Complement deficiency
Complement deficiency is an immunodeficiency of absent or suboptimal functioning of one of the complement system proteins. Because of redundancies in the immune system, many complement disorders are never diagnosed. Some studies estimate that less than 10% are identified. Hypocomplementemia may be used more generally to refer to decreased complement levels, while secondary complement disorder means decreased complement levels that are not directly due to a genetic cause but secondary to another medical condition.
Types
- Disorders of the proteins that act to inhibit the complement system can lead to an overactive response, causing conditions such as hereditary angioedema.
- Disorders of the proteins that act to activate the complement system can lead to an underactive response, causing greater susceptibility to infections.
Signs and symptoms
Complications
for encapsulated organisms is crucial for preventing infections in complement deficiencies. Among the possible complications are the following:- Deficiencies of the terminal complement components increases susceptibility to infections by Neisseria.
Causes
Inherited
- Properdin deficiency is an X-linked disorder that also causes susceptibility to Neisseria infections.
- C1-inhibitor deficiency or hereditary angioedema will have low C4 with normal C1 levels.
Acquired
Mechanism
The mechanism of complement deficiency consists of:- C2: In regard to C2 deficiency, about 5 different mutations in the C2 gene are responsible. In turn, immune function decreases and infection opportunities increase. One of the most common mutations deletes 28 DNA nucleotides from the C2 gene. Therefore, no C2 protein which can help make C3-convertase is produced. Ultimately, this delays/decreases immune response.
- C3: In terms of deficiency of C3, it has been found that 17 mutations in the C3 gene cause problems with C3. This rare condition mutates or prevents C3 protein from forming, lowering the immune system's ability to protect.
- C4: C4 deficiency is highly associated with systemic lupus erythematosus. Aβ42, a protein involved in Alzheimer's disease, can cause activation of C4. At least one study indicates that the genetic variation of C4 plays a role in schizophrenia.
Diagnosis
- CH50 measurement
- Immunochemical methods/test
- C3 deficiency screening
- Mannose-binding lectin
- Plasma levels/regulatory proteins
Treatment
Pneumococcus and Haemophilus infections can be prevented via immunization. Epsilon-aminocaproic acid could be used to treat hereditary C1-INH deficiency, though the possible side effect of intravascular thrombosis should be weighed.