Publication Date:
2013-07-19
Description:
Fetal/neonatal alloimmune thrombocytopenia (FNAIT) is often caused by maternal alloantibodies against the human platelet antigen (HPA)–1a, which opsonizes fetal platelets (PLTs). Subsequent PLT destruction is mediated via the Fc part of the alloantibodies. The monoclonal antibody (mAb) SZ21 binds to the HPA-1a epitope and inhibits the binding of maternal alloantibodies. However, it also promotes complement activation and phagocytosis. Deglycosylation of antibodies abrogates the Fc-related effector functions. We modified the N -glycan of SZ21 by endoglycosidase F. The in vivo transplacental transport of N -glycan–modified (NGM)-SZ21 was not impaired. When injected into pregnant mice, both native-SZ21 and NGM-SZ21 were transported equally into fetal circulation (8.9% vs 8.7%, respectively, P = .58). Neither the binding properties of NGM-SZ21 to HPA-1a in surface plasmon resonance, nor the inhibition of anti–HPA-1a–induced PLT phagocytosis, were affected by N -glycan modification. NGM-SZ21 prevented PLT destruction induced by maternal anti–HPA-1a antibodies in vivo in a mouse model (PLT clearance after 5 hours; 18% vs 62%, in the presence or absence of NGM-SZ21, respectively, P = .013). Deglycosylation of SZ21 abrogates Fc-effector functions without interfering with placental transport or the ability to block anti–HPA-1a binding. Humanized, deglycosylated anti–HPA-1a mAbs may represent a novel treatment strategy to prevent anti–HPA-1a–mediated PLT destruction in FNAIT.
Keywords:
Pediatric Hematology, Thrombocytopenia, Plenary Papers, Free Research Articles, Platelets and Thrombopoiesis
Print ISSN:
0006-4971
Electronic ISSN:
1528-0020
Topics:
Biology
,
Medicine
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