{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,23]],"date-time":"2026-10-23T01:05:43Z","timestamp":1792717543965,"version":"4.5.0"},"reference-count":42,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2013,7,5]],"date-time":"2013-07-05T00:00:00Z","timestamp":1372982400000},"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":[[2014,3]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>Hemolysis may follow intravenous immunoglobulin (<jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content>), with product, dosing, and host factors contributing. The importance of recipient features remains unclear.<\/jats:p><\/jats:sec><jats:sec><jats:title>Case Report<\/jats:title><jats:p>A 52\u2010year\u2010old obese woman, 10 years after <jats:styled-content style=\"fixed-case\">ABO<\/jats:styled-content>\u2010mismatched (recipient <jats:styled-content style=\"fixed-case\">O<\/jats:styled-content>, donor <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>) marrow transplantation, presented with immune thrombocytopenia (<jats:styled-content style=\"fixed-case\">ITP<\/jats:styled-content>). <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> at 100\u2009g\/day\u2009\u00d7\u20092 days was followed by hemoglobinuria and angina and dyspnea, with frank hemoglobinemia and anemia (hemoglobin 12.9 to 8.4 over 24\u2009hr, to a nadir of 6.9\u2009g\/<jats:styled-content style=\"fixed-case\">dL<\/jats:styled-content>).<\/jats:p><\/jats:sec><jats:sec><jats:title>Study Design and Methods<\/jats:title><jats:p>Serologic methods established <jats:styled-content style=\"fixed-case\">ABO<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>1, <jats:styled-content style=\"fixed-case\">L<\/jats:styled-content>ewis, and <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>ecretor type, while monocyte monolayer assay (<jats:styled-content style=\"fixed-case\">MMA<\/jats:styled-content>) examined erythrophagocytosis with control or patient monocytes, and the implicated <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> lot to opsonize control (group <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>1, <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>2, <jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>, <jats:styled-content style=\"fixed-case\">O<\/jats:styled-content>) or patient red blood cells (RBCs). Baseline, hemolytic, and convalescent markers (including cytokines) were assessed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Passive anti\u2010<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content> was identified on reverse type and eluted from sensitized RBCs (immunoglobulin\u2009<jats:styled-content style=\"fixed-case\">G<\/jats:styled-content> 1+, <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>3d\u2013). <jats:styled-content style=\"fixed-case\">L<\/jats:styled-content>e(a\u2013b+) typing and saliva confirmed <jats:styled-content style=\"fixed-case\">H S<\/jats:styled-content>ecretor status. <jats:styled-content style=\"fixed-case\">MMA<\/jats:styled-content> revealed significant activity between patient RBCs, monocytes, and <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content>. However, normal <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>1 cells opsonized with <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> were not significantly phagocytosed by either normal or patient monocytes. Proinflammatory markers were significantly elevated before and after <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>Synergizing host factors (including obesity\u2010unadjusted dosing and existing inflammation) marked this severe post\u2010<jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> hemolytic crisis. Group <jats:styled-content style=\"fixed-case\">A<\/jats:styled-content> antigen restriction to myeloid tissues, with <jats:styled-content style=\"fixed-case\">H S<\/jats:styled-content>ecretor phenotype, may have contributed, rendering this bone marrow transplant chimera vulnerable to anti\u2010<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content> in a manner analogous to the idiosyncratic effect of therapeutic anti\u2010<jats:styled-content style=\"fixed-case\">D<\/jats:styled-content> in certain <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>+ <jats:styled-content style=\"fixed-case\">ITP<\/jats:styled-content> recipients. However, <jats:styled-content style=\"fixed-case\">MMA<\/jats:styled-content> suggested a macrophage activation state as contributory, perhaps precipitated by existing inflammation.<\/jats:p><\/jats:sec>","DOI":"10.1111\/trf.12329","type":"journal-article","created":{"date-parts":[[2013,7,5]],"date-time":"2013-07-05T12:10:16Z","timestamp":1373026216000},"page":"681-690","source":"Crossref","is-referenced-by-count":31,"title":["Acute hemolysis after intravenous immunoglobulin amid host factors of <scp>ABO<\/scp>\u2010mismatched bone marrow transplantation, inflammation, and activated mononuclear phagocytes"],"prefix":"10.1111","volume":"54","author":[{"given":"Fotios V.","family":"Michelis","sequence":"first","affiliation":[{"name":"Blood and Marrow Transplant Program Princess Margaret Hospital University Health Network  Toronto Ontario Canada"},{"name":"Research &amp; Development Canadian Blood Services  Toronto Ontario Canada"},{"name":"Transfusion Medicine Laboratory University Health Network University of Toronto  Toronto Ontario Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Donald R.","family":"Branch","sequence":"additional","affiliation":[{"name":"Blood and Marrow Transplant Program Princess Margaret Hospital University Health Network  Toronto Ontario Canada"},{"name":"Research &amp; 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