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Microbiology · Immunology: complement levels in active lupus
Sample itemA patient with systemic lupus erythematosus develops a flare with nephritis, and serum C3 and C4 are both markedly low. What is the best explanation?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Immune complexes consume complement through the classical pathway
In active lupus, circulating and deposited immune complexes activate the classical pathway, consuming C1q, C4 and C3, so levels fall as disease activity rises. Serial complement levels and anti-dsDNA titres are used to follow disease activity. Low C4 with normal C3 is more characteristic of hereditary angioedema.
Option by option
A. Immune complexes consume complement through the classical pathway (correct)
Correct. Classical pathway activation by immune complexes depletes C4 and C3.
B. Loss of CD59 from red cells
CD59 loss is the defect in paroxysmal nocturnal haemoglobinuria and does not lower serum complement.
C. Inherited absence of C1 inhibitor
C1 inhibitor deficiency causes hereditary angioedema, with low C4 but usually normal C3.
D. Failure of hepatic synthesis of all complement proteins
Hepatic synthetic failure is not the mechanism of low complement in a lupus flare.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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