Literature DB >> 22183929

Natalizumab remains detectable in patients with multiple sclerosis long after treatment is stopped.

Theo Rispens1, Anke Vennegoor, Gert Jan Wolbink, Chris H Polman, Joep Killestein.   

Abstract

Natalizumab is frequently used as a treatment for multiple sclerosis (MS). The occurrence of progressive multifocal leukoencephalopathy (PML) in natalizumab-treated patients indicates that its prominent beneficial effects need to be balanced against the risks. Also, cessation of the drug seems to be associated with recurrence of disease activity. Both the moment of rebound disease activity and the outcome of PML are related to clearance of the drug. Specific features of this IgG4 antibody (i.e. half-antibody exchange) may result in underestimated drug levels. Here, we demonstrate natalizumab levels in 10 patients with relapsing MS, using a recently developed sensitive assay. Remarkably, natalizumab was detectable up to 200 days after cessation of therapy.

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Year:  2011        PMID: 22183929     DOI: 10.1177/1352458511431073

Source DB:  PubMed          Journal:  Mult Scler        ISSN: 1352-4585            Impact factor:   6.312


  12 in total

Review 1.  Monoclonal antibodies as disease modifying therapy in multiple sclerosis.

Authors:  Erin E Longbrake; Becky J Parks; Anne H Cross
Journal:  Curr Neurol Neurosci Rep       Date:  2013-11       Impact factor: 5.081

2.  The S228P mutation prevents in vivo and in vitro IgG4 Fab-arm exchange as demonstrated using a combination of novel quantitative immunoassays and physiological matrix preparation.

Authors:  John-Paul Silva; Olivia Vetterlein; Joby Jose; Shirley Peters; Hishani Kirby
Journal:  J Biol Chem       Date:  2015-01-07       Impact factor: 5.157

3.  High interindividual variability in the CD4/CD8 T cell ratio and natalizumab concentration levels in the cerebrospinal fluid of patients with multiple sclerosis.

Authors:  A Harrer; G Pilz; P Wipfler; K Oppermann; J Sellner; W Hitzl; E Haschke-Becher; S Afazel; T Rispens; D van der Kleij; E Trinka; J Kraus
Journal:  Clin Exp Immunol       Date:  2015-04-27       Impact factor: 4.330

Review 4.  Monoclonal antibody therapies for the treatment of relapsing-remitting multiple sclerosis: differentiating mechanisms and clinical outcomes.

Authors:  Jan Lycke
Journal:  Ther Adv Neurol Disord       Date:  2015-11       Impact factor: 6.570

5.  Assessment of immune functions and MRI disease activity in relapsing-remitting multiple sclerosis patients switching from natalizumab to fingolimod (ToFingo-Successor).

Authors:  Luisa Klotz; Berit Grützke; Maria Eveslage; Michael Deppe; Catharina C Gross; Lucienne Kirstein; Anita Posevitz-Fejfar; Tilman Schneider-Hohendorf; Nicholas Schwab; Sven G Meuth; Heinz Wiendl
Journal:  BMC Neurol       Date:  2015-06-23       Impact factor: 2.474

6.  PML-IRIS during Fingolimod Diagnosed after Natalizumab Discontinuation.

Authors:  J Killestein; A Vennegoor; A E L van Golde; R L J H Bourez; M L B Wijlens; M P Wattjes
Journal:  Case Rep Neurol Med       Date:  2014-11-23

7.  The majority of natalizumab-treated MS patients have high natalizumab concentrations at time of re-dosing.

Authors:  Zoé LE van Kempen; Cyra E Leurs; Birgit I Witte; Annick de Vries; Mike P Wattjes; Theo Rispens; Joep Killestein
Journal:  Mult Scler       Date:  2017-05-09       Impact factor: 6.312

8.  New insights into the pharmacokinetics and pharmacodynamics of natalizumab treatment for patients with multiple sclerosis, obtained from clinical and in vitro studies.

Authors:  T Sehr; U Proschmann; K Thomas; M Marggraf; E Straube; H Reichmann; A Chan; T Ziemssen
Journal:  J Neuroinflammation       Date:  2016-06-27       Impact factor: 8.322

9.  Severe inflammatory disease activity 14 months after cessation of Natalizumab in a patient with Leber's optic neuropathy and multiple sclerosis - a case report.

Authors:  Trygve Holmøy; Antonie G Beiske; Svetozar Zarnovicky; Aija Zuleron Myro; Egil Røsjø; Emilia Kerty
Journal:  BMC Neurol       Date:  2016-10-18       Impact factor: 2.474

10.  Disease activity following pregnancy-related discontinuation of natalizumab in MS.

Authors:  Iris Kleerekooper; Zoé L E van Kempen; Cyra E Leurs; Iris Dekker; Theo Rispens; Birgit I Lissenberg-Witte; Caspar E P van Munster; Brigit A de Jong; Bob W van Oosten; Bernard M J Uitdehaag; Mike P Wattjes; Joep Killestein
Journal:  Neurol Neuroimmunol Neuroinflamm       Date:  2017-12-05
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