“…An additional critical issue is the potential Th2 suppression with secondary dysregulation of Th1/17 in patients with MS. Recently, a temporal association was observed between flare-up of relapsing-remitting MS and treatment with dupilumab in an AD patient, who had a long-term untreated MS. 16 In this regard, the authors hypothesized that dupilumab's inhibition of the effects of IL-4 downstream actions may have altered the patient's cytokine milieu, shifting the balance of Th profiles in favor of Th1/17 pathways, which is, the T-cell phenotype thought to drive MS pathogenesis. 16 However, it is frequent that in young women the MS disease course is characterized by incoming, relapsing, and unstable episodes of multiple disease localization, especially if not treated, thus the clear attribution of a causal link seems undue.…”