Possible alternative strategies to implement basophil activation testing in multicentric studies
The Basophil Activation Test (BAT) enables flow cytometry characterization of basophil reactivity against specific allergenic molecules. The focus now revolves around democratizing this tool, but, as blood sample stability could be challenging, after having developed a simplified approach, herein, w...
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Veröffentlicht in: | Cytometry. Part B, Clinical cytometry Clinical cytometry, 2024-09, Vol.106 (5), p.392-404 |
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creator | Bourgoin, Pénélope Dupont, Thomas Agabriel, Chantal Carsin, Ania Verles, Aurélie Cabanski, Maciej Vitaliti, Alessandra Busnel, Jean‐Marc |
description | The Basophil Activation Test (BAT) enables flow cytometry characterization of basophil reactivity against specific allergenic molecules. The focus now revolves around democratizing this tool, but, as blood sample stability could be challenging, after having developed a simplified approach, herein, we aimed to characterize two strategies for implementing BAT in multicentric studies: store and ship blood before or after sample processing. Fresh heparin‐ and EDTA‐anticoagulated whole blood samples followed both BAT workflows: “collect, store, process & analyze” or “collect, process, store & analyze”. Storage temperatures of 18–25 °C or 2–8 °C and preservation times from 0 to 7 days were considered. Interleukin‐3 was also evaluated. With the “collect, store, process & analyze” workflow, heparin‐anticoagulated blood and 18–25 °C storage were better than other conditions. While remaining possible, basophil activation exhibited a possible reactivity decay after 24 h. Under the conditions tested, interleukin‐3 had no role in enhancing basophil reactivity after storage. Conversely, the “collect, process, store & analyze” workflow demonstrated that either heparin‐ or EDTA‐anticoagulated blood can be processed and kept up to 7 days at 18–25 °C or 2–8 °C before being analyzed. Various strategies can be implemented to integrate BAT in multicentric studies. The “collect, store, process & analyze” workflow remains a simplified logistical approach, but depending on time required to ship from the clinical centers to the reference laboratories, it might not be applicable, or should be used with caution. The “collect, process, store & analyze” workflow may constitute a workflow improvement to provide significant flexibility without impact on basophil reactivity. |
doi_str_mv | 10.1002/cyto.b.22172 |
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The focus now revolves around democratizing this tool, but, as blood sample stability could be challenging, after having developed a simplified approach, herein, we aimed to characterize two strategies for implementing BAT in multicentric studies: store and ship blood before or after sample processing. Fresh heparin‐ and EDTA‐anticoagulated whole blood samples followed both BAT workflows: “collect, store, process & analyze” or “collect, process, store & analyze”. Storage temperatures of 18–25 °C or 2–8 °C and preservation times from 0 to 7 days were considered. Interleukin‐3 was also evaluated. With the “collect, store, process & analyze” workflow, heparin‐anticoagulated blood and 18–25 °C storage were better than other conditions. While remaining possible, basophil activation exhibited a possible reactivity decay after 24 h. Under the conditions tested, interleukin‐3 had no role in enhancing basophil reactivity after storage. Conversely, the “collect, process, store & analyze” workflow demonstrated that either heparin‐ or EDTA‐anticoagulated blood can be processed and kept up to 7 days at 18–25 °C or 2–8 °C before being analyzed. Various strategies can be implemented to integrate BAT in multicentric studies. The “collect, store, process & analyze” workflow remains a simplified logistical approach, but depending on time required to ship from the clinical centers to the reference laboratories, it might not be applicable, or should be used with caution. The “collect, process, store & analyze” workflow may constitute a workflow improvement to provide significant flexibility without impact on basophil reactivity.]]></description><identifier>ISSN: 1552-4949</identifier><identifier>ISSN: 1552-4957</identifier><identifier>EISSN: 1552-4957</identifier><identifier>DOI: 10.1002/cyto.b.22172</identifier><identifier>PMID: 38572669</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>basophil activation testing ; basophil reactivity ; Blood ; blood sample stability ; Cytokines ; Edetic acid ; Ethylenediaminetetraacetic acids ; Flow cytometry ; Heparin ; Impact analysis ; Interleukins ; interleukin‐3 ; Leukocytes (basophilic) ; multicentric studies ; Reactivity ; Workflow</subject><ispartof>Cytometry. Part B, Clinical cytometry, 2024-09, Vol.106 (5), p.392-404</ispartof><rights>2024 International Clinical Cytometry Society.</rights><rights>2024 International Clinical Cytometry Society</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3212-ac729bbdad6b1b61833fe807e65b06d991152f8e9a12cf900e4a893e54dab04a3</cites><orcidid>0000-0002-9970-2680</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcyto.b.22172$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcyto.b.22172$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38572669$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bourgoin, Pénélope</creatorcontrib><creatorcontrib>Dupont, Thomas</creatorcontrib><creatorcontrib>Agabriel, Chantal</creatorcontrib><creatorcontrib>Carsin, Ania</creatorcontrib><creatorcontrib>Verles, Aurélie</creatorcontrib><creatorcontrib>Cabanski, Maciej</creatorcontrib><creatorcontrib>Vitaliti, Alessandra</creatorcontrib><creatorcontrib>Busnel, Jean‐Marc</creatorcontrib><title>Possible alternative strategies to implement basophil activation testing in multicentric studies</title><title>Cytometry. Part B, Clinical cytometry</title><addtitle>Cytometry B Clin Cytom</addtitle><description><![CDATA[The Basophil Activation Test (BAT) enables flow cytometry characterization of basophil reactivity against specific allergenic molecules. The focus now revolves around democratizing this tool, but, as blood sample stability could be challenging, after having developed a simplified approach, herein, we aimed to characterize two strategies for implementing BAT in multicentric studies: store and ship blood before or after sample processing. Fresh heparin‐ and EDTA‐anticoagulated whole blood samples followed both BAT workflows: “collect, store, process & analyze” or “collect, process, store & analyze”. Storage temperatures of 18–25 °C or 2–8 °C and preservation times from 0 to 7 days were considered. Interleukin‐3 was also evaluated. With the “collect, store, process & analyze” workflow, heparin‐anticoagulated blood and 18–25 °C storage were better than other conditions. While remaining possible, basophil activation exhibited a possible reactivity decay after 24 h. Under the conditions tested, interleukin‐3 had no role in enhancing basophil reactivity after storage. Conversely, the “collect, process, store & analyze” workflow demonstrated that either heparin‐ or EDTA‐anticoagulated blood can be processed and kept up to 7 days at 18–25 °C or 2–8 °C before being analyzed. Various strategies can be implemented to integrate BAT in multicentric studies. The “collect, store, process & analyze” workflow remains a simplified logistical approach, but depending on time required to ship from the clinical centers to the reference laboratories, it might not be applicable, or should be used with caution. The “collect, process, store & analyze” workflow may constitute a workflow improvement to provide significant flexibility without impact on basophil reactivity.]]></description><subject>basophil activation testing</subject><subject>basophil reactivity</subject><subject>Blood</subject><subject>blood sample stability</subject><subject>Cytokines</subject><subject>Edetic acid</subject><subject>Ethylenediaminetetraacetic acids</subject><subject>Flow cytometry</subject><subject>Heparin</subject><subject>Impact analysis</subject><subject>Interleukins</subject><subject>interleukin‐3</subject><subject>Leukocytes (basophilic)</subject><subject>multicentric studies</subject><subject>Reactivity</subject><subject>Workflow</subject><issn>1552-4949</issn><issn>1552-4957</issn><issn>1552-4957</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp90DtPwzAYhWELgWgpbMzIEgsDLb7k5hEqbhISDDAwGdv5Aq6cpMQOqP8eQ0oHBiZ7ePTKPggdUjKjhLAzswrtTM8YoznbQmOapmyaiDTf3twTMUJ73i8I4WmS5btoxIs0Z1kmxujlofXeagdYuQBdo4L9AOxDpwK8WvA4tNjWSwc1NAFr5dvlm3VYmeiibRscwAfbvGLb4Lp3wZoIO2tioy9jYB_tVMp5OFifE_R0dfk4v5ne3V_fzs_vpoYzyqbK5ExoXaoy01RntOC8goLkkKWaZKUQlKasKkAoykwlCIFEFYJDmpRKk0TxCToZusuufe_jm2RtvQHnVANt7yUnnBOSM84jPf5DF20fv-6iopSShImMRHU6KNPFiTqo5LKztepWkhL5vbz8Xl5q-bN85EfraK9rKDf4d-oIkgF8Wgerf2Ny_vx4fzF0vwDwx5Gf</recordid><startdate>202409</startdate><enddate>202409</enddate><creator>Bourgoin, Pénélope</creator><creator>Dupont, Thomas</creator><creator>Agabriel, Chantal</creator><creator>Carsin, Ania</creator><creator>Verles, Aurélie</creator><creator>Cabanski, Maciej</creator><creator>Vitaliti, Alessandra</creator><creator>Busnel, Jean‐Marc</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9970-2680</orcidid></search><sort><creationdate>202409</creationdate><title>Possible alternative strategies to implement basophil activation testing in multicentric studies</title><author>Bourgoin, Pénélope ; Dupont, Thomas ; Agabriel, Chantal ; Carsin, Ania ; Verles, Aurélie ; Cabanski, Maciej ; Vitaliti, Alessandra ; Busnel, Jean‐Marc</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3212-ac729bbdad6b1b61833fe807e65b06d991152f8e9a12cf900e4a893e54dab04a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>basophil activation testing</topic><topic>basophil reactivity</topic><topic>Blood</topic><topic>blood sample stability</topic><topic>Cytokines</topic><topic>Edetic acid</topic><topic>Ethylenediaminetetraacetic acids</topic><topic>Flow cytometry</topic><topic>Heparin</topic><topic>Impact analysis</topic><topic>Interleukins</topic><topic>interleukin‐3</topic><topic>Leukocytes (basophilic)</topic><topic>multicentric studies</topic><topic>Reactivity</topic><topic>Workflow</topic><toplevel>online_resources</toplevel><creatorcontrib>Bourgoin, Pénélope</creatorcontrib><creatorcontrib>Dupont, Thomas</creatorcontrib><creatorcontrib>Agabriel, Chantal</creatorcontrib><creatorcontrib>Carsin, Ania</creatorcontrib><creatorcontrib>Verles, Aurélie</creatorcontrib><creatorcontrib>Cabanski, Maciej</creatorcontrib><creatorcontrib>Vitaliti, Alessandra</creatorcontrib><creatorcontrib>Busnel, Jean‐Marc</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cytometry. 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The focus now revolves around democratizing this tool, but, as blood sample stability could be challenging, after having developed a simplified approach, herein, we aimed to characterize two strategies for implementing BAT in multicentric studies: store and ship blood before or after sample processing. Fresh heparin‐ and EDTA‐anticoagulated whole blood samples followed both BAT workflows: “collect, store, process & analyze” or “collect, process, store & analyze”. Storage temperatures of 18–25 °C or 2–8 °C and preservation times from 0 to 7 days were considered. Interleukin‐3 was also evaluated. With the “collect, store, process & analyze” workflow, heparin‐anticoagulated blood and 18–25 °C storage were better than other conditions. While remaining possible, basophil activation exhibited a possible reactivity decay after 24 h. Under the conditions tested, interleukin‐3 had no role in enhancing basophil reactivity after storage. Conversely, the “collect, process, store & analyze” workflow demonstrated that either heparin‐ or EDTA‐anticoagulated blood can be processed and kept up to 7 days at 18–25 °C or 2–8 °C before being analyzed. Various strategies can be implemented to integrate BAT in multicentric studies. The “collect, store, process & analyze” workflow remains a simplified logistical approach, but depending on time required to ship from the clinical centers to the reference laboratories, it might not be applicable, or should be used with caution. The “collect, process, store & analyze” workflow may constitute a workflow improvement to provide significant flexibility without impact on basophil reactivity.]]></abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>38572669</pmid><doi>10.1002/cyto.b.22172</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-9970-2680</orcidid></addata></record> |
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subjects | basophil activation testing basophil reactivity Blood blood sample stability Cytokines Edetic acid Ethylenediaminetetraacetic acids Flow cytometry Heparin Impact analysis Interleukins interleukin‐3 Leukocytes (basophilic) multicentric studies Reactivity Workflow |
title | Possible alternative strategies to implement basophil activation testing in multicentric studies |
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