» Articles » PMID: 22379454

Autoimmune Neuromuscular Disorders

Overview
Date 2012 Mar 2
PMID 22379454
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Autoimmune neuromuscular disorders affecting peripheral nerves, neuromuscular junction or muscle have a wide clinical spectrum with diverse pathogenetic mechanisms. Peripheral nervous system may be targeted in the context of complex immune reactions involving different cytokines, antigen-presenting cells, B cells and different types of T cells. Various immunomodulating and cytotoxic treatments block proliferation or activation of immune cells by different mechanisms attempting to control the response of the immune system and limit target organ injury. Most treatment protocols for autoimmune neuromuscular disorders are based on the use of corticosteroids, intravenous immunoglobulins and plasmapheresis, with cytotoxic agents mostly used as steroid-sparing medications. More recently, development of specific monoclonal antibodies targeting individual cell types allowed a different approach targeting specific immune pathways, but these new treatments are also associated with various adverse effects and their long-term efficacy is still unknown.

Citing Articles

Decoding Neuromuscular Disorders Using Phenotypic Clusters Obtained From Co-Occurrence Networks.

Diaz-Santiago E, Claros M, Yahyaoui R, de Diego-Otero Y, Calvo R, Hoenicka J Front Mol Biosci. 2021; 8:635074.

PMID: 34046427 PMC: 8147726. DOI: 10.3389/fmolb.2021.635074.


Of rAAV and Men: From Genetic Neuromuscular Disorder Efficacy and Toxicity Preclinical Studies to Clinical Trials and Back.

Buscara L, Gross D, Daniele N J Pers Med. 2020; 10(4).

PMID: 33260623 PMC: 7768510. DOI: 10.3390/jpm10040258.


Expanding the Role of the Pharmacist: Immunoglobulin Therapy and Disease Management in Neuromuscular Disorders.

Tichy E, Prosser B, Doyle D J Pharm Pract. 2020; 35(1):106-119.

PMID: 32677504 PMC: 8822190. DOI: 10.1177/0897190020938212.


Unusual reactions to hymenoptera stings: what should we keep in mind?.

Mingomataj E, Bakiri A, Ibranji A, Sturm G Clin Rev Allergy Immunol. 2014; 47(1):91-9.

PMID: 24962710 DOI: 10.1007/s12016-014-8434-y.

References
1.
Kupersmith M . Ocular myasthenia gravis: treatment successes and failures in patients with long-term follow-up. J Neurol. 2009; 256(8):1314-20. DOI: 10.1007/s00415-009-5120-8. View

2.
Burns T, Dyck P, Aksamit A, Dyck P . The natural history and long-term outcome of 57 limb sarcoidosis neuropathy cases. J Neurol Sci. 2006; 244(1-2):77-87. DOI: 10.1016/j.jns.2006.01.014. View

3.
. Assessment of plasmapheresis. Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. 1996; 47(3):840-3. View

4.
Lozeron P, Denier C, Lacroix C, Adams D . Long-term course of demyelinating neuropathies occurring during tumor necrosis factor-alpha-blocker therapy. Arch Neurol. 2009; 66(4):490-7. DOI: 10.1001/archneurol.2009.11. View

5.
Dyck P, OBrien P, Swanson C, Low P, Daube J . Combined azathioprine and prednisone in chronic inflammatory-demyelinating polyneuropathy. Neurology. 1985; 35(8):1173-6. DOI: 10.1212/wnl.35.8.1173. View