Secondary rituximab-associated versus primary immunodeficiencies: The enigmatic border
Giorgio Ottaviano1, Mayla Sgrulletti2,3, Viviana Moschese2
1Molecular and Cellular Immunology Unit, UCL Institute of Child Health, London, UK.
Rituximab treatment can cause prolonged B-cell deficiency and hypogammaglobulinemia. Identifying patients at risk is crucial for tailored immunology follow-up to detect underlying primary immune deficiencies.
Area of Science:
- Immunology
- Pharmacology
- Genetics
Background:
- Rituximab (RTX) targets CD20-positive cells for immune-related disorders.
- RTX treatment typically allows B-cell reconstitution within months.
- Prolonged B-cell deficiency and hypogammaglobulinemia post-RTX have emerged.
Purpose of the Study:
- To review evidence on post-RTX hypogammaglobulinemia.
- To provide a guideline for identifying high-risk patients.
- To highlight potential inborn errors of immunity.
Main Methods:
- Literature review of studies on RTX and hypogammaglobulinemia.
- Analysis of clinical and immunological manifestations.
- Development of risk stratification criteria.
Main Results:
- Increased incidence of hypogammaglobulinemia reported, especially in children.
- Atypical presentations suggest underlying primary immune deficiencies.
- Identifying RTX-associated hypogammaglobulinemia aids in diagnosing inborn errors of immunity.
Conclusions:
- Post-RTX hypogammaglobulinemia requires careful monitoring.
- Risk stratification can identify patients needing specialized immunology follow-up.
- RTX may unmask genetic immunological disorders.
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