Humans with mutations in the FOXP3 gene (Xp11.23-q13.3) suffer from a severe autoimmune disorder known as IPEX syndrome (immune dysregulation, polyendocrinopathy, enteropathy, and X-linked), which manifests in lymphoproliferation, multiorgan lymphocytic infiltration, and systemic autoimmune inflammation; the disease is incompatible with life [6, 7]. This evidence concerns the gene FOXP3 and Autoimmunity.