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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
Main Authors: Natorska, Joanna, PhD, Marek, Grzegorz, MD, PhD, Sadowski, Jerzy, MD, PhD, Undas, Anetta, MD, PhD
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creator Natorska, Joanna, PhD
Marek, Grzegorz, MD, PhD
Sadowski, Jerzy, MD, PhD
Undas, Anetta, MD, PhD
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.
doi_str_mv 10.1016/j.jjcc.2015.05.002
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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. 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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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