{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,2]],"date-time":"2026-09-02T11:32:10Z","timestamp":1788348730021,"version":"build-2803163510"},"reference-count":46,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2013,4,29]],"date-time":"2013-04-29T00:00:00Z","timestamp":1367193600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Transfusion"],"published-print":{"date-parts":[[2014,1]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>Red blood cell (<jats:styled-content style=\"fixed-case\">RBC<\/jats:styled-content>) alloantibodies to nonself antigens may develop after transfusion or pregnancy, leading to morbidity and mortality in the form of hemolytic transfusion reactions or hemolytic disease of the newborn. A better understanding of the mechanisms of <jats:styled-content style=\"fixed-case\">RBC<\/jats:styled-content> alloantibody induction, or strategies to mitigate the consequences of such antibodies, may ultimately improve transfusion safety. However, such studies are inherently difficult in humans.<\/jats:p><\/jats:sec><jats:sec><jats:title>Study Design and Methods<\/jats:title><jats:p>We recently generated transgenic mice with <jats:styled-content style=\"fixed-case\">RBC<\/jats:styled-content>\u2010specific expression of the human <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content> glycoprotein, specifically the <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content>2 or <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content>1 antigens. Herein, we investigate recipient alloimmune responses to transfused <jats:styled-content style=\"fixed-case\">RBCs<\/jats:styled-content> in this system.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Transfusion of <jats:styled-content style=\"fixed-case\">RBCs<\/jats:styled-content> from <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content>2 donors into wild\u2010type recipients (lacking the human <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content> protein but expressing the murine <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content> ortholog) resulted in dose\u2010dependent anti\u2010<jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content> glycoprotein immunoglobulin (<jats:styled-content style=\"fixed-case\">Ig<\/jats:styled-content>)<jats:styled-content style=\"fixed-case\">M<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">IgG<\/jats:styled-content> antibody responses, enhanced by recipient inflammation with poly(<jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>:<jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>). Boostable responses were evident upon repeat transfusion, with morbid\u2010appearing alloimmunized recipients experiencing rapid clearance of transfused <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content>2 but not control <jats:styled-content style=\"fixed-case\">RBCs<\/jats:styled-content>. Although <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content>1 <jats:styled-content style=\"fixed-case\">RBCs<\/jats:styled-content> were also immunogenic after transfusion into wild\u2010type recipients, transfusion of <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content>1 <jats:styled-content style=\"fixed-case\">RBCs<\/jats:styled-content> into <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content>2 recipients or vice versa failed to lead to detectable anti\u2010<jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content>1 or anti\u2010<jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content>2 responses.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>This murine model, with reproducible and clinically significant <jats:styled-content style=\"fixed-case\">KEL<\/jats:styled-content> glycoprotein alloantibody responses, provides a platform for future mechanistic studies of <jats:styled-content style=\"fixed-case\">RBC<\/jats:styled-content> alloantibody induction and consequences. Long\u2010term translational goals of these studies include improving transfusion safety for at\u2010risk patients.<\/jats:p><\/jats:sec>","DOI":"10.1111\/trf.12217","type":"journal-article","created":{"date-parts":[[2013,4,29]],"date-time":"2013-04-29T08:01:53Z","timestamp":1367222513000},"page":"179-189","source":"Crossref","is-referenced-by-count":53,"title":["Transfusion of murine red blood cells expressing the human <scp>KEL<\/scp> glycoprotein induces clinically significant alloantibodies"],"prefix":"10.1111","volume":"54","author":[{"given":"Sean R.","family":"Stowell","sequence":"first","affiliation":[{"name":"Department of Pathology Emory University  Atlanta Georgia"},{"name":"Aflac Cancer and Blood Disorders Center Department of Pediatrics Emory University  Atlanta Georgia"},{"name":"Puget Sound Blood Center Research Institute  Seattle Washington"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kathryn R.","family":"Girard\u2010Pierce","sequence":"additional","affiliation":[{"name":"Department of Pathology Emory University  Atlanta Georgia"},{"name":"Aflac Cancer and Blood Disorders Center Department of Pediatrics Emory University  Atlanta Georgia"},{"name":"Puget Sound Blood Center Research Institute  Seattle Washington"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nicole H.","family":"Smith","sequence":"additional","affiliation":[{"name":"Department of Pathology Emory University  Atlanta Georgia"},{"name":"Aflac Cancer and Blood Disorders Center Department of Pediatrics Emory University  Atlanta Georgia"},{"name":"Puget Sound Blood Center Research Institute  Seattle Washington"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kate L.","family":"Henry","sequence":"additional","affiliation":[{"name":"Department of Pathology Emory University  Atlanta Georgia"},{"name":"Aflac Cancer and Blood Disorders Center Department of Pediatrics Emory University  Atlanta Georgia"},{"name":"Puget Sound Blood Center Research Institute  Seattle Washington"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C. 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