Summary.-Local injection (i.e. injection at the site of tumour inoculation) of strains of C. Parvum which have a significant anti-tumour effect when given systemically (i.e. intravenously or, in the case of subcutaneous tumour transplant, intraperitoneally) strongly inhibits the growth of isogeneic transplants of a fibrosarcoma in intact CBA mice but has little or no effect on subcutaneous transplants of the same tumour in T-cell deprived mice. The anti-tumour effect of local injection of C. parvum, unlike that of systemic injection in this particular tumour system, thus appears to be T-cell dependent.PRELIMINARY observations of our own with a mouse fibrosarcoma, and experiments with other mouse tumours recently reported by Likhite and Halpern (1974) and Scott (1974), have shown that intratumour injection of C. parvum may strongly inhibit tumour growth and under some conditions cause complete regression.The present experiments were designed to investigate this phenomenon further, using both subcutaneous and intraperitoneal tumour transplants. To exclude purely mechanical effects we have compared the degree of tumour inhibition resulting from local injection of 3 anaerobic coryneforms which differ markedly in their effect on tumour growth when given systemically, and of an aerobic organism, C. diphtheriae.We have used as tumour hosts both intact and T-cell deprived mice, because in our own experience (Wooodruff and Dunbar, 1972;Woodruff, Dunbar and Ghaffar, 1973), the anti-tumour effect of systemic injections of active strains of C. parvum in respect of cholanthrene induced sarcomata is maintained in T-cell deficient mice, whereas Scott (1974) has reported that the growth of a mastocytoma, is inhibited by intratumour injection of C. parvum in intact mice but not in T-cell deprived mice.
MATERIALS AND METHODSMice.-The recipient mice were either intact adult CBA females (20-22 g) or T-cell deprived CBA females prepared as described previously (Woodruff et al., 1973).Tumour. The tumour was originally induced in a female CBA mouse with methylcholanthrene. It was stored in liquid nitrogen after 1]5 transplant generations and was transplanted once more before being used in the experiments. The properties of this tumour have been summarized in a recent review (Woodruff, 1975). It was transplanted subcutaneously (right foreleg) or intraperitoneally, or by both these routes, in the form of a cell suspension prepared with pronase in a dosage (unless otherwise stated) of 104 cells.The mice were inspected and weighed every 2 days. If a subcutaneous tumour was present, its width in 2 directions at rightangles was measured with a caliper and the mean was recorded. Where appropriate, the diameters of subcutaneous tumours were summed, as described previously (Woodruff et al., 1973), up to the day when some of the tumours in control mice were 18-20 mm in diameter, and the group mean sums were compared by Student's t-test. In many cases, however, the differences between groups were sufficiently clearcut to make this unnecessary.