Journal article

Blockade of maternal anti-HPA-1a-mediated platelet clearance by an HPA-1a epitope-specific F(ab')2 in an in vivo mouse model of alloimmune thrombocytopenia


Authors listBakchoul, Tamam; Boylan, Brian; Sachs, Ulrich J. H.; Bein, Gregor; Ruan, Changgeng; Santoso, Sentot; Newman, Peter J.

Publication year2009

Pages265-270

JournalTransfusion

Volume number49

Issue number2

ISSN0041-1132

Open access statusGreen

DOI Linkhttps://doi.org/10.1111/j.1537-2995.2008.01972.x

PublisherWiley


Abstract

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.

Resting human PLTs from HPA-1ab heterozygous donors were injected into nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice. Purified F(ab')(2) fragments of SZ21 or control immunoglobulin G (IgG) were injected intraperitoneally 30 minutes before introduction of HPA-1a antibodies. Blood samples were taken periodically and analyzed by flow cytometry to determine the percentage of circulating human PLTs.

Anti-HPA-1a IgG from NAIT cases were able to efficiently clear HPA-1a-positive PLTs from murine circulation. Administration of SZ21 F(ab')(2) fragments not only inhibited binding of HPA-1a antibodies to circulating human PLTs, preventing their clearance, but also displaced bound HPA-1a antibodies from the PLT surface.

F(ab')(2) fragments of HPA-1a-selective MoAb SZ21 effectively inhibit anti-HPA-1a-mediated clearance of human PLT circulating in an in vivo NOD/SCID mouse model. These results suggest that agents that inhibit binding of anti-HPA-1a to PLTs may have therapeutic potential in the treatment of NAIT.




Citation Styles

Harvard Citation styleBakchoul, T., Boylan, B., Sachs, U., Bein, G., Ruan, C., Santoso, S., et al. (2009) Blockade of maternal anti-HPA-1a-mediated platelet clearance by an HPA-1a epitope-specific F(ab')2 in an in vivo mouse model of alloimmune thrombocytopenia, Transfusion, 49(2), pp. 265-270. https://doi.org/10.1111/j.1537-2995.2008.01972.x

APA Citation styleBakchoul, T., Boylan, B., Sachs, U., Bein, G., Ruan, C., Santoso, S., & Newman, P. (2009). Blockade of maternal anti-HPA-1a-mediated platelet clearance by an HPA-1a epitope-specific F(ab')2 in an in vivo mouse model of alloimmune thrombocytopenia. Transfusion. 49(2), 265-270. https://doi.org/10.1111/j.1537-2995.2008.01972.x



Keywords


FETALGPVIIIIaP1(A1)

Last updated on 2025-10-06 at 09:46