Summary of Complement deficiency
Transcript for Complement deficiency
Content Reviewers:Rishi Desai, MD, MPH, Yifan Xiao, MD, Pauline Rowsome, Tanner Marshall, MS, Sam Gillespie, Thomas Bush
Complement deficiencies can either be acquired or inherited, and often result in a weaker immune response to infections.
So let’s start with the proteins that make up the classical pathway - C1, C2, C3, C4, C5, C6, C7, C8, and C9.
And parts of these proteins are designated with lower case letters like “a” or “b”. Pretty easy right?
Now these were numbered, in the order they were discovered, but not the order in which they function.
Generally speaking, each complement protein is normally inactive, and it becomes activated when it’s cleaved - in other words when some part of it breaks free.
A bit like how a fire extinguisher isn’t “active” until a pin is pulled out.
The complement system helps with three important immune processes: inflammation, phagocytosis, and the creation of membrane attack complexes or MACs.
Inflammation is when chemicals and cells collect to protect a damaged or infected area; phagocytosis is when certain white blood cells called phagocytes engulf and digest antigens; and membrane attack complexes are structures which dig into antigen surfaces and lyse them, or rupture and kill them.
There are actually three complement pathways: The classical pathway - called that because it was discovered first, the alternative pathway which was found second and is always at work, and the Lectin binding pathway - which was found third and when folks got more descriptive with their naming.
So all three pathways start out a bit differently, but end the same way - with a membrane attack complex which is a protein complex that creates a hole in a bacterial cell membrane - effectively destroying mainly gram negative bacteria.
The various complement fragments contribute to these three pathways, but also play other additional roles as well.
For example, C3b serves as an opsonin - which means that it helps immune cells phagocytose debris.
C5a and C3a also act as chemotaxins which recruit neutrophils, eosinophils, monocytes, and macrophages to the site of inflammation.
C5a and C3a are also anaphylatoxins which means that they help basophils and mast cells degranulate, releasing proinflammatory molecules like histamine and heparin into an area.
This can cause contraction of the smooth muscles, bronchial constriction, and increased vascular permeability.
Finally, because C1, C2, C3, and C4 are all involved in removing antigen-antibody complexes, individuals that lack any of these proteins can experience a lupus-like illness, chronic renal disease, and repeated infections.
Individuals who are deficient in C5, C6, C7, or C8 suffer from repeated Neisseria infections and are at higher risk for developing gonorrhea or meningitis.
Interestingly, individuals who are deficient in C9 seem to have no problems because C5,C6, C7, C8 can lyse a bacterium all on their own, with C9 being icing on the cake!
In complement deficiency, there’s either too little of one or more of these complement system proteins, or they just don’t function properly.
This can cause an underactive immune response, like in C3 deficiency, since C3 would normally activate the complement system.
In fact, a C3 deficiency causes severe clinical manifestations, because C3 is needed in large quantities.