1. The Etiology of the Antiphospholipid Syndrome
- Author
-
Sara De Carolis, Rotem Inbar, Yehuda Shoenfeld, C. Garufi, Miri Blank, and Giuseppina Monteleone
- Subjects
biology ,business.industry ,medicine.medical_treatment ,Congenital cytomegalovirus infection ,medicine.disease_cause ,medicine.disease ,Molecular mimicry ,immune system diseases ,Antiphospholipid syndrome ,Hemostasis ,Fibrinolysis ,Immunology ,biology.protein ,medicine ,Platelet ,Antibody ,business ,neoplasms ,Protein C ,medicine.drug - Abstract
Antiphospholipid syndrome (APS) is a systemic syndrome whose etiology involves both environmental and genetic factors. Infections may play an important part in the etiology by using different mechanisms, predominantly molecular mimicry, to induce antiphospholipid antibodies (aPL). aPL are often associated with false-positive serological tests for toxoplasmosis, rubella, cytomegalovirus, herpes, human immunodeficiency virus, Lyme disease, and syphilis. A higher prevalence of aPL has been seen in the serum of patients of similar descent, and in mouse models. The hypercoagulable state in APS involves all three major components governing hemostasis: platelets, fibrinolysis, and the coagulation cascade. aPL inhibit both protein C activation and the function of activated protein C, thereby preventing the inactivation of activated factor V and VIII. Potentiation of the procoagulant activity of human umbilical vein endothelial cells by aPL is strongly decreased after depleting IgG from the serum.
- Published
- 2020
- Full Text
- View/download PDF