Joanna, PhD</creatorcontrib><creatorcontrib>Marek, Grzegorz, MD, PhD</creatorcontrib><creatorcontrib>Sadowski, Jerzy, MD, PhD</creatorcontrib><creatorcontrib>Undas, Anetta, MD, PhD</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Natorska, Joanna, PhD</au><au>Marek, Grzegorz, MD, PhD</au><au>Sadowski, Jerzy, MD, PhD</au><au>Undas, Anetta, MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Presence of B cells within aortic valves in patients with aortic stenosis: Relation to severity of the disease</atitle><jtitle>Journal of cardiology</jtitle><addtitle>J Cardiol</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>67</volume><issue>1</issue><spage>80</spage><epage>85</epage><pages>80-85</pages><issn>0914-5087</issn><eissn>1876-4738</eissn><abstract>Abstract Background Aortic stenosis (AS) shares several similarities with atherosclerosis. Recent reports showed that B cells are implicated in atherosclerosis progression through macrophage–B cells bidirectional interaction. We aimed to study the in loco presence of B cells within aortic valves and to determine its modulators. Methods Thirty-seven patients with severe AS were studied. Immunohistochemistry was performed on valve leaflets using antibodies against CD20, B cell-activating factor of the tumor necrosis factor family receptor (BAFF-R) and CD68. Plasma inflammatory markers were also determined. Results The B cells were detected within aortic leaflets from 5 to 31/mm2 (17.9 ± 11.6/mm2 ). Double-staining showed that 27 ± 13.5% of B cells express BAFF-R. There were positive correlations between the number of B cells and macrophages ( r = 0.45, p = 0.018), and between macrophages and B cell-associated BAFF-R expression ( r = 0.66, p = 0.002). The number of B cells was associated with the valve calcification ( r = 0.41, p = 0.039), and with the maximum transvalvular gradient ( r = 0.63, p = 0.02). The BAFF-R expression was positively correlated with maximum transvalvular gradient ( r = 0.39, p = 0.031) and negatively with aortic valve area ( r = −0.41, p = 0.048). There were no correlations between the number of B cells and plasma markers. Conclusions It might be hypothesized that, like in atherosclerosis, increasing number of B cells within aortic valves may accelerate inflammation and thus potentiate the progression of AS.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>26068299</pmid><doi>10.1016/j.jjcc.2015.05.002</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aortic stenosis Aortic Valve - metabolism Aortic Valve - pathology Aortic Valve Stenosis - pathology B cells B-Cell Activation Factor Receptor - metabolism B-Lymphocytes - pathology Calcification Calcinosis - pathology Cardiovascular Female Humans Immunohistochemistry Inflammation Macrophages - metabolism Male Middle Aged Severity of Illness Index |
title | Presence of B cells within aortic valves in patients with aortic stenosis: Relation to severity of the disease |
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