Neurofilament light antibodies in serum reflect response to natalizumab treatment in multiple sclerosis

Author:

Amor Sandra12,van der Star Baukje J2,Bosca Isabel13,Raffel Joel1,Gnanapavan Sharmilee1,Watchorn Jonathan1,Kuhle Jens1,Giovannoni Gavin1,Baker David1,Malaspina Andrea1,Puentes Fabiola1

Affiliation:

1. Neuroimmunology Unit, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK

2. Department of Pathology, VU University Medical Center and MS Center, Amsterdam, The Netherlands

3. MS Unit, Neurology Department, La Fe University Hospital, Valencia, Spain

Abstract

Background: Increased levels of antibodies to neurofilament light protein (NF-L) in biological fluids have been found to reflect neuroinflammatory responses and neurodegeneration in multiple sclerosis (MS). Objective: To evaluate whether levels of serum antibodies against NF-L correlate with clinical variants and treatment response in MS. Methods: The autoantibody reactivity to NF-L protein was tested in serum samples from patients with relapsing–remitting MS (RRMS) ( n=22) and secondary progressive MS (SPMS) ( n=26). Two other cohorts of RRMS patients under treatment with natalizumab were analysed cross-sectionally ( n=16) and longitudinally ( n=24). The follow-up samples were taken at 6, 12, 18 and 24 months after treatment, and the NF-L antibody levels were compared against baseline levels. Results: NF-L antibodies were higher in MS clinical groups than healthy controls and in RRMS compared to SPMS patients ( p<0.001). NF-L antibody levels were lower in natalizumab treated than in untreated patients ( p<0.001). In the longitudinal series, NF-L antibody levels decreased over time and a significant difference was found following 24 months of treatment compared with baseline measurements ( p=0.001). Conclusions: Drug efficacy in MS treatment indicates the potential use of monitoring the content of antibodies against the NF-L chain as a predictive biomarker of treatment response in MS.

Publisher

SAGE Publications

Subject

Clinical Neurology,Neurology

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