Loading…

Detection of engraftment of donor-derived antibody producing cells in a lung transplant recipient by anti-cytomegalovirus IgG avidity test

Transplant recipients become immunocompromised through the use of immunosuppressive therapy to prevent allograft rejection. These recipients readily experience human cytomegalovirus (CMV) infection or reactivation. Therefore, CMV represents a life-threatening pathogen in transplant recipients. To de...

Full description

Saved in:
Bibliographic Details
Published in:Transplant immunology 2019-04, Vol.53, p.34-37
Main Authors: Koshizuka, Tetsuo, Matsuda, Yasushi, Suzuki, Hirotoshi, Kanno, Ryoko, Ikuta, Kazufumi, Kobayashi, Takahiro, Kondo, Takashi, Okada, Yoshinori, Suzutani, Tatsuo
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c422t-b38be4083d31b7538772a3cc71dbe809004b4ac9a5a95331d5f91cd00b0eb3c03
cites cdi_FETCH-LOGICAL-c422t-b38be4083d31b7538772a3cc71dbe809004b4ac9a5a95331d5f91cd00b0eb3c03
container_end_page 37
container_issue
container_start_page 34
container_title Transplant immunology
container_volume 53
creator Koshizuka, Tetsuo
Matsuda, Yasushi
Suzuki, Hirotoshi
Kanno, Ryoko
Ikuta, Kazufumi
Kobayashi, Takahiro
Kondo, Takashi
Okada, Yoshinori
Suzutani, Tatsuo
description Transplant recipients become immunocompromised through the use of immunosuppressive therapy to prevent allograft rejection. These recipients readily experience human cytomegalovirus (CMV) infection or reactivation. Therefore, CMV represents a life-threatening pathogen in transplant recipients. To demonstrate the serostatus and course of IgG maturation against CMV in transplant patients, we measured the transition of anti-CMV IgG and its affinity (avidity index; AI) as criteria for antibody maturation. Among 31 lung transplant recipients, 26 were infected with CMV before transplantation and maintained anti-CMV IgG and high AI values throughout the study period. Four of the 31 experienced primary infection with CMV through the allograft, with two of the 4 recipients presented high AI values even after 6 month post-transplantation. A significant portion of donor-derived plasma cells were detectable in one recipient. These results suggested that the plasma cells from donors are carried in through the transplanted lung and lymph nodes and produce matured high-avidity IgG from the early stage of transplantation.
doi_str_mv 10.1016/j.trim.2018.12.003
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2157674412</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0966327418301709</els_id><sourcerecordid>2157674412</sourcerecordid><originalsourceid>FETCH-LOGICAL-c422t-b38be4083d31b7538772a3cc71dbe809004b4ac9a5a95331d5f91cd00b0eb3c03</originalsourceid><addsrcrecordid>eNp9kc1q3DAUhUVoaKZpXyCLomU3dq4k_0I3JWmTQKCbdi30cz1osK2pJA_4FfrUkTtpl12JC9854pxDyA2DkgFrbg9lCm4qObCuZLwEEBdkx7q2K-qq52_IDvqmKQRvqyvyLsYDAPC6b9-SKwF1zfu-2ZHf95jQJOdn6geK8z6oIU04p-20fvahsBjcCS1Vc3La25Ueg7eLcfOeGhzHSN1MFR2XfKeg5ngcM0kDGnd0m5Fe_0gLsyY_4V6N_uTCEunT_oGqk7MurTRhTO_J5aDGiB9e32vy89vXH3ePxfP3h6e7L8-FqThPhRadxgo6YQXTbS26tuVKGNMyq7GDHqDSlTK9qlVfC8FsPfTMWAANqIUBcU0-nX1zjl9L_lhOLm5J1Ix-iZKzum3aqmI8o_yMmuBjDDjIY25chVUykNsG8iC3DeS2gWRc5g2y6OOr_6IntP8kf0vPwOczgDnlyWGQ0eSmDFqXW0vSevc__xeLfptM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2157674412</pqid></control><display><type>article</type><title>Detection of engraftment of donor-derived antibody producing cells in a lung transplant recipient by anti-cytomegalovirus IgG avidity test</title><source>Elsevier</source><creator>Koshizuka, Tetsuo ; Matsuda, Yasushi ; Suzuki, Hirotoshi ; Kanno, Ryoko ; Ikuta, Kazufumi ; Kobayashi, Takahiro ; Kondo, Takashi ; Okada, Yoshinori ; Suzutani, Tatsuo</creator><creatorcontrib>Koshizuka, Tetsuo ; Matsuda, Yasushi ; Suzuki, Hirotoshi ; Kanno, Ryoko ; Ikuta, Kazufumi ; Kobayashi, Takahiro ; Kondo, Takashi ; Okada, Yoshinori ; Suzutani, Tatsuo</creatorcontrib><description>Transplant recipients become immunocompromised through the use of immunosuppressive therapy to prevent allograft rejection. These recipients readily experience human cytomegalovirus (CMV) infection or reactivation. Therefore, CMV represents a life-threatening pathogen in transplant recipients. To demonstrate the serostatus and course of IgG maturation against CMV in transplant patients, we measured the transition of anti-CMV IgG and its affinity (avidity index; AI) as criteria for antibody maturation. Among 31 lung transplant recipients, 26 were infected with CMV before transplantation and maintained anti-CMV IgG and high AI values throughout the study period. Four of the 31 experienced primary infection with CMV through the allograft, with two of the 4 recipients presented high AI values even after 6 month post-transplantation. A significant portion of donor-derived plasma cells were detectable in one recipient. These results suggested that the plasma cells from donors are carried in through the transplanted lung and lymph nodes and produce matured high-avidity IgG from the early stage of transplantation.</description><identifier>ISSN: 0966-3274</identifier><identifier>EISSN: 1878-5492</identifier><identifier>DOI: 10.1016/j.trim.2018.12.003</identifier><identifier>PMID: 30552996</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Anit-CMV IgG ; Avidity index ; Donor-derived plasma cells ; Lung transplantation</subject><ispartof>Transplant immunology, 2019-04, Vol.53, p.34-37</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-b38be4083d31b7538772a3cc71dbe809004b4ac9a5a95331d5f91cd00b0eb3c03</citedby><cites>FETCH-LOGICAL-c422t-b38be4083d31b7538772a3cc71dbe809004b4ac9a5a95331d5f91cd00b0eb3c03</cites><orcidid>0000-0001-6810-8892</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30552996$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Koshizuka, Tetsuo</creatorcontrib><creatorcontrib>Matsuda, Yasushi</creatorcontrib><creatorcontrib>Suzuki, Hirotoshi</creatorcontrib><creatorcontrib>Kanno, Ryoko</creatorcontrib><creatorcontrib>Ikuta, Kazufumi</creatorcontrib><creatorcontrib>Kobayashi, Takahiro</creatorcontrib><creatorcontrib>Kondo, Takashi</creatorcontrib><creatorcontrib>Okada, Yoshinori</creatorcontrib><creatorcontrib>Suzutani, Tatsuo</creatorcontrib><title>Detection of engraftment of donor-derived antibody producing cells in a lung transplant recipient by anti-cytomegalovirus IgG avidity test</title><title>Transplant immunology</title><addtitle>Transpl Immunol</addtitle><description>Transplant recipients become immunocompromised through the use of immunosuppressive therapy to prevent allograft rejection. These recipients readily experience human cytomegalovirus (CMV) infection or reactivation. Therefore, CMV represents a life-threatening pathogen in transplant recipients. To demonstrate the serostatus and course of IgG maturation against CMV in transplant patients, we measured the transition of anti-CMV IgG and its affinity (avidity index; AI) as criteria for antibody maturation. Among 31 lung transplant recipients, 26 were infected with CMV before transplantation and maintained anti-CMV IgG and high AI values throughout the study period. Four of the 31 experienced primary infection with CMV through the allograft, with two of the 4 recipients presented high AI values even after 6 month post-transplantation. A significant portion of donor-derived plasma cells were detectable in one recipient. These results suggested that the plasma cells from donors are carried in through the transplanted lung and lymph nodes and produce matured high-avidity IgG from the early stage of transplantation.</description><subject>Anit-CMV IgG</subject><subject>Avidity index</subject><subject>Donor-derived plasma cells</subject><subject>Lung transplantation</subject><issn>0966-3274</issn><issn>1878-5492</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kc1q3DAUhUVoaKZpXyCLomU3dq4k_0I3JWmTQKCbdi30cz1osK2pJA_4FfrUkTtpl12JC9854pxDyA2DkgFrbg9lCm4qObCuZLwEEBdkx7q2K-qq52_IDvqmKQRvqyvyLsYDAPC6b9-SKwF1zfu-2ZHf95jQJOdn6geK8z6oIU04p-20fvahsBjcCS1Vc3La25Ueg7eLcfOeGhzHSN1MFR2XfKeg5ngcM0kDGnd0m5Fe_0gLsyY_4V6N_uTCEunT_oGqk7MurTRhTO_J5aDGiB9e32vy89vXH3ePxfP3h6e7L8-FqThPhRadxgo6YQXTbS26tuVKGNMyq7GDHqDSlTK9qlVfC8FsPfTMWAANqIUBcU0-nX1zjl9L_lhOLm5J1Ix-iZKzum3aqmI8o_yMmuBjDDjIY25chVUykNsG8iC3DeS2gWRc5g2y6OOr_6IntP8kf0vPwOczgDnlyWGQ0eSmDFqXW0vSevc__xeLfptM</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Koshizuka, Tetsuo</creator><creator>Matsuda, Yasushi</creator><creator>Suzuki, Hirotoshi</creator><creator>Kanno, Ryoko</creator><creator>Ikuta, Kazufumi</creator><creator>Kobayashi, Takahiro</creator><creator>Kondo, Takashi</creator><creator>Okada, Yoshinori</creator><creator>Suzutani, Tatsuo</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6810-8892</orcidid></search><sort><creationdate>20190401</creationdate><title>Detection of engraftment of donor-derived antibody producing cells in a lung transplant recipient by anti-cytomegalovirus IgG avidity test</title><author>Koshizuka, Tetsuo ; Matsuda, Yasushi ; Suzuki, Hirotoshi ; Kanno, Ryoko ; Ikuta, Kazufumi ; Kobayashi, Takahiro ; Kondo, Takashi ; Okada, Yoshinori ; Suzutani, Tatsuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-b38be4083d31b7538772a3cc71dbe809004b4ac9a5a95331d5f91cd00b0eb3c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Anit-CMV IgG</topic><topic>Avidity index</topic><topic>Donor-derived plasma cells</topic><topic>Lung transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Koshizuka, Tetsuo</creatorcontrib><creatorcontrib>Matsuda, Yasushi</creatorcontrib><creatorcontrib>Suzuki, Hirotoshi</creatorcontrib><creatorcontrib>Kanno, Ryoko</creatorcontrib><creatorcontrib>Ikuta, Kazufumi</creatorcontrib><creatorcontrib>Kobayashi, Takahiro</creatorcontrib><creatorcontrib>Kondo, Takashi</creatorcontrib><creatorcontrib>Okada, Yoshinori</creatorcontrib><creatorcontrib>Suzutani, Tatsuo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplant immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Koshizuka, Tetsuo</au><au>Matsuda, Yasushi</au><au>Suzuki, Hirotoshi</au><au>Kanno, Ryoko</au><au>Ikuta, Kazufumi</au><au>Kobayashi, Takahiro</au><au>Kondo, Takashi</au><au>Okada, Yoshinori</au><au>Suzutani, Tatsuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of engraftment of donor-derived antibody producing cells in a lung transplant recipient by anti-cytomegalovirus IgG avidity test</atitle><jtitle>Transplant immunology</jtitle><addtitle>Transpl Immunol</addtitle><date>2019-04-01</date><risdate>2019</risdate><volume>53</volume><spage>34</spage><epage>37</epage><pages>34-37</pages><issn>0966-3274</issn><eissn>1878-5492</eissn><abstract>Transplant recipients become immunocompromised through the use of immunosuppressive therapy to prevent allograft rejection. These recipients readily experience human cytomegalovirus (CMV) infection or reactivation. Therefore, CMV represents a life-threatening pathogen in transplant recipients. To demonstrate the serostatus and course of IgG maturation against CMV in transplant patients, we measured the transition of anti-CMV IgG and its affinity (avidity index; AI) as criteria for antibody maturation. Among 31 lung transplant recipients, 26 were infected with CMV before transplantation and maintained anti-CMV IgG and high AI values throughout the study period. Four of the 31 experienced primary infection with CMV through the allograft, with two of the 4 recipients presented high AI values even after 6 month post-transplantation. A significant portion of donor-derived plasma cells were detectable in one recipient. These results suggested that the plasma cells from donors are carried in through the transplanted lung and lymph nodes and produce matured high-avidity IgG from the early stage of transplantation.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>30552996</pmid><doi>10.1016/j.trim.2018.12.003</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0001-6810-8892</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0966-3274
ispartof Transplant immunology, 2019-04, Vol.53, p.34-37
issn 0966-3274
1878-5492
language eng
recordid cdi_proquest_miscellaneous_2157674412
source Elsevier
subjects Anit-CMV IgG
Avidity index
Donor-derived plasma cells
Lung transplantation
title Detection of engraftment of donor-derived antibody producing cells in a lung transplant recipient by anti-cytomegalovirus IgG avidity test
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T03%3A50%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Detection%20of%20engraftment%20of%20donor-derived%20antibody%20producing%20cells%20in%20a%20lung%20transplant%20recipient%20by%20anti-cytomegalovirus%20IgG%20avidity%20test&rft.jtitle=Transplant%20immunology&rft.au=Koshizuka,%20Tetsuo&rft.date=2019-04-01&rft.volume=53&rft.spage=34&rft.epage=37&rft.pages=34-37&rft.issn=0966-3274&rft.eissn=1878-5492&rft_id=info:doi/10.1016/j.trim.2018.12.003&rft_dat=%3Cproquest_cross%3E2157674412%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c422t-b38be4083d31b7538772a3cc71dbe809004b4ac9a5a95331d5f91cd00b0eb3c03%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2157674412&rft_id=info:pmid/30552996&rfr_iscdi=true