Literature DB >> 31587244

Current Anti-HPA-1a Standard Antibodies React with the β3 Integrin Subunit but not with αIIbβ3 and αvβ3 Complexes.

Behnaz Bayat1, Annalena Traum1, Heike Berghöfer1, Silke Werth1, Jieging Zhu2, Gregor Bein1, Ulrich J Sachs1,3, Sentot Santoso1.   

Abstract

BACKGROUND: Fetal/neonatal alloimmune thrombocytopenia (FNAIT) results from maternal alloantibodies (abs) reacting with fetal platelets expressing paternal human platelet antigens (HPAs), mostly HPA-1a. Anti-HPA-1a abs, are the most frequent cause of severe thrombocytopenia and intracranial hemorrhage (ICH).
OBJECTIVES: Titration of anti-HPA-1a in maternal serum using standard National Institute for Biological Standards and Control (NIBSC) 03/152 is one diagnostic approach to predict the severity of FNAIT. Recently, we found three anti-HPA-1a subtypes reacting with the β3 subunit independently or dependently from complexes with αIIb and αv. Endothelial cell-reactive anti-αvβ3 abs were found predominantly in cases with ICH. Our aim was to assess whether available standard material represents all anti-HPA-1a subtypes.
MATERIALS AND METHODS: In this study, anti-HPA-1a sera (NIBSC 03/152) and human monoclonal antibodies (moabs) against HPA-1a (moabs 26.4 and 813) were evaluated using transfected cell lines expressing αIIbβ3, αvβ3 or monomeric cβ3.
RESULTS: Flow cytometry analyses with well-characterized murine moabs recognizing αIIbβ3, αvβ3, or β3 alone demonstrated that AP3 reacts compound-independently, whereas compound-dependent moabs Gi5 and 23C6 reacted only with complexes. NIBSC 03/152, moabs 26.4, and 813 against HPA-1a reacted like AP3, same results were obtained with monomeric cβ3 in immunoblotting. Antigen capture assay targeting endothelial cells showed anti-HPA-1a reactivity disappearance after cβ3 beads adsorption. Furthermore, in contrast to anti-HPA-1a abs from ICH cases, none of NIBSC 03/152, 26.4, and 813 inhibited tube formation.
CONCLUSION: These results suggest that current anti-HPA-1a standard material contains only the anti-β3 subtype. The absence of anti-αvβ3 makes NIBSC 03/152 less suitable as standard to predict the severity of FNAIT. Georg Thieme Verlag KG Stuttgart · New York.

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Year:  2019        PMID: 31587244      PMCID: PMC6827430          DOI: 10.1055/s-0039-1696716

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  31 in total

Review 1.  A review of pathophysiology and current treatment for neonatal alloimmune thrombocytopenia (NAIT) and introducing the Australian NAIT registry.

Authors:  Zoe K McQuilten; Erica M Wood; Helen Savoia; Stephen Cole
Journal:  Aust N Z J Obstet Gynaecol       Date:  2011-02-14       Impact factor: 2.100

2.  Receptor patching and capping of platelet membranes induced by monoclonal antibodies.

Authors:  S Santoso; U Zimmermann; J Neppert; C Mueller-Eckhardt
Journal:  Blood       Date:  1986-02       Impact factor: 22.113

3.  High-resolution mapping of the polyclonal immune response to the human platelet alloantigen HPA-1a (PlA1).

Authors:  Huiying Zhi; Maria Therese Ahlen; Aye Myat Myat Thinn; Hartmut Weiler; Brian R Curtis; Bjørn Skogen; Jieqing Zhu; Peter J Newman
Journal:  Blood Adv       Date:  2018-11-13

Review 4.  Fetal and neonatal alloimmune thrombocytopenia: harvesting the evidence to develop a clinical approach to management.

Authors:  Amanda Symington; Bosco Paes
Journal:  Am J Perinatol       Date:  2010-08-10       Impact factor: 1.862

5.  Clinical and diagnostic comparison of neonatal alloimmune thrombocytopenia to non-immune cases of thrombocytopenia.

Authors:  James B Bussel; Stergios Zacharoulis; Kim Kramer; Janice G McFarland; Joanne Pauliny; Cecile Kaplan
Journal:  Pediatr Blood Cancer       Date:  2005-08       Impact factor: 3.167

6.  The human platelet alloantigens, PlA1 and PlA2, are associated with a leucine33/proline33 amino acid polymorphism in membrane glycoprotein IIIa, and are distinguishable by DNA typing.

Authors:  P J Newman; R S Derbes; R H Aster
Journal:  J Clin Invest       Date:  1989-05       Impact factor: 14.808

7.  HPA-1a alloantibodies reduce endothelial cell spreading and monolayer integrity.

Authors:  Janine M van Gils; Janine Stutterheim; Trynette J van Duijn; Jaap Jan Zwaginga; Leendert Porcelijn; Masja de Haas; Peter L Hordijk
Journal:  Mol Immunol       Date:  2008-11-26       Impact factor: 4.407

8.  Developing recombinant HPA-1a-specific antibodies with abrogated Fcgamma receptor binding for the treatment of fetomaternal alloimmune thrombocytopenia.

Authors:  Cedric Ghevaert; David A Wilcox; Juan Fang; Kathryn L Armour; Mike R Clark; Willem H Ouwehand; Lorna M Williamson
Journal:  J Clin Invest       Date:  2008-08       Impact factor: 14.808

9.  Structure of an extended β3 integrin.

Authors:  Dongwen Zhou; Aye Myat Myat Thinn; Yan Zhao; Zhengli Wang; Jieqing Zhu
Journal:  Blood       Date:  2018-07-17       Impact factor: 22.113

10.  Characterization of a human platelet antigen-1a-specific monoclonal antibody derived from a B cell from a woman alloimmunized in pregnancy.

Authors:  Mariana Eksteen; Heidi Tiller; Maria Averina; Gøril Heide; Mette Kjaer; Cedric Ghevaert; Terje E Michaelsen; Øistein Ihle; Anne Husebekk; Bjørn Skogen; Tor B Stuge
Journal:  J Immunol       Date:  2015-05-13       Impact factor: 5.422

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  1 in total

1.  Naturally occurring point mutation Cys460Trp located in the I-EGF1 domain of integrin β3 alters the binding of some anti-HPA-1a antibodies.

Authors:  Sarah Theresa Holzwarth; Behnaz Bayat; Jieqing Zhu; Roongaroon Phuangtham; Lars Fischer; Doris Boeckelmann; Lida Röder; Heike Berghöfer; Silke Schmidt; Gregor Bein; Sentot Santoso
Journal:  Transfusion       Date:  2020-08-08       Impact factor: 3.157

  1 in total

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