Circulating Immune Complexes and Glomerulonephritis in a Patient with Congenital Absence of the Third Component of Complement

Abstract
THE third component of complement (C3) is critically involved in host defense and the maintenance of normal immunologic homeostasis.1 , 2 It is a central component of both the classical and alternative pathways of complement, and its major cleavage product, C3b, serves as an important serum opsonin.1 , 2 Another cleavage product, C3a, is a potent anaphylatoxin that is thought to be important in the initiation of local inflammatory processes.1 , 2 Therefore, attention has focused on infection as the major clinical problem in the rare patients with congenital C3 deficiency3 4 5 6 7 or marked C3 consumption.8 , 9 In the present report, we describe a patient with a congenital . . .