Basic and Clinical Researches of Antiphospholipid Syndrome: 2nd Edition

A special issue of Biomedicines (ISSN 2227-9059). This special issue belongs to the section "Immunology and Immunotherapy".

Deadline for manuscript submissions: closed (30 June 2024) | Viewed by 154

Special Issue Editor


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Guest Editor
Immunology Laboratory, Department of Rheumatology, University Medical Centre, Ljubljana, Slovenia
Interests: antiphospholipid syndrome; autoantibodies; diagnostic biomarkers; extracellular vesicles
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

We cordially invite you to contribute your research to the Special Issue titled “Basic and Clinical Researches of Antiphospholipid Syndrome: 2nd Edition”.

Antiphospholipid syndrome (APS) is a systemic autoimmune disorder known as acquired thrombophilia, characterized by vascular thrombosis and/or pregnancy-related morbidity in the presence of persistently positive antiphospholipid antibodies. "Seronegative APS" represents patients who have only clinical manifestations without laboratory confirmation, i.e., those that do not meet the standard classification criteria for APS and are therefore less likely to be treated, which carries the risk of recurrent thrombosis and/or pregnancy loss.

The heterogeneity and non-specificity of potential clinical signs highlight that APS is a true systemic autoimmune disease and underscores the need for a better understanding of disease mechanisms to facilitate a personalized treatment approach. In the general population, the incidence of clinical manifestations of APS is high and could often be triggered by many other underlying factors. Therefore, the diagnosis of APS primarily relies on laboratory measurements. However, current laboratory tests are hampered by technical limitations in the preanalytical and analytical phases.

This Special Issue aims to collate research articles and reviews on the pathogenic mechanisms underlying APS in order to provide new insights at the molecular level and refine understanding on disease development and progression, with the hope of consequently improving APS diagnosis.

Dr. Polona Žigon
Guest Editor

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Keywords

  • antiphospholipid snydrome
  • antiphospholipid antibodies
  • thrombosis
  • obstetric morbidity
  • thrombophilia
  • APS novel markers
  • non-criteria manifestations
  • pathogenesis

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