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Single Cell Collection of Trophoblast Cells in Peri-implantation Stage Human Embryos
Published on: June 12, 2020
Antiphospholipid antibodies in implantation failures
1HLA-Vascular Biology Laboratory, St Francis Hospital and Health Centers, Indiana/Purdue Universities at Indianapolis, Indianapolis, IN 46107, USA. john.mcintyre@ssfhs.org
Antiphospholipid antibodies (aPL), particularly those targeting phosphatidylserine (aPS) and phosphatidylethanolamine (aPE), are implicated in implantation failure and recurrent pregnancy loss. These antibodies can disrupt trophoblast function and potentially interfere with early embryonic development.
Area of Science:
- Immunology
- Cell Biology
- Reproductive Biology
Background:
- Plasma membranes exhibit asymmetric distribution of amino phospholipids like phosphatidylserine (PS) and phosphatidylethanolamine (PE).
- This asymmetry is maintained by aminophospholipid translocase (flipase) and disrupted by scramblase during cell activation, injury, or apoptosis.
- Developing trophoblasts uniquely externalize PS during differentiation.
Purpose of the Study:
- To review the role of antiphospholipid antibodies (aPL) in implantation failure and pregnancy loss.
- To explore the impact of antibodies to PS (aPS) and PE (aPE) on trophoblast function and early embryogenesis.
Main Methods:
- Analysis of published and unpublished data.
- Review of experimental models (animal and in vitro) investigating aPL effects on trophoblast.
- Consideration of cell division mechanisms involving PE.
Main Results:
- Antiphospholipid antibodies (aPL), especially aPS, target trophoblasts, leading to destruction, inhibited syncytium formation, reduced hCG production, and limited invasion.
- Anticardiolipin (aCL) antibodies, though not present on trophoblasts, are implicated in pathology and cross-react with aPS.
- Antibodies to PE (aPE) are associated with recurrent pregnancy loss and may interfere with embryonic cell division.
Conclusions:
- A role for aPL in implantation failure and occult pregnancy loss is proposed.
- Further investigation into the mechanisms of aPE in early pregnancy complications is warranted.
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