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Advanced Diagnostic Laboratories

Factor I Level


Test Code

FIL

Description

The complement system is part of our innate immune response. It is vital to our defense against invasive microorganisms. Complement activation can occur through the classical, lectin and alternative pathway, which then converge to a common terminal pathway. Complement activation is controlled by multiple proteins at various steps in each pathway to prevent injury to autologous tissues. Factor I is the key regulator of the complement pathways due to its ability to degrade activated complement proteins C3b and C4b in the presence of cofactors such as factor H, C4b-binding protein, complement receptor 1 or CD46. 

The factor I RID assay is a method for quantitation of the complement regulatory factor I protein. Complete deficiency of factor I can lead to complement consumption resulting in severe recurrent infections, glomerulonephritis or autoimmune disease. Low or absent factor I levels can be associated with low C3 levels