Literature DB >> 15623671

Other therapy options and future strategies for treating patients with multiple sclerosis.

Syed A Rizvi1, Khurram Bashir.   

Abstract

Research into therapy for multiple sclerosis (MS) is occurring at a rapid pace, and current treatment options approved by the FDA specifically target the inflammatory phase of MS. However, drugs that are not FDA-approved are routinely used to treat MS. One example is corticosteroids, which are commonly used to treat acute relapses. Other drugs that are commonly used to treat patients who do not respond to the FDA-approved agents include the following: methotrexate, azathioprine, cyclophosphamide, and pulse steroids. Drugs being studied as possible therapeutic agents include the statins, mycophenolate mofetil, various monoclonal antibodies (e.g., alemtuzumab, daclzumab, natalizumab, and rituximab), antibiotics and antivirals, and the pregnancy hormone estriol. Disease modifying agents (DMAs) that promote remyelination would be beneficial for preventing long-term disability, and such agents are also under active investigation (e.g., IV immunoglobulin G and stem cell transplantation). Combination therapy with DMAs with different mechanisms of action may be advantageous in the future for providing optimal treatment that both delays the progression of disability and promotes repair and remyelination.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15623671     DOI: 10.1212/wnl.63.12_suppl_6.s47

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  7 in total

1.  Pneumocystis Pneumonia during Rituximab Treatment in Children with Autoimmune Nerve System Diseases.

Authors:  Ji Zhou; Yao Zhang; Yiwen Jin; Taoyun Ji; Xinhua Bao; Yuehua Zhang; Hui Xiong; Xinzhi Chang; Yuwu Jiang; Ye Wu
Journal:  J Neuroimmune Pharmacol       Date:  2018-05-17       Impact factor: 4.147

2.  IVIG enters the central nervous system during treatment of experimental autoimmune encephalomyelitis and is localised to inflammatory lesions.

Authors:  Signe Humle Jorgensen; Nicolas Storm; Poul Erik Hyldgaard Jensen; Henning Laursen; Per Soelberg Sorensen
Journal:  Exp Brain Res       Date:  2006-11-08       Impact factor: 1.972

Review 3.  [Update on pathophysiologic and immunotherapeutic approaches for the treatment of multiple sclerosis].

Authors:  C Kleinschnitz; S G Meuth; B C Kieseier; H Wiendl
Journal:  Nervenarzt       Date:  2007-08       Impact factor: 1.214

Review 4.  Oral disease-modifying treatments for multiple sclerosis: the story so far.

Authors:  Bernd C Kieseier; Heinz Wiendl
Journal:  CNS Drugs       Date:  2007       Impact factor: 5.749

5.  Overexpression of GSN could decrease inflammation and apoptosis in EAE and may enhance vitamin D therapy on EAE/MS.

Authors:  Jifang Gao; Zhaoyu Qin; Xinyuan Guan; Juanjuan Guo; Huaqing Wang; Shilian Liu
Journal:  Sci Rep       Date:  2017-04-04       Impact factor: 4.379

6.  Rifampicin attenuates experimental autoimmune encephalomyelitis by inhibiting pathogenic Th17 cells responses.

Authors:  Ke Ma; Xi Chen; Jia-Cheng Chen; Ying Wang; Xi-Meng Zhang; Fan Huang; Jun-Jiong Zheng; Xiong Chen; Wei Yu; Ke-Ling Cheng; Yan-Qing Feng; Huai-Yu Gu
Journal:  J Neurochem       Date:  2016-11-29       Impact factor: 5.372

Review 7.  Multiple sclerosis therapy: an update on recently finished trials.

Authors:  Christoph Kleinschnitz; Sven G Meuth; Olaf Stüve; Bernd Kieseier; Heinz Wiendl
Journal:  J Neurol       Date:  2007-11-15       Impact factor: 6.682

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.