Susceptibility to LPS mitogenicity, an apparent B-cell function, was increased relatively and absolutely. The B-cell function of anti-SR BC production was also increased. Colonyforming units increased in number, but they were insuficient to account for significant proportions of the spleen cell population. It was concluded that the animal bearing a primary MCA tumor is deficient in neither T nor B cells and that the effect of the tumor upon immune function is stimulatory.In the course of experiments designed to explore further apparent manifestations of immuno deficiency in tumor-bearing animals (Adler el al., 1971b, a model system was developed in which the spleen and lymph nodes of mice bearing transplanted, syngeneic, methylcholanthreneinduced sarcomas were examined for evidence of competence at the cellular level (Smith and Konda, 1972; Konda and Smith, 1973a; Konda et al., 1973b;Forbes et al., 1973). Contrary to expectations, the absolute size of both the T-and B-cell subpopulations was increased in the spleen and lymph nodes. These conclusions were based upon both the assessment of cells bearing marker antigens and the numbers of cells capable of T-and B-cell functions. It could be argued, however, that the transplanted syngeneic tumor has a different effect on lympho-reticular function from that of a primary tumor, particularly in view of evidence that chemical carcinogens may have an immunodepressive effect (Stjernsward, 1966).Immunologic functions in animals developing primary tumors induced by methylcholanthrene were tested, therefore. In this report methylcholanthrene was used to induce tumors in five different mouse strains; the resultant tumors had varying latency periods and immunogenicity. The effect of these primary tumors upon immunologic functions at the cellular level was stimulatory and similar to those evoked by transplanted syngeneic tumors in each circumstance.