Natalizumab in cerebrospinal fluid and breastmilk of patients with multiple sclerosis

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Ilaria Callegari - , University of Basel (Author)
  • Mika Schneider - , University of Basel (Author)
  • Vera Aebischer - , University of Basel (Author)
  • Margarete M Voortman - , Medical University of Graz (Author)
  • Undine Proschmann - , Department of Neurology, Neuroimmunological Lab, Center of Clinical Neuroscience (Author)
  • Tjalf Ziemssen - , Department of Neurology, Neuroimmunological Lab, Center of Clinical Neuroscience (Author)
  • Raija Lindberg - , University of Basel (Author)
  • Bettina Fischer-Barnicol - , University of Basel (Author)
  • Michael Khalil - , Medical University of Graz (Author)
  • Ludwig Kappos - , University of Basel (Author)
  • Jens Kuhle - , University of Basel (Author)
  • Nicholas S R Sanderson - , University of Basel (Author)
  • Tobias Derfuss - , University of Basel (Author)

Abstract

BACKGROUND: Natalizumab is a highly effective monoclonal antibody for the treatment of multiple sclerosis (MS), which can diffuse in different anatomical compartments, including cerebrospinal fluid (CSF) and milk.

OBJECTIVES: Starting from incidental detection of natalizumab in the CSF of MS patients, the objective of this study was to develope a flow-cytometry-based assay and apply it to quantify natalizumab in body fluids, including milk collected from nursing patients over 180 days and in patients with neutralizing antibodies against natalizumab.

METHODS: CSF, milk and sera samples from patients with multiple sclerosis were tested by flow-cytometry for binding to a VLA-4 expressing cell line or to a control cell line. A standard curve was prepared by incubating the same cells with natalizumab at 50 μg/ml and serially diluted to 0.005 ng/ml. Binding specificity was confirmed using an anti-natalizumab neutralizing antibody.

RESULTS: Our assay was sensitive enough to detect natalizumab in CSF, with a lower detection limit of 1.5 ng/ml. Neutralizing antibodies against natalizumab inhibited binding to the cell line. In breastmilk, the peak concentration was observed during the first 2 weeks after infusion and the average concentration over the observation time was 173.3 ng/ml, with a trend toward increased average milk concentration over subsequent administrations.

CONCLUSION: Routine use of such an assay would enable a better understanding of the safety of therapeutic antibody administration during pregnancy and lactation.

Details

Original languageEnglish
Pages (from-to)1-8
Number of pages8
JournalTherapeutic advances in neurological disorders
Volume16 (2023)
Publication statusPublished - 30 Jan 2023
Peer-reviewedYes

External IDs

PubMedCentral PMC9896084
Scopus 85147170797
Mendeley 03939f21-cc7b-330a-9dd0-ae93535767eb
ORCID /0000-0001-8799-8202/work/171553548

Keywords

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