“…There is substantial evidence indicating that immune responses, which should otherwise suppress or eliminate oral cancer cells, are inhibited by properties and functions of oral cancers. NK cells and cytotoxic T-cells, which play crucial effector functions in the host defense against neoplasia, are functionaly inactivated in oral cancers (Trinchieri, 1989;Jewett et al, , 1997Jewett et al, , 2003Jewett et al, , 2006aLaad et al, 1996). Regressing tumor grafts of oral origin contain significantly larger numbers of functional NK and T-cells than those associated with the primary tumors (Thomas et al, 1995), while patients with metastasis of head and neck cancers have low NK and T-cell activity (Schantz et al, 1986).…”