Close

Acquired Drivers of Dysregulation of Complement in C3G

Acquired Drivers of Dysregulation of Complement in C3G

A number of different autoantibodies recognising complement components and their regulators have been identified in C3G. The most common finding is a C3 nephritic factor. These are antibodies that bind to and stabilise C3 convertase resulting in over-activity of the complement system. C3 nephritic factors are found in many cases C3G, typically in ~80% of cases of DDD and ~50% of cases of C3GN. 

Autoantibodies to complement factor H can be found in ~ 15% of cases of C3G. Many of these have been shown to impair the regulatory function of FH resulting in over-activation of complement. More recently, autoantibodies have been identified to the complement components C3 and factor B. Studies have demonstrated their ability to cause dysregulation of complement. 

find out more

Genetic Causes of C3G

find out more

Diagnostic Testing in C3G

find out more

Treatments in C3G

Find out more
Skip to content