“…Previous studies have associated the induction of cytokines such as IFN-␥ or tumor necrosis factor alpha, as well as the increased expression of mucosal IL-4 in mucosal lesions with the pathogenesis of the disease (5,6,13,26). Thus, it is likely that the observed exacerbated hypersensitivity to leishmanial antigens in ML associated with high production of both cytokine types may have a detrimental effect, contributing to the severity of the disease (5,6,13,27). Indeed, stronger intradermal leishmanin test and lymphoproliferative responses, as well as higher frequencies of L. braziliensis-reactive T cells and higher specific cytotoxic activity have been observed in patients with ML compared to patients with CL (3,5,6,8,28).…”