{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,13]],"date-time":"2026-10-13T12:29:32Z","timestamp":1791894572649,"version":"4.3.4"},"reference-count":24,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2014,11,13]],"date-time":"2014-11-13T00:00:00Z","timestamp":1415836800000},"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":[[2015,4]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p>Anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content> autoantibodies are among the most frequently detected autoantibodies and have traditionally been associated with <jats:styled-content style=\"fixed-case\">S<\/jats:styled-content>j\u00f6gren's syndrome (<jats:styled-content style=\"fixed-case\">SjS<\/jats:styled-content>) and systemic lupus erythematosus. The unexpected finding of anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content> antibodies in a patient with common variable immunodeficiency disorder (<jats:styled-content style=\"fixed-case\">CVID<\/jats:styled-content>) treated with intravenous immunoglobulin (<jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content>), who developed discoid lupus erythematosus, prompted us to investigate the presence of anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content> antibodies in <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> preparations. Since anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content> antibodies may be present in apparently healthy individuals without overt autoimmune features, <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> preparations may also contain anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content> antibodies.<\/jats:p><\/jats:sec><jats:sec><jats:title>Study Design and Methods<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> consists of polyclonal immunoglobulin\u2009<jats:styled-content style=\"fixed-case\">G<\/jats:styled-content> isolated from the plasma of more than 1000 blood donors. Several <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> batches from different suppliers and serum samples of patients receiving these <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> products were tested for the presence of anti\u2010nuclear antibodies (<jats:styled-content style=\"fixed-case\">ANAs<\/jats:styled-content>) and extractable nuclear antibodies (<jats:styled-content style=\"fixed-case\">ENAs<\/jats:styled-content>). In addition, we tested several plasma pools for the presence of anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content> and subsequent serum samples of individual donors.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Several <jats:styled-content style=\"fixed-case\">CVID<\/jats:styled-content>\u2010patients receiving <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> tested positive for <jats:styled-content style=\"fixed-case\">ANA<\/jats:styled-content> and anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content>. The <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> products administered also contained clearly detectable concentrations of these antibodies. The frequency of apparently healthy blood donors with anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content> positivity was 0.69% and one of 1894 donors (0.05%) showed a very high titer of anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content> of more than 10,000\u2009<jats:styled-content style=\"fixed-case\">U<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">mL<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Anti\u2010<jats:styled-content style=\"fixed-case\">SSA<\/jats:styled-content> is present in <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> products and in blood donors without clinical symptoms. <jats:styled-content style=\"fixed-case\">IVIG<\/jats:styled-content> replacement can interfere with <jats:styled-content style=\"fixed-case\">ANA<\/jats:styled-content> and <jats:styled-content style=\"fixed-case\">ENA<\/jats:styled-content> serology by passive transfer of autoantibodies. We hypothesize that such autoantibodies may be causally related to disease manifestations in some recipients.<\/jats:p><\/jats:sec>","DOI":"10.1111\/trf.12922","type":"journal-article","created":{"date-parts":[[2014,11,13]],"date-time":"2014-11-13T08:35:18Z","timestamp":1415867718000},"page":"832-837","source":"Crossref","is-referenced-by-count":23,"title":["Anti\u2010<scp>SSA<\/scp> antibodies are present in immunoglobulin preparations"],"prefix":"10.1111","volume":"55","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-3113-6587","authenticated-orcid":false,"given":"Renate G.","family":"van der Molen","sequence":"first","affiliation":[{"name":"Department of Laboratory Medicine Laboratory for Medical Immunology Radboud University Medical Center  Nijmegen the Netherlands"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D\u00f6rte","family":"Hamann","sequence":"additional","affiliation":[{"name":"Department of Immunopathology and Blood Coagulation Sanquin Diagnostic 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