Platelet Activation Mechanisms and Consequences of Immune Thrombocytopenia

• Published in: Cells (Basel, Switzerland) Switzerland), 2021-12, Vol.10 (12), p.3386
• Main Authors: Sun, Siyu, Urbanus, Rolf T, Ten Cate, Hugo, de Groot, Philip G, de Laat, Bas, Heemskerk, Johan W M, Roest, Mark
• Format: Article
• Language: English
• Subjects: Adaptive immunity; Animals; Antibodies; Antigen-antibody complexes; Antiphospholipid syndrome; Apoptosis; auto-antibodies; Autoantibodies; Autoimmune diseases; autoimmune disorders; Blood clots; Blood platelets; Bone marrow; Complement activation; COVID-19 vaccines; Glycoproteins; Heparin; Humans; Idiopathic thrombocytopenic purpura; Immune clearance; Immune response; immune thrombocytopenia; Immunoglobulins; Immunomodulation; Models, Biological; Molecular modelling; platelet; Platelet Activation; Platelets; Purpura; Purpura, Thrombocytopenic, Idiopathic - blood; Review; Signal Transduction; Structure-function relationships; Systemic lupus erythematosus; Thrombocytopenia; Thrombosis; Vaccines
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells10123386

Autoimmune disorders are often associated with low platelet count or thrombocytopenia. In immune-induced thrombocytopenia (IIT), a common mechanism is increased platelet activity, which can have an increased risk of thrombosis. In addition, or alternatively, auto-antibodies suppress platelet formation or augment platelet clearance. Effects of the auto-antibodies are linked to the unique structural and functional characteristics of platelets. Conversely, prior platelet activation may contribute to the innate and adaptive immune responses. Extensive interplay between platelets, coagulation and complement activation processes may aggravate the pathology. Here, we present an overview of the reported molecular causes and consequences of IIT in the most common forms of autoimmune disorders. These include idiopathic thrombocytopenic purpura (ITP), systemic lupus erythematosus (SLE), antiphospholipid syndrome (APS), drug-induced thrombocytopenia (DITP), heparin-induced thrombocytopenia (HIT), COVID-19 vaccine-induced thrombosis with thrombocytopenia (VITT), thrombotic thrombocytopenia purpura (TTP), and hemolysis, the elevated liver enzymes and low platelet (HELLP) syndrome. We focus on the platelet receptors that bind auto-antibodies, the immune complexes, damage-associated molecular patterns (DAMPs) and complement factors. In addition, we review how circulating platelets serve as a reservoir of immunomodulatory molecules. By this update on the molecular mechanisms and the roles of platelets in the pathogenesis of autoimmune diseases, we highlight platelet-based pathways that can predispose for thrombocytopenia and are linked thrombotic or bleeding events.