Pooling, room temperature, and extended storage time increase the release of adult‐specific biologic response modifiers in platelet concentrates: a hidden transfusion risk for neonates?
BACKGROUND Adult donor platelets (PLTs) are frequently transfused to prevent or stop bleeding in neonates with thrombocytopenia. There is evidence for PLT transfusion–related morbidity and mortality, leading to the hypothesis on immunomodulatory effects of transfusing adult PLTs into neonates. Candi...
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Veröffentlicht in: | Transfusion (Philadelphia, Pa.) Pa.), 2020-08, Vol.60 (8), p.1828-1836 |
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creator | Waubert de Puiseau, Miriam Sciesielski, Lina K. Meyer, Oliver Liu, Zhi‐Jian Badur, Chiara‐Aiyleen Schönfeld, Helge Tauber, Rudolf Pruß, Axel Sola‐Visner, Martha C. Dame, Christof |
description | BACKGROUND
Adult donor platelets (PLTs) are frequently transfused to prevent or stop bleeding in neonates with thrombocytopenia. There is evidence for PLT transfusion–related morbidity and mortality, leading to the hypothesis on immunomodulatory effects of transfusing adult PLTs into neonates. Candidate factors are biologic response modifiers (BRMs) that are expressed at higher rates in adult than in neonatal PLTs. This study investigated whether storage conditions or preparation methods impact on the release of those differentially expressed BRMs.
STUDY DESIGN AND METHODS
Pooled PLT concentrates (PCs) and apheresis PCs (APCs) were stored under agitation for up to 7 days at room temperature (RT) or at 2 to 8°C. The BRMs CCL5/RANTES, TGFβ1, TSP1, and DKK1 were measured in PCsʼ supernatant, lysate, and corresponding plasma. PLT function was assessed by light transmission aggregometry.
RESULTS
Concerning the preparation method, higher concentrations of DKK1 were found in pooled PCs compared to APCs. In supernatants, the concentrations of CCL5, TGFβ1, TSP1, and DKK1 significantly increased, both over standard (≤4 days) and over extended storage times (7 days). Each of the four BRMs showed an up to twofold increase in concentration after storage at RT compared to cold storage (CS). There was no difference in the aggregation capacity.
CONCLUSION
This analysis shows that the release of adult‐specific BRMs during storage is lowest in short‐ and CS APCs. Our study points to strategies for reducing the exposure of sick neonates to BRMs that can be specifically associated to PLT transfusion–related morbidity. |
doi_str_mv | 10.1111/trf.15827 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2395612255</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2395612255</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4547-ca54482ab04a21820645ceb3d858679e1168033b69ea76c0795fa1aa8f0326bd3</originalsourceid><addsrcrecordid>eNp1kc9qFTEUh4Mo9ra68AUk4Eah0-bvzMSNSLEqFBSp65BJztymziRjkkG76yP4Pr6NT2LaW10IZpOT5DtfDvwQekLJEa3ruKTxiMqedffQhkreNUwpeR9tCBG0oZSzPbSf8yUhhClCH6I9zjhXnKgN-vkxxsmH7SFOMc64wLxAMmVNcIhNcBi-FwgOHM4lJrMFXPwM2AebwOR6ugCcYLqt44iNW6fy6_pHXsD60Vs8-DjFbS0S5CWGSs3R1RdIuUrwMplSuwu2MVgIpf4M-SU2-MI7BwHXi5DHNfsYcPL5Cx5jwgFiuOFePUIPRjNleHy3H6DPp2_OT941Zx_evj95fdZYIUXXWCOF6JkZiDCM9oy0QloYuOtl33YKKG17wvnQKjBda0mn5GioMf1IOGsHxw_Q8513SfHrCrno2WcL02TqKGvWjCvZUsakrOizf9DLuKZQp9NMcKaEakVfqRc7yqaYc4JRL8nPJl1pSvRNoromqm8TrezTO-M6zOD-kn8irMDxDvjmJ7j6v0mffzrdKX8Dtp2u6Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2432949648</pqid></control><display><type>article</type><title>Pooling, room temperature, and extended storage time increase the release of adult‐specific biologic response modifiers in platelet concentrates: a hidden transfusion risk for neonates?</title><source>Access via Wiley Online Library</source><creator>Waubert de Puiseau, Miriam ; Sciesielski, Lina K. ; Meyer, Oliver ; Liu, Zhi‐Jian ; Badur, Chiara‐Aiyleen ; Schönfeld, Helge ; Tauber, Rudolf ; Pruß, Axel ; Sola‐Visner, Martha C. ; Dame, Christof</creator><creatorcontrib>Waubert de Puiseau, Miriam ; Sciesielski, Lina K. ; Meyer, Oliver ; Liu, Zhi‐Jian ; Badur, Chiara‐Aiyleen ; Schönfeld, Helge ; Tauber, Rudolf ; Pruß, Axel ; Sola‐Visner, Martha C. ; Dame, Christof</creatorcontrib><description>BACKGROUND
Adult donor platelets (PLTs) are frequently transfused to prevent or stop bleeding in neonates with thrombocytopenia. There is evidence for PLT transfusion–related morbidity and mortality, leading to the hypothesis on immunomodulatory effects of transfusing adult PLTs into neonates. Candidate factors are biologic response modifiers (BRMs) that are expressed at higher rates in adult than in neonatal PLTs. This study investigated whether storage conditions or preparation methods impact on the release of those differentially expressed BRMs.
STUDY DESIGN AND METHODS
Pooled PLT concentrates (PCs) and apheresis PCs (APCs) were stored under agitation for up to 7 days at room temperature (RT) or at 2 to 8°C. The BRMs CCL5/RANTES, TGFβ1, TSP1, and DKK1 were measured in PCsʼ supernatant, lysate, and corresponding plasma. PLT function was assessed by light transmission aggregometry.
RESULTS
Concerning the preparation method, higher concentrations of DKK1 were found in pooled PCs compared to APCs. In supernatants, the concentrations of CCL5, TGFβ1, TSP1, and DKK1 significantly increased, both over standard (≤4 days) and over extended storage times (7 days). Each of the four BRMs showed an up to twofold increase in concentration after storage at RT compared to cold storage (CS). There was no difference in the aggregation capacity.
CONCLUSION
This analysis shows that the release of adult‐specific BRMs during storage is lowest in short‐ and CS APCs. Our study points to strategies for reducing the exposure of sick neonates to BRMs that can be specifically associated to PLT transfusion–related morbidity.</description><identifier>ISSN: 0041-1132</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1111/trf.15827</identifier><identifier>PMID: 32339309</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Apheresis ; Bleeding ; Cold storage ; Dkk1 protein ; Immunomodulation ; Light transmission ; Morbidity ; Neonates ; Platelets ; RANTES ; Room temperature ; Storage conditions ; Thrombocytopenia ; Transforming growth factor-b1 ; Transfusion</subject><ispartof>Transfusion (Philadelphia, Pa.), 2020-08, Vol.60 (8), p.1828-1836</ispartof><rights>2020 The Authors. published by Wiley Periodicals, Inc. on behalf of AABB.</rights><rights>2020 The Authors. Transfusion published by Wiley Periodicals, Inc. on behalf of AABB.</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4547-ca54482ab04a21820645ceb3d858679e1168033b69ea76c0795fa1aa8f0326bd3</citedby><cites>FETCH-LOGICAL-c4547-ca54482ab04a21820645ceb3d858679e1168033b69ea76c0795fa1aa8f0326bd3</cites><orcidid>0000-0003-3458-0309 ; 0000-0002-7303-6667</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%2Ftrf.15827$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftrf.15827$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32339309$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Waubert de Puiseau, Miriam</creatorcontrib><creatorcontrib>Sciesielski, Lina K.</creatorcontrib><creatorcontrib>Meyer, Oliver</creatorcontrib><creatorcontrib>Liu, Zhi‐Jian</creatorcontrib><creatorcontrib>Badur, Chiara‐Aiyleen</creatorcontrib><creatorcontrib>Schönfeld, Helge</creatorcontrib><creatorcontrib>Tauber, Rudolf</creatorcontrib><creatorcontrib>Pruß, Axel</creatorcontrib><creatorcontrib>Sola‐Visner, Martha C.</creatorcontrib><creatorcontrib>Dame, Christof</creatorcontrib><title>Pooling, room temperature, and extended storage time increase the release of adult‐specific biologic response modifiers in platelet concentrates: a hidden transfusion risk for neonates?</title><title>Transfusion (Philadelphia, Pa.)</title><addtitle>Transfusion</addtitle><description>BACKGROUND
Adult donor platelets (PLTs) are frequently transfused to prevent or stop bleeding in neonates with thrombocytopenia. There is evidence for PLT transfusion–related morbidity and mortality, leading to the hypothesis on immunomodulatory effects of transfusing adult PLTs into neonates. Candidate factors are biologic response modifiers (BRMs) that are expressed at higher rates in adult than in neonatal PLTs. This study investigated whether storage conditions or preparation methods impact on the release of those differentially expressed BRMs.
STUDY DESIGN AND METHODS
Pooled PLT concentrates (PCs) and apheresis PCs (APCs) were stored under agitation for up to 7 days at room temperature (RT) or at 2 to 8°C. The BRMs CCL5/RANTES, TGFβ1, TSP1, and DKK1 were measured in PCsʼ supernatant, lysate, and corresponding plasma. PLT function was assessed by light transmission aggregometry.
RESULTS
Concerning the preparation method, higher concentrations of DKK1 were found in pooled PCs compared to APCs. In supernatants, the concentrations of CCL5, TGFβ1, TSP1, and DKK1 significantly increased, both over standard (≤4 days) and over extended storage times (7 days). Each of the four BRMs showed an up to twofold increase in concentration after storage at RT compared to cold storage (CS). There was no difference in the aggregation capacity.
CONCLUSION
This analysis shows that the release of adult‐specific BRMs during storage is lowest in short‐ and CS APCs. Our study points to strategies for reducing the exposure of sick neonates to BRMs that can be specifically associated to PLT transfusion–related morbidity.</description><subject>Apheresis</subject><subject>Bleeding</subject><subject>Cold storage</subject><subject>Dkk1 protein</subject><subject>Immunomodulation</subject><subject>Light transmission</subject><subject>Morbidity</subject><subject>Neonates</subject><subject>Platelets</subject><subject>RANTES</subject><subject>Room temperature</subject><subject>Storage conditions</subject><subject>Thrombocytopenia</subject><subject>Transforming growth factor-b1</subject><subject>Transfusion</subject><issn>0041-1132</issn><issn>1537-2995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNp1kc9qFTEUh4Mo9ra68AUk4Eah0-bvzMSNSLEqFBSp65BJztymziRjkkG76yP4Pr6NT2LaW10IZpOT5DtfDvwQekLJEa3ruKTxiMqedffQhkreNUwpeR9tCBG0oZSzPbSf8yUhhClCH6I9zjhXnKgN-vkxxsmH7SFOMc64wLxAMmVNcIhNcBi-FwgOHM4lJrMFXPwM2AebwOR6ugCcYLqt44iNW6fy6_pHXsD60Vs8-DjFbS0S5CWGSs3R1RdIuUrwMplSuwu2MVgIpf4M-SU2-MI7BwHXi5DHNfsYcPL5Cx5jwgFiuOFePUIPRjNleHy3H6DPp2_OT941Zx_evj95fdZYIUXXWCOF6JkZiDCM9oy0QloYuOtl33YKKG17wvnQKjBda0mn5GioMf1IOGsHxw_Q8513SfHrCrno2WcL02TqKGvWjCvZUsakrOizf9DLuKZQp9NMcKaEakVfqRc7yqaYc4JRL8nPJl1pSvRNoromqm8TrezTO-M6zOD-kn8irMDxDvjmJ7j6v0mffzrdKX8Dtp2u6Q</recordid><startdate>202008</startdate><enddate>202008</enddate><creator>Waubert de Puiseau, Miriam</creator><creator>Sciesielski, Lina K.</creator><creator>Meyer, Oliver</creator><creator>Liu, Zhi‐Jian</creator><creator>Badur, Chiara‐Aiyleen</creator><creator>Schönfeld, Helge</creator><creator>Tauber, Rudolf</creator><creator>Pruß, Axel</creator><creator>Sola‐Visner, Martha C.</creator><creator>Dame, Christof</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</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>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3458-0309</orcidid><orcidid>https://orcid.org/0000-0002-7303-6667</orcidid></search><sort><creationdate>202008</creationdate><title>Pooling, room temperature, and extended storage time increase the release of adult‐specific biologic response modifiers in platelet concentrates: a hidden transfusion risk for neonates?</title><author>Waubert de Puiseau, Miriam ; Sciesielski, Lina K. ; Meyer, Oliver ; Liu, Zhi‐Jian ; Badur, Chiara‐Aiyleen ; Schönfeld, Helge ; Tauber, Rudolf ; Pruß, Axel ; Sola‐Visner, Martha C. ; Dame, Christof</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4547-ca54482ab04a21820645ceb3d858679e1168033b69ea76c0795fa1aa8f0326bd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Apheresis</topic><topic>Bleeding</topic><topic>Cold storage</topic><topic>Dkk1 protein</topic><topic>Immunomodulation</topic><topic>Light transmission</topic><topic>Morbidity</topic><topic>Neonates</topic><topic>Platelets</topic><topic>RANTES</topic><topic>Room temperature</topic><topic>Storage conditions</topic><topic>Thrombocytopenia</topic><topic>Transforming growth factor-b1</topic><topic>Transfusion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Waubert de Puiseau, Miriam</creatorcontrib><creatorcontrib>Sciesielski, Lina K.</creatorcontrib><creatorcontrib>Meyer, Oliver</creatorcontrib><creatorcontrib>Liu, Zhi‐Jian</creatorcontrib><creatorcontrib>Badur, Chiara‐Aiyleen</creatorcontrib><creatorcontrib>Schönfeld, Helge</creatorcontrib><creatorcontrib>Tauber, Rudolf</creatorcontrib><creatorcontrib>Pruß, Axel</creatorcontrib><creatorcontrib>Sola‐Visner, Martha C.</creatorcontrib><creatorcontrib>Dame, Christof</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Waubert de Puiseau, Miriam</au><au>Sciesielski, Lina K.</au><au>Meyer, Oliver</au><au>Liu, Zhi‐Jian</au><au>Badur, Chiara‐Aiyleen</au><au>Schönfeld, Helge</au><au>Tauber, Rudolf</au><au>Pruß, Axel</au><au>Sola‐Visner, Martha C.</au><au>Dame, Christof</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pooling, room temperature, and extended storage time increase the release of adult‐specific biologic response modifiers in platelet concentrates: a hidden transfusion risk for neonates?</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><addtitle>Transfusion</addtitle><date>2020-08</date><risdate>2020</risdate><volume>60</volume><issue>8</issue><spage>1828</spage><epage>1836</epage><pages>1828-1836</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><abstract>BACKGROUND
Adult donor platelets (PLTs) are frequently transfused to prevent or stop bleeding in neonates with thrombocytopenia. There is evidence for PLT transfusion–related morbidity and mortality, leading to the hypothesis on immunomodulatory effects of transfusing adult PLTs into neonates. Candidate factors are biologic response modifiers (BRMs) that are expressed at higher rates in adult than in neonatal PLTs. This study investigated whether storage conditions or preparation methods impact on the release of those differentially expressed BRMs.
STUDY DESIGN AND METHODS
Pooled PLT concentrates (PCs) and apheresis PCs (APCs) were stored under agitation for up to 7 days at room temperature (RT) or at 2 to 8°C. The BRMs CCL5/RANTES, TGFβ1, TSP1, and DKK1 were measured in PCsʼ supernatant, lysate, and corresponding plasma. PLT function was assessed by light transmission aggregometry.
RESULTS
Concerning the preparation method, higher concentrations of DKK1 were found in pooled PCs compared to APCs. In supernatants, the concentrations of CCL5, TGFβ1, TSP1, and DKK1 significantly increased, both over standard (≤4 days) and over extended storage times (7 days). Each of the four BRMs showed an up to twofold increase in concentration after storage at RT compared to cold storage (CS). There was no difference in the aggregation capacity.
CONCLUSION
This analysis shows that the release of adult‐specific BRMs during storage is lowest in short‐ and CS APCs. Our study points to strategies for reducing the exposure of sick neonates to BRMs that can be specifically associated to PLT transfusion–related morbidity.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>32339309</pmid><doi>10.1111/trf.15827</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3458-0309</orcidid><orcidid>https://orcid.org/0000-0002-7303-6667</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Apheresis Bleeding Cold storage Dkk1 protein Immunomodulation Light transmission Morbidity Neonates Platelets RANTES Room temperature Storage conditions Thrombocytopenia Transforming growth factor-b1 Transfusion |
title | Pooling, room temperature, and extended storage time increase the release of adult‐specific biologic response modifiers in platelet concentrates: a hidden transfusion risk for neonates? |
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