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Updated: Jan 12, 2026

Anti-Nuclear Antibody Screening Using HEp-2 Cells
Published on: June 23, 2014
[Anti-rituximab antibodies in autoimmune diseases and hematologic malignancies: An update]
Maxime Teisseyre1, Marco Allinovi2, Michael Levraut3
1Centre de référence maladies rares - syndrome néphrotique idiopathique et glomérulonéphrite extra-membraneuse, Centre Hospitalier Universitaire de Nice, Université Côte d'Azur, Nice, France; Laboratoire d'immunologie et de thérapie cellulaire, Centre Hospitalier Universitaire de Nice, Université Côte d'Azur, Nice, France; Service de néphrologie, dialyse et transplantation, Centre Hospitalier Universitaire de Nice, Université Côte d'Azur, Nice, France; Institut de recherche sur le cancer et vieillissement, UMR7284, CNRS, Inserm U1081, Université Côte d'Azur, Nice, France.
Abstract:
Rituximab, a chimeric monoclonal antibody targeting the CD20, is a key therapy for treating haematological malignancies and numerous autoimmune diseases. However, its use may be complicated by the occurrence of anti-drug antibodies (ADA), which reflect its immunogenicity. This immunogenicity varies depending on the clinical context: it remains rare in oncology, but is more common in autoimmune diseases. These ADAs may be neutralising or non-neutralising and may influence pharmacokinetics, B-cell depletion, clinical efficacy and the risk of hypersensitivity reactions. Their occurrence is influenced by multiple factors: drug characteristics, administration methods, treatment regimen, but also patient-specific parameters. To limit immunogenicity, several approaches are being studied, such as optimising treatment regimens, combining with immunosuppressants, or using alternative humanised or fully human antibodies. This review provides an updated summary of anti-rituximab antibodies and highlights the importance of a personalised monitoring strategy to optimise the management of patients treated with rituximab.
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