Journalartikel
Autorenliste: Kjaer, Mette; Geisen, Christof; Akkok, Cigdem Akalin; Wikman, Agneta; Sachs, Ulrich; Bussel, James B.; Nielsen, Kaspar; Walles, Katarina; Curtis, Brian R.; Vidarsson, Gestur; Jaras, Kerstin; Skogen, Bjorn
Jahr der Veröffentlichung: 2020
Zeitschrift: Transfusion and Apheresis Science
Bandnummer: 59
Heftnummer: 1
ISSN: 1473-0502
Open Access Status: Hybrid
DOI Link: https://doi.org/10.1016/j.transci.2019.102712
Verlag: Elsevier
Anti-HPA-1a-antibodies are the main cause of fetal and neonatal alloimmune thrombocytopenia (FNAIT) which may result in intracranial hemorrhage (ICH) and death among fetuses and newborns. Advances in understanding the pathogenesis of FNAIT and proof of concept for prophylaxis to prevent immunization suggest that development of hyperimmune anti-HPA-1a IgG aimed at preventing immunization against HPA-1a and FNAIT is feasible. Anti-HPA-1a IgG can be obtained either by isolating immunoglobulin from already-immunized women or by development of monoclonal anti-HPA-1a antibodies. Here we discuss recent advances that may lead to the development of a prenatal and postnatal prophylactic treatment for the prevention of HPA-1a-associated FNAIT and life-threatening FNAIT-induced complications.
Abstract:
Zitierstile
Harvard-Zitierstil: Kjaer, M., Geisen, C., Akkok, C., Wikman, A., Sachs, U., Bussel, J., et al. (2020) Strategies to develop a prophylaxis for the prevention of HPA-1a immunization and fetal and neonatal alloimmune thrombocytopenia, Transfusion and Apheresis Science, 59(1), Article 102712. https://doi.org/10.1016/j.transci.2019.102712
APA-Zitierstil: Kjaer, M., Geisen, C., Akkok, C., Wikman, A., Sachs, U., Bussel, J., Nielsen, K., Walles, K., Curtis, B., Vidarsson, G., Jaras, K., & Skogen, B. (2020). Strategies to develop a prophylaxis for the prevention of HPA-1a immunization and fetal and neonatal alloimmune thrombocytopenia. Transfusion and Apheresis Science. 59(1), Article 102712. https://doi.org/10.1016/j.transci.2019.102712
Schlagwörter
FC-GAMMA-RIII; FETUS; FNAIT; FUCOSYLATION; GLYCOPROTEIN IIIA; HEMOLYTIC-DISEASE; HPA-1a; HUMAN PLATELET ALLOANTIGEN; IGG