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Physiology · Immunity: complement
Sample itemA 20-year-old man has had two episodes of meningococcal meningitis. A total haemolytic complement (CH50) assay is near zero. Which defect is most likely?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. Deficiency of a terminal component, C5 to C9, preventing membrane attack complex formation
The membrane attack complex formed by C5b to C9 punctures the outer membrane of Gram-negative diplococci such as Neisseria. Terminal complement deficiency causes recurrent Neisseria infection with a very low CH50. Other complement defects present differently.
Option by option
A. Deficiency of C1 esterase inhibitor
C1 esterase inhibitor deficiency causes hereditary angioedema, not recurrent meningitis.
B. Deficiency of a terminal component, C5 to C9, preventing membrane attack complex formation (correct)
Correct. Loss of the membrane attack complex leaves Neisseria insufficiently lysed.
C. Deficiency of decay accelerating factor (CD55)
CD55 deficiency causes complement-mediated lysis of red cells in paroxysmal nocturnal haemoglobinuria.
D. Deficiency of the immunoglobulin heavy chain gene
A heavy chain defect gives agammaglobulinaemia, with a normal CH50.
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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