Donor specific anti-hla antibodies with antibody mediated rejection and long-term outcomes following heart transplantation

Introduction Donor specific anti-HLA antibodies (DSA) are common following heart transplantation and are associated with rejection, cardiac allograft vasculopathy (CAV), and mortality. Currently a non-invasive diagnostic test for pathologic AMR (pAMR) does not exist. Methods 221 consecutive adult pa...

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Veröffentlicht in:The Journal of heart and lung transplantation 2017-05, Vol.36 (5), p.540-545
Hauptverfasser: Clerkin, Kevin J., MD, Farr, Maryjane A., MD, MSc, Restaino, Susan W., MD, Zorn, Emmanuel, PhD, Latif, Farhana, MD, Vasilescu, Elena R., MD, Marboe, Charles C., MD, Colombo, Paolo C., MD, Mancini, Donna M., MD
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container_end_page 545
container_issue 5
container_start_page 540
container_title The Journal of heart and lung transplantation
container_volume 36
creator Clerkin, Kevin J., MD
Farr, Maryjane A., MD, MSc
Restaino, Susan W., MD
Zorn, Emmanuel, PhD
Latif, Farhana, MD
Vasilescu, Elena R., MD
Marboe, Charles C., MD
Colombo, Paolo C., MD
Mancini, Donna M., MD
description Introduction Donor specific anti-HLA antibodies (DSA) are common following heart transplantation and are associated with rejection, cardiac allograft vasculopathy (CAV), and mortality. Currently a non-invasive diagnostic test for pathologic AMR (pAMR) does not exist. Methods 221 consecutive adult patients underwent heart transplantation from January 1st , 2010 through August 31th , 2013 and followed through October 1st , 2015. The primary objective was to determine whether the presence of DSA could detect AMR at the time of pathologic diagnosis. Secondary analyses included the association of DSA (stratified by MHC Class and de-novo status) during AMR with new graft dysfunction, graft loss (mortality or retransplantation), and development of CAV. Results During the study period 69 individual patients (31.2%) had DSA (24% had de-novo DSA) and there were 74 episodes of pAMR in 38 unique patients. The sensitivity of DSA at any MFI to detect concurrent pAMR was only 54.3%. The presence of any DSA during pAMR increased the odds of graft dysfunction (OR 5.37, 95% CI 1.34-21.47, p=0.018), adjusting for age, gender, and timing of AMR. Circulating Class II DSA after transplantation increased the risk of future pAMR (HR 2.97, 95% CI 1.31-6.73, p=0.009). Patients who developed de-novo Class II DSA had a 151% increase in risk of graft loss (contingent on 30-day survival) compared with those who did not have DSA (95% CI 1.11-5.69, p=0.027). Conclusions DSA were inadequate to diagnose pAMR, but Class II DSA provided prognostic information regarding future pAMR, graft dysfunction with pAMR, and graft loss.
doi_str_mv 10.1016/j.healun.2016.10.016
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Currently a non-invasive diagnostic test for pathologic AMR (pAMR) does not exist. Methods 221 consecutive adult patients underwent heart transplantation from January 1st , 2010 through August 31th , 2013 and followed through October 1st , 2015. The primary objective was to determine whether the presence of DSA could detect AMR at the time of pathologic diagnosis. Secondary analyses included the association of DSA (stratified by MHC Class and de-novo status) during AMR with new graft dysfunction, graft loss (mortality or retransplantation), and development of CAV. Results During the study period 69 individual patients (31.2%) had DSA (24% had de-novo DSA) and there were 74 episodes of pAMR in 38 unique patients. The sensitivity of DSA at any MFI to detect concurrent pAMR was only 54.3%. The presence of any DSA during pAMR increased the odds of graft dysfunction (OR 5.37, 95% CI 1.34-21.47, p=0.018), adjusting for age, gender, and timing of AMR. Circulating Class II DSA after transplantation increased the risk of future pAMR (HR 2.97, 95% CI 1.31-6.73, p=0.009). Patients who developed de-novo Class II DSA had a 151% increase in risk of graft loss (contingent on 30-day survival) compared with those who did not have DSA (95% CI 1.11-5.69, p=0.027). Conclusions DSA were inadequate to diagnose pAMR, but Class II DSA provided prognostic information regarding future pAMR, graft dysfunction with pAMR, and graft loss.</description><identifier>ISSN: 1053-2498</identifier><identifier>EISSN: 1557-3117</identifier><identifier>DOI: 10.1016/j.healun.2016.10.016</identifier><identifier>PMID: 27916323</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Allografts - immunology ; antibody mediated rejection ; Antibody Specificity - immunology ; cardiac allograft vasculopathy ; Cohort Studies ; donor specific antibodies ; Female ; Follow-Up Studies ; Graft Rejection - immunology ; heart transplant ; Heart Transplantation - adverse effects ; Heart Transplantation - methods ; HLA Antigens - immunology ; Humans ; Isoantibodies - immunology ; Kaplan-Meier Estimate ; Male ; Middle Aged ; mortality ; Proportional Hazards Models ; Reoperation ; Retrospective Studies ; Risk Assessment ; Surgery ; Survival Analysis ; Tissue Donors ; Transplantation Immunology - physiology ; United States</subject><ispartof>The Journal of heart and lung transplantation, 2017-05, Vol.36 (5), p.540-545</ispartof><rights>2017 International Society for Heart and Lung Transplantation</rights><rights>Copyright © 2017 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c518t-aafee0865fb6dfdab2c91a197bde6eadabf978f6c528e63aedaa68c48df5b4643</citedby><cites>FETCH-LOGICAL-c518t-aafee0865fb6dfdab2c91a197bde6eadabf978f6c528e63aedaa68c48df5b4643</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S105324981630403X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27916323$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Clerkin, Kevin J., MD</creatorcontrib><creatorcontrib>Farr, Maryjane A., MD, MSc</creatorcontrib><creatorcontrib>Restaino, Susan W., MD</creatorcontrib><creatorcontrib>Zorn, Emmanuel, PhD</creatorcontrib><creatorcontrib>Latif, Farhana, MD</creatorcontrib><creatorcontrib>Vasilescu, Elena R., MD</creatorcontrib><creatorcontrib>Marboe, Charles C., MD</creatorcontrib><creatorcontrib>Colombo, Paolo C., MD</creatorcontrib><creatorcontrib>Mancini, Donna M., MD</creatorcontrib><title>Donor specific anti-hla antibodies with antibody mediated rejection and long-term outcomes following heart transplantation</title><title>The Journal of heart and lung transplantation</title><addtitle>J Heart Lung Transplant</addtitle><description>Introduction Donor specific anti-HLA antibodies (DSA) are common following heart transplantation and are associated with rejection, cardiac allograft vasculopathy (CAV), and mortality. Currently a non-invasive diagnostic test for pathologic AMR (pAMR) does not exist. Methods 221 consecutive adult patients underwent heart transplantation from January 1st , 2010 through August 31th , 2013 and followed through October 1st , 2015. The primary objective was to determine whether the presence of DSA could detect AMR at the time of pathologic diagnosis. Secondary analyses included the association of DSA (stratified by MHC Class and de-novo status) during AMR with new graft dysfunction, graft loss (mortality or retransplantation), and development of CAV. Results During the study period 69 individual patients (31.2%) had DSA (24% had de-novo DSA) and there were 74 episodes of pAMR in 38 unique patients. The sensitivity of DSA at any MFI to detect concurrent pAMR was only 54.3%. The presence of any DSA during pAMR increased the odds of graft dysfunction (OR 5.37, 95% CI 1.34-21.47, p=0.018), adjusting for age, gender, and timing of AMR. Circulating Class II DSA after transplantation increased the risk of future pAMR (HR 2.97, 95% CI 1.31-6.73, p=0.009). Patients who developed de-novo Class II DSA had a 151% increase in risk of graft loss (contingent on 30-day survival) compared with those who did not have DSA (95% CI 1.11-5.69, p=0.027). Conclusions DSA were inadequate to diagnose pAMR, but Class II DSA provided prognostic information regarding future pAMR, graft dysfunction with pAMR, and graft loss.</description><subject>Adult</subject><subject>Allografts - immunology</subject><subject>antibody mediated rejection</subject><subject>Antibody Specificity - immunology</subject><subject>cardiac allograft vasculopathy</subject><subject>Cohort Studies</subject><subject>donor specific antibodies</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Graft Rejection - immunology</subject><subject>heart transplant</subject><subject>Heart Transplantation - adverse effects</subject><subject>Heart Transplantation - methods</subject><subject>HLA Antigens - immunology</subject><subject>Humans</subject><subject>Isoantibodies - immunology</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Middle Aged</subject><subject>mortality</subject><subject>Proportional Hazards Models</subject><subject>Reoperation</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Surgery</subject><subject>Survival Analysis</subject><subject>Tissue Donors</subject><subject>Transplantation Immunology - physiology</subject><subject>United States</subject><issn>1053-2498</issn><issn>1557-3117</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUstu1DAUjRCIlsIfIJQlmwx-xE6yQUIFClIlFoDEznLs6xkHxx5sp9Xw9XWYtjw2rO7znHuvj6vqOUYbjDB_NW12IN3iN6REJbUp5kF1ihnrGopx97D4iNGGtEN_Uj1JaUIIEcrI4-qEdAPmlNDT6ufb4EOs0x6UNVbV0mfb7Jz85YxBW0j1tc27u_hQz6CtzKDrCBOobIMvNV274LdNhjjXYckqzAVngnPh2vptXTaNuc5R-rR3hUmusKfVIyNdgme39qz6-v7dl_MPzeWni4_nby4bxXCfGykNAOo5MyPXRsuRqAFLPHSjBg6yJMzQ9YYrRnrgVIKWkveq7bVhY8tbela9PvLul7Esr8CXRZzYRzvLeBBBWvF3xdud2IYrwThrKaaF4OUtQQw_FkhZzDYpcOUSCEsSuG85IpzQtbU9tqoYUopg7sdgJFbZxCSOsolVtjVbTIG9-HPFe9CdTr9vgPJQVxaiSMqCV0WLWEQQOtj_TfiXQDnrrZLuOxwgTWGJvoggsEhEIPF5_TrrzylQ1CL6jd4A5VbGKw</recordid><startdate>20170501</startdate><enddate>20170501</enddate><creator>Clerkin, Kevin J., MD</creator><creator>Farr, Maryjane A., MD, MSc</creator><creator>Restaino, Susan W., MD</creator><creator>Zorn, Emmanuel, PhD</creator><creator>Latif, Farhana, MD</creator><creator>Vasilescu, Elena R., MD</creator><creator>Marboe, Charles C., MD</creator><creator>Colombo, Paolo C., MD</creator><creator>Mancini, Donna M., MD</creator><general>Elsevier Inc</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><scope>5PM</scope></search><sort><creationdate>20170501</creationdate><title>Donor specific anti-hla antibodies with antibody mediated rejection and long-term outcomes following heart transplantation</title><author>Clerkin, Kevin J., MD ; Farr, Maryjane A., MD, MSc ; Restaino, Susan W., MD ; Zorn, Emmanuel, PhD ; Latif, Farhana, MD ; Vasilescu, Elena R., MD ; Marboe, Charles C., MD ; Colombo, Paolo C., MD ; Mancini, Donna M., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c518t-aafee0865fb6dfdab2c91a197bde6eadabf978f6c528e63aedaa68c48df5b4643</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Allografts - immunology</topic><topic>antibody mediated rejection</topic><topic>Antibody Specificity - immunology</topic><topic>cardiac allograft vasculopathy</topic><topic>Cohort Studies</topic><topic>donor specific antibodies</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Graft Rejection - immunology</topic><topic>heart transplant</topic><topic>Heart Transplantation - adverse effects</topic><topic>Heart Transplantation - methods</topic><topic>HLA Antigens - immunology</topic><topic>Humans</topic><topic>Isoantibodies - immunology</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Middle Aged</topic><topic>mortality</topic><topic>Proportional Hazards Models</topic><topic>Reoperation</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Surgery</topic><topic>Survival Analysis</topic><topic>Tissue Donors</topic><topic>Transplantation Immunology - physiology</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Clerkin, Kevin J., MD</creatorcontrib><creatorcontrib>Farr, Maryjane A., MD, MSc</creatorcontrib><creatorcontrib>Restaino, Susan W., MD</creatorcontrib><creatorcontrib>Zorn, Emmanuel, PhD</creatorcontrib><creatorcontrib>Latif, Farhana, MD</creatorcontrib><creatorcontrib>Vasilescu, Elena R., MD</creatorcontrib><creatorcontrib>Marboe, Charles C., MD</creatorcontrib><creatorcontrib>Colombo, Paolo C., MD</creatorcontrib><creatorcontrib>Mancini, Donna M., MD</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of heart and lung transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Clerkin, Kevin J., MD</au><au>Farr, Maryjane A., MD, MSc</au><au>Restaino, Susan W., MD</au><au>Zorn, Emmanuel, PhD</au><au>Latif, Farhana, MD</au><au>Vasilescu, Elena R., MD</au><au>Marboe, Charles C., MD</au><au>Colombo, Paolo C., MD</au><au>Mancini, Donna M., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Donor specific anti-hla antibodies with antibody mediated rejection and long-term outcomes following heart transplantation</atitle><jtitle>The Journal of heart and lung transplantation</jtitle><addtitle>J Heart Lung Transplant</addtitle><date>2017-05-01</date><risdate>2017</risdate><volume>36</volume><issue>5</issue><spage>540</spage><epage>545</epage><pages>540-545</pages><issn>1053-2498</issn><eissn>1557-3117</eissn><abstract>Introduction Donor specific anti-HLA antibodies (DSA) are common following heart transplantation and are associated with rejection, cardiac allograft vasculopathy (CAV), and mortality. Currently a non-invasive diagnostic test for pathologic AMR (pAMR) does not exist. Methods 221 consecutive adult patients underwent heart transplantation from January 1st , 2010 through August 31th , 2013 and followed through October 1st , 2015. The primary objective was to determine whether the presence of DSA could detect AMR at the time of pathologic diagnosis. Secondary analyses included the association of DSA (stratified by MHC Class and de-novo status) during AMR with new graft dysfunction, graft loss (mortality or retransplantation), and development of CAV. Results During the study period 69 individual patients (31.2%) had DSA (24% had de-novo DSA) and there were 74 episodes of pAMR in 38 unique patients. The sensitivity of DSA at any MFI to detect concurrent pAMR was only 54.3%. The presence of any DSA during pAMR increased the odds of graft dysfunction (OR 5.37, 95% CI 1.34-21.47, p=0.018), adjusting for age, gender, and timing of AMR. Circulating Class II DSA after transplantation increased the risk of future pAMR (HR 2.97, 95% CI 1.31-6.73, p=0.009). Patients who developed de-novo Class II DSA had a 151% increase in risk of graft loss (contingent on 30-day survival) compared with those who did not have DSA (95% CI 1.11-5.69, p=0.027). Conclusions DSA were inadequate to diagnose pAMR, but Class II DSA provided prognostic information regarding future pAMR, graft dysfunction with pAMR, and graft loss.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27916323</pmid><doi>10.1016/j.healun.2016.10.016</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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ispartof The Journal of heart and lung transplantation, 2017-05, Vol.36 (5), p.540-545
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Adult
Allografts - immunology
antibody mediated rejection
Antibody Specificity - immunology
cardiac allograft vasculopathy
Cohort Studies
donor specific antibodies
Female
Follow-Up Studies
Graft Rejection - immunology
heart transplant
Heart Transplantation - adverse effects
Heart Transplantation - methods
HLA Antigens - immunology
Humans
Isoantibodies - immunology
Kaplan-Meier Estimate
Male
Middle Aged
mortality
Proportional Hazards Models
Reoperation
Retrospective Studies
Risk Assessment
Surgery
Survival Analysis
Tissue Donors
Transplantation Immunology - physiology
United States
title Donor specific anti-hla antibodies with antibody mediated rejection and long-term outcomes following heart transplantation
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