Major Histocompatibility Complex Class I and II Expression in Idiopathic Inflammatory Myopathy
Das, Leena
Peter C. FRCPA,FRACP†; Manavis,Jim BSc (Hons)†; Limaye,Vidya S. MBBS,FRACP,PhD‡,Blumbergs P,Manavis J,Limaye V
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Introduction: We sought to study the intensity and pattern of major histocompatibility complex (MHC) I and II expression in muscle from patients with biopsy-proven idiopathic inflammatory myositis (IIM) including the subgroups, polymyositis (PM), dermatomyositis (DM), and inclusion body myositis (IBM).
Methods: A total of 120 muscle biopsies (61 PM, 14 DM, and 45 IBM) were immunostained for MHC I and II. Staining was graded as follows. 0: no staining, 1+: ≤10% fibers, 2+: 10% to 25%, 3+: 25% to 50%, 4+: 50% to 99%, and 5+ 100%.
Results: All IIM biopsies showed MHC I positivity; 93% showed MHC II positivity. The proportion of patients with MHC II score ≥3+ was higher in IBM than DM or PM. In DM, MHC I expression showed a perifascicular pattern. All IBM biopsies were immunopositive for MHC I and II; 30/45 were scored 5+.
Discussion: Immunostaining for MHC I and II is a useful adjunctive test in diagnosis and subclassification of IIM.
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Applied Immunohistochemistry & Molecular Morphology:
December 2013 - Volume 21 - Issue 6 - p 539–542
2013
http://journals.lww.com/appliedimmunohist/Abstract/2013/12000/Major_Histocompatibility_Complex_Class_I_and_II.10.aspx