Literature DB >> 20397968

Glatiramer acetate and the glatiramoid class of immunomodulator drugs in multiple sclerosis: an update.

Kenneth P Johnson1.   

Abstract

IMPORTANCE OF THE FIELD: MS is a chronic progressive inflammatory and neurodegenerative disease associated with autoimmune dysregulation. Glatiramer acetate (GA), a complex polypeptides mixture and first member of the glatiramoid class, is a first-line therapy for relapsing MS. New glatiramoids are under development. AREAS COVERED IN THIS REVIEW: Studies from a PubMed search with terms 'glatiramer' and 'glatiramoid' were evaluated, focussing on studies conducted between 2007 and 2010. WHAT THE READER WILL GAIN: We review newly discovered GA effects on innate and acquired immunity and results of recent clinical studies. GA delays conversion from a clinically isolated syndrome to definite MS and has clinical benefits comparable to those of IFN-beta drugs, but is more cost-effective and improves quality of life. Preclinical studies of protiramer, a higher molecular mass glatiramoid, showed unexpected toxicity in animals, resulting in discontinuation of drug development. TAKE HOME MESSAGES: GA is a cost-effective, safe and efficacious MS treatment with pleiotropic immunomodulation activity, is best prescribed early and may safely enhance outcomes when used with other immunomodulators. Protiramer experience indicates the potential for unexpected toxicity associated with new glatiramoids. The safety, efficacy and immunogenicity of new glatiramoids must be evaluated thoroughly.

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Year:  2010        PMID: 20397968     DOI: 10.1517/17425251003752715

Source DB:  PubMed          Journal:  Expert Opin Drug Metab Toxicol        ISSN: 1742-5255            Impact factor:   4.481


  6 in total

1.  Glatiramer acetate (copaxone) modulates platelet activation and inhibits thrombin-induced calcium influx: possible role of copaxone in targeting platelets during autoimmune neuroinflammation.

Authors:  Sarah C Starossom; Tatyana Veremeyko; Marina Dukhinova; Amanda W Y Yung; Eugene D Ponomarev
Journal:  PLoS One       Date:  2014-05-02       Impact factor: 3.240

2.  Metabolic response to glatiramer acetate therapy in multiple sclerosis patients.

Authors:  Lidia De Riccardis; Alessandra Ferramosca; Antonio Danieli; Giorgio Trianni; Vincenzo Zara; Francesca De Robertis; Michele Maffia
Journal:  BBA Clin       Date:  2016-10-18

Review 3.  Development of Glatopa® (Glatiramer Acetate): The First FDA-Approved Generic Disease-Modifying Therapy for Relapsing Forms of Multiple Sclerosis.

Authors:  Christine Bell; James Anderson; Tanmoy Ganguly; James Prescott; Ishan Capila; Jonathan C Lansing; Richard Sachleben; Mani Iyer; Ian Fier; James Roach; Kristina Storey; Paul Miller; Steven Hall; Daniel Kantor; Benjamin M Greenberg; Kavita Nair; Joseph Glajch
Journal:  J Pharm Pract       Date:  2017-08-29

Review 4.  Treatment Challenges in Multiple Sclerosis - A Continued Role for Glatiramer Acetate?

Authors:  Massimiliano Mirabella; Pietro Annovazzi; Wallace Brownlee; Jeffrey A Cohen; Christoph Kleinschnitz; Christian Wolf
Journal:  Front Neurol       Date:  2022-04-15       Impact factor: 4.086

Review 5.  A Comprehensive Review on Copemyl®.

Authors:  Pietro Annovazzi; Antonio Bertolotto; Vincenzo Brescia Morra; Claudio Gasperini; Enrico Montanari; Pierluigi Navarra; Francesco Patti; Maria Pia Sormani; Angelo Ghezzi
Journal:  Neurol Ther       Date:  2017-07-31

6.  Glatiramer acetate as a clinically and cost-effective treatment of relapsing multiple sclerosis over 10 years of use within the National Health Service: Final results from the UK Risk Sharing Scheme.

Authors:  G Giovannoni; P A Brex; D Dhiraj; J Fullarton; M Freddi; B Rodgers-Gray; K Schmierer
Journal:  Mult Scler J Exp Transl Clin       Date:  2019-12-05
  6 in total

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