Recent approaches to the development of antigen-specific immunotherapies for myasthenia gravis
Autor: | Konstantinos Lazaridis, Paraskevi Zisimopoulou, Konstantinos Poulas, Socrates J. Tzartos, Gregory Kordas, George Lagoumintzis |
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Jazyk: | angličtina |
Rok vydání: | 2010 |
Předmět: |
animal structures
medicine.medical_treatment Immunology Neuromuscular transmission Receptors Nicotinic Autoantigens Neuromuscular junction 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Myasthenia Gravis Animals Humans Immunology and Allergy Medicine Autoantibodies 030304 developmental biology Acetylcholine receptor 0303 health sciences Plasma Exchange business.industry Therapies Investigational Antibodies Monoclonal Immunoglobulins Intravenous Thymectomy medicine.disease Acetylcholinesterase Myasthenia gravis 3. Good health Nicotinic acetylcholine receptor Nicotinic agonist medicine.anatomical_structure chemistry Blood Component Removal Immunotherapy Immunosorbents business Immunosuppressive Agents 030217 neurology & neurosurgery |
Zdroj: | Autoimmunity; Vol 43 Autoimmunity |
ISSN: | 0891-6934 |
DOI: | 10.3109/08916930903518099 |
Popis: | Acquired autoimmune myasthenia gravis (MG) is the most common disease that affects the neuromuscular junction (NMJ). MG is associated with autoantibodies (auto-Abs) to components of the NMJ. About 85-90% of MG patients have auto-Abs against the muscle nicotinic acetylcholine receptor (AChR), while about half of the remaining patients have auto-Abs against muscle-specific kinase. Auto-Abs, in combination with local deposition of complement, reduce the number of available post-synaptic nicotinic AChRs and thereby impair neuromuscular transmission. Current medications for MG are non-specific and include acetylcholinesterase inhibitors, immunosuppressants, plasma exchange, intravenous Ig administration and thymectomy. Treatments that selectively target the anti-AChR auto-Abs may prove to be more effective and free of side-effects. We here review two approaches aimed at the development of antigen-specific therapies for MG. The first is specific apheresis of Abs from patients' sera using immobilised recombinant AChR domains as immunoadsorbents. Indeed, we have recently shown that the combined recombinant extracellular domains of all human AChR subunits are capable of specifically immunoadsorbing the majority of pathogenic auto-Abs from several MG sera. The second therapeutic approach is the development of non-pathogenic anti-AChR monoclonal Abs that could potentially be used as protective agents by blocking the binding of patients' auto-Abs to the AChR. |
Databáze: | OpenAIRE |
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