Literature DB >> 21124072

Monoclonal antibody therapy in multiple sclerosis: Paradigm shifts and emerging challenges.

Paulo Fontoura1.   

Abstract

Therapeutic approaches to multiple sclerosis (MS) are based on altering the functions of the immune system, either by using broad immunosuppressive drugs used for transplantation rejection and rheumatology, or by modulating them more discreetly with beta interferon and synthetic amino-acid copolymers. These strategies are only partially successful, have important safety and tolerability limitations, and have shown to be mostly effective in earlier stages of the disease, in which acute relapses dominate the clinical picture. For progressive phenotypes of MS there are currently no effective therapeutic options. As very specific and potent immunosuppressive agents, monoclonal antibodies (mAbs) may offer considerable advantages over other therapies for MS. During the last decade, anti-a4 integrin natalizumab became the first approved mAb for treatment of relapsing MS, after convincingly demonstrating clinically significant effects on two large Phase 3 trials. Moreover, the concept of disease remission was introduced for the first time, to describe patients that show no signs of clinical or imaging markers of disease activity during therapy with natalizumab. Of the mAbs under development for MS, alemtuzumab and rituximab have also shown promising evidence of effectiveness, and potentially expanded the therapeutic horizon to reversal of disease progression in early relapsing patients, and progressive patients who previously had not been studied. However, the appearance of progressive multifocal leukoencephalopathy (PML) in natalizumab-treated MS patients, as well as in patients with lymphoma, lupus and rheumatoid arthritis treated with rituximab, and autoimmune-type complications in alemtuzumab-treated MS patients underlines the fact that extended efficacy comes with significant clinical risks. The challenge is then how best to utilize therapies that have evidently superior efficacy in a chronic disease of young adults, to obtain the best benefit-risk ratio, and how to monitor and prevent emergent safety concerns.

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Year:  2010        PMID: 21124072      PMCID: PMC3011221          DOI: 10.4161/mabs.2.6.13270

Source DB:  PubMed          Journal:  MAbs        ISSN: 1942-0862            Impact factor:   5.857


  87 in total

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Review 3.  Assessment: the use of natalizumab (Tysabri) for the treatment of multiple sclerosis (an evidence-based review): report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology.

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Journal:  Neurology       Date:  2008-09-02       Impact factor: 9.910

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Review 6.  Natalizumab (Tysabri) treatment for relapsing multiple sclerosis.

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Review 7.  LINGO-1 antagonists as therapy for multiple sclerosis: in vitro and in vivo evidence.

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Review 9.  Natalizumab treatment for multiple sclerosis: recommendations for patient selection and monitoring.

Authors:  Ludwig Kappos; David Bates; Hans-Peter Hartung; Eva Havrdova; David Miller; Chris H Polman; Mads Ravnborg; Stephen L Hauser; Richard A Rudick; Howard L Weiner; Paul W O'Connor; John King; Ernst Wilhelm Radue; Tarek Yousry; Eugene O Major; David B Clifford
Journal:  Lancet Neurol       Date:  2007-05       Impact factor: 44.182

10.  Alemtuzumab vs. interferon beta-1a in early multiple sclerosis.

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Journal:  N Engl J Med       Date:  2008-10-23       Impact factor: 91.245

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Journal:  Ther Adv Drug Saf       Date:  2012-10

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4.  Preclinical and early clinical development of GNbAC1, a humanized IgG4 monoclonal antibody targeting endogenous retroviral MSRV-Env protein.

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5.  CD98 is a potential target for ablating B cell clonal expansion and autoantibody in multiple sclerosis.

Authors:  Joseph M Cantor
Journal:  J Neuroimmunol       Date:  2014-06-26       Impact factor: 3.478

6.  Risk-benefit considerations in the treatment of relapsing-remitting multiple sclerosis.

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Review 7.  Daclizumab: A Review in Relapsing Multiple Sclerosis.

Authors:  Matt Shirley
Journal:  Drugs       Date:  2017-03       Impact factor: 11.431

8.  Italian multicentre observational study of the prevalence of CCSVI in multiple sclerosis (CoSMo study): rationale, design, and methodology.

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Review 9.  Monoclonal Antibody Therapies for Hematological Malignancies: Not Just Lineage-Specific Targets.

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Review 10.  The Development of Cladribine Tablets for the Treatment of Multiple Sclerosis: A Comprehensive Review.

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  10 in total

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