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Challenging the dogma: Red blood cell-directed autoimmunity as risk factor for red blood cell alloimmunisation after blood transfusion.
Oud, Josine A; de Haas, Masja; de Vooght, Karen M K; van de Kerkhof, Daan; Som, Nel; Péquériaux, Nathalie C V; Hudig, Francisca; van der Bom, Johanna G; Evers, Dorothea; Zwaginga, Jaap Jan.
Affiliation
  • Oud JA; Center for Clinical Transfusion Research, Sanquin Research, Leiden, The Netherlands.
  • de Haas M; Department of Haematology, Leiden University Medical Center, Leiden, The Netherlands.
  • de Vooght KMK; Department of Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
  • van de Kerkhof D; Center for Clinical Transfusion Research, Sanquin Research, Leiden, The Netherlands.
  • Som N; Department of Haematology, Leiden University Medical Center, Leiden, The Netherlands.
  • Péquériaux NCV; Department of Immunohaematology Diagnostics, Sanquin, Amsterdam, The Netherlands.
  • Hudig F; Central Diagnostic Laboratory, University Medical Center Utrecht, Utrecht, The Netherlands.
  • van der Bom JG; Department of Clinical Chemistry and Haematology, Catharina Hospital, Eindhoven, The Netherlands.
  • Evers D; Department of Clinical Chemistry, Amsterdam University Medical Center, Location VUmc, Amsterdam, The Netherlands.
  • Zwaginga JJ; Department of Clinical Chemistry and Haematology, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.
Br J Haematol ; 204(5): 2103-2111, 2024 May.
Article in En | MEDLINE | ID: mdl-38494337
ABSTRACT
Red blood cell autoimmunity and alloimmunity are potentially linked. Quantification of this association can tailor extensively matched red blood cell transfusions in patients with autoimmunity. Using an incident new-user cohort comprising 47 285 previously non-transfused, non-alloimmunised patients, we compared transfusion-induced red blood cell alloimmunisation incidences in direct antiglobulin test (DAT)-positive and control patients. Additionally, we performed case-control analyses to handle potential confounding by clinical immunomodulators. Among (IgG and/or C3d) DAT-positive patients (N = 380), cumulative red blood cell alloimmunisation incidences after 10 units transfused reached 4.5% (95% confidence interval [CI] 2.5-8.2) versus 4.2% (CI 3.9-4.5, p = 0.88) in controls. In case-control analyses, alloimmunisation relative risks among DAT-positive patients increased to 1.7 (CI 1.1-2.8). Additional adjustments for pre-DAT transfusion exposure or the extent of Rh/K mismatching did not impact results. In conclusion, while patients with DAT positivity show an intrinsically increased alloimmune red blood cell response, their absolute risk is comparable to control patients due to counteracting co-existing immunosuppressive conditions. Consequently, isolated DAT positivity in patients lacking overt haemolysis or complicated alloantibody testing does not seem to warrant extended matching strategies.
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Full text: 1 Database: MEDLINE Main subject: Autoimmunity / Erythrocyte Transfusion / Erythrocytes Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Br J Haematol / Br. j. haematol / British journal of haematology Year: 2024 Type: Article Affiliation country: Netherlands

Full text: 1 Database: MEDLINE Main subject: Autoimmunity / Erythrocyte Transfusion / Erythrocytes Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Br J Haematol / Br. j. haematol / British journal of haematology Year: 2024 Type: Article Affiliation country: Netherlands