Indoleamine 2,3-Dioxygenase in Lung Allograft Tolerance
Background Indoleamine 2,3-dioxygenase (IDO), an enzyme involved in the degradation of tryptophan (Try) to kynurenine (Kyn), is thought to suppress T-cell activity. Although a few experimental studies have suggested a role for IDO in graft acceptance, human data are scarce and inconclusive. We sough...
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Veröffentlicht in: | The Journal of heart and lung transplantation 2009-11, Vol.28 (11), p.1185-1192 |
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creator | Meloni, Federica, MD, PhD Giuliano, Serena, ScD Solari, Nadia, ScD, PhD Draghi, Paola, ScD Miserere, Simona, ScD Bardoni, Anna Maria, ScD Salvini, Roberta, ScD Bini, Francesco, MD Fietta, Anna Maria, ScD |
description | Background Indoleamine 2,3-dioxygenase (IDO), an enzyme involved in the degradation of tryptophan (Try) to kynurenine (Kyn), is thought to suppress T-cell activity. Although a few experimental studies have suggested a role for IDO in graft acceptance, human data are scarce and inconclusive. We sought to establish whether, in lung transplant recipients (LTRs), plasma IDO activity mirrors the level of graft acceptance. Methods We measured the plasma Kyn/Try ratio, reflecting IDO activity, by high-performance liquid chromatography (HPLC) in 90 LTRs, including 26 patients who were still functionally/clinically stable for >36 post-transplant months (stable LTRs) and 64 LTRs with bronchiolitis obliterans syndrome (BOS, Grades 0-p to 3). Twenty-four normal healthy controls (NHCs) were also included. Results The Kyn/Try ratio in stable LTRs resembled that observed in NHCs, whereas, unexpectedly, patients with BOS, who had lower counts of peripheral CD4+ T-regulatory cells and tolerogenic plasmacytoid dendritic cells than stable LTRs, showed an increased plasma Kyn/Try ratio compared with both NHCs and stable LTRs. IDO expression by in vitro–stimulated peripheral blood mononuclear cells (PBMC) did not vary between BOS and stable LTRs. Furthermore, BOS patients displayed signs of chronic systemic inflammation (increased plasma levels of interleukin-8 and tumor necrosis factor-alpha) and higher T-cell activation (increased frequency of peripheral interferon-γ–producing clones). Conclusions Our results suggest that, in vivo, in lung transplantation, plasma IDO activity does not reflect the degree of lung graft acceptance, but instead is correlated with the degree of chronic inflammation. |
doi_str_mv | 10.1016/j.healun.2009.07.023 |
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Although a few experimental studies have suggested a role for IDO in graft acceptance, human data are scarce and inconclusive. We sought to establish whether, in lung transplant recipients (LTRs), plasma IDO activity mirrors the level of graft acceptance. Methods We measured the plasma Kyn/Try ratio, reflecting IDO activity, by high-performance liquid chromatography (HPLC) in 90 LTRs, including 26 patients who were still functionally/clinically stable for >36 post-transplant months (stable LTRs) and 64 LTRs with bronchiolitis obliterans syndrome (BOS, Grades 0-p to 3). Twenty-four normal healthy controls (NHCs) were also included. Results The Kyn/Try ratio in stable LTRs resembled that observed in NHCs, whereas, unexpectedly, patients with BOS, who had lower counts of peripheral CD4+ T-regulatory cells and tolerogenic plasmacytoid dendritic cells than stable LTRs, showed an increased plasma Kyn/Try ratio compared with both NHCs and stable LTRs. IDO expression by in vitro–stimulated peripheral blood mononuclear cells (PBMC) did not vary between BOS and stable LTRs. Furthermore, BOS patients displayed signs of chronic systemic inflammation (increased plasma levels of interleukin-8 and tumor necrosis factor-alpha) and higher T-cell activation (increased frequency of peripheral interferon-γ–producing clones). Conclusions Our results suggest that, in vivo, in lung transplantation, plasma IDO activity does not reflect the degree of lung graft acceptance, but instead is correlated with the degree of chronic inflammation.</description><identifier>ISSN: 1053-2498</identifier><identifier>EISSN: 1557-3117</identifier><identifier>DOI: 10.1016/j.healun.2009.07.023</identifier><identifier>PMID: 19783182</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Biological and medical sciences ; Biomarkers - blood ; Bronchiolitis Obliterans - blood ; Bronchiolitis Obliterans - enzymology ; Cardiology. Vascular system ; Chromatography, High Pressure Liquid ; Enzyme-Linked Immunosorbent Assay ; Flow Cytometry ; Follow-Up Studies ; Humans ; Indoleamine-Pyrrole 2,3,-Dioxygenase - blood ; Interleukin-8 - blood ; Kynurenine - blood ; Lung Transplantation - physiology ; Medical sciences ; Postoperative Complications - blood ; Postoperative Complications - enzymology ; Reference Values ; Surgery ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the heart ; T-Lymphocyte Subsets - enzymology ; Time Factors ; Transplantation Tolerance - physiology ; Transplantation, Homologous - physiology ; Tryptophan - blood</subject><ispartof>The Journal of heart and lung transplantation, 2009-11, Vol.28 (11), p.1185-1192</ispartof><rights>International Society for Heart and Lung Transplantation</rights><rights>2009 International Society for Heart and Lung Transplantation</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-245f8e12084d5333861fee9df63642b5c11b48763ffc0a0a25be006af4d38ff3</citedby><cites>FETCH-LOGICAL-c446t-245f8e12084d5333861fee9df63642b5c11b48763ffc0a0a25be006af4d38ff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.healun.2009.07.023$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27911,27912,45982</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22108428$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19783182$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meloni, Federica, MD, PhD</creatorcontrib><creatorcontrib>Giuliano, Serena, ScD</creatorcontrib><creatorcontrib>Solari, Nadia, ScD, PhD</creatorcontrib><creatorcontrib>Draghi, Paola, ScD</creatorcontrib><creatorcontrib>Miserere, Simona, ScD</creatorcontrib><creatorcontrib>Bardoni, Anna Maria, ScD</creatorcontrib><creatorcontrib>Salvini, Roberta, ScD</creatorcontrib><creatorcontrib>Bini, Francesco, MD</creatorcontrib><creatorcontrib>Fietta, Anna Maria, ScD</creatorcontrib><title>Indoleamine 2,3-Dioxygenase in Lung Allograft Tolerance</title><title>The Journal of heart and lung transplantation</title><addtitle>J Heart Lung Transplant</addtitle><description>Background Indoleamine 2,3-dioxygenase (IDO), an enzyme involved in the degradation of tryptophan (Try) to kynurenine (Kyn), is thought to suppress T-cell activity. Although a few experimental studies have suggested a role for IDO in graft acceptance, human data are scarce and inconclusive. We sought to establish whether, in lung transplant recipients (LTRs), plasma IDO activity mirrors the level of graft acceptance. Methods We measured the plasma Kyn/Try ratio, reflecting IDO activity, by high-performance liquid chromatography (HPLC) in 90 LTRs, including 26 patients who were still functionally/clinically stable for >36 post-transplant months (stable LTRs) and 64 LTRs with bronchiolitis obliterans syndrome (BOS, Grades 0-p to 3). Twenty-four normal healthy controls (NHCs) were also included. Results The Kyn/Try ratio in stable LTRs resembled that observed in NHCs, whereas, unexpectedly, patients with BOS, who had lower counts of peripheral CD4+ T-regulatory cells and tolerogenic plasmacytoid dendritic cells than stable LTRs, showed an increased plasma Kyn/Try ratio compared with both NHCs and stable LTRs. IDO expression by in vitro–stimulated peripheral blood mononuclear cells (PBMC) did not vary between BOS and stable LTRs. Furthermore, BOS patients displayed signs of chronic systemic inflammation (increased plasma levels of interleukin-8 and tumor necrosis factor-alpha) and higher T-cell activation (increased frequency of peripheral interferon-γ–producing clones). Conclusions Our results suggest that, in vivo, in lung transplantation, plasma IDO activity does not reflect the degree of lung graft acceptance, but instead is correlated with the degree of chronic inflammation.</description><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Bronchiolitis Obliterans - blood</subject><subject>Bronchiolitis Obliterans - enzymology</subject><subject>Cardiology. Vascular system</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Flow Cytometry</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Indoleamine-Pyrrole 2,3,-Dioxygenase - blood</subject><subject>Interleukin-8 - blood</subject><subject>Kynurenine - blood</subject><subject>Lung Transplantation - physiology</subject><subject>Medical sciences</subject><subject>Postoperative Complications - blood</subject><subject>Postoperative Complications - enzymology</subject><subject>Reference Values</subject><subject>Surgery</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the heart</subject><subject>T-Lymphocyte Subsets - enzymology</subject><subject>Time Factors</subject><subject>Transplantation Tolerance - physiology</subject><subject>Transplantation, Homologous - physiology</subject><subject>Tryptophan - blood</subject><issn>1053-2498</issn><issn>1557-3117</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU2P0zAQhi0EYpfCP0AoF8SFhPFHEueCtFq-VqrEgd4t1xkXF9dZ7AZt_z0TtQKJCyfP4Zl3PM8w9pJDw4F37_bNd7RxTo0AGBroGxDyEbvmbdvXkvP-MdXQylqoQV-xZ6XsAQhpxVN2xYdeS67FNevv0jhFtIeQsBJvZf0hTA-nHSZbsAqpWs9pV93EOO2y9cdqQ2y2yeFz9sTbWPDF5V2xzaePm9sv9frr57vbm3XtlOqONLz1GrkArcZWSqk77hGH0XeyU2LbOs63Sved9N6BBSvaLQJ01qtRau_lir05x97n6eeM5WgOoTiM0Sac5mJ6qTitRdErps6ky1MpGb25z-Fg88lwMIswszdnYWYRZqA3ZIPaXl0GzNsDjn-bLoYIeH0BbHE2-mX7UP5wQnDaTWji3p85JBu_AmZTXEAyNYaM7mjGKfzvJ_8GuBhSoJk_8IRlP805kWnDTREGzLfluMttYSBhghJ-Aw2Hnbo</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Meloni, Federica, MD, PhD</creator><creator>Giuliano, Serena, ScD</creator><creator>Solari, Nadia, ScD, PhD</creator><creator>Draghi, Paola, ScD</creator><creator>Miserere, Simona, ScD</creator><creator>Bardoni, Anna Maria, ScD</creator><creator>Salvini, Roberta, ScD</creator><creator>Bini, Francesco, MD</creator><creator>Fietta, Anna Maria, ScD</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>20091101</creationdate><title>Indoleamine 2,3-Dioxygenase in Lung Allograft Tolerance</title><author>Meloni, Federica, MD, PhD ; Giuliano, Serena, ScD ; Solari, Nadia, ScD, PhD ; Draghi, Paola, ScD ; Miserere, Simona, ScD ; Bardoni, Anna Maria, ScD ; Salvini, Roberta, ScD ; Bini, Francesco, MD ; Fietta, Anna Maria, ScD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-245f8e12084d5333861fee9df63642b5c11b48763ffc0a0a25be006af4d38ff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Bronchiolitis Obliterans - blood</topic><topic>Bronchiolitis Obliterans - enzymology</topic><topic>Cardiology. Vascular system</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Flow Cytometry</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Indoleamine-Pyrrole 2,3,-Dioxygenase - blood</topic><topic>Interleukin-8 - blood</topic><topic>Kynurenine - blood</topic><topic>Lung Transplantation - physiology</topic><topic>Medical sciences</topic><topic>Postoperative Complications - blood</topic><topic>Postoperative Complications - enzymology</topic><topic>Reference Values</topic><topic>Surgery</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the heart</topic><topic>T-Lymphocyte Subsets - enzymology</topic><topic>Time Factors</topic><topic>Transplantation Tolerance - physiology</topic><topic>Transplantation, Homologous - physiology</topic><topic>Tryptophan - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meloni, Federica, MD, PhD</creatorcontrib><creatorcontrib>Giuliano, Serena, ScD</creatorcontrib><creatorcontrib>Solari, Nadia, ScD, PhD</creatorcontrib><creatorcontrib>Draghi, Paola, ScD</creatorcontrib><creatorcontrib>Miserere, Simona, ScD</creatorcontrib><creatorcontrib>Bardoni, Anna Maria, ScD</creatorcontrib><creatorcontrib>Salvini, Roberta, ScD</creatorcontrib><creatorcontrib>Bini, Francesco, MD</creatorcontrib><creatorcontrib>Fietta, Anna Maria, ScD</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>The Journal of heart and lung transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meloni, Federica, MD, PhD</au><au>Giuliano, Serena, ScD</au><au>Solari, Nadia, ScD, PhD</au><au>Draghi, Paola, ScD</au><au>Miserere, Simona, ScD</au><au>Bardoni, Anna Maria, ScD</au><au>Salvini, Roberta, ScD</au><au>Bini, Francesco, MD</au><au>Fietta, Anna Maria, ScD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Indoleamine 2,3-Dioxygenase in Lung Allograft Tolerance</atitle><jtitle>The Journal of heart and lung transplantation</jtitle><addtitle>J Heart Lung Transplant</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>28</volume><issue>11</issue><spage>1185</spage><epage>1192</epage><pages>1185-1192</pages><issn>1053-2498</issn><eissn>1557-3117</eissn><abstract>Background Indoleamine 2,3-dioxygenase (IDO), an enzyme involved in the degradation of tryptophan (Try) to kynurenine (Kyn), is thought to suppress T-cell activity. Although a few experimental studies have suggested a role for IDO in graft acceptance, human data are scarce and inconclusive. We sought to establish whether, in lung transplant recipients (LTRs), plasma IDO activity mirrors the level of graft acceptance. Methods We measured the plasma Kyn/Try ratio, reflecting IDO activity, by high-performance liquid chromatography (HPLC) in 90 LTRs, including 26 patients who were still functionally/clinically stable for >36 post-transplant months (stable LTRs) and 64 LTRs with bronchiolitis obliterans syndrome (BOS, Grades 0-p to 3). Twenty-four normal healthy controls (NHCs) were also included. Results The Kyn/Try ratio in stable LTRs resembled that observed in NHCs, whereas, unexpectedly, patients with BOS, who had lower counts of peripheral CD4+ T-regulatory cells and tolerogenic plasmacytoid dendritic cells than stable LTRs, showed an increased plasma Kyn/Try ratio compared with both NHCs and stable LTRs. IDO expression by in vitro–stimulated peripheral blood mononuclear cells (PBMC) did not vary between BOS and stable LTRs. Furthermore, BOS patients displayed signs of chronic systemic inflammation (increased plasma levels of interleukin-8 and tumor necrosis factor-alpha) and higher T-cell activation (increased frequency of peripheral interferon-γ–producing clones). Conclusions Our results suggest that, in vivo, in lung transplantation, plasma IDO activity does not reflect the degree of lung graft acceptance, but instead is correlated with the degree of chronic inflammation.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>19783182</pmid><doi>10.1016/j.healun.2009.07.023</doi><tpages>8</tpages></addata></record> |
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subjects | Biological and medical sciences Biomarkers - blood Bronchiolitis Obliterans - blood Bronchiolitis Obliterans - enzymology Cardiology. Vascular system Chromatography, High Pressure Liquid Enzyme-Linked Immunosorbent Assay Flow Cytometry Follow-Up Studies Humans Indoleamine-Pyrrole 2,3,-Dioxygenase - blood Interleukin-8 - blood Kynurenine - blood Lung Transplantation - physiology Medical sciences Postoperative Complications - blood Postoperative Complications - enzymology Reference Values Surgery Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the heart T-Lymphocyte Subsets - enzymology Time Factors Transplantation Tolerance - physiology Transplantation, Homologous - physiology Tryptophan - blood |
title | Indoleamine 2,3-Dioxygenase in Lung Allograft Tolerance |
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