Mus exemplar idiopathicae inflammationis myopathy (IIM)
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Mus exemplar idiopathicae inflammationis myopathy (IIM)

Inflammatoriae myopathiae idiopathicae (IIM) sunt coetus heterogeneorum musculorum autoimmunerum acquisitorum morborum musculorum, infirmitatis inflammatoriis, cellulae infiltrationis inflammatoriae, et productione autoanticorporum myositis-specialis. Subtypes includunt dermatomyositis (DM), polymyositis (PM), inclusio corporis myositis (IBM), necrotantibus myopathy immune-mediatis (IMNM), et syndrome antisynthetasis (ASSD). HKeyBio exemplar myosin IIM in Balb/c murium bene convalidum praebet. Immunitatem ad interdum musculi (myosin) autoimmune responsionis contra musculum sceletum, et recapitulat clavem IIM humanarum notarum, inter pondus damnum, vires musculi decrescentes, cytokinos inflammatores elevatos (IL-6, IL-17A), et histopathologiam musculi (inflammatoriam infiltratam, myofiber necrosis). Hoc exemplar praebet validum suggestum ad efficaciam preclinicalis probationis novae immunomodulatoriae et anti-inflammatorii therapiae pro myositis et morbis musculi autoimmune affinis.
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