Ontology highlight
ABSTRACT: Background
Neonatal alloimmune thrombocytopenia (NAIT) is most commonly caused by transplacental passage of maternal human platelet-specific alloantigen (HPA)-1a antibodies that bind to fetal platelets (PLTs) and mediate their clearance. SZ21, a monoclonal antibody (MoAb) directed against PLT glycoprotein IIIa, competitively inhibits the binding of anti-HPA-1a alloantibodies to PLTs in vitro. The purpose of this investigation was to determine whether SZ21 F(ab')(2) fragments might be therapeutically effective in inhibiting or displacing maternal HPA-1a antibodies from the fetal PLT surface and preventing their clearance from circulation.Study design and methods
Resting human PLTs from HPA-1ab heterozygous donors were injected into nonobese diabetic/severe combined immunodef
SUBMITTER: Bakchoul T
PROVIDER: S-EPMC4154534 | biostudies-literature | 2009 Feb
REPOSITORIES: biostudies-literature