Early Microchimerism in Peripheral Blood Following Kidney Transplantation

Abstract Background The role of microchimerism found in the peripheral blood of renal transplant recipients remains a matter of debate. We assessed the frequency of microchimerism after kidney transplantation and examined its influence on clinical courses over a 12-month follow-up period. Patients a...

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Veröffentlicht in:Transplantation proceedings 2014, Vol.46 (2), p.388-390
Hauptverfasser: Kishikawa, H, Kinoshita, T, Yonemoto, S, Kawamura, M, Nakazawa, S, Ueda, N, Hirai, T, Nishimura, K, Hashimoto, M, Ichikawa, Y
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container_end_page 390
container_issue 2
container_start_page 388
container_title Transplantation proceedings
container_volume 46
creator Kishikawa, H
Kinoshita, T
Yonemoto, S
Kawamura, M
Nakazawa, S
Ueda, N
Hirai, T
Nishimura, K
Hashimoto, M
Ichikawa, Y
description Abstract Background The role of microchimerism found in the peripheral blood of renal transplant recipients remains a matter of debate. We assessed the frequency of microchimerism after kidney transplantation and examined its influence on clinical courses over a 12-month follow-up period. Patients and Methods Ten single-kidney recipients underwent microchimerism detection at 2 days, 2 weeks, and 1, 3, 6, and 12 months after transplantation, with mismatch human leukocyte antigen (HLA)-A, -B, and -C used as markers. Results Microchimerism was detected in 8 (80%) patients at 2 days after kidney transplantation. In 3 of those, microchimerism became negative within 3 months after transplantation, whereas it remained present for up to 12 months in 3 patients (33 %). There was 1 acute rejection episode in a patient in whom microchimerism became negative within 3 months. Protocol renal graft biopsy specimens obtained 3 months after transplantation revealed no acute cellular-mediated rejection (ACMR) or acute antibody-mediated rejection (AAMR) in the 5 patients positive for microchimerism at 3 months. Conclusions Microchimerism was frequently detected after kidney transplantation. Microchimerism that remained for more than 3 months post-transplantation might be correlated with a lower incidence of rejection, thus its monitoring may help identify recipients with a low rejection risk.
doi_str_mv 10.1016/j.transproceed.2013.12.036
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We assessed the frequency of microchimerism after kidney transplantation and examined its influence on clinical courses over a 12-month follow-up period. Patients and Methods Ten single-kidney recipients underwent microchimerism detection at 2 days, 2 weeks, and 1, 3, 6, and 12 months after transplantation, with mismatch human leukocyte antigen (HLA)-A, -B, and -C used as markers. Results Microchimerism was detected in 8 (80%) patients at 2 days after kidney transplantation. In 3 of those, microchimerism became negative within 3 months after transplantation, whereas it remained present for up to 12 months in 3 patients (33 %). There was 1 acute rejection episode in a patient in whom microchimerism became negative within 3 months. Protocol renal graft biopsy specimens obtained 3 months after transplantation revealed no acute cellular-mediated rejection (ACMR) or acute antibody-mediated rejection (AAMR) in the 5 patients positive for microchimerism at 3 months. Conclusions Microchimerism was frequently detected after kidney transplantation. Microchimerism that remained for more than 3 months post-transplantation might be correlated with a lower incidence of rejection, thus its monitoring may help identify recipients with a low rejection risk.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2013.12.036</identifier><identifier>PMID: 24655970</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Biomarkers - blood ; Chimerism ; Female ; HLA Antigens - blood ; HLA Antigens - genetics ; Humans ; Kidney Transplantation ; Male ; Middle Aged ; Surgery</subject><ispartof>Transplantation proceedings, 2014, Vol.46 (2), p.388-390</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c435t-6304b427b6461b8ea52e67bbb7a07de4cd0f86a9deff1e2fd24c61c7b94b52683</citedby><cites>FETCH-LOGICAL-c435t-6304b427b6461b8ea52e67bbb7a07de4cd0f86a9deff1e2fd24c61c7b94b52683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.transproceed.2013.12.036$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24655970$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kishikawa, H</creatorcontrib><creatorcontrib>Kinoshita, T</creatorcontrib><creatorcontrib>Yonemoto, S</creatorcontrib><creatorcontrib>Kawamura, M</creatorcontrib><creatorcontrib>Nakazawa, S</creatorcontrib><creatorcontrib>Ueda, N</creatorcontrib><creatorcontrib>Hirai, T</creatorcontrib><creatorcontrib>Nishimura, K</creatorcontrib><creatorcontrib>Hashimoto, M</creatorcontrib><creatorcontrib>Ichikawa, Y</creatorcontrib><title>Early Microchimerism in Peripheral Blood Following Kidney Transplantation</title><title>Transplantation proceedings</title><addtitle>Transplant Proc</addtitle><description>Abstract Background The role of microchimerism found in the peripheral blood of renal transplant recipients remains a matter of debate. We assessed the frequency of microchimerism after kidney transplantation and examined its influence on clinical courses over a 12-month follow-up period. Patients and Methods Ten single-kidney recipients underwent microchimerism detection at 2 days, 2 weeks, and 1, 3, 6, and 12 months after transplantation, with mismatch human leukocyte antigen (HLA)-A, -B, and -C used as markers. Results Microchimerism was detected in 8 (80%) patients at 2 days after kidney transplantation. In 3 of those, microchimerism became negative within 3 months after transplantation, whereas it remained present for up to 12 months in 3 patients (33 %). There was 1 acute rejection episode in a patient in whom microchimerism became negative within 3 months. Protocol renal graft biopsy specimens obtained 3 months after transplantation revealed no acute cellular-mediated rejection (ACMR) or acute antibody-mediated rejection (AAMR) in the 5 patients positive for microchimerism at 3 months. Conclusions Microchimerism was frequently detected after kidney transplantation. Microchimerism that remained for more than 3 months post-transplantation might be correlated with a lower incidence of rejection, thus its monitoring may help identify recipients with a low rejection risk.</description><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers - blood</subject><subject>Chimerism</subject><subject>Female</subject><subject>HLA Antigens - blood</subject><subject>HLA Antigens - genetics</subject><subject>Humans</subject><subject>Kidney Transplantation</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Surgery</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1vEzEQhi0EoqHwF9CKE5ddPLbXm3BAgn5A1SKQKGfLH7PUwWsHe1OUf49DWglx6sm2_L4z8z5DyCugHVCQb9bdnHUsm5wsousYBd4B6yiXj8gClgNvmWT8MVlQKqAFLvoj8qyUNa1vJvhTcsSE7PvVQBfk4kznsGs-e1ur3fgJsy9T42Pztd42N5h1aD6ElFxznkJIv3380Vx6F3HXXP8dIug469mn-Jw8GXUo-OLuPCbfz8-uTz61V18-Xpy8v2qt4P3cSk6FEWwwUkgwS9Q9QzkYYwZNB4fCOjoupV45HEdANjomrAQ7mJUwPZNLfkxeH-rW_L-2WGY1-WIx1EEwbYuCvkICGARU6duDtIYrJeOoNtlPOu8UULVHqdbqX5Rqj1IBUxVlNb-867M1U_27t96zq4LTgwBr2luPWRXrMVp0PqOdlUv-YX3e_VfGBh-91eEn7rCs0zbHylOBKtWgvu2Xut8pcAqCM8b_AMWYoao</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Kishikawa, H</creator><creator>Kinoshita, T</creator><creator>Yonemoto, S</creator><creator>Kawamura, M</creator><creator>Nakazawa, S</creator><creator>Ueda, N</creator><creator>Hirai, T</creator><creator>Nishimura, K</creator><creator>Hashimoto, M</creator><creator>Ichikawa, Y</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></search><sort><creationdate>2014</creationdate><title>Early Microchimerism in Peripheral Blood Following Kidney Transplantation</title><author>Kishikawa, H ; Kinoshita, T ; Yonemoto, S ; Kawamura, M ; Nakazawa, S ; Ueda, N ; Hirai, T ; Nishimura, K ; Hashimoto, M ; Ichikawa, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-6304b427b6461b8ea52e67bbb7a07de4cd0f86a9deff1e2fd24c61c7b94b52683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biomarkers - blood</topic><topic>Chimerism</topic><topic>Female</topic><topic>HLA Antigens - blood</topic><topic>HLA Antigens - genetics</topic><topic>Humans</topic><topic>Kidney Transplantation</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kishikawa, H</creatorcontrib><creatorcontrib>Kinoshita, T</creatorcontrib><creatorcontrib>Yonemoto, S</creatorcontrib><creatorcontrib>Kawamura, M</creatorcontrib><creatorcontrib>Nakazawa, S</creatorcontrib><creatorcontrib>Ueda, N</creatorcontrib><creatorcontrib>Hirai, T</creatorcontrib><creatorcontrib>Nishimura, K</creatorcontrib><creatorcontrib>Hashimoto, M</creatorcontrib><creatorcontrib>Ichikawa, Y</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 proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kishikawa, H</au><au>Kinoshita, T</au><au>Yonemoto, S</au><au>Kawamura, M</au><au>Nakazawa, S</au><au>Ueda, N</au><au>Hirai, T</au><au>Nishimura, K</au><au>Hashimoto, M</au><au>Ichikawa, Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Early Microchimerism in Peripheral Blood Following Kidney Transplantation</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2014</date><risdate>2014</risdate><volume>46</volume><issue>2</issue><spage>388</spage><epage>390</epage><pages>388-390</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><abstract>Abstract Background The role of microchimerism found in the peripheral blood of renal transplant recipients remains a matter of debate. We assessed the frequency of microchimerism after kidney transplantation and examined its influence on clinical courses over a 12-month follow-up period. Patients and Methods Ten single-kidney recipients underwent microchimerism detection at 2 days, 2 weeks, and 1, 3, 6, and 12 months after transplantation, with mismatch human leukocyte antigen (HLA)-A, -B, and -C used as markers. Results Microchimerism was detected in 8 (80%) patients at 2 days after kidney transplantation. In 3 of those, microchimerism became negative within 3 months after transplantation, whereas it remained present for up to 12 months in 3 patients (33 %). There was 1 acute rejection episode in a patient in whom microchimerism became negative within 3 months. Protocol renal graft biopsy specimens obtained 3 months after transplantation revealed no acute cellular-mediated rejection (ACMR) or acute antibody-mediated rejection (AAMR) in the 5 patients positive for microchimerism at 3 months. 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subjects Adult
Aged
Biomarkers - blood
Chimerism
Female
HLA Antigens - blood
HLA Antigens - genetics
Humans
Kidney Transplantation
Male
Middle Aged
Surgery
title Early Microchimerism in Peripheral Blood Following Kidney Transplantation
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