Persistent hypogammaglobulinemia after rituximab therapy in pediatric patients, prevalence and clinical outcomes

• Over 50 % of children had low IgG levels and/or required IGRT following rituximab therapy. • Persistent hypogammaglobulinemia was linked to low baseline IgG/IgM and recurrent infections. • Children with hypogammaglobulinemia after RTX often require IGRT, face recurrent infections, and may develop Ig class-switch defects. Hypogammaglobulinemia is a known side effect of rituximab (RTX) in adults, but its prevalence and persistence in children remain underexplored. This retrospective cohort study at a tertiary care center examines the prevalence and clinical outcomes of hypogammaglobulinemia in pediatric patients after RTX therapy. Patients aged ≤ 18 years treated with RTX for various indications between 2000 and 2020 were included. Patients were classified as having hypogammaglobulinemia when (1) IgG levels were <-2 SD below reference for age, or (2) when they received immunoglobulin replacement therapy (IGRT) for the indication hypogammaglobulinemia. Hypogammaglobulinemia after RTX treatment was observed in 74/134 patients (55.2 %). Persistent hypogammaglobulinemia (>6 months) was observed in 46/91 patients (50.5 %), of whom 9 patients remained hypogammaglobulinemic >5 years. Low baseline IgG and IgM levels were significantly associated with persistent hypogammaglobulinemia, while patients receiving RTX therapy for autoimmune diseases were less frequently affected. CD19 + B cells reconstituted in a median of 11 months ( IQR =[7.3–18.0]), while CD19 + CD27 + IgG + switched memory B cells took significantly longer, with a median of 1.8 years ( IQR =[1.0–2.9]). Three patients developed class-switch recombination-deficiencies and never recovered. Recurrent infections, of which two fatal, were recorded in 18 patients and were significantly more prevalent in those with persistent hypogammaglobulinemia. In conclusion, over half of children had low IgG levels and/or required IGRT for hypogammaglobulinemia following RTX therapy. Persistent hypogammaglobulinemia was associated with low pre-RTX IgG and/or IgM levels. Children with hypogammaglobulinemia after RTX are often IGRT-dependent, experience recurrent (and sometimes fatal) infections, and may develop secondary immunoglobulin class-switch defects.

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Publication Details

Journal
Clinical Immunology Communications
Published
2025-04-29
DOI
https://doi.org/10.1016/j.clicom.2025.04.001
Citations
1
Primary Topic
Immunodeficiency and Autoimmune Disorders
Type
article
Field-Weighted Citation Impact
0.80
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article

Persistent hypogammaglobulinemia after rituximab therapy in pediatric patients, prevalence and clinical outcomes

Jaap Jan Boelens, Joris M. van Montfrans, Saskia Haitjema, Marc H.A. Jansen et al.
1 citations
Clinical Immunology Communications
Immunodeficiency and Autoimmune Disorders
0.80
article

Persistent hypogammaglobulinemia after rituximab therapy in pediatric patients, prevalence and clinical outcomes

Jaap Jan Boelens, Joris M. van Montfrans, Saskia Haitjema, Marc H.A. Jansen, Mark de Groot, Caroline A. Lindemans, Julia Drylewicz, Annet van Royen‐Kerkhof, Saskia R Veldkamp, Susanna P.C. Höppener
article en
1 citations

Abstract

• Over 50 % of children had low IgG levels and/or required IGRT following rituximab therapy. • Persistent hypogammaglobulinemia was linked to low baseline IgG/IgM and recurrent infections. • Children with hypogammaglobulinemia after RTX often require IGRT, face recurrent infections, and may develop Ig class-switch defects. Hypogammaglobulinemia is a known side effect of rituximab (RTX) in adults, but its prevalence and persistence in children remain underexplored. This retrospective cohort study at a tertiary care center examines the prevalence and clinical outcomes of hypogammaglobulinemia in pediatric patients after RTX therapy. Patients aged ≤ 18 years treated with RTX for various indications between 2000 and 2020 were included. Patients were classified as having hypogammaglobulinemia when (1) IgG levels were <-2 SD below reference for age, or (2) when they received immunoglobulin replacement therapy (IGRT) for the indication hypogammaglobulinemia. Hypogammaglobulinemia after RTX treatment was observed in 74/134 patients (55.2 %). Persistent hypogammaglobulinemia (>6 months) was observed in 46/91 patients (50.5 %), of whom 9 patients remained hypogammaglobulinemic >5 years. Low baseline IgG and IgM levels were significantly associated with persistent hypogammaglobulinemia, while patients receiving RTX therapy for autoimmune diseases were less frequently affected. CD19 + B cells reconstituted in a median of 11 months ( IQR =[7.3–18.0]), while CD19 + CD27 + IgG + switched memory B cells took significantly longer, with a median of 1.8 years ( IQR =[1.0–2.9]). Three patients developed class-switch recombination-deficiencies and never recovered. Recurrent infections, of which two fatal, were recorded in 18 patients and were significantly more prevalent in those with persistent hypogammaglobulinemia. In conclusion, over half of children had low IgG levels and/or required IGRT for hypogammaglobulinemia following RTX therapy. Persistent hypogammaglobulinemia was associated with low pre-RTX IgG and/or IgM levels. Children with hypogammaglobulinemia after RTX are often IGRT-dependent, experience recurrent (and sometimes fatal) infections, and may develop secondary immunoglobulin class-switch defects.

Clinical Immunology CommunicationsVol. 7
Memorial Sloan Kettering Cancer Center (US), Utrecht University (NL), University Medical Center Utrecht (NL), Princess Máxima Center (NL), Wilhelmina Children's Hospital (NL)
Openalex Percentile: Top 29%
Immunodeficiency and Autoimmune Disorders
0.80
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