C-Reactive Protein in Bronchoalveolar Lavage Fluid is Associated With Markers of Airway Inflammation After Lung Transplantation

Abstract Background C-reactive protein (CRP), an acute-phase marker of systemic inflammation, may also be a local regulator of the pulmonary immune system. Its role in lung transplantation (LT), however, is unclear. We hypothesized that CRP in bronchoalveolar lavage (BAL) fluid might be associated w...

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Veröffentlicht in:Transplantation proceedings 2009-10, Vol.41 (8), p.3409-3413
Hauptverfasser: Vos, R, Vanaudenaerde, B.M, De Vleeschauwer, S.I, Willems-Widyastuti, A, Dupont, L.J, Van Raemdonck, D.E, Verleden, G.M
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container_end_page 3413
container_issue 8
container_start_page 3409
container_title Transplantation proceedings
container_volume 41
creator Vos, R
Vanaudenaerde, B.M
De Vleeschauwer, S.I
Willems-Widyastuti, A
Dupont, L.J
Van Raemdonck, D.E
Verleden, G.M
description Abstract Background C-reactive protein (CRP), an acute-phase marker of systemic inflammation, may also be a local regulator of the pulmonary immune system. Its role in lung transplantation (LT), however, is unclear. We hypothesized that CRP in bronchoalveolar lavage (BAL) fluid might be associated with airway inflammation or remodeling. Therefore, it could play a role in the development of bronchiolitis obliterans syndrome (BOS). Patients and Methods A total of 100 LT recipients who had undergone transplantation between August 2001 and August 2005 were included in the current cross-sectional study. Patients who were evaluated at 90 days after LT were categorized as either stable (n = 36), colonized (n = 25), or suffering from infection (n = 16) or acute rejection (n = 23). BAL CRP, cell differentials, and interleukin (IL), IL8, transforming growth factor β (TGFβ), and vascular endothelial growth factor (VEGF) protein levels, as well as blood leukocytosis, plasma CRP, and forced expiratory value in 1 second (FEV1 ; % predicted) were compared between groups. We analyzed the correlation of BAL CRP with inflammatory or remodeling markers and FEV1. Results Compared with stable LT recipients, BAL CRP was significantly increased in patients with infection or acute rejection ( P < .0001), but not in those with colonization. Generally, BAL CRP levels positively correlated with BAL total cell count, neutrophilia, and IL8 levels, as well as with plasma CRP levels ( P < .0001). An inverse correlation was observed with BAL macrophages ( P < .01), VEGF ( P < .0001), and FEV1 ( P < .0001). Only a trend for a positive, respectively inverse correlation was seen for BAL IL6 and TGFβ. Conclusions The current data corroborate a possible role for CRP in airway inflammation after LT. Its importance for BOS should therefore be further elucidated.
doi_str_mv 10.1016/j.transproceed.2009.09.029
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Its role in lung transplantation (LT), however, is unclear. We hypothesized that CRP in bronchoalveolar lavage (BAL) fluid might be associated with airway inflammation or remodeling. Therefore, it could play a role in the development of bronchiolitis obliterans syndrome (BOS). Patients and Methods A total of 100 LT recipients who had undergone transplantation between August 2001 and August 2005 were included in the current cross-sectional study. Patients who were evaluated at 90 days after LT were categorized as either stable (n = 36), colonized (n = 25), or suffering from infection (n = 16) or acute rejection (n = 23). BAL CRP, cell differentials, and interleukin (IL), IL8, transforming growth factor β (TGFβ), and vascular endothelial growth factor (VEGF) protein levels, as well as blood leukocytosis, plasma CRP, and forced expiratory value in 1 second (FEV1 ; % predicted) were compared between groups. We analyzed the correlation of BAL CRP with inflammatory or remodeling markers and FEV1. Results Compared with stable LT recipients, BAL CRP was significantly increased in patients with infection or acute rejection ( P &lt; .0001), but not in those with colonization. Generally, BAL CRP levels positively correlated with BAL total cell count, neutrophilia, and IL8 levels, as well as with plasma CRP levels ( P &lt; .0001). An inverse correlation was observed with BAL macrophages ( P &lt; .01), VEGF ( P &lt; .0001), and FEV1 ( P &lt; .0001). Only a trend for a positive, respectively inverse correlation was seen for BAL IL6 and TGFβ. Conclusions The current data corroborate a possible role for CRP in airway inflammation after LT. Its importance for BOS should therefore be further elucidated.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2009.09.029</identifier><identifier>PMID: 19857759</identifier><identifier>CODEN: TRPPA8</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Adult ; Airway Obstruction - diagnosis ; Biological and medical sciences ; Biomarkers - analysis ; Bronchoalveolar Lavage Fluid - chemistry ; C-Reactive Protein - analysis ; Cross-Sectional Studies ; Female ; Forced Expiratory Volume ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Graft Rejection - epidemiology ; Humans ; Immunosuppressive Agents - therapeutic use ; Infection - epidemiology ; Inflammation - diagnosis ; Lung Diseases - classification ; Lung Diseases - surgery ; Lung Transplantation - adverse effects ; Lung Transplantation - immunology ; Male ; Medical sciences ; Middle Aged ; Postoperative Complications - epidemiology ; Respiratory Function Tests ; Retrospective Studies ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Tissue, organ and graft immunology</subject><ispartof>Transplantation proceedings, 2009-10, Vol.41 (8), p.3409-3413</ispartof><rights>Elsevier Inc.</rights><rights>2009 Elsevier Inc.</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c464t-789df168dec0bb62d0cf6e3503caba4ee9f23dd24d168701ec41aeb3e73f266b3</citedby><cites>FETCH-LOGICAL-c464t-789df168dec0bb62d0cf6e3503caba4ee9f23dd24d168701ec41aeb3e73f266b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.transproceed.2009.09.029$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,780,784,789,790,3550,23930,23931,25140,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22076081$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19857759$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vos, R</creatorcontrib><creatorcontrib>Vanaudenaerde, B.M</creatorcontrib><creatorcontrib>De Vleeschauwer, S.I</creatorcontrib><creatorcontrib>Willems-Widyastuti, A</creatorcontrib><creatorcontrib>Dupont, L.J</creatorcontrib><creatorcontrib>Van Raemdonck, D.E</creatorcontrib><creatorcontrib>Verleden, G.M</creatorcontrib><title>C-Reactive Protein in Bronchoalveolar Lavage Fluid is Associated With Markers of Airway Inflammation After Lung Transplantation</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>Abstract Background C-reactive protein (CRP), an acute-phase marker of systemic inflammation, may also be a local regulator of the pulmonary immune system. Its role in lung transplantation (LT), however, is unclear. We hypothesized that CRP in bronchoalveolar lavage (BAL) fluid might be associated with airway inflammation or remodeling. Therefore, it could play a role in the development of bronchiolitis obliterans syndrome (BOS). Patients and Methods A total of 100 LT recipients who had undergone transplantation between August 2001 and August 2005 were included in the current cross-sectional study. Patients who were evaluated at 90 days after LT were categorized as either stable (n = 36), colonized (n = 25), or suffering from infection (n = 16) or acute rejection (n = 23). BAL CRP, cell differentials, and interleukin (IL), IL8, transforming growth factor β (TGFβ), and vascular endothelial growth factor (VEGF) protein levels, as well as blood leukocytosis, plasma CRP, and forced expiratory value in 1 second (FEV1 ; % predicted) were compared between groups. We analyzed the correlation of BAL CRP with inflammatory or remodeling markers and FEV1. Results Compared with stable LT recipients, BAL CRP was significantly increased in patients with infection or acute rejection ( P &lt; .0001), but not in those with colonization. Generally, BAL CRP levels positively correlated with BAL total cell count, neutrophilia, and IL8 levels, as well as with plasma CRP levels ( P &lt; .0001). An inverse correlation was observed with BAL macrophages ( P &lt; .01), VEGF ( P &lt; .0001), and FEV1 ( P &lt; .0001). Only a trend for a positive, respectively inverse correlation was seen for BAL IL6 and TGFβ. Conclusions The current data corroborate a possible role for CRP in airway inflammation after LT. Its importance for BOS should therefore be further elucidated.</description><subject>Adult</subject><subject>Airway Obstruction - diagnosis</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - analysis</subject><subject>Bronchoalveolar Lavage Fluid - chemistry</subject><subject>C-Reactive Protein - analysis</subject><subject>Cross-Sectional Studies</subject><subject>Female</subject><subject>Forced Expiratory Volume</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Graft Rejection - epidemiology</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Infection - epidemiology</subject><subject>Inflammation - diagnosis</subject><subject>Lung Diseases - classification</subject><subject>Lung Diseases - surgery</subject><subject>Lung Transplantation - adverse effects</subject><subject>Lung Transplantation - immunology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Postoperative Complications - epidemiology</subject><subject>Respiratory Function Tests</subject><subject>Retrospective Studies</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Tissue, organ and graft immunology</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkl9rFDEUxYModq1-BQmC-DRr_sxOZnwQ1tVqYUXRio8hk9y02c4mbZJZ2Se_upnuUsQn4UII93fPPRwuQi8omVNCm9ebeY7Kp5sYNICZM0K6-VSse4BmtBW8Yg3jD9GMkJpWlNeLE_QkpQ0pf1bzx-iEdu1CiEU3Q79X1TdQOrsd4K8xZHAel3oXg9dXQQ07CIOKeK126hLw2TA6g13Cy5SCdiqDwT9dvsKfVbyGmHCweOniL7XH594OartV2QWPlzZDERn9Jb64sz4on-9aT9Ejq4YEz47vKfpx9uFi9alaf_l4vlquK103da5E2xlLm9aAJn3fMEO0bYAvCNeqVzVAZxk3htWmQIJQ0DVV0HMQ3LKm6fkpenXQLandjpCy3LqkYShGIIxJCl5TwlrGCvnmQOoYUopg5U10WxX3khI55S838u_85ZS_nIp1Zfj5cc3Yb0vvfvQYeAFeHgGVtBpsEdIu3XOMEdGQlhbu_YGDEsrOQZRJO_AajIugszTB_Z-ft__I6MF5VzZfwx7SJozRl9gllYlJIr9PFzMdDOkIZUJ0_A8M6sIn</recordid><startdate>20091001</startdate><enddate>20091001</enddate><creator>Vos, R</creator><creator>Vanaudenaerde, B.M</creator><creator>De Vleeschauwer, S.I</creator><creator>Willems-Widyastuti, A</creator><creator>Dupont, L.J</creator><creator>Van Raemdonck, D.E</creator><creator>Verleden, G.M</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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>20091001</creationdate><title>C-Reactive Protein in Bronchoalveolar Lavage Fluid is Associated With Markers of Airway Inflammation After Lung Transplantation</title><author>Vos, R ; Vanaudenaerde, B.M ; De Vleeschauwer, S.I ; Willems-Widyastuti, A ; Dupont, L.J ; Van Raemdonck, D.E ; Verleden, G.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c464t-789df168dec0bb62d0cf6e3503caba4ee9f23dd24d168701ec41aeb3e73f266b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Airway Obstruction - diagnosis</topic><topic>Biological and medical sciences</topic><topic>Biomarkers - analysis</topic><topic>Bronchoalveolar Lavage Fluid - chemistry</topic><topic>C-Reactive Protein - analysis</topic><topic>Cross-Sectional Studies</topic><topic>Female</topic><topic>Forced Expiratory Volume</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Graft Rejection - epidemiology</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Infection - epidemiology</topic><topic>Inflammation - diagnosis</topic><topic>Lung Diseases - classification</topic><topic>Lung Diseases - surgery</topic><topic>Lung Transplantation - adverse effects</topic><topic>Lung Transplantation - immunology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Postoperative Complications - epidemiology</topic><topic>Respiratory Function Tests</topic><topic>Retrospective Studies</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Tissue, organ and graft immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vos, R</creatorcontrib><creatorcontrib>Vanaudenaerde, B.M</creatorcontrib><creatorcontrib>De Vleeschauwer, S.I</creatorcontrib><creatorcontrib>Willems-Widyastuti, A</creatorcontrib><creatorcontrib>Dupont, L.J</creatorcontrib><creatorcontrib>Van Raemdonck, D.E</creatorcontrib><creatorcontrib>Verleden, G.M</creatorcontrib><collection>Pascal-Francis</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>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vos, R</au><au>Vanaudenaerde, B.M</au><au>De Vleeschauwer, S.I</au><au>Willems-Widyastuti, A</au><au>Dupont, L.J</au><au>Van Raemdonck, D.E</au><au>Verleden, G.M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>C-Reactive Protein in Bronchoalveolar Lavage Fluid is Associated With Markers of Airway Inflammation After Lung Transplantation</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2009-10-01</date><risdate>2009</risdate><volume>41</volume><issue>8</issue><spage>3409</spage><epage>3413</epage><pages>3409-3413</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><coden>TRPPA8</coden><abstract>Abstract Background C-reactive protein (CRP), an acute-phase marker of systemic inflammation, may also be a local regulator of the pulmonary immune system. Its role in lung transplantation (LT), however, is unclear. We hypothesized that CRP in bronchoalveolar lavage (BAL) fluid might be associated with airway inflammation or remodeling. Therefore, it could play a role in the development of bronchiolitis obliterans syndrome (BOS). Patients and Methods A total of 100 LT recipients who had undergone transplantation between August 2001 and August 2005 were included in the current cross-sectional study. Patients who were evaluated at 90 days after LT were categorized as either stable (n = 36), colonized (n = 25), or suffering from infection (n = 16) or acute rejection (n = 23). BAL CRP, cell differentials, and interleukin (IL), IL8, transforming growth factor β (TGFβ), and vascular endothelial growth factor (VEGF) protein levels, as well as blood leukocytosis, plasma CRP, and forced expiratory value in 1 second (FEV1 ; % predicted) were compared between groups. We analyzed the correlation of BAL CRP with inflammatory or remodeling markers and FEV1. Results Compared with stable LT recipients, BAL CRP was significantly increased in patients with infection or acute rejection ( P &lt; .0001), but not in those with colonization. Generally, BAL CRP levels positively correlated with BAL total cell count, neutrophilia, and IL8 levels, as well as with plasma CRP levels ( P &lt; .0001). An inverse correlation was observed with BAL macrophages ( P &lt; .01), VEGF ( P &lt; .0001), and FEV1 ( P &lt; .0001). Only a trend for a positive, respectively inverse correlation was seen for BAL IL6 and TGFβ. Conclusions The current data corroborate a possible role for CRP in airway inflammation after LT. Its importance for BOS should therefore be further elucidated.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>19857759</pmid><doi>10.1016/j.transproceed.2009.09.029</doi><tpages>5</tpages></addata></record>
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source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Adult
Airway Obstruction - diagnosis
Biological and medical sciences
Biomarkers - analysis
Bronchoalveolar Lavage Fluid - chemistry
C-Reactive Protein - analysis
Cross-Sectional Studies
Female
Forced Expiratory Volume
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Graft Rejection - epidemiology
Humans
Immunosuppressive Agents - therapeutic use
Infection - epidemiology
Inflammation - diagnosis
Lung Diseases - classification
Lung Diseases - surgery
Lung Transplantation - adverse effects
Lung Transplantation - immunology
Male
Medical sciences
Middle Aged
Postoperative Complications - epidemiology
Respiratory Function Tests
Retrospective Studies
Surgery
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Tissue, organ and graft immunology
title C-Reactive Protein in Bronchoalveolar Lavage Fluid is Associated With Markers of Airway Inflammation After Lung Transplantation
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