FOXP3 and neoplasm: Treg cells have been shown to express inflammatory chemokine receptors and adhesion molecules suggestive of an enhanced capacity to migrate to inflamed tissues.19–23 Whether this accounts for the enrichment of Treg cells observed in tumours is not clear as, to our knowledge, few studies have performed a side-by-side analysis of chemokine receptor expression by both tumour-infiltrating Foxp3+ and Foxp3− CD4+ T cells.