Complement deficiency

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Complement deficiency

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With complement deficiency, there’s a deficiency in one or more of the complement proteins, which are part of the immune system.

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.

Summary

A complement deficiency is a condition in which the body doesn't have enough of the proteins called complements, which work together to fight infection. Complement deficiencies can be inherited or acquired. Inherited complement deficiencies are caused by a change (mutation) in the gene that codes for one of the proteins in the complement system. Acquired complement deficiencies can be caused by infections, cancer, and autoimmune diseases such as lupus. People with an inherited or acquired complement deficiency are at risk of severe infections, including meningitis, sepsis, and pneumonia.

Sources

  1. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  2. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  3. "Yen & Jaffe's Reproductive Endocrinology" Saunders W.B. (2018)
  4. "Bates' Guide to Physical Examination and History Taking" LWW (2016)
  5. "Robbins Basic Pathology" Elsevier (2017)
  6. "THE METABOLISM OF C3 AND C4 IN PATIENTS WITH IMMUNE COMPLEXES AND NORMAL COMPLEMENT LEVELS" Australian and New Zealand Journal of Medicine (1989)
  7. "Clinical Significance of Complement Deficiencies" Annals of the New York Academy of Sciences (2009)
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