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[Cancer Research 32, 2201-2211, October 1, 1972]
© 1972 American Association for Cancer Research

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In Vivo and in Vitro Studies of the Influence of the Immune Status of C3Hf/Bu Mice on the Effectiveness of Local Irradiation of a Methylcholanthrene-induced Fibrosarcoma1

Mislav Jurin2 and Herman D. Suit3

Section of Experimental Radiotherapy, The University of Texas at Houston, M. D. Anderson Hospital and Tumor Institute, Houston, Texas 77025

The influence of the immune status of C3Hf/Bu mice on the effectiveness of local irradiation of a transplanted, methylcholanthrene-induced fibrosarcoma was studied. The numbers of tumor cells that transplanted the tumor into one-half of the recipients were 3.0 x 104, 2.9 x 102, and 5.7 x 105 for normal, immunodepressed, or immunized recipients, respectively. A tumor reached 12 mm in diameter more quickly when transplanted into immunized recipients than when transplanted into control animals. Also, the radiation dose that controlled one-half of the treated 12-mm tumors was about 1000 rads higher in immunized than in normal recipients. In vitro studies showed that lymphoid cells from tumorous mice were effective in inhibiting colony formation by fibrosarcoma cells. The degree of inhibition of colony formation by the lymphocytes decreased according to the size of tumor borne by the lymphocytes donor. Also, lymphocytes collected from tumor-bearing donors were less effective if the donor had been immunized prior to transplantation. The most effective lymphoid cells came from preimmunized but non-tumor-bearing donors. Serum from tumorous but not from immunized mice contained blocking antibodies, i.e., abolished inhibition of colony growth by lymphoid cells.

1 This work was supported in part by USPHS Grants CA 05047 and CA 6294.

2 Present address: Department of Biology, Rudjer Boskovic Institute, Zagreb, Croatia, Yugoslavia.

3 Present address: Department of Radiation of Radiation Medicine, Massachusetts General Hospital, Boston, Mass. 02114.

Received 2/25/72. Accepted 6/21/72.







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Copyright © 1972 by the American Association for Cancer Research.