Cellular and Molecular Mechanisms of Anti-Phospholipid Syndrome

Autor: Debendra Pattanaik, Marko Z. Radic
Jazyk: angličtina
Rok vydání: 2018
Předmět:
lcsh:Immunologic diseases. Allergy
0301 basic medicine
autoantibodies
Cell
Immunology
neutrophil extracellular traps
Antigen-Antibody Complex
Review
030204 cardiovascular system & hematology
Extracellular Traps
Pathogenesis
Mice
03 medical and health sciences
0302 clinical medicine
Immune system
systemic lupus erythematosus
Pregnancy
medicine
Animals
Humans
beta2 glycoprotein I
Immunology and Allergy
Genetic Predisposition to Disease
Platelet
phospholipids
thrombosis
Coagulation Protein Disorders
coagulation protein disorders
biology
Chemistry
Cell Membrane
Neutrophil extracellular traps
Antiphospholipid Syndrome
Immunity
Innate

Chromatin
Cell biology
anti-phospholipid syndrome
030104 developmental biology
medicine.anatomical_structure
beta 2-Glycoprotein I
Antibodies
Antiphospholipid

biology.protein
Female
Antibody
lcsh:RC581-607
Signal Transduction
Zdroj: Frontiers in Immunology
Frontiers in Immunology, Vol 9 (2018)
ISSN: 1664-3224
DOI: 10.3389/fimmu.2018.00969
Popis: The primary anti-phospholipid syndrome (APS) is characterized by the production of antibodies that bind the phospholipid-binding protein β2 glycoprotein I (β2GPI) or that directly recognize negatively charged membrane phospholipids in a manner that may contribute to arterial or venous thrombosis. Clinically, the binding of antibodies to β2GPI could contribute to pathogenesis by formation of immune complexes or modification of coagulation steps that operate along cell surfaces. However, additional events are likely to play a role in pathogenesis, including platelet and endothelial cell activation. Recent studies focus on neutrophil release of chromatin in the form of neutrophil extracellular traps as an important disease contributor. Jointly, the participation of both the innate and adaptive arms of the immune system in aspects of the APS make the complete understanding of crucial steps in pathogenesis extremely difficult. Only coordinated and comprehensive analyses, carried out in different clinical and research settings, are likely to advance the understanding of this complex disease condition.
Databáze: OpenAIRE