What is the role of the complement system in the immune response?
The complement system enhances the immune response by opsonizing pathogens for phagocytosis, promoting inflammation, and forming membrane attack complexes to directly lyse pathogen cell membranes. It bridges innate and adaptive immunity through facilitating immune clearance and maintaining homeostasis.
How does the complement system get activated in the body?
The complement system is activated via three pathways: the classical pathway triggered by antibody-antigen complexes, the lectin pathway activated by mannose-binding lectin binding to pathogen surfaces, and the alternative pathway initiated by spontaneous complement protein hydrolysis and interaction with pathogen surfaces.
What are the components of the complement system?
The complement system consists of over 30 proteins, primarily including C1-C9 (complement components 1 through 9), regulatory proteins, and receptors. The system is activated via three pathways: classical, lectin, and alternative, which play essential roles in immune response, inflammation, and opsonization.
What diseases are associated with dysfunction of the complement system?
Diseases associated with dysfunction of the complement system include autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis, and vasculitis. Additionally, atypical hemolytic uremic syndrome, hereditary angioedema, and age-related macular degeneration can be linked to complement system abnormalities.
How does the complement system interact with antibodies?
The complement system interacts with antibodies primarily through the classical pathway, where antibodies bound to antigens on pathogen surfaces activate complement proteins. This leads to a cascade of reactions that enhance phagocytosis, promote inflammation, and ultimately form a membrane attack complex that can lyse target cells.