CD4+/CD8+ T‐cell ratio correlates with the graft fate in pig‐to‐non‐human primate islet xenotransplantation

Background Xenogeneic islet transplantation using porcine pancreata has been a promising option for substituting human islet transplantation. Moreover, recent advances in pre‐clinical results have put islet xenotransplantation closer to the possibility of clinical application. While preparing for th...

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Veröffentlicht in:Xenotransplantation (Københaven) 2020-03, Vol.27 (2), p.e12562-n/a
Hauptverfasser: Chung, Hyunwoo, Kim, Hyun‐Je, Kim, Jung‐Sik, Yoon, Il‐Hee, Min, Byoung‐Hoon, Shin, Jun‐Seop, Kim, Jong‐Min, Lee, Won‐Woo, Park, Chung‐Gyu
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container_issue 2
container_start_page e12562
container_title Xenotransplantation (Københaven)
container_volume 27
creator Chung, Hyunwoo
Kim, Hyun‐Je
Kim, Jung‐Sik
Yoon, Il‐Hee
Min, Byoung‐Hoon
Shin, Jun‐Seop
Kim, Jong‐Min
Lee, Won‐Woo
Park, Chung‐Gyu
description Background Xenogeneic islet transplantation using porcine pancreata has been a promising option for substituting human islet transplantation. Moreover, recent advances in pre‐clinical results have put islet xenotransplantation closer to the possibility of clinical application. While preparing for the era of clinical xenotransplantation, developing non‐invasive immune monitoring method which could predict the graft fate could benefit the patient. However, there are few reports showing predictive immune parameters associated with the fate of the graft in islet xenotransplantation. Methods The absolute number and ratio of T‐cell subsets have been measured via flow cytometry from the peripheral blood of 16 rhesus monkeys before and after porcine islet xenotransplantation. The correlation between the graft survival and the absolute number or ratio of T cells was retrospectively analyzed. Results The ratio of CD4+ versus CD8+ T cells was significantly reduced due to CD8+ effector memory cells’ increase. Correlation analyses revealed that CD4+/CD8+, CD4+/CD8+ naïve, CD4+ naïve/CD8+ naïve, and CD4+ central memory/CD8+ naïve cell ratios negatively correlated with the duration of graft survival. Conversely, further analyses discovered strong, positive correlation of CD4+/CD8+ cell ratios within the early graft‐rejected monkeys (≤60 days). Conclusions This retrospective study demonstrated that CD4+/CD8+ ratios correlated with graft survival, especially in recipients which rejected the graft in early post‐transplantation periods. CD4+/CD8+ ratios could be used as a surrogate marker to predict the graft fate in pig‐to‐NHP islet xenotransplantation.
doi_str_mv 10.1111/xen.12562
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Moreover, recent advances in pre‐clinical results have put islet xenotransplantation closer to the possibility of clinical application. While preparing for the era of clinical xenotransplantation, developing non‐invasive immune monitoring method which could predict the graft fate could benefit the patient. However, there are few reports showing predictive immune parameters associated with the fate of the graft in islet xenotransplantation. Methods The absolute number and ratio of T‐cell subsets have been measured via flow cytometry from the peripheral blood of 16 rhesus monkeys before and after porcine islet xenotransplantation. The correlation between the graft survival and the absolute number or ratio of T cells was retrospectively analyzed. Results The ratio of CD4+ versus CD8+ T cells was significantly reduced due to CD8+ effector memory cells’ increase. Correlation analyses revealed that CD4+/CD8+, CD4+/CD8+ naïve, CD4+ naïve/CD8+ naïve, and CD4+ central memory/CD8+ naïve cell ratios negatively correlated with the duration of graft survival. Conversely, further analyses discovered strong, positive correlation of CD4+/CD8+ cell ratios within the early graft‐rejected monkeys (≤60 days). Conclusions This retrospective study demonstrated that CD4+/CD8+ ratios correlated with graft survival, especially in recipients which rejected the graft in early post‐transplantation periods. CD4+/CD8+ ratios could be used as a surrogate marker to predict the graft fate in pig‐to‐NHP islet xenotransplantation.</description><identifier>ISSN: 0908-665X</identifier><identifier>EISSN: 1399-3089</identifier><identifier>DOI: 10.1111/xen.12562</identifier><identifier>PMID: 31642566</identifier><language>eng</language><publisher>Denmark: Wiley Subscription Services, Inc</publisher><subject>biomarker ; CD4 antigen ; CD8 antigen ; Effector cells ; Flow cytometry ; immune monitoring ; Islet cells ; Lymphocytes T ; Memory cells ; non‐human primate ; Pancreas ; pancreatic islet ; Pancreatic islet transplantation ; Peripheral blood ; Xenografts ; xenotransplantation</subject><ispartof>Xenotransplantation (Københaven), 2020-03, Vol.27 (2), p.e12562-n/a</ispartof><rights>2019 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><rights>2020 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3882-4dccb79b2a35c55ba4d024436d6a610a781f2498005c06b8ff353be7b2644d93</citedby><cites>FETCH-LOGICAL-c3882-4dccb79b2a35c55ba4d024436d6a610a781f2498005c06b8ff353be7b2644d93</cites><orcidid>0000-0003-4083-8791 ; 0000-0003-0906-0117</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fxen.12562$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fxen.12562$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27911,27912,45561,45562</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31642566$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chung, Hyunwoo</creatorcontrib><creatorcontrib>Kim, Hyun‐Je</creatorcontrib><creatorcontrib>Kim, Jung‐Sik</creatorcontrib><creatorcontrib>Yoon, Il‐Hee</creatorcontrib><creatorcontrib>Min, Byoung‐Hoon</creatorcontrib><creatorcontrib>Shin, Jun‐Seop</creatorcontrib><creatorcontrib>Kim, Jong‐Min</creatorcontrib><creatorcontrib>Lee, Won‐Woo</creatorcontrib><creatorcontrib>Park, Chung‐Gyu</creatorcontrib><title>CD4+/CD8+ T‐cell ratio correlates with the graft fate in pig‐to‐non‐human primate islet xenotransplantation</title><title>Xenotransplantation (Københaven)</title><addtitle>Xenotransplantation</addtitle><description>Background Xenogeneic islet transplantation using porcine pancreata has been a promising option for substituting human islet transplantation. Moreover, recent advances in pre‐clinical results have put islet xenotransplantation closer to the possibility of clinical application. While preparing for the era of clinical xenotransplantation, developing non‐invasive immune monitoring method which could predict the graft fate could benefit the patient. However, there are few reports showing predictive immune parameters associated with the fate of the graft in islet xenotransplantation. Methods The absolute number and ratio of T‐cell subsets have been measured via flow cytometry from the peripheral blood of 16 rhesus monkeys before and after porcine islet xenotransplantation. The correlation between the graft survival and the absolute number or ratio of T cells was retrospectively analyzed. Results The ratio of CD4+ versus CD8+ T cells was significantly reduced due to CD8+ effector memory cells’ increase. Correlation analyses revealed that CD4+/CD8+, CD4+/CD8+ naïve, CD4+ naïve/CD8+ naïve, and CD4+ central memory/CD8+ naïve cell ratios negatively correlated with the duration of graft survival. Conversely, further analyses discovered strong, positive correlation of CD4+/CD8+ cell ratios within the early graft‐rejected monkeys (≤60 days). Conclusions This retrospective study demonstrated that CD4+/CD8+ ratios correlated with graft survival, especially in recipients which rejected the graft in early post‐transplantation periods. CD4+/CD8+ ratios could be used as a surrogate marker to predict the graft fate in pig‐to‐NHP islet xenotransplantation.</description><subject>biomarker</subject><subject>CD4 antigen</subject><subject>CD8 antigen</subject><subject>Effector cells</subject><subject>Flow cytometry</subject><subject>immune monitoring</subject><subject>Islet cells</subject><subject>Lymphocytes T</subject><subject>Memory cells</subject><subject>non‐human primate</subject><subject>Pancreas</subject><subject>pancreatic islet</subject><subject>Pancreatic islet transplantation</subject><subject>Peripheral blood</subject><subject>Xenografts</subject><subject>xenotransplantation</subject><issn>0908-665X</issn><issn>1399-3089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kctKAzEUQIMoWh8Lf0ACbpQybd6TLKU-QXTThbshM5OxI9OkJhnUnZ_gN_olpq26EMziBi7nHu4DgEOMRji98auxI0y4IBtggKlSGUVSbYIBUkhmQvCHHbAbwhNCiHLJt8EOxYIlXgxAmJyz4XhyLodw-vn-UZmug17H1sHKeW86HU2AL22cwTgz8NHrJsImJWFr4aJ9TCXRpWCdTXHWz3VK-3a-IkJnIky9uei1DYtO27g0232w1egumIPvfw9MLy-mk-vs9v7qZnJ2m1VUSpKxuqrKXJVEU15xXmpWI8IYFbXQAiOdS9wQpiRCvEKilE1DOS1NXhLBWK3oHjhZaxfePfcmxGLehuWA2hrXh4KkLeE854Qk9PgP-uR6b1NziZKKU67oUni6pirvQvCmKVaj-rcCo2J5iCINW6wOkdijb2Nfzk39S_5sPgHjNfDSdubtf1PxcHG3Vn4BgnGVSQ</recordid><startdate>202003</startdate><enddate>202003</enddate><creator>Chung, Hyunwoo</creator><creator>Kim, Hyun‐Je</creator><creator>Kim, Jung‐Sik</creator><creator>Yoon, Il‐Hee</creator><creator>Min, Byoung‐Hoon</creator><creator>Shin, Jun‐Seop</creator><creator>Kim, Jong‐Min</creator><creator>Lee, Won‐Woo</creator><creator>Park, Chung‐Gyu</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4083-8791</orcidid><orcidid>https://orcid.org/0000-0003-0906-0117</orcidid></search><sort><creationdate>202003</creationdate><title>CD4+/CD8+ T‐cell ratio correlates with the graft fate in pig‐to‐non‐human primate islet xenotransplantation</title><author>Chung, Hyunwoo ; Kim, Hyun‐Je ; Kim, Jung‐Sik ; Yoon, Il‐Hee ; Min, Byoung‐Hoon ; Shin, Jun‐Seop ; Kim, Jong‐Min ; Lee, Won‐Woo ; Park, Chung‐Gyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3882-4dccb79b2a35c55ba4d024436d6a610a781f2498005c06b8ff353be7b2644d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>biomarker</topic><topic>CD4 antigen</topic><topic>CD8 antigen</topic><topic>Effector cells</topic><topic>Flow cytometry</topic><topic>immune monitoring</topic><topic>Islet cells</topic><topic>Lymphocytes T</topic><topic>Memory cells</topic><topic>non‐human primate</topic><topic>Pancreas</topic><topic>pancreatic islet</topic><topic>Pancreatic islet transplantation</topic><topic>Peripheral blood</topic><topic>Xenografts</topic><topic>xenotransplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chung, Hyunwoo</creatorcontrib><creatorcontrib>Kim, Hyun‐Je</creatorcontrib><creatorcontrib>Kim, Jung‐Sik</creatorcontrib><creatorcontrib>Yoon, Il‐Hee</creatorcontrib><creatorcontrib>Min, Byoung‐Hoon</creatorcontrib><creatorcontrib>Shin, Jun‐Seop</creatorcontrib><creatorcontrib>Kim, Jong‐Min</creatorcontrib><creatorcontrib>Lee, Won‐Woo</creatorcontrib><creatorcontrib>Park, Chung‐Gyu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Xenotransplantation (Københaven)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chung, Hyunwoo</au><au>Kim, Hyun‐Je</au><au>Kim, Jung‐Sik</au><au>Yoon, Il‐Hee</au><au>Min, Byoung‐Hoon</au><au>Shin, Jun‐Seop</au><au>Kim, Jong‐Min</au><au>Lee, Won‐Woo</au><au>Park, Chung‐Gyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CD4+/CD8+ T‐cell ratio correlates with the graft fate in pig‐to‐non‐human primate islet xenotransplantation</atitle><jtitle>Xenotransplantation (Københaven)</jtitle><addtitle>Xenotransplantation</addtitle><date>2020-03</date><risdate>2020</risdate><volume>27</volume><issue>2</issue><spage>e12562</spage><epage>n/a</epage><pages>e12562-n/a</pages><issn>0908-665X</issn><eissn>1399-3089</eissn><abstract>Background Xenogeneic islet transplantation using porcine pancreata has been a promising option for substituting human islet transplantation. Moreover, recent advances in pre‐clinical results have put islet xenotransplantation closer to the possibility of clinical application. While preparing for the era of clinical xenotransplantation, developing non‐invasive immune monitoring method which could predict the graft fate could benefit the patient. However, there are few reports showing predictive immune parameters associated with the fate of the graft in islet xenotransplantation. Methods The absolute number and ratio of T‐cell subsets have been measured via flow cytometry from the peripheral blood of 16 rhesus monkeys before and after porcine islet xenotransplantation. The correlation between the graft survival and the absolute number or ratio of T cells was retrospectively analyzed. Results The ratio of CD4+ versus CD8+ T cells was significantly reduced due to CD8+ effector memory cells’ increase. Correlation analyses revealed that CD4+/CD8+, CD4+/CD8+ naïve, CD4+ naïve/CD8+ naïve, and CD4+ central memory/CD8+ naïve cell ratios negatively correlated with the duration of graft survival. Conversely, further analyses discovered strong, positive correlation of CD4+/CD8+ cell ratios within the early graft‐rejected monkeys (≤60 days). Conclusions This retrospective study demonstrated that CD4+/CD8+ ratios correlated with graft survival, especially in recipients which rejected the graft in early post‐transplantation periods. CD4+/CD8+ ratios could be used as a surrogate marker to predict the graft fate in pig‐to‐NHP islet xenotransplantation.</abstract><cop>Denmark</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31642566</pmid><doi>10.1111/xen.12562</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-4083-8791</orcidid><orcidid>https://orcid.org/0000-0003-0906-0117</orcidid><oa>free_for_read</oa></addata></record>
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subjects biomarker
CD4 antigen
CD8 antigen
Effector cells
Flow cytometry
immune monitoring
Islet cells
Lymphocytes T
Memory cells
non‐human primate
Pancreas
pancreatic islet
Pancreatic islet transplantation
Peripheral blood
Xenografts
xenotransplantation
title CD4+/CD8+ T‐cell ratio correlates with the graft fate in pig‐to‐non‐human primate islet xenotransplantation
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