CD4+ CD25+ T regulatory (Treg) cells inhibit immunopathology and autoimmune disease in vivo. CD4+ CD25+ Treg cells’ capacity to inhibit conventional T cells in vitro is dependent upon cell-cell contact; however, the cell surface molecules mediating this cell: cell contact have not yet been identified. LFA-1 (CD11a/CD18) is an adhesion molecule that plays an established role in T cell-mediated cell contact and in T cell activation. Although expressed at high levels on murine CD4+ CD25+ Treg cells, the role of LFA-1 in these cells has not been defined previously. We hypothesized that LFA-1 may play a role in murine CD4+ CD25+ Treg function. To evaluate this, we analyzed LFA-1-deficient (CD18−/−) CD4+ CD25+ T cells. We show that CD18−/− mice demonstrate a propensity to autoimmunity. Absence of CD18 led to diminished CD4+ CD25+ T cell numbers and affected both thymic and peripheral development of these cells. LFA-1-deficient CD4+ CD25+ T cells were deficient in mediating suppression in vitro and in mediating protection from colitis induced by the transfer of CD4+ CD25− T cells into lymphopenic hosts. Therefore, we define a crucial role for CD18 in optimal CD4+ CD25+ Treg development and function.