4.2 Article

Emerging Therapies in Antiphospholipid Syndrome

Journal

CURRENT RHEUMATOLOGY REPORTS
Volume 18, Issue 4, Pages -

Publisher

SPRINGER
DOI: 10.1007/s11926-016-0566-z

Keywords

Antiphospholipid syndrome (APS); Pathogenesis; Warfarin; Oral anticoagulants; New treatments; Immunoregulatory agents; In vitro studies; Animal models; Clinical studies

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Antiphospholipid syndrome (APS) is a hypercoagulable state characterized by arterial and venous thromboses and pregnancy morbidity in the presence of antiphospholipid antibodies. Although warfarin remains the main therapeutic choice in APS, there is still concern about its efficacy, safety, and patient compliance. Patients with refractory APS to conventional therapy as well as patients with non-classical manifestations of APS may have alternative treatment approaches. APS pathogenesis has been further elucidated over the past years identifying new molecules as potential new treatment targets. This review summarizes available data from in vitro and animal models and clinical studies on the role of new potential treatment approaches including new oral anticoagulants and immunoregulatory agents: direct thrombin or factor Xa inhibitors, hydroxychloroquine, statins, B cell inhibition, complement inhibition, peptide therapy, nuclear factor kappa B and p38 mitogen-activated kinase inhibitors, defibrotide, abciximab, mTOR inhibitor, and other potential targets. Large multicenter prospective studies of well-characterized APS patients are needed to assess the efficacy and safety profile of these potential treatment alternatives.

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