| Literature DB >> 34064035 |
Laura Dresser1, Richard Wlodarski1, Kourosh Rezania1, Betty Soliven1.
Abstract
Myasthenia gravis (MG) is an autoimmune neurological disorder characterized by defective transmission at the neuromuscular junction. The incidence of the disease is 4.1 to 30 cases per million person-years, and the prevalence rate ranges from 150 to 200 cases per million. MG is considered a classic example of antibody-mediated autoimmune disease. Most patients with MG have autoantibodies against the acetylcholine receptors (AChRs). Less commonly identified autoantibodies include those targeted to muscle-specific kinase (MuSK), low-density lipoprotein receptor-related protein 4 (Lrp4), and agrin. These autoantibodies disrupt cholinergic transmission between nerve terminals and muscle fibers by causing downregulation, destruction, functional blocking of AChRs, or disrupting the clustering of AChRs in the postsynaptic membrane. The core clinical manifestation of MG is fatigable muscle weakness, which may affect ocular, bulbar, respiratory and limb muscles. Clinical manifestations vary according to the type of autoantibody, and whether a thymoma is present.Entities:
Keywords: B cells; T cells; acetylcholine receptor; autoantibodies; cytokines; myasthenia gravis
Year: 2021 PMID: 34064035 DOI: 10.3390/jcm10112235
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241