Literature DB >> 20627553

Overlapping and distinct mechanisms of action of multiple sclerosis therapies.

J J Graber1, C A McGraw, D Kimbrough, S Dhib-Jalbut.   

Abstract

In the last two decades MS has changed from an idiopathic condition with only symptomatic treatments to a disease with better characterized pathophysiologic underpinnings and several treatments that modify its long-term course based on specific mechanisms of action. There are now several FDA approved options for therapy at the onset of disease, and discussions have begun on choosing the best treatment in individual patients and what option to choose next in patients who are failing their current treatment. Numerous studies have begun to highlight that the underlying pathology of CNS damage may be different in subsets of patients, raising the possibility that some may respond to a treatment with a mechanism of action that is targeted to 'their' MS. Trials are ongoing of numerous new agents with different mechanisms of action and some combination therapies. A better understanding of how each therapy works may guide decisions on initiating, combining or changing therapy in a more rational way to improve patient outcomes. Further knowledge of underlying mechanisms of disease in different patients with 'the same' disease may lead to more targeted therapies, as will biomarkers that predict clinical response to therapy. Studies of the effects of various agents used in MS reveal both overlapping and distinct mechanisms of actions that may be relevant to their efficacy and side effects in individual patients. However, it is important to remember that most agents are approved based on their reduction of MRI lesions and relapse rates over a short time frame. These measures only partially correlate with long-term disability, which may be the most relevant clinical outcome for people with MS. Fixed disability requires years to become apparent, and there is a lack of large studies of biomarkers for chronic outcomes. In addition, few large studies correlate response to therapy with cognitive outcomes, which are a major cause of chronic disability. This review will attempt to summarize clinically relevant knowledge of the mechanisms of action of current FDA approved therapies for MS in the context of ongoing clinical trials of combination therapy and address rational approaches to changing therapy in a patient suspected to be 'unresponsive' to their current treatment.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20627553     DOI: 10.1016/j.clineuro.2010.05.002

Source DB:  PubMed          Journal:  Clin Neurol Neurosurg        ISSN: 0303-8467            Impact factor:   1.876


  11 in total

1.  The synthetic cannabinoid R(+)WIN55,212-2 augments interferon-β expression via peroxisome proliferator-activated receptor-α.

Authors:  Eric J Downer; Eileen Clifford; Sylvie Amu; Padraic G Fallon; Paul N Moynagh
Journal:  J Biol Chem       Date:  2012-05-31       Impact factor: 5.157

2.  Circulating levels of interleukin-35 in patients with multiple sclerosis: evaluation of the influences of FOXP3 gene polymorphism and treatment program.

Authors:  A Jafarzadeh; M Jamali; R Mahdavi; H A Ebrahimi; H Hajghani; A Khosravimashizi; M Nemati; H Najafipour; A Sheikhi; M M Mohammadi; H Daneshvar
Journal:  J Mol Neurosci       Date:  2014-10-19       Impact factor: 3.444

3.  Interferon-β regulates dendritic cell activation and migration in experimental autoimmune encephalomyelitis.

Authors:  Leesa M Pennell; Eleanor N Fish
Journal:  Immunology       Date:  2017-07-21       Impact factor: 7.397

4.  Randomized study combining interferon and glatiramer acetate in multiple sclerosis.

Authors:  Fred D Lublin; Stacey S Cofield; Gary R Cutter; Robin Conwit; Ponnada A Narayana; Flavia Nelson; Amber R Salter; Tarah Gustafson; Jerry S Wolinsky
Journal:  Ann Neurol       Date:  2013-03-11       Impact factor: 10.422

5.  Rapamycin Augments Immunomodulatory Properties of Bone Marrow-Derived Mesenchymal Stem Cells in Experimental Autoimmune Encephalomyelitis.

Authors:  Mansoureh Togha; Mehrdad Jahanshahi; Leila Alizadeh; Soodeh Razeghi Jahromi; Gelareh Vakilzadeh; Bahram Alipour; Ali Gorji; Amir Ghaemi
Journal:  Mol Neurobiol       Date:  2016-03-12       Impact factor: 5.590

6.  IFNAR signaling directly modulates T lymphocyte activity, resulting in milder experimental autoimmune encephalomyelitis development.

Authors:  Nadia Kavrochorianou; Maria Evangelidou; Melina Markogiannaki; Michael Tovey; George Thyphronitis; Sylva Haralambous
Journal:  J Leukoc Biol       Date:  2015-07-31       Impact factor: 4.962

Review 7.  Interferon beta and glatiramer acetate therapy.

Authors:  Corey A McGraw; Fred D Lublin
Journal:  Neurotherapeutics       Date:  2013-01       Impact factor: 7.620

Review 8.  Therapeutic Prospects of Cannabinoids in the Immunomodulation of Prevalent Autoimmune Diseases.

Authors:  Xandy Melissa Rodríguez Mesa; Andrés Felipe Moreno Vergara; Leonardo Andrés Contreras Bolaños; Natalia Guevara Moriones; Antonio Luis Mejía Piñeros; Sandra Paola Santander González
Journal:  Cannabis Cannabinoid Res       Date:  2021-05-24

Review 9.  Vaccine Considerations for Multiple Sclerosis in the COVID-19 Era.

Authors:  Patricia K Coyle; Anne Gocke; Megan Vignos; Scott D Newsome
Journal:  Adv Ther       Date:  2021-06-01       Impact factor: 3.845

Review 10.  Role of regulatory T cells in pathogenesis and biological therapy of multiple sclerosis.

Authors:  Milan Buc
Journal:  Mediators Inflamm       Date:  2013-05-12       Impact factor: 4.711

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.