Secondary Hypogammaglobulinaemia — RACP Adult Medicine MCQ
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Correct answer: D — Immunoglobulin replacement therapy
Secondary hypogammaglobulinaemia can occur with B-cell depleting therapies (rituximab most commonly) and other immunosuppressants. When IgG is significantly reduced (<4 g/L) with recurrent infections, immunoglobulin replacement therapy (IVIg or SCIg) should be considered. This allows continuation of effective immunosuppressive therapy while reducing infection risk. Simply stopping immunosuppression may lead to disease flare without resolving the hypogammaglobulinaemia.
Reference: eTG – 2025 – Immunology; ASCIA – 2024 – Secondary Immunodeficiency Guidelines