By George Klein, Sidney Weinhouse, Alexander Haddow (Eds.)
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HALL adopting this procedure, one of us (Hall and Glover, unpublished) was able to retard the growth of primary rat sarcomata which had merely been biopsied but which had not been irradiated. I n other words, the sporadic effects observed by Haddow (1965) were converted into a response seen in 60% of the treated animals by changing to a more widespread regime for the immunization. The advantage of multiple over single sites of immunization, even when the total number of irradiated tumor cells used is the same, was also apparent from experiments (Parr, 1970) involving the arrest of mouse lymphomas.
Ezptl. Biol. Med. 125, 96% 968. Parr. I. (1970). Proc. 4th Conf. Cancer. Immunity Tolerance Oncogeneszs. , Perugia, Italy (in press). , Muller-Eberhard, H. J.. and Manni. J. A. (1969). Science 163, 937-939. Pilch, Y. , and Riggins, R. S. (1966). Cancer Res. 26, 871-875. Prehn, R. T. (1963). J . Natl. Cancer Inst. 31, 791-805. Prendergast, R. A. (1964). J . E x p t l . Med. 119, 377-388. Rudenstam, C. M. (1970). Proc. 4th Conf. Cancer. Immunity Tolerance Oncogenesis. , Perugia, Italy (in press).
The advantage of multiple over single sites of immunization, even when the total number of irradiated tumor cells used is the same, was also apparent from experiments (Parr, 1970) involving the arrest of mouse lymphomas. In one of the tumors, a n effect was only seen following multiple immunization, and a single immunization failed t o arrest the growth of even a very small innoculum of 100 cells. I n the studies of human malignant melanoma to which reference has already been made (see p. 281, an effect of autografting on immunity was only observed in those patients who were injected with irradiated tumor cells a t many different sites.