Efficient neutralization of daratumumab in pretransfusion samples using a novel recombinant monoclonal anti‐idiotype antibody
Background Anti‐CD38 antibodies such as daratumumab (DARA) are critical therapies for multiple myeloma and other diseases. Unfortunately, anti‐CD38 antibodies cause panreactivity in indirect antiglobulin tests (IATs), complicating blood compatibility testing. The anti‐CD38 interference is most often...
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Veröffentlicht in: | Transfusion (Philadelphia, Pa.) Pa.), 2022-08, Vol.62 (8), p.1511-1518 |
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creator | Aung, Fleur Spencer, Jeff Potter, David Pham, Thuy‐Dung Farooqui, Naheed Platt, Kathryn R. Zayat, Raja Oliveira, Melanie Smeland‐Wagman, Robin Petersen, Eric Kaufman, Richard M. |
description | Background
Anti‐CD38 antibodies such as daratumumab (DARA) are critical therapies for multiple myeloma and other diseases. Unfortunately, anti‐CD38 antibodies cause panreactivity in indirect antiglobulin tests (IATs), complicating blood compatibility testing. The anti‐CD38 interference is most often mitigated by treating reagent red blood cells (RBCs) with dithiothreitol (DTT). However, when using the DTT method, not all RBC antibody specificities can be detected (e.g., anti‐K), and the DTT method is impractical for some transfusion services. We evaluated the ability of a new anti‐idiotype antibody to neutralize DARA in vitro and eliminate the anti‐CD38 interference.
Study Design and Methods
A recombinant monoclonal rabbit anti‐DARA idiotype antibody (“anti‐DARA”) was generated. The ratio of anti‐DARA required to neutralize DARA in spiked samples was evaluated in IATs performed in gel. IATs performed in tube were used to demonstrate that anti‐DARA allows alloantibody detection in the presence of DARA. Plasma samples from 29 patients receiving DARA were treated with a fixed quantity of anti‐DARA (120 μg) before performing antibody detection tests (screens) in tube.
Results
Anti‐DARA used at or above a 1:1 ratio with DARA eliminated the DARA interference with IATs. Anti‐DARA allowed detection of both alloanti‐E and alloanti‐K in the presence of DARA. In 27/29 (93.1%) clinical samples, 120 μg anti‐DARA was sufficient to neutralize the DARA in 100 μl patient plasma.
Discussion
An anti‐DARA:DARA ratio as low as 1:1 is sufficient to neutralize DARA in solution. A fixed amount of anti‐DARA eliminates the anti‐CD38 interference in most patient samples. |
doi_str_mv | 10.1111/trf.17006 |
format | Article |
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Anti‐CD38 antibodies such as daratumumab (DARA) are critical therapies for multiple myeloma and other diseases. Unfortunately, anti‐CD38 antibodies cause panreactivity in indirect antiglobulin tests (IATs), complicating blood compatibility testing. The anti‐CD38 interference is most often mitigated by treating reagent red blood cells (RBCs) with dithiothreitol (DTT). However, when using the DTT method, not all RBC antibody specificities can be detected (e.g., anti‐K), and the DTT method is impractical for some transfusion services. We evaluated the ability of a new anti‐idiotype antibody to neutralize DARA in vitro and eliminate the anti‐CD38 interference.
Study Design and Methods
A recombinant monoclonal rabbit anti‐DARA idiotype antibody (“anti‐DARA”) was generated. The ratio of anti‐DARA required to neutralize DARA in spiked samples was evaluated in IATs performed in gel. IATs performed in tube were used to demonstrate that anti‐DARA allows alloantibody detection in the presence of DARA. Plasma samples from 29 patients receiving DARA were treated with a fixed quantity of anti‐DARA (120 μg) before performing antibody detection tests (screens) in tube.
Results
Anti‐DARA used at or above a 1:1 ratio with DARA eliminated the DARA interference with IATs. Anti‐DARA allowed detection of both alloanti‐E and alloanti‐K in the presence of DARA. In 27/29 (93.1%) clinical samples, 120 μg anti‐DARA was sufficient to neutralize the DARA in 100 μl patient plasma.
Discussion
An anti‐DARA:DARA ratio as low as 1:1 is sufficient to neutralize DARA in solution. A fixed amount of anti‐DARA eliminates the anti‐CD38 interference in most patient samples.</description><identifier>ISSN: 0041-1132</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1111/trf.17006</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Alloantibodies ; Antibodies ; CD38 antigen ; Dithiothreitol ; Erythrocytes ; Immunotherapy ; Interference ; Monoclonal antibodies ; Multiple myeloma ; Neutralization ; Patients ; Reagents ; Targeted cancer therapy ; Transfusion</subject><ispartof>Transfusion (Philadelphia, Pa.), 2022-08, Vol.62 (8), p.1511-1518</ispartof><rights>2022 AABB.</rights><rights>2022 AABB</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2606-ca4d77c0386958b15641fe2127c68bbeae1768e9e9ed954f5daa6b6d31599ec03</citedby><cites>FETCH-LOGICAL-c2606-ca4d77c0386958b15641fe2127c68bbeae1768e9e9ed954f5daa6b6d31599ec03</cites><orcidid>0000-0002-0041-804X</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.17006$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Ftrf.17006$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids></links><search><creatorcontrib>Aung, Fleur</creatorcontrib><creatorcontrib>Spencer, Jeff</creatorcontrib><creatorcontrib>Potter, David</creatorcontrib><creatorcontrib>Pham, Thuy‐Dung</creatorcontrib><creatorcontrib>Farooqui, Naheed</creatorcontrib><creatorcontrib>Platt, Kathryn R.</creatorcontrib><creatorcontrib>Zayat, Raja</creatorcontrib><creatorcontrib>Oliveira, Melanie</creatorcontrib><creatorcontrib>Smeland‐Wagman, Robin</creatorcontrib><creatorcontrib>Petersen, Eric</creatorcontrib><creatorcontrib>Kaufman, Richard M.</creatorcontrib><title>Efficient neutralization of daratumumab in pretransfusion samples using a novel recombinant monoclonal anti‐idiotype antibody</title><title>Transfusion (Philadelphia, Pa.)</title><description>Background
Anti‐CD38 antibodies such as daratumumab (DARA) are critical therapies for multiple myeloma and other diseases. Unfortunately, anti‐CD38 antibodies cause panreactivity in indirect antiglobulin tests (IATs), complicating blood compatibility testing. The anti‐CD38 interference is most often mitigated by treating reagent red blood cells (RBCs) with dithiothreitol (DTT). However, when using the DTT method, not all RBC antibody specificities can be detected (e.g., anti‐K), and the DTT method is impractical for some transfusion services. We evaluated the ability of a new anti‐idiotype antibody to neutralize DARA in vitro and eliminate the anti‐CD38 interference.
Study Design and Methods
A recombinant monoclonal rabbit anti‐DARA idiotype antibody (“anti‐DARA”) was generated. The ratio of anti‐DARA required to neutralize DARA in spiked samples was evaluated in IATs performed in gel. IATs performed in tube were used to demonstrate that anti‐DARA allows alloantibody detection in the presence of DARA. Plasma samples from 29 patients receiving DARA were treated with a fixed quantity of anti‐DARA (120 μg) before performing antibody detection tests (screens) in tube.
Results
Anti‐DARA used at or above a 1:1 ratio with DARA eliminated the DARA interference with IATs. Anti‐DARA allowed detection of both alloanti‐E and alloanti‐K in the presence of DARA. In 27/29 (93.1%) clinical samples, 120 μg anti‐DARA was sufficient to neutralize the DARA in 100 μl patient plasma.
Discussion
An anti‐DARA:DARA ratio as low as 1:1 is sufficient to neutralize DARA in solution. A fixed amount of anti‐DARA eliminates the anti‐CD38 interference in most patient samples.</description><subject>Alloantibodies</subject><subject>Antibodies</subject><subject>CD38 antigen</subject><subject>Dithiothreitol</subject><subject>Erythrocytes</subject><subject>Immunotherapy</subject><subject>Interference</subject><subject>Monoclonal antibodies</subject><subject>Multiple myeloma</subject><subject>Neutralization</subject><subject>Patients</subject><subject>Reagents</subject><subject>Targeted cancer therapy</subject><subject>Transfusion</subject><issn>0041-1132</issn><issn>1537-2995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp10ctKxDAUBuAgCo6XhW8QcKOLatJMk8lSxBsIgozrkqYnkiFNatIq40YfwWf0SczMuBJMFuGH7xwIP0JHlJzRfM6HaM6oIIRvoQmtmChKKattNCFkSgtKWbmL9lJaEEJKSegEfVwZY7UFP2AP4xCVs-9qsMHjYHCrohrGbuxUg63HfYQMfDJjWoGkut5Bwjn5Z6ywD6_gcAQdusZ6lTd2wQftglcO52i_P79sa8Ow7GGdm9AuD9COUS7B4e-7j56ur-aXt8X9w83d5cV9oUtOeKHVtBVCEzbjspo1tOJTaqCkpdB81jSggAo-A5lvK6upqVqleMNbRispIc_to5PN3j6GlxHSUHc2aXBOeQhjqksumRBMMJbp8R-6CGPMn1grSZkkcqVON0rHkFIEU_fRdioua0rqVRV1rqJeV5Ht-ca-WQfL_2E9f7zeTPwAF5eO1A</recordid><startdate>202208</startdate><enddate>202208</enddate><creator>Aung, Fleur</creator><creator>Spencer, Jeff</creator><creator>Potter, David</creator><creator>Pham, Thuy‐Dung</creator><creator>Farooqui, Naheed</creator><creator>Platt, Kathryn R.</creator><creator>Zayat, Raja</creator><creator>Oliveira, Melanie</creator><creator>Smeland‐Wagman, Robin</creator><creator>Petersen, Eric</creator><creator>Kaufman, Richard M.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><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/0000-0002-0041-804X</orcidid></search><sort><creationdate>202208</creationdate><title>Efficient neutralization of daratumumab in pretransfusion samples using a novel recombinant monoclonal anti‐idiotype antibody</title><author>Aung, Fleur ; Spencer, Jeff ; Potter, David ; Pham, Thuy‐Dung ; Farooqui, Naheed ; Platt, Kathryn R. ; Zayat, Raja ; Oliveira, Melanie ; Smeland‐Wagman, Robin ; Petersen, Eric ; Kaufman, Richard M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2606-ca4d77c0386958b15641fe2127c68bbeae1768e9e9ed954f5daa6b6d31599ec03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Alloantibodies</topic><topic>Antibodies</topic><topic>CD38 antigen</topic><topic>Dithiothreitol</topic><topic>Erythrocytes</topic><topic>Immunotherapy</topic><topic>Interference</topic><topic>Monoclonal antibodies</topic><topic>Multiple myeloma</topic><topic>Neutralization</topic><topic>Patients</topic><topic>Reagents</topic><topic>Targeted cancer therapy</topic><topic>Transfusion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aung, Fleur</creatorcontrib><creatorcontrib>Spencer, Jeff</creatorcontrib><creatorcontrib>Potter, David</creatorcontrib><creatorcontrib>Pham, Thuy‐Dung</creatorcontrib><creatorcontrib>Farooqui, Naheed</creatorcontrib><creatorcontrib>Platt, Kathryn R.</creatorcontrib><creatorcontrib>Zayat, Raja</creatorcontrib><creatorcontrib>Oliveira, Melanie</creatorcontrib><creatorcontrib>Smeland‐Wagman, Robin</creatorcontrib><creatorcontrib>Petersen, Eric</creatorcontrib><creatorcontrib>Kaufman, Richard M.</creatorcontrib><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>Aung, Fleur</au><au>Spencer, Jeff</au><au>Potter, David</au><au>Pham, Thuy‐Dung</au><au>Farooqui, Naheed</au><au>Platt, Kathryn R.</au><au>Zayat, Raja</au><au>Oliveira, Melanie</au><au>Smeland‐Wagman, Robin</au><au>Petersen, Eric</au><au>Kaufman, Richard M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient neutralization of daratumumab in pretransfusion samples using a novel recombinant monoclonal anti‐idiotype antibody</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><date>2022-08</date><risdate>2022</risdate><volume>62</volume><issue>8</issue><spage>1511</spage><epage>1518</epage><pages>1511-1518</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><abstract>Background
Anti‐CD38 antibodies such as daratumumab (DARA) are critical therapies for multiple myeloma and other diseases. Unfortunately, anti‐CD38 antibodies cause panreactivity in indirect antiglobulin tests (IATs), complicating blood compatibility testing. The anti‐CD38 interference is most often mitigated by treating reagent red blood cells (RBCs) with dithiothreitol (DTT). However, when using the DTT method, not all RBC antibody specificities can be detected (e.g., anti‐K), and the DTT method is impractical for some transfusion services. We evaluated the ability of a new anti‐idiotype antibody to neutralize DARA in vitro and eliminate the anti‐CD38 interference.
Study Design and Methods
A recombinant monoclonal rabbit anti‐DARA idiotype antibody (“anti‐DARA”) was generated. The ratio of anti‐DARA required to neutralize DARA in spiked samples was evaluated in IATs performed in gel. IATs performed in tube were used to demonstrate that anti‐DARA allows alloantibody detection in the presence of DARA. Plasma samples from 29 patients receiving DARA were treated with a fixed quantity of anti‐DARA (120 μg) before performing antibody detection tests (screens) in tube.
Results
Anti‐DARA used at or above a 1:1 ratio with DARA eliminated the DARA interference with IATs. Anti‐DARA allowed detection of both alloanti‐E and alloanti‐K in the presence of DARA. In 27/29 (93.1%) clinical samples, 120 μg anti‐DARA was sufficient to neutralize the DARA in 100 μl patient plasma.
Discussion
An anti‐DARA:DARA ratio as low as 1:1 is sufficient to neutralize DARA in solution. A fixed amount of anti‐DARA eliminates the anti‐CD38 interference in most patient samples.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1111/trf.17006</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-0041-804X</orcidid></addata></record> |
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subjects | Alloantibodies Antibodies CD38 antigen Dithiothreitol Erythrocytes Immunotherapy Interference Monoclonal antibodies Multiple myeloma Neutralization Patients Reagents Targeted cancer therapy Transfusion |
title | Efficient neutralization of daratumumab in pretransfusion samples using a novel recombinant monoclonal anti‐idiotype antibody |
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