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Dynamic nature of maternal multiple RBC alloantibodies after vaccination: Case report and immunological mechanisms
Hana Safić Stanić1, Zrinka Kruhonja Galić1, Iva Lucija Burnać2
1Department for RBC Imunohematology, Croatian Institute for Transfusion Medicine, Zagreb, Croatia.
Red blood cell (RBC) alloimmunization in pregnancy remains a major cause of hemolytic disease of the fetus and newborn (HDFN). Multiple maternal alloantibodies are uncommon and present significant diagnostic, and transfusion challenges. We report a case of a 35-year-old gravida, with anti-D, anti-C, anti-Fya, and anti-M alloantibodies detected at 10 weeks gestation. Initial titers of anti-D and anti-C were low and stable under serial monitoring. Non-invasive fetal genotyping confirmed an RHD-positive fetus. Following routine maternal vaccination against influenza (28 weeks), pertussis (30 weeks), and RSV (32 weeks), a rapid rise in anti-D and anti-C titers was observed at 31-32 weeks, accompanied by increased serologic reactivity of anti-Fya and anti-M. Middle cerebral artery peak systolic velocity (MCA-PSV) rose to 1.7 MoM, indicating fetal anemia. Two intrauterine transfusions with antigen-negative RBCs were performed. The patient delivered at 37 weeks. The neonate required phototherapy, IVIG, and transfusion support but had a favorable outcome. The temporal association between vaccination and antibody escalation raised the question of immune modulation. Although molecular mimicry is unlikely, non-specific polyclonal immune activation with bystander stimulation of memory B cells may represent a biologically plausible mechanism. However, causality cannot be established. This case highlights the dynamic nature of multiple maternal alloimmunizations, the critical role of serial monitoring and logistical challenges of providing antigen-negative blood for IUT.
Red blood cell (RBC) alloimmunization in pregnancy remains a major cause of hemolytic disease of the fetus and newborn (HDFN). Multiple maternal alloantibodies are uncommon and present significant diagnostic, and transfusion challenges. We report a case of a 35-year-old gravida, with anti-D, anti-C, anti-Fya, and anti-M alloantibodies detected at 10 weeks gestation. Initial titers of anti-D and anti-C were low and stable under serial monitoring. Non-invasive fetal genotyping confirmed an RHD-positive fetus. Following routine maternal vaccination against influenza (28 weeks), pertussis (30 weeks), and RSV (32 weeks), a rapid rise in anti-D and anti-C titers was observed at 31-32 weeks, accompanied by increased serologic reactivity of anti-Fya and anti-M. Middle cerebral artery peak systolic velocity (MCA-PSV) rose to 1.7 MoM, indicating fetal anemia. Two intrauterine transfusions with antigen-negative RBCs were performed. The patient delivered at 37 weeks. The neonate required phototherapy, IVIG, and transfusion support but had a favorable outcome. The temporal association between vaccination and antibody escalation raised the question of immune modulation. Although molecular mimicry is unlikely, non-specific polyclonal immune activation with bystander stimulation of memory B cells may represent a biologically plausible mechanism. However, causality cannot be established. This case highlights the dynamic nature of multiple maternal alloimmunizations, the critical role of serial monitoring and logistical challenges of providing antigen-negative blood for IUT.
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