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Title: | Immunotherapeutic strategies in antiphospholipid syndrome | Austin Authors: | Hoi, Alberta Y ;Ross, Laura;Day, Jessica;Buchanan, Russell R C | Affiliation: | Austin Health, Heidelberg, Victoria, Australia Department of Rheumatology, Austin Health, Heidelberg, Victoria, Australia Department of Rheumatology, Monash Health, Melbourne, Victoria, Australia School of Clinical Sciences, Monash University, Victoria, Australia |
Issue Date: | Mar-2017 | Date: | 2016-08-30 | Publication information: | Internal Medicine Journal 2016; 47(3): 250-256 | Abstract: | Antiphospholipid syndrome (APS) is an autoimmune condition, characterized by the persistent presence of antiphospholipid antibodies (aPL) and either thrombosis or obstetric morbidity. The cornerstone of therapy is long-term anticoagulation to reduce morbidity and mortality; however, better understanding of the immunological pathways may direct us to develop future therapeutic strategies. We provide an overview of the current understanding of the immunopathogenesis of this perplexing condition and its associated morbidities and current evidence for some of the immunotherapeutic strategies. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/16247 | DOI: | 10.1111/imj.13245 | Journal: | Internal Medicine Journal | PubMed URL: | https://pubmed.ncbi.nlm.nih.gov/27572264 | Type: | Journal Article | Subjects: | CAPS antiphospholipid syndrome therapeutic options |
Appears in Collections: | Journal articles |
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