The Role of Defective Complement Control in Hemolytic Uremic Syndrome

ABSTRACT

Atypical hemolytic uremic syndrome (HUS) is a severe disease that is characterized by microangiopathic hemolytic anemia, thrombocytopenia, and acute renal failure. Recent evidence has shown that defective complement activation and defective complement control is a cause of HUS. So far, mutations in single genes coding for the cofactor and complement regulator factor H, the membrane cofactor protein (MCP/CD46), the serine protease factor I, and autoantibodies to factor H have been linked to HUS. All of these proteins affect the same enzyme the alternative pathway convertase C3bBb. This article explains how alternative pathway activation proceeds and how defective control increases activation, which ultimately leads to endothelial cell damage.

KEYWORDS

Complement control - alternative pathway - hemolytic uremic syndrome (HUS) - membrane-proliferative glomerulonephritis (MPGN) - factor H - membrane cofactor protein (MCP) - factor I - autoantibodies

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