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Updated: Jun 23, 2026
Development of Antibiotic Resistance
Published on: June 12, 2025
The lupus anticoagulant/antiphospholipid syndrome
1Cardeza Foundation for Hematologic Research, Department of Medicine, Jefferson Medical College of Thomas Jefferson University, Philadelphia, Pennsylvania 19107-5099, USA.
Antiphospholipid syndrome involves antibodies targeting protein-phospholipid complexes, increasing risks of thrombosis and fetal loss. Current management focuses on long-term anticoagulation for thrombotic risk.
Area of Science:
- Immunology
- Hematology
- Obstetrics
Background:
- Antiphospholipid syndrome (APS) is linked to thrombosis, recurrent fetal loss, and thrombocytopenia.
- Pathogenesis of APS remains poorly understood despite strong clinical associations.
Purpose of the Study:
- To review diagnostic methods for APS.
- To discuss current understanding of APS pathogenesis.
- To outline anticoagulation strategies for managing thrombotic risk in APS.
Main Methods:
- Review of current literature on antiphospholipid antibodies and APS.
- Analysis of diagnostic assays for lupus anticoagulants (LACs) and anticardiolipin antibodies (ACAs).
- Discussion of emerging pathogenetic mechanisms and therapeutic approaches.
Main Results:
- Lupus anticoagulants and anticardiolipin antibodies are likely directed against protein-phospholipid complexes, not phospholipids alone.
- Other unrecognized protein-phospholipid complexes may contribute to APS.
- Long-term anticoagulation is the primary treatment for thrombotic risk.
Conclusions:
- Understanding APS pathogenesis is evolving, shifting focus to protein-phospholipid interactions.
- Accurate diagnosis and risk stratification are crucial for managing APS.
- Anticoagulation remains the cornerstone of thrombotic risk management in APS.
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