Natalizumab in cerebrospinal fluid and breastmilk of patients with multiple sclerosis

Author:

Callegari Ilaria12ORCID,Schneider Mika1,Aebischer Vera1,Voortman Margarete M.3,Proschmann Undine4ORCID,Ziemssen Tjalf4,Lindberg Raija1,Fischer-Barnicol Bettina2,Khalil Michael3,Kappos Ludwig2ORCID,Kuhle Jens2,Sanderson Nicholas S.R.12,Derfuss Tobias5

Affiliation:

1. Department of Biomedicine, University of Basel and University Hospital Basel, Basel, Switzerland

2. Neurologic Clinic and Policlinic, MS Center and Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University of Basel, Basel, Switzerland

3. Department of Neurology, Medical University of Graz, Graz, Austria

4. Neuroimmunological Lab, Center of Clinical Neuroscience, Department of Neurology, University Hospital Carl Gustav Carus, Technical University Dresden, Dresden, Germany

5. Department of Biomedicine, University of Basel and University Hospital Basel, Neurologic Clinic and Policlinic, MS Center Petersgraben 4, 4031 Basel, Switzerland

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.

Funder

Schweizerische Multiple Sklerose Gesellschaft

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology,Pharmacology

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