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Anti-Phospholipid Antibodies And Infertility

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Abstract

Antiphospholipid syndrome (APS) or the presence of antiphospholipid antibodies (aPL), usually presents as pregnancy loss. However, aPL have also been reported to affect implantation, placentation, and early embryonic development. The binding of aPl to β2GP1 may lead to breakdown of the phospholipid adhesion molecules between different elements of trophoblast. As aPL affect placental growth and function, aPl may prevent implantation presenting as infertility. Lupus anticoagulant and anticardiolipin antibody have been implicated in the prothrombotic effects of APS. Antibodies to other phospholipids such as anti-phosphatidylserine, phosphatidyl ethanolamine, phosphatidyl choline, phosphatidyl glycerol, phosphatidyl Inositol etc. may be more relevant in infertility. Their role remains to be clarified. There is theoretical evidence from animal models and clinical infertility practice that aPL has a role in infertility. However, a large-scale meta-analysis has failed to confirm the association. To determine whether infertility or even pregnancy loss is associated with aPL, it is necessary to know that the embryo is chromosomally normal. Pregestational diagnosis has shown that up to 60% of embryos may be chromosomally aneuploid in failed in vitro fertilization (IVF); hence, may confound our understanding concerning the association between aPL and infertility, failed IVF or even pregnancy loss.

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Authors and Affiliations

  1. Department of Obstetrics & Gynecology, Sheba Medical Center, Tel Hashomer, 52621, Israel

    H. J. A. Carp

  2. University of Tel Aviv, Tel Aviv, Israel

    H. J. A. Carp

  3. Department of Internal Medicine B and Center for Autoimmune Diseases, Sheba Medical Center, Tel Hashomer, Israel

    Y. Shoenfeld

  4. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

    Y. Shoenfeld

Authors
  1. H. J. A. Carp
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  2. Y. Shoenfeld
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Correspondence to H. J. A. Carp.

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Carp, H.J.A., Shoenfeld, Y. Anti-Phospholipid Antibodies And Infertility. Clinic Rev Allerg Immunol 32, 159–161 (2007). https://doi.org/10.1007/s12016-007-0010-2

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