Onset and progression of de novo donor-specific anti-human leukocyte antigen antibodies after BK polyomavirus and preemptive immunosuppression reduction

Background BK polyomavirus (BKPyV) viremia/nephropathy and reduction in immunosuppression following viremia may increase the risk of alloimmune activation and allograft rejection. This study investigates the impact of BKPyV viremia on de novo donor anti‐human leukocyte antigen (HLA)‐specific antibod...

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Veröffentlicht in:Transplant infectious disease 2015-12, Vol.17 (6), p.848-858
Hauptverfasser: Dieplinger, G., Everly, M.J., Briley, K.P., Haisch, C.E., Bolin, P., Maldonado, A.Q., Kendrick, W.T., Kendrick, S.A., Morgan, C., Terasaki, P.I., Rebellato, L.M.
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container_end_page 858
container_issue 6
container_start_page 848
container_title Transplant infectious disease
container_volume 17
creator Dieplinger, G.
Everly, M.J.
Briley, K.P.
Haisch, C.E.
Bolin, P.
Maldonado, A.Q.
Kendrick, W.T.
Kendrick, S.A.
Morgan, C.
Terasaki, P.I.
Rebellato, L.M.
description Background BK polyomavirus (BKPyV) viremia/nephropathy and reduction in immunosuppression following viremia may increase the risk of alloimmune activation and allograft rejection. This study investigates the impact of BKPyV viremia on de novo donor anti‐human leukocyte antigen (HLA)‐specific antibodies (dnDSA). Patients and methods All primary renal transplants at East Carolina University from March 1999 to December 2010, with at least 1 post‐transplant BKPyV viral load testing, were analyzed. Patients were negative for anti‐HLA antibodies to donor antigens (tested via single antigen beads) at transplantation and at first BKPyV testing. Results Nineteen of 174 patients (11%) tested positive for BKPyV viremia. Within 24 months of BKPyV viremia detection, 79% of BKPyV‐viremic patients developed dnDSA. Only 20% of BKPyV viremia‐persistent cases, compared to 86% of BKPyV viremia‐resolved cases, developed dnDSA (P = 0.03). Poor allograft survival was evident in BKPyV viremia‐persistent patients (60% failure by 2 years post BKPyV diagnosis) and in BKPyV viremia‐resolved patients with dnDSA (5‐year post BKPyV diagnosis allograft survival of 48%). Conclusions Post‐transplant BKPyV viremia and preemptive immunosuppression reduction is associated with high rates of dnDSA. When preemptively treating BKPyV viremia, dnDSA should be monitored to prevent allograft consequences.
doi_str_mv 10.1111/tid.12467
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This study investigates the impact of BKPyV viremia on de novo donor anti‐human leukocyte antigen (HLA)‐specific antibodies (dnDSA). Patients and methods All primary renal transplants at East Carolina University from March 1999 to December 2010, with at least 1 post‐transplant BKPyV viral load testing, were analyzed. Patients were negative for anti‐HLA antibodies to donor antigens (tested via single antigen beads) at transplantation and at first BKPyV testing. Results Nineteen of 174 patients (11%) tested positive for BKPyV viremia. Within 24 months of BKPyV viremia detection, 79% of BKPyV‐viremic patients developed dnDSA. Only 20% of BKPyV viremia‐persistent cases, compared to 86% of BKPyV viremia‐resolved cases, developed dnDSA (P = 0.03). Poor allograft survival was evident in BKPyV viremia‐persistent patients (60% failure by 2 years post BKPyV diagnosis) and in BKPyV viremia‐resolved patients with dnDSA (5‐year post BKPyV diagnosis allograft survival of 48%). Conclusions Post‐transplant BKPyV viremia and preemptive immunosuppression reduction is associated with high rates of dnDSA. When preemptively treating BKPyV viremia, dnDSA should be monitored to prevent allograft consequences.</description><identifier>ISSN: 1398-2273</identifier><identifier>EISSN: 1399-3062</identifier><identifier>DOI: 10.1111/tid.12467</identifier><identifier>PMID: 26442607</identifier><language>eng</language><publisher>Denmark: Blackwell Publishing Ltd</publisher><subject>Adult ; anti-human leukocyte antigen antibody ; Antibodies - blood ; BK Virus - isolation &amp; purification ; Dose-Response Relationship, Drug ; Female ; HLA Antigens - immunology ; Humans ; immunosuppression ; Immunosuppression - adverse effects ; Immunosuppressive Agents - administration &amp; dosage ; Immunosuppressive Agents - therapeutic use ; Kidney Transplantation - adverse effects ; Male ; Middle Aged ; polyomavirus ; Polyomavirus Infections - blood ; Polyomavirus Infections - immunology ; transplantation ; Tumor Virus Infections - blood ; Tumor Virus Infections - immunology ; Viremia</subject><ispartof>Transplant infectious disease, 2015-12, Vol.17 (6), p.848-858</ispartof><rights>2015 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2015 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><rights>2015 Wiley Periodicals, Inc</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3917-a9630fb8808a5b79abeeb021ddfbf516837f6787d2a1d8fbb4698b6055db7acf3</citedby><cites>FETCH-LOGICAL-c3917-a9630fb8808a5b79abeeb021ddfbf516837f6787d2a1d8fbb4698b6055db7acf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Ftid.12467$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftid.12467$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26442607$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dieplinger, G.</creatorcontrib><creatorcontrib>Everly, M.J.</creatorcontrib><creatorcontrib>Briley, K.P.</creatorcontrib><creatorcontrib>Haisch, C.E.</creatorcontrib><creatorcontrib>Bolin, P.</creatorcontrib><creatorcontrib>Maldonado, A.Q.</creatorcontrib><creatorcontrib>Kendrick, W.T.</creatorcontrib><creatorcontrib>Kendrick, S.A.</creatorcontrib><creatorcontrib>Morgan, C.</creatorcontrib><creatorcontrib>Terasaki, P.I.</creatorcontrib><creatorcontrib>Rebellato, L.M.</creatorcontrib><title>Onset and progression of de novo donor-specific anti-human leukocyte antigen antibodies after BK polyomavirus and preemptive immunosuppression reduction</title><title>Transplant infectious disease</title><addtitle>Transpl Infect Dis</addtitle><description>Background BK polyomavirus (BKPyV) viremia/nephropathy and reduction in immunosuppression following viremia may increase the risk of alloimmune activation and allograft rejection. This study investigates the impact of BKPyV viremia on de novo donor anti‐human leukocyte antigen (HLA)‐specific antibodies (dnDSA). Patients and methods All primary renal transplants at East Carolina University from March 1999 to December 2010, with at least 1 post‐transplant BKPyV viral load testing, were analyzed. Patients were negative for anti‐HLA antibodies to donor antigens (tested via single antigen beads) at transplantation and at first BKPyV testing. Results Nineteen of 174 patients (11%) tested positive for BKPyV viremia. Within 24 months of BKPyV viremia detection, 79% of BKPyV‐viremic patients developed dnDSA. Only 20% of BKPyV viremia‐persistent cases, compared to 86% of BKPyV viremia‐resolved cases, developed dnDSA (P = 0.03). Poor allograft survival was evident in BKPyV viremia‐persistent patients (60% failure by 2 years post BKPyV diagnosis) and in BKPyV viremia‐resolved patients with dnDSA (5‐year post BKPyV diagnosis allograft survival of 48%). Conclusions Post‐transplant BKPyV viremia and preemptive immunosuppression reduction is associated with high rates of dnDSA. When preemptively treating BKPyV viremia, dnDSA should be monitored to prevent allograft consequences.</description><subject>Adult</subject><subject>anti-human leukocyte antigen antibody</subject><subject>Antibodies - blood</subject><subject>BK Virus - isolation &amp; purification</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>HLA Antigens - immunology</subject><subject>Humans</subject><subject>immunosuppression</subject><subject>Immunosuppression - adverse effects</subject><subject>Immunosuppressive Agents - administration &amp; dosage</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Male</subject><subject>Middle Aged</subject><subject>polyomavirus</subject><subject>Polyomavirus Infections - blood</subject><subject>Polyomavirus Infections - immunology</subject><subject>transplantation</subject><subject>Tumor Virus Infections - blood</subject><subject>Tumor Virus Infections - immunology</subject><subject>Viremia</subject><issn>1398-2273</issn><issn>1399-3062</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1TAQhSMEoqWw4AWQJTawSGs7iZ0saYG2cEWFVGBp2fG4uE3s1I4v3Dfp49a9P10g4c0cjb85Y-sUxWuCD0k-R7PVh4TWjD8p9knVdWWFGX261m1JKa_2ihcxXmNMeFd3z4s9yuqaMsz3i7sLF2FG0mk0BX8VIEbrHfIGaUDOLz3S3vlQxgl6a2yfydmWv9MoHRog3fh-NcO6eQVuXZXXFiKSZoaAjr-iyQ8rP8qlDSlu9wCM02yXgOw4Judjmqbd4gA69XNWL4tnRg4RXm3rQfHj86fLk7NycXF6fvJhUfZVR3gpO1Zho9oWt7JRvJMKQGFKtDbKNIS1FTeMt1xTSXRrlKpZ1yqGm0YrLntTHRTvNr75-7cJ4ixGG3sYBunApygIZ7htOkppRt_-g177FFx-XaYaznHdUpKp9xuqDz7GAEZMwY4yrATB4iEukeMS67gy-2brmNQI-pHc5ZOBow3wxw6w-r-TuDz_uLMsNxM2zvD3cUKGG5FveSN-fTsVP6sF_n78hWdxD2Ywsi4</recordid><startdate>201512</startdate><enddate>201512</enddate><creator>Dieplinger, G.</creator><creator>Everly, M.J.</creator><creator>Briley, K.P.</creator><creator>Haisch, C.E.</creator><creator>Bolin, P.</creator><creator>Maldonado, A.Q.</creator><creator>Kendrick, W.T.</creator><creator>Kendrick, S.A.</creator><creator>Morgan, C.</creator><creator>Terasaki, P.I.</creator><creator>Rebellato, L.M.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7QO</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201512</creationdate><title>Onset and progression of de novo donor-specific anti-human leukocyte antigen antibodies after BK polyomavirus and preemptive immunosuppression reduction</title><author>Dieplinger, G. ; 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Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transplant infectious disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dieplinger, G.</au><au>Everly, M.J.</au><au>Briley, K.P.</au><au>Haisch, C.E.</au><au>Bolin, P.</au><au>Maldonado, A.Q.</au><au>Kendrick, W.T.</au><au>Kendrick, S.A.</au><au>Morgan, C.</au><au>Terasaki, P.I.</au><au>Rebellato, L.M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Onset and progression of de novo donor-specific anti-human leukocyte antigen antibodies after BK polyomavirus and preemptive immunosuppression reduction</atitle><jtitle>Transplant infectious disease</jtitle><addtitle>Transpl Infect Dis</addtitle><date>2015-12</date><risdate>2015</risdate><volume>17</volume><issue>6</issue><spage>848</spage><epage>858</epage><pages>848-858</pages><issn>1398-2273</issn><eissn>1399-3062</eissn><abstract>Background BK polyomavirus (BKPyV) viremia/nephropathy and reduction in immunosuppression following viremia may increase the risk of alloimmune activation and allograft rejection. This study investigates the impact of BKPyV viremia on de novo donor anti‐human leukocyte antigen (HLA)‐specific antibodies (dnDSA). Patients and methods All primary renal transplants at East Carolina University from March 1999 to December 2010, with at least 1 post‐transplant BKPyV viral load testing, were analyzed. Patients were negative for anti‐HLA antibodies to donor antigens (tested via single antigen beads) at transplantation and at first BKPyV testing. Results Nineteen of 174 patients (11%) tested positive for BKPyV viremia. Within 24 months of BKPyV viremia detection, 79% of BKPyV‐viremic patients developed dnDSA. Only 20% of BKPyV viremia‐persistent cases, compared to 86% of BKPyV viremia‐resolved cases, developed dnDSA (P = 0.03). Poor allograft survival was evident in BKPyV viremia‐persistent patients (60% failure by 2 years post BKPyV diagnosis) and in BKPyV viremia‐resolved patients with dnDSA (5‐year post BKPyV diagnosis allograft survival of 48%). Conclusions Post‐transplant BKPyV viremia and preemptive immunosuppression reduction is associated with high rates of dnDSA. When preemptively treating BKPyV viremia, dnDSA should be monitored to prevent allograft consequences.</abstract><cop>Denmark</cop><pub>Blackwell Publishing Ltd</pub><pmid>26442607</pmid><doi>10.1111/tid.12467</doi><tpages>11</tpages></addata></record>
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subjects Adult
anti-human leukocyte antigen antibody
Antibodies - blood
BK Virus - isolation & purification
Dose-Response Relationship, Drug
Female
HLA Antigens - immunology
Humans
immunosuppression
Immunosuppression - adverse effects
Immunosuppressive Agents - administration & dosage
Immunosuppressive Agents - therapeutic use
Kidney Transplantation - adverse effects
Male
Middle Aged
polyomavirus
Polyomavirus Infections - blood
Polyomavirus Infections - immunology
transplantation
Tumor Virus Infections - blood
Tumor Virus Infections - immunology
Viremia
title Onset and progression of de novo donor-specific anti-human leukocyte antigen antibodies after BK polyomavirus and preemptive immunosuppression reduction
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