In addition, and association with assessment of PFA, established pathophysiological concepts of DM such as increased ISGs (see above), can be used to highlight perifascicular pathology such as stains against MxA or ISG15, which may even be more sensible to identify DM-specific (perifascicular) pathology (44) than established MHC class 1 (61). The gene discussed is MX1; the disease is dermatomyositis.