Disclaimer:
This website is intended to assist with patient education and should not be used as a diagnostic, treatment or prescription service, forum or platform. Always consult your own healthcare practitioner for a more personalised and detailed opinion
To determine whether deficiencies or abnormalities in complement system proteins are contributing to increased infections or increased autoimmune activity; to help monitor the activity and treatment of autoimmune diseases and immune complex-related diseases
When you have recurrent microbial (usually bacterial) infections, unexplained inflammation or edema, or symptoms related to an autoimmune disorder; periodically to help monitor a known acute or chronic condition that affects the complement system
A blood sample drawn from a vein in your arm
None
The complement system is complex and composed of a set of more than 30 circulating blood proteins that work together to promote immune and inflammatory responses. Its principal role is to destroy foreign pathogens like bacteria and viruses. The complement system can also be activated when the body makes antibodies against its own tissues that it thinks are foreign (autoantibodies) as happens in autoimmune diseases. Complement tests measure the quantity or activity of complement proteins in the blood.
The complement system is part of the body's innate immune system. Unlike the acquired immune system, which produces antibodies that target and protect against specific threats, the innate immune system is non-specific and can quickly respond to foreign substances. It does not require previous exposure to an invading microorganism or substance and does not maintain a memory of previous encounters.
There are nine primary complement proteins that are designated C1 through C9. These components, in addition to the remaining proteins, work together in a cascade manner by activating, amplifying, breaking apart, and forming complexes that respond to infections, non-self tissues (transplants), dead cells (apoptosis), or inflammation.
Complement activation may be initiated in several different ways.These are termed classical, alternative or lectin pathways.However, the final product from all activation pathways is the same – the formation of the membrane attack complex (MAC).Complement activation causes several things to happen ("complement cascade"):
Complement tests measure the quantity or the function (activity) of complement proteins in the blood.Complement components may be measured individually or together to determine whether the system is functioning normally.C3 and C4 are the most frequently measured complement proteins.Total complement activity (CH50 or CH100) can be measured if a health practitioner suspects a deficiency that is not measured by C3 or C4.CH50 measures the function of the complete classical complement pathway, C1 – C9.If this measurement is outside the normal range, then each of the nine different complement levels can be measured individually to look for hereditary or acquired deficiencies.
A blood sample is obtained by inserting a needle into a vein in the arm.
No test preparation is needed.