Frontiers in Immunology (Aug 2023)

Natalizumab-immunogenicity evaluation in patients with infusion related events or disease exacerbations

  • Nicolás Lundahl Ciano-Petersen,
  • Nicolás Lundahl Ciano-Petersen,
  • Pablo Aliaga-Gaspar,
  • Isaac Hurtado-Guerrero,
  • Virginia Reyes,
  • Virginia Reyes,
  • José Luis Rodriguez-Bada,
  • Eva Rodriguez-Traver,
  • Isabel Brichette-Mieg,
  • Laura Leyva Fernández,
  • Laura Leyva Fernández,
  • Pedro Serrano-Castro,
  • Pedro Serrano-Castro,
  • Pedro Serrano-Castro,
  • Ana Alonso,
  • Ana Alonso,
  • Begoña Oliver-Martos,
  • Begoña Oliver-Martos,
  • Begoña Oliver-Martos

DOI
https://doi.org/10.3389/fimmu.2023.1242508
Journal volume & issue
Vol. 14

Abstract

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IntroductionNatalizumab is a biologic drug for relapsing-remitting multiple sclerosis that may induce the generation of anti-drug antibodies in some patients. Anti-natalizumab antibodies (ANA) increase the risk of adverse events and reduce efficacy, being useful biomarkers for monitoring treatment response.MethodsRetrospective observational study including MS patients treated with natalizumab that experienced infusion-related events (IRE) or disease exacerbations (DE). ANA were tested by Elisa including a screening and a confirmation assay. Patients were further classified as transient (one positive result) or persistent (two or more positive results) ANA.ResultsA total of 1251 MS patients were included and 153 (12.3%) had ANA with at least one single point determination, which were more frequent among patients with IRE compared to those with DE (21,6% vs.10.8%) during the first six infusions. Two or more determinations ANA were performed in 184 patients, being 31.5% permanently positive and 7.1% transiently positive. Interestingly, 26.1% of patients that experienced DE had persistent ANA, while 2.6% were transient. In contrast, 43% of patients with IRE had persistent ANA, and 9.3% had transient antibodies. Patients with persistent antibodies had more frequently high levels at the first sampling compared to patients with transient ANA.ConclusionReal-world evidence shows that the presence of ANA is behind an important percentage of patients treated with natalizumab that experience IRE, as well as DE but in a lower degree. These findings support the need to systematically evaluate ANA towards a personalized management of these patients to avoid undesired complications.

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