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Human Reproduction Update Advance Access published online on November 11, 2006

Human Reproduction Update, doi:10.1093/humupd/dml051
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© The Author 2006. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
Received July 13, 2006
Revised September 18, 2006
Accepted October 9, 2006

Article

Pathogenic role of anti-{beta}2-glycoprotein I antibodies on human placenta: functional effects related to implantation and roles of heparin

N. Di Simone 1 *, P.L. Meroni 2, M. D’Asta 1, F. Di Nicuolo 1, M.C. D’Alessio 1, and A. Caruso 1

1 Department of Obstetrics and Gynecology, Catholic University of Sacred Heart, Rome, Italy
2 Allergy, Clinical Immunology and Rheumatology Unit, IRCCS, Istituto Auxologico Italiano, Milan, Italy

* To whom correspondence should be addressed.
N. Di Simone, E-mail: nicolettadisimone{at}rm.unicatt.it


   Abstract

Most of the clinical manifestations of the antiphospholipid syndrome (APS) can be related to thrombotic events; however, placental thrombosis cannot explain all of the pregnancy complications that occur in women with this syndrome. In this regard, it has been hypothesized that antiphospholipid (aPL) antibodies can directly attack trophoblasts, but it is still unclear what pathogenetic mechanisms play a role and which aPL antibodies subpopulations are involved. Although it has been assumed that aPL antibodies are directed against anionic phospholipids (PLs), current advances in the field suggest that antibodies to PL-binding plasma protein such as {beta}2-glycoprotein-I ({beta}2-GPI) are the clinically relevant aPL antibodies. It appears that following the attachment of {beta}2-GPI to PLs, both molecules undergo conformational changes that result in the exposure of cryptic epitopes within the structure of {beta}2- GPI allowing the subsequent binding of antibodies. aPL antibodies detected by anti-{beta}2-GPI assays are associated with fetal loss. However, there is still debate on how the antibodies might induce the obstetrical manifestations. The significantly improved outcome of pregnancies treated with heparin has stimulated interest in the drug’s mechanisms of action. Several mechanisms could explain its beneficial effects, because in addition to a direct effect of heparin on the coagulation cascade, it might protect pregnancies by reducing the binding of aPL antibodies, reducing inflammation, facilitating implantation and/or inhibiting complement activation. Further investigations are needed to better understand how aPL antibodies induce obstetric complications and to better clarify the functional role of heparin in the human placenta leading to more successful therapeutic options.

Keywords: placenta/antiphospholipid syndrome/{beta}2-glycoprotein I/heparin/antiphospholipid antibodies.
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Ann. N. Y. Acad. Sci.Home page
N. DI SIMONE, M. P. LUIGI, D. MARCO, D. N. FIORELLA, D. SILVIA, D. M. CLARA, and C. ALESSANDRO
Pregnancies Complicated with Antiphospholipid Syndrome: The Pathogenic Mechanism of Antiphospholipid Antibodies: A Review of the Literature
Ann. N.Y. Acad. Sci., June 1, 2007; 1108(1): 505 - 514.
[Abstract] [Full Text] [PDF]



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