Plasma IL-10 Levels to Guide Antiviral Prophylaxis Prevention of Late-Onset Cytomegalovirus Disease, in High Risk Solid Kidney and Liver Transplant Recipients

BACKGROUNDImmune measurements that distinguish solid organ transplantation (SOT) recipients who control cytomegalovirus (CMV) infection from those who progress to CMV-disease (CMV-dz) may be clinically useful in guiding tailored prevention strategies. We previously reported that elevated plasma leve...

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Veröffentlicht in:Transplantation 2016-01, Vol.100 (1), p.210-216
Hauptverfasser: Limaye, Ajit P, La Rosa, Corinna, Longmate, Jeff, Diamond, Don J
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creator Limaye, Ajit P
La Rosa, Corinna
Longmate, Jeff
Diamond, Don J
description BACKGROUNDImmune measurements that distinguish solid organ transplantation (SOT) recipients who control cytomegalovirus (CMV) infection from those who progress to CMV-disease (CMV-dz) may be clinically useful in guiding tailored prevention strategies. We previously reported that elevated plasma levels of the immune-modulator IL-10 are associated with late CMV-dz. Here we evaluate whether IL-10 levels measured soon after prophylaxis discontinuation are predictive of CMV-dz risk. METHODSPlasma IL-10 levels were quantitatively measured by ELISA kit in 40 D/R SOT patients. All 40 D/R high-risk patients were prospectively followed for at least 12 months post-SOT13 subjects developed CMV-dz, all within 6 months of prophylaxis discontinuation. RESULTSIL-10 was detectable at the first post-prophylaxis measurement for 11 of 13 subjects who developed CMV-dz. In contrast, IL-10 was detectable in only 6 of 27 CMV asymptomatic patients. Monitoring IL-10 plasma levels within 1 month prophylaxis suspension appeared to have clinically useful level of 85% sensitivity and 78% specificity. CONCLUSIONSThe exact role of IL-10 with its multiple immunoregulatory effects during CMV infection is not clear. Moreover, IL-10 production can be influenced by pathological and infectious contexts, and/or anti-rejection immunosuppressant therapy. Despite mechanisms of IL-10 dysregulation may substantially differ among SOT patients, our findings suggest that measurable plasma IL-10 soon after prophylaxis discontinuation may be an adequate indicator of subsequent CMV-dz. If a similar prognostic performance is confirmed in a larger D/R cohort, IL-10 plasma levels could be used to guide the length of prophylaxis, providing a clinically useful means to reduce the incidence of CMV-dz in high risk patients.
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We previously reported that elevated plasma levels of the immune-modulator IL-10 are associated with late CMV-dz. Here we evaluate whether IL-10 levels measured soon after prophylaxis discontinuation are predictive of CMV-dz risk. METHODSPlasma IL-10 levels were quantitatively measured by ELISA kit in 40 D/R SOT patients. All 40 D/R high-risk patients were prospectively followed for at least 12 months post-SOT13 subjects developed CMV-dz, all within 6 months of prophylaxis discontinuation. RESULTSIL-10 was detectable at the first post-prophylaxis measurement for 11 of 13 subjects who developed CMV-dz. In contrast, IL-10 was detectable in only 6 of 27 CMV asymptomatic patients. Monitoring IL-10 plasma levels within 1 month prophylaxis suspension appeared to have clinically useful level of 85% sensitivity and 78% specificity. CONCLUSIONSThe exact role of IL-10 with its multiple immunoregulatory effects during CMV infection is not clear. Moreover, IL-10 production can be influenced by pathological and infectious contexts, and/or anti-rejection immunosuppressant therapy. Despite mechanisms of IL-10 dysregulation may substantially differ among SOT patients, our findings suggest that measurable plasma IL-10 soon after prophylaxis discontinuation may be an adequate indicator of subsequent CMV-dz. If a similar prognostic performance is confirmed in a larger D/R cohort, IL-10 plasma levels could be used to guide the length of prophylaxis, providing a clinically useful means to reduce the incidence of CMV-dz in high risk patients.</description><identifier>ISSN: 0041-1337</identifier><identifier>EISSN: 1534-6080</identifier><identifier>DOI: 10.1097/TP.0000000000000816</identifier><identifier>PMID: 26680375</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Antiviral Agents - administration &amp; dosage ; Biomarkers - blood ; Cytomegalovirus Infections - blood ; Cytomegalovirus Infections - diagnosis ; Cytomegalovirus Infections - immunology ; Cytomegalovirus Infections - prevention &amp; control ; Drug Administration Schedule ; Drug Monitoring - methods ; Enzyme-Linked Immunosorbent Assay ; Ganciclovir - administration &amp; dosage ; Ganciclovir - analogs &amp; derivatives ; Humans ; Interleukin-10 - blood ; Kidney Transplantation - adverse effects ; Liver Transplantation - adverse effects ; Predictive Value of Tests ; Prospective Studies ; Risk Assessment ; Risk Factors ; Time Factors ; Transplant Recipients ; Treatment Outcome ; Up-Regulation</subject><ispartof>Transplantation, 2016-01, Vol.100 (1), p.210-216</ispartof><rights>Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4646-6eb76a21920d7d6fccf912a43dee8439442eda557f3aa970b6f77711984ebde3</citedby><cites>FETCH-LOGICAL-c4646-6eb76a21920d7d6fccf912a43dee8439442eda557f3aa970b6f77711984ebde3</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/26680375$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Limaye, Ajit P</creatorcontrib><creatorcontrib>La Rosa, Corinna</creatorcontrib><creatorcontrib>Longmate, Jeff</creatorcontrib><creatorcontrib>Diamond, Don J</creatorcontrib><title>Plasma IL-10 Levels to Guide Antiviral Prophylaxis Prevention of Late-Onset Cytomegalovirus Disease, in High Risk Solid Kidney and Liver Transplant Recipients</title><title>Transplantation</title><addtitle>Transplantation</addtitle><description>BACKGROUNDImmune measurements that distinguish solid organ transplantation (SOT) recipients who control cytomegalovirus (CMV) infection from those who progress to CMV-disease (CMV-dz) may be clinically useful in guiding tailored prevention strategies. We previously reported that elevated plasma levels of the immune-modulator IL-10 are associated with late CMV-dz. Here we evaluate whether IL-10 levels measured soon after prophylaxis discontinuation are predictive of CMV-dz risk. METHODSPlasma IL-10 levels were quantitatively measured by ELISA kit in 40 D/R SOT patients. All 40 D/R high-risk patients were prospectively followed for at least 12 months post-SOT13 subjects developed CMV-dz, all within 6 months of prophylaxis discontinuation. RESULTSIL-10 was detectable at the first post-prophylaxis measurement for 11 of 13 subjects who developed CMV-dz. In contrast, IL-10 was detectable in only 6 of 27 CMV asymptomatic patients. Monitoring IL-10 plasma levels within 1 month prophylaxis suspension appeared to have clinically useful level of 85% sensitivity and 78% specificity. CONCLUSIONSThe exact role of IL-10 with its multiple immunoregulatory effects during CMV infection is not clear. Moreover, IL-10 production can be influenced by pathological and infectious contexts, and/or anti-rejection immunosuppressant therapy. Despite mechanisms of IL-10 dysregulation may substantially differ among SOT patients, our findings suggest that measurable plasma IL-10 soon after prophylaxis discontinuation may be an adequate indicator of subsequent CMV-dz. If a similar prognostic performance is confirmed in a larger D/R cohort, IL-10 plasma levels could be used to guide the length of prophylaxis, providing a clinically useful means to reduce the incidence of CMV-dz in high risk patients.</description><subject>Antiviral Agents - administration &amp; dosage</subject><subject>Biomarkers - blood</subject><subject>Cytomegalovirus Infections - blood</subject><subject>Cytomegalovirus Infections - diagnosis</subject><subject>Cytomegalovirus Infections - immunology</subject><subject>Cytomegalovirus Infections - prevention &amp; control</subject><subject>Drug Administration Schedule</subject><subject>Drug Monitoring - methods</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Ganciclovir - administration &amp; dosage</subject><subject>Ganciclovir - analogs &amp; derivatives</subject><subject>Humans</subject><subject>Interleukin-10 - blood</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Liver Transplantation - adverse effects</subject><subject>Predictive Value of Tests</subject><subject>Prospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Time Factors</subject><subject>Transplant Recipients</subject><subject>Treatment Outcome</subject><subject>Up-Regulation</subject><issn>0041-1337</issn><issn>1534-6080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFu1DAQhi0EotvCEyAhHzmQYseOnRyrBdqKSF2V3CNvPOmaOnHwJFv2ZXjWGm1BiANzmZHm-_8Z6SfkDWfnnFX6Q7M5Z39XydUzsuKFkJliJXtOVoxJnnEh9Ak5RfyWmEJo_ZKc5EqVTOhiRX5uvMHB0Os644zWsAePdA70cnEW6MU4u72LxtNNDNPu4M0Ph2lOWNqEkYae1maG7GZEmOn6MIcB7owPSbQg_egQDMJ76kZ65e529NbhPf0avLP0i7MjHKgZLa3dHiJtohlx8mac6S10bnLpBL4iL3rjEV4_9TPSfP7UrK-y-ubyen1RZ51UUmUKtlqZnFc5s9qqvuv6iudGCgtQSlFJmYM1RaF7YUyl2Vb1WmvOq1LC1oI4I--OtlMM3xfAuR0cduDTNxAWbLkuWLKplEyoOKJdDIgR-naKbjDx0HLW_sqlbTbtv7kk1dunA8t2APtH8zuIBOgj8BD8DBHv_fIAsd2B8fPuv9aPtyGaxg</recordid><startdate>201601</startdate><enddate>201601</enddate><creator>Limaye, Ajit P</creator><creator>La Rosa, Corinna</creator><creator>Longmate, Jeff</creator><creator>Diamond, Don J</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</general><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>201601</creationdate><title>Plasma IL-10 Levels to Guide Antiviral Prophylaxis Prevention of Late-Onset Cytomegalovirus Disease, in High Risk Solid Kidney and Liver Transplant Recipients</title><author>Limaye, Ajit P ; La Rosa, Corinna ; Longmate, Jeff ; Diamond, Don J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4646-6eb76a21920d7d6fccf912a43dee8439442eda557f3aa970b6f77711984ebde3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Antiviral Agents - administration &amp; dosage</topic><topic>Biomarkers - blood</topic><topic>Cytomegalovirus Infections - blood</topic><topic>Cytomegalovirus Infections - diagnosis</topic><topic>Cytomegalovirus Infections - immunology</topic><topic>Cytomegalovirus Infections - prevention &amp; control</topic><topic>Drug Administration Schedule</topic><topic>Drug Monitoring - methods</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Ganciclovir - administration &amp; dosage</topic><topic>Ganciclovir - analogs &amp; derivatives</topic><topic>Humans</topic><topic>Interleukin-10 - blood</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Liver Transplantation - adverse effects</topic><topic>Predictive Value of Tests</topic><topic>Prospective Studies</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Time Factors</topic><topic>Transplant Recipients</topic><topic>Treatment Outcome</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Limaye, Ajit P</creatorcontrib><creatorcontrib>La Rosa, Corinna</creatorcontrib><creatorcontrib>Longmate, Jeff</creatorcontrib><creatorcontrib>Diamond, Don J</creatorcontrib><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</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Limaye, Ajit P</au><au>La Rosa, Corinna</au><au>Longmate, Jeff</au><au>Diamond, Don J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma IL-10 Levels to Guide Antiviral Prophylaxis Prevention of Late-Onset Cytomegalovirus Disease, in High Risk Solid Kidney and Liver Transplant Recipients</atitle><jtitle>Transplantation</jtitle><addtitle>Transplantation</addtitle><date>2016-01</date><risdate>2016</risdate><volume>100</volume><issue>1</issue><spage>210</spage><epage>216</epage><pages>210-216</pages><issn>0041-1337</issn><eissn>1534-6080</eissn><abstract>BACKGROUNDImmune measurements that distinguish solid organ transplantation (SOT) recipients who control cytomegalovirus (CMV) infection from those who progress to CMV-disease (CMV-dz) may be clinically useful in guiding tailored prevention strategies. We previously reported that elevated plasma levels of the immune-modulator IL-10 are associated with late CMV-dz. Here we evaluate whether IL-10 levels measured soon after prophylaxis discontinuation are predictive of CMV-dz risk. METHODSPlasma IL-10 levels were quantitatively measured by ELISA kit in 40 D/R SOT patients. All 40 D/R high-risk patients were prospectively followed for at least 12 months post-SOT13 subjects developed CMV-dz, all within 6 months of prophylaxis discontinuation. RESULTSIL-10 was detectable at the first post-prophylaxis measurement for 11 of 13 subjects who developed CMV-dz. In contrast, IL-10 was detectable in only 6 of 27 CMV asymptomatic patients. Monitoring IL-10 plasma levels within 1 month prophylaxis suspension appeared to have clinically useful level of 85% sensitivity and 78% specificity. CONCLUSIONSThe exact role of IL-10 with its multiple immunoregulatory effects during CMV infection is not clear. Moreover, IL-10 production can be influenced by pathological and infectious contexts, and/or anti-rejection immunosuppressant therapy. Despite mechanisms of IL-10 dysregulation may substantially differ among SOT patients, our findings suggest that measurable plasma IL-10 soon after prophylaxis discontinuation may be an adequate indicator of subsequent CMV-dz. If a similar prognostic performance is confirmed in a larger D/R cohort, IL-10 plasma levels could be used to guide the length of prophylaxis, providing a clinically useful means to reduce the incidence of CMV-dz in high risk patients.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>26680375</pmid><doi>10.1097/TP.0000000000000816</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Antiviral Agents - administration & dosage
Biomarkers - blood
Cytomegalovirus Infections - blood
Cytomegalovirus Infections - diagnosis
Cytomegalovirus Infections - immunology
Cytomegalovirus Infections - prevention & control
Drug Administration Schedule
Drug Monitoring - methods
Enzyme-Linked Immunosorbent Assay
Ganciclovir - administration & dosage
Ganciclovir - analogs & derivatives
Humans
Interleukin-10 - blood
Kidney Transplantation - adverse effects
Liver Transplantation - adverse effects
Predictive Value of Tests
Prospective Studies
Risk Assessment
Risk Factors
Time Factors
Transplant Recipients
Treatment Outcome
Up-Regulation
title Plasma IL-10 Levels to Guide Antiviral Prophylaxis Prevention of Late-Onset Cytomegalovirus Disease, in High Risk Solid Kidney and Liver Transplant Recipients
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