Persistently positive antiphospholipid antibodies (aPL) in association with thromboses and/or pregnancy morbidity is the hallmark of the antiphospholipid syndrome (APS). The management of aPL-positive patients has been focused on utilizing traditional antithrombotic medications, such as heparin or warfarin. Given that our understanding of the molecular mechanisms of aPL-mediated thrombosis has been growing, this chapter reviews potential “immunomodulatory” approaches (tissue factor inhibition, P38 mitogen-activated protein kinase inhibition, nuclear factor-κB inhibition, platelet glycoprotein receptor inhibition, hydroxychloroquine, statins, inhibition of b2-glycoprotein-I β2GPI and/or anti-β2 GPI binding to target cells, complement inhibition, and B cell inhibition) as well as new oral thrombin and factor Xa inhibitors that will most likely have an important future role in the management of aPL-positive patients.
CITATION STYLE
Erkan, D., Rahman, A., Cohen, H., Machin, S. J., & Pierangeli, S. S. (2012). What are the potential future treatments in antiphospholipid syndrome? In Antiphospholipid Syndrome: Insights and Highlights from the 13Th International Congress on Antiphospholipid Antibodies (pp. 261–287). Springer US. https://doi.org/10.1007/978-1-4614-3194-7_18
Mendeley helps you to discover research relevant for your work.