N aturally occurring CD4⁺CD25^hiFoxp3⁺ Tregs (nTregs) are highly proliferative in blood. However, the kinetics of their accumulation and proliferation during a localized antigen-specific T cell response is currently unknown. To explore this, we used a human experimental system whereby tuberculin purified protein derivative (PPD) was injected into the skin and the local T cell response analyzed over time. The numbers of both CD4⁺Foxp3^– (memory) and CD4⁺Foxp3⁺ (putative nTreg) T cells increased in parallel, with the 2 populations proliferating at the same relative rate. In contrast to CD4⁺Foxp3^– T cell populations, skin CD4⁺Foxp3⁺ T cells expressed typical Treg markers (i.e., they were CD25^hi, CD127^lo, CD27⁺, and CD39⁺) and did not synthesize IL-2 or IFN-γ after restimulation in vitro, indicating that they were not recently activated effector cells. To determine whether CD4⁺Foxp3⁺ T cells in skin could be induced from memory CD4⁺ T cells, we expanded skin-derived memory CD4⁺ T cells in vitro and anergized them. These cells expressed high levels of CD25 and Foxp3 and suppressed the proliferation of skin-derived responder T cells to PPD challenge. Our data therefore demonstrate that memory and CD4⁺ Treg populations are regulated in tandem during a secondary antigenic response. Furthermore, it is possible to isolate effector CD4⁺ T cell populations from inflamed tissues and manipulate them to generate Tregs with the potential to suppress inflammatory responses.