Natalizumab in multiple sclerosis: discontinuation, progressive multifocal leukoencephalopathy and possible use in children
Document Type
Article
Abstract
In the early 1990s, attention was drawn to the migration of immune cells into the central nervous system via the blood-brain barrier. The literature showed that lymphocytes binding to the endothelium were successfully inhibited by an antibody against α4β1 integrin. These biological findings resulted in the development of a humanized antibody to α4 integrin - natalizumab (NTZ) - to treat multiple sclerosis (MS). Here, we provide a systematic review and meta-analysis on the efficacy and safety of natalizumab, trying to answer the question whether its use may be recommended both in adult and in pediatric age groups as standard MS treatment. Our results highlight the improvement of clinical and radiological findings in treated patients (p < 0.005), confirming NTZ efficacy. Nevertheless, if NTZ is shown to be efficient, further studies should be performed to evaluate its safety and to target the MS profile that could benefit from this treatment.
Medical Subject Headings
Antibodies, Monoclonal, Humanized (administration & dosage, therapeutic use); Child; Clinical Protocols; Humans; Leukoencephalopathy, Progressive Multifocal (drug therapy); Multiple Sclerosis (drug therapy); Natalizumab (administration & dosage, therapeutic use)
Publication Date
1-1-2015
Publication Title
Expert review of neurotherapeutics
E-ISSN
1744-8360
Volume
15
Issue
11
First Page
1321
Last Page
41
PubMed ID
26513633
Digital Object Identifier (DOI)
10.1586/14737175.2015.1102061
Recommended Citation
Vitaliti, Giovanna; Matin, Nassim; Tabatabaie, Omidreza; Di Traglia, Mario; Pavone, Piero; Lubrano, Riccardo; and Falsaperla, Raffaele, "Natalizumab in multiple sclerosis: discontinuation, progressive multifocal leukoencephalopathy and possible use in children" (2015). Neurology. 1511.
https://scholar.barrowneuro.org/neurology/1511