作者: Miri Pass-Rozner , Anat Faber-Elmann , Michael Sela , Edna Mozes
DOI: 10.1007/978-94-011-4060-7_17
关键词: Experimental autoimmune encephalomyelitis 、 Acetylcholine receptor 、 Immunology 、 Chemistry 、 Inositol phosphate 、 Lymphocyte 、 Myasthenia gravis 、 Immune system 、 Peptide ligand 、 Nicotinic acetylcholine receptor
摘要: Myasthenia gravis (MG) and its experimental animal model, autoimmune myasthenia (EAMG), are immune disorders characterized by circulating antibodies lymphocyte autoreactivity to nicotinic acetylcholine receptor (AChR). Although the production of specific is directly attributed B cells, there extensive evidence that T cells have a key role in etiopathology disease humans animals [1-4]. Since α-subunit AChR was shown be predominant for cell epitopes [2], we used peptides representing different sequences human study initiation, development immunomodulation gravis.