Storage of murine red blood cells enhances alloantibody responses to an erythroid-specific model antigen
Red blood cell (RBC) alloimmunization can be a serious complication of blood transfusion, but factors influencing the development of alloantibodies are only partially understood. Within FDA-approved time limits, RBCs are generally transfused without regard to length of storage. However, recent studi...
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Veröffentlicht in: | Transfusion (Philadelphia, Pa.) Pa.), 2010-03, Vol.50 (3), p.642-648 |
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description | Red blood cell (RBC) alloimmunization can be a serious complication of blood transfusion, but factors influencing the development of alloantibodies are only partially understood. Within FDA-approved time limits, RBCs are generally transfused without regard to length of storage. However, recent studies have raised concerns that RBCs stored for more than 14 days have altered biologic properties that may affect medical outcomes. To test the hypothesis that storage time alters RBC immunogenicity, we utilized a murine model of RBC storage and alloimmunization.
Blood from transgenic HOD donor mice, which express a model antigen (hen egg lysozyme [HEL]) specifically on RBCs, was filter leukoreduced and stored for 14 days under conditions similar to those used for human RBCs. Fresh or 14-day-stored RBCs were transfused into wild-type recipients. The stability of the HOD antigen and posttransfusion RBC survival were analyzed by flow cytometry. RBC alloimmunization was monitored by measuring circulating anti-HEL immunoglobulin levels.
Transfusion of 14-day-stored, leukoreduced HOD RBCs resulted in 10- to 100-fold higher levels of anti-HEL alloantibodies as detected by enzyme-linked immunosorbent assay than transfusion of freshly collected, leukoreduced RBCs. RBC expression of the HOD antigen was stable during storage.
These findings demonstrate that HOD murine RBCs become more immunogenic with storage and generate the rationale for clinical trials to test if the same phenomenon is observed in humans. Length of storage of RBCs may represent a previously unappreciated variable in whether or not a transfusion recipient becomes alloimmunized. |
doi_str_mv | 10.1111/j.1537-2995.2009.02481.x |
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Blood from transgenic HOD donor mice, which express a model antigen (hen egg lysozyme [HEL]) specifically on RBCs, was filter leukoreduced and stored for 14 days under conditions similar to those used for human RBCs. Fresh or 14-day-stored RBCs were transfused into wild-type recipients. The stability of the HOD antigen and posttransfusion RBC survival were analyzed by flow cytometry. RBC alloimmunization was monitored by measuring circulating anti-HEL immunoglobulin levels.
Transfusion of 14-day-stored, leukoreduced HOD RBCs resulted in 10- to 100-fold higher levels of anti-HEL alloantibodies as detected by enzyme-linked immunosorbent assay than transfusion of freshly collected, leukoreduced RBCs. RBC expression of the HOD antigen was stable during storage.
These findings demonstrate that HOD murine RBCs become more immunogenic with storage and generate the rationale for clinical trials to test if the same phenomenon is observed in humans. Length of storage of RBCs may represent a previously unappreciated variable in whether or not a transfusion recipient becomes alloimmunized.</description><identifier>ISSN: 0041-1132</identifier><identifier>EISSN: 1537-2995</identifier><identifier>DOI: 10.1111/j.1537-2995.2009.02481.x</identifier><identifier>PMID: 19906034</identifier><identifier>CODEN: TRANAT</identifier><language>eng</language><publisher>Hoboken, NJ: Wiley</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Animals ; Biological and medical sciences ; Blood Group Incompatibility - genetics ; Blood Group Incompatibility - immunology ; Blood Preservation ; Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis ; Erythrocyte Transfusion ; Erythrocytes - immunology ; Hematology ; Humans ; Investigative techniques, diagnostic techniques (general aspects) ; Isoantibodies - immunology ; Isoantigens - genetics ; Isoantigens - immunology ; Medical sciences ; Mice ; Mice, Transgenic ; Models, Immunological ; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques ; Time Factors ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><ispartof>Transfusion (Philadelphia, Pa.), 2010-03, Vol.50 (3), p.642-648</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22541691$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19906034$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>HENDRICKSON, Jeanne E</creatorcontrib><creatorcontrib>HOD, Eldad A</creatorcontrib><creatorcontrib>SPITALNIK, Steven L</creatorcontrib><creatorcontrib>HILLYER, Christopher D</creatorcontrib><creatorcontrib>ZIMRING, James C</creatorcontrib><title>Storage of murine red blood cells enhances alloantibody responses to an erythroid-specific model antigen</title><title>Transfusion (Philadelphia, Pa.)</title><addtitle>Transfusion</addtitle><description>Red blood cell (RBC) alloimmunization can be a serious complication of blood transfusion, but factors influencing the development of alloantibodies are only partially understood. Within FDA-approved time limits, RBCs are generally transfused without regard to length of storage. However, recent studies have raised concerns that RBCs stored for more than 14 days have altered biologic properties that may affect medical outcomes. To test the hypothesis that storage time alters RBC immunogenicity, we utilized a murine model of RBC storage and alloimmunization.
Blood from transgenic HOD donor mice, which express a model antigen (hen egg lysozyme [HEL]) specifically on RBCs, was filter leukoreduced and stored for 14 days under conditions similar to those used for human RBCs. Fresh or 14-day-stored RBCs were transfused into wild-type recipients. The stability of the HOD antigen and posttransfusion RBC survival were analyzed by flow cytometry. RBC alloimmunization was monitored by measuring circulating anti-HEL immunoglobulin levels.
Transfusion of 14-day-stored, leukoreduced HOD RBCs resulted in 10- to 100-fold higher levels of anti-HEL alloantibodies as detected by enzyme-linked immunosorbent assay than transfusion of freshly collected, leukoreduced RBCs. RBC expression of the HOD antigen was stable during storage.
These findings demonstrate that HOD murine RBCs become more immunogenic with storage and generate the rationale for clinical trials to test if the same phenomenon is observed in humans. Length of storage of RBCs may represent a previously unappreciated variable in whether or not a transfusion recipient becomes alloimmunized.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Group Incompatibility - genetics</subject><subject>Blood Group Incompatibility - immunology</subject><subject>Blood Preservation</subject><subject>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</subject><subject>Erythrocyte Transfusion</subject><subject>Erythrocytes - immunology</subject><subject>Hematology</subject><subject>Humans</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Isoantibodies - immunology</subject><subject>Isoantigens - genetics</subject><subject>Isoantigens - immunology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Models, Immunological</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</subject><subject>Time Factors</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><issn>0041-1132</issn><issn>1537-2995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkE9r3DAQxUVpaTZpv0LRpfRkV_8sW5dACWkTCPTQ9mwka7SrIEuO5C3Zbx-FbpZmLgMzv3mPeQhhSlpa6-t9SzveN0yprmWEqJYwMdD28Q3anBZv0YYQQRtKOTtD56XcE0KYIvQ9OqNKEUm42KDdrzVlvQWcHJ732UfAGSw2ISWLJwihYIg7HScoWIeQdFy9SfZQqbKkWOp4TVhHDPmw7nLytikLTN75Cc_JQsDPF1uIH9A7p0OBj8d-gf58v_59ddPc_fxxe_XtrlmY6tZGO2YGOhjujOW9ElQ6IqeeMkGd5D0MIJwiljpquLGa971UskZiOB80gOAX6PKf7rI3M9gJ4pp1GJfsZ50PY9J-fL2Jfjdu09-Rd3JQQlWBL0eBnB72UNZx9uU5CR0h7cvYcy47SoSs5Kf_rU4eL-lW4PMR0GXSweWaoy8njrGu_qcofwI-Uo2w</recordid><startdate>20100301</startdate><enddate>20100301</enddate><creator>HENDRICKSON, Jeanne E</creator><creator>HOD, Eldad A</creator><creator>SPITALNIK, Steven L</creator><creator>HILLYER, Christopher D</creator><creator>ZIMRING, James C</creator><general>Wiley</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20100301</creationdate><title>Storage of murine red blood cells enhances alloantibody responses to an erythroid-specific model antigen</title><author>HENDRICKSON, Jeanne E ; HOD, Eldad A ; SPITALNIK, Steven L ; HILLYER, Christopher D ; ZIMRING, James C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p295t-af2b818b3fbd379416f06c71241f637e8e4f90d1f1b3bda377696111b338aee43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Group Incompatibility - genetics</topic><topic>Blood Group Incompatibility - immunology</topic><topic>Blood Preservation</topic><topic>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</topic><topic>Erythrocyte Transfusion</topic><topic>Erythrocytes - immunology</topic><topic>Hematology</topic><topic>Humans</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Isoantibodies - immunology</topic><topic>Isoantigens - genetics</topic><topic>Isoantigens - immunology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Models, Immunological</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Time Factors</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HENDRICKSON, Jeanne E</creatorcontrib><creatorcontrib>HOD, Eldad A</creatorcontrib><creatorcontrib>SPITALNIK, Steven L</creatorcontrib><creatorcontrib>HILLYER, Christopher D</creatorcontrib><creatorcontrib>ZIMRING, James C</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Transfusion (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HENDRICKSON, Jeanne E</au><au>HOD, Eldad A</au><au>SPITALNIK, Steven L</au><au>HILLYER, Christopher D</au><au>ZIMRING, James C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Storage of murine red blood cells enhances alloantibody responses to an erythroid-specific model antigen</atitle><jtitle>Transfusion (Philadelphia, Pa.)</jtitle><addtitle>Transfusion</addtitle><date>2010-03-01</date><risdate>2010</risdate><volume>50</volume><issue>3</issue><spage>642</spage><epage>648</epage><pages>642-648</pages><issn>0041-1132</issn><eissn>1537-2995</eissn><coden>TRANAT</coden><abstract>Red blood cell (RBC) alloimmunization can be a serious complication of blood transfusion, but factors influencing the development of alloantibodies are only partially understood. Within FDA-approved time limits, RBCs are generally transfused without regard to length of storage. However, recent studies have raised concerns that RBCs stored for more than 14 days have altered biologic properties that may affect medical outcomes. To test the hypothesis that storage time alters RBC immunogenicity, we utilized a murine model of RBC storage and alloimmunization.
Blood from transgenic HOD donor mice, which express a model antigen (hen egg lysozyme [HEL]) specifically on RBCs, was filter leukoreduced and stored for 14 days under conditions similar to those used for human RBCs. Fresh or 14-day-stored RBCs were transfused into wild-type recipients. The stability of the HOD antigen and posttransfusion RBC survival were analyzed by flow cytometry. RBC alloimmunization was monitored by measuring circulating anti-HEL immunoglobulin levels.
Transfusion of 14-day-stored, leukoreduced HOD RBCs resulted in 10- to 100-fold higher levels of anti-HEL alloantibodies as detected by enzyme-linked immunosorbent assay than transfusion of freshly collected, leukoreduced RBCs. RBC expression of the HOD antigen was stable during storage.
These findings demonstrate that HOD murine RBCs become more immunogenic with storage and generate the rationale for clinical trials to test if the same phenomenon is observed in humans. Length of storage of RBCs may represent a previously unappreciated variable in whether or not a transfusion recipient becomes alloimmunized.</abstract><cop>Hoboken, NJ</cop><pub>Wiley</pub><pmid>19906034</pmid><doi>10.1111/j.1537-2995.2009.02481.x</doi><tpages>7</tpages></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Animals Biological and medical sciences Blood Group Incompatibility - genetics Blood Group Incompatibility - immunology Blood Preservation Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis Erythrocyte Transfusion Erythrocytes - immunology Hematology Humans Investigative techniques, diagnostic techniques (general aspects) Isoantibodies - immunology Isoantigens - genetics Isoantigens - immunology Medical sciences Mice Mice, Transgenic Models, Immunological Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques Time Factors Transfusions. Complications. Transfusion reactions. Cell and gene therapy |
title | Storage of murine red blood cells enhances alloantibody responses to an erythroid-specific model antigen |
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