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ABSTRACT: Purpose
Sporadic inclusion body myositis (sIBM) is an autoimmune degenerative disease of the muscle, with inflammatory infiltrates and inclusion vacuoles. Its pathogenesis is not fully understood and the diagnosis is hampered by its imprecise characteristics, at times indistinguishable from other idiopathic inflammatory myopathies such as polymyositis and dermatomyositis. The diagnosis may be assisted by the detection of autoantibodies targeting Mup44, a skeletal muscle antigen identified as cytosolic 5'-nucleotidase 1A (cN-1A, NT5C1A). A novel standardized anti-cN-1A IgG ELISA was developed and its diagnostic performance was evaluated by two reference laboratories.Methods
Recombinant human full-length cN-1A was expressed and purified, and subsequently utilized to set up a
SUBMITTER: Kramp SL
PROVIDER: S-EPMC5114199 | biostudies-literature | 2016 Dec
REPOSITORIES: biostudies-literature