The beneficial effect of yoghurt consumption on health and on the improvement of the mucosal immune system is well established, as is the diet-associated risk of colon cancer. In an experimental model in BALB=c mice we demonstrated that yoghurt added to the diet for 10 consecutive days, with the procedure repeated each 10 days for 6 months, inhibited the development of a colorectal carcinoma induced by 1,2 dimethylhydrazine (DMH). The immunoregulatory mechanisms involved in the inhibition of tumour growth by yoghurt were also examined in these studies. We determined B lymphocytes IgA þ and IgG þ , as well as CD4 þ and CD8 þ T cells in the large intestine. We measured cellular apoptosis and the cytokines TNF-a, IFN-g and IL-10. An increase in the number of IgA þ (P < 0.01) was observed, but not in IgG þ (P < 0.01), or in the CD4 þ population (P < 0.01) in the mice treated with DMH and yoghurt. While in the group with the carcinogen there was an enhancement in the IgG þ B cells (P < 0.01) and CD8 þ T cells (P < 0.01). Yoghurt increased the number of apoptotic cells and induced IFN-g and TNFa cytokine release, their production being regulated by an increase in IL-10 (P < 0.001). We demonstrated that yoghurt may exert antitumour activity by a decrease in the inflammatory immune response mediated by IgA þ increase, apoptosis induction and IL-10 release.