Age, Low Immunoglobulin G, and M Serum Levels Predict Infections in People With <scp>AQP4</scp> ‐ <scp>IgG</scp> + <scp>NMOSD</scp> Treated With Rituximab—A Multicenter Cohort Study From the German Neuromyelitis Optica Study Group ( <scp>NEMOS</scp> )

Daniel W. Engels(LMU Klinikum), Mariella Herfurth(Leipzig University), Joachim Havla(LMU Klinikum), Patrick Schindler(Humboldt-Universität zu Berlin), Klemens Ruprecht(Humboldt-Universität zu Berlin), Carolin Schwake(St. Josef-Hospital), Marius Ringelstein(Düsseldorf University Hospital), Katinka Fischer(Düsseldorf University Hospital), Charlotte Schubert(Universität Hamburg), Insa Schiffmann(Universität Hamburg), Martin W. Hümmert(Medizinische Hochschule Hannover), Katrin Giglhuber(TUM Klinikum), Sven Jarius(Heidelberg University), Ioannis Vardakas(Universität Ulm), Matthias Grothe(Universität Greifswald), Thorleif Etgen(Kreisklinik Trostberg), C Warnke(Philipps University of Marburg), Jasmin Naumann(Knappschaftsklinikum Saar), FrankA Hoffmann(Martha-Maria Hospital), Makbule Senel(Universität Ulm), Brigitte Wildemann(Heidelberg University), Achim Berthele(TUM Klinikum), Corinna Trebst(Medizinische Hochschule Hannover), Vivien Häußler(Universität Hamburg), Orhan Aktas(Düsseldorf University Hospital), Ilya Ayzenberg(St. Josef-Hospital), Judith Bellmann‐Strobl(Max Delbrück Center), F. Then Bergh(Leipzig University), Tania Kümpfel(LMU Klinikum), Neuromyelitis Optica Study Group (NEMOS)
European Journal of Neurology
February 1, 2026
Cited by 0Open Access
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Abstract

INTRODUCTION: Rituximab is effective and widely used as long-term treatment in aquaporin-4-IgG-positive neuromyelitis optica spectrum disorder (AQP4-IgG+ NMOSD). However, infections remain a significant concern during rituximab treatment. METHODS: We conducted a retrospective multicenter cohort study within the NMO Study Group (NEMOS) in Germany, analyzing demographic and clinical data from people with AQP4-IgG+ NMOSD receiving rituximab or azathioprine by retrospective chart, and compared infection occurrence and severity. For rituximab-treated patients, we collected laboratory data (blood lymphocytes, B-cell counts, serum IgG, IgM, and IgA levels), assessed risk factors for infections, and determined the probability of infection within a 3-month window before and after the laboratory assessment. RESULTS: In 92/170 rituximab and in 12/33 azathioprine treatment episodes, one or more infections were documented. Rituximab and azathioprine showed comparable types and risk of infection (HR = 1.24, 95% CI: 0.68-2.25). Rituximab-treated individuals older than 60 years had a higher risk of infection (HR = 1.62, 95% CI: 1.02-2.57). Hypogammaglobulinemia (IgG < 6.0 g/L: OR = 2.27, 95% CI: 1.15-4.48; IgM < 0.3 g/L: OR = 2.08, 95% CI: 1.05-4.09) predicted infections and the occurrence of both low IgG and IgM serum levels further increased the risk of infection (OR = 2.77, 95% CI: 1.10-6.98) during rituximab treatment. Low IgG and IgA serum levels as well as lymphopenia predicted infection-related hospitalizations. CONCLUSION: Age > 60 years and immunoglobulin serum levels during rituximab treatment may serve as predictors for infection and help to individualize treatment decisions in NMOSD.


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