While suppression assays and cytokine expression are most commonly used to evaluate Treg function, other methods employed to monitor Treg function in clinical trials include evaluating serum cytokine levels, evaluating tumor biopsies for expression of suppressive factors such as IDO, or evaluating the methylation status of the Foxp3 promoter as a surrogate for Treg activity (Polansky et al., 2008; Wieczorek et al., 2009). This evidence concerns the gene FOXP3 and neoplasm.