Abstract

Background: There is a lack of knowledge about the evolution of cerebrospinal fluid (CSF) markers in multiple sclerosis (MS) patients undergoing natalizumab treatment. Aim: We aimed to evaluate the effect of natalizumab on basic inflammatory CSF and MRI measures. Methods: Together, 411 patients were screened for eligibility and 93 subjects with ≥2 CSF examinations ≤6 months before and ≥12 months after natalizumab initiation were recruited. The effect of natalizumab on CSF as well as clinical and paraclinical measures was analyzed using adjusted mixed models. Results: Natalizumab induced a decrease in CSF leukocytes (p < 1 × 10−15), CSF protein (p = 0.00007), the albumin quotient (p = 0.007), the IgG quotient (p = 6 × 10−15), the IgM quotient (p = 0.0002), the IgG index (p = 0.0004), the IgM index (p = 0.003) and the number of CSF-restricted oligoclonal bands (OCBs) (p = 0.0005). CSF-restricted OCBs positivity dropped from 94.6% to 86% but 26 patients (28%) had an increased number of OCBs at the follow-up. The baseline to follow-up EDSS and T2-LV were stable; a decrease in the relapse rate was consistent with a decrease in the CSF inflammatory markers and previous knowledge about the effectiveness of natalizumab. The average annualized brain volume loss during the follow-up was −0.50% (IQR = −0.96, −0.16) and was predicted by the baseline IgM index (B = −0.37; p = 0.003). Conclusions: Natalizumab is associated with a reduction of basic CSF inflammatory measures supporting its strong anti-inflammatory properties. The IgM index at the baseline predicted future brain volume loss during the course of natalizumab treatment.

Highlights

  • Multiple sclerosis (MS) is a chronic, demyelinating autoimmune disease

  • The majority of patients were treated with low efficacy disease modifying therapies (DMT) before

  • NTZ induced a reduction of a wide spectrum of basic cerebrospinal fluid (CSF) inflammatory measures such as the number of CSF leukocytes, CSF proteins, albumin quotients and IgG

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Summary

Introduction

Multiple sclerosis (MS) is a chronic, demyelinating autoimmune disease. It is multifactorial in nature due to an interaction between environmental factors and an underlying genetic susceptibility. Natalizumab (NTZ) is a humanized recombinant antibody against α4-integrin and is highly effective in reducing disability progression, relapses and radiological disease activity in RRMS [1,2,3,4]. It acts primarily by inhibiting the interaction between very late activating antigen 4 (VLA-4) (expressed on all leukocytes except neutrophils) and vascular cell adhesion molecule 1 (VCAM-1) (expressed on endothelial cells) and inhibits leukocyte adhesion and migration across the blood-brain barrier (BBB) into the central nervous system (CNS). Markers in multiple sclerosis (MS) patients undergoing natalizumab treatment. CSF-restricted OCBs positivity dropped from 94.6% to 86% but 26 patients (28%)

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