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Embryo-derived teratocarcinomas elicit splenomegaly in syngeneic host

Abstract

MOUSE egg-cylinders transplanted to extrauterine sites develop either as teratomas (benign tumours composed of adult tissues) or as teratocarcinomas (retransplantable malignant tumours containing, in addition, undifferentiated embryonic carcinoma cells)1–4. Rat egg-cylinders similarly transplanted, however, always develop as teratoma5. When transplanted to a syngeneic host, C57BL mouse egg-cylinders develop as teratomas but when transplanted to (C3H × C57BL)F1 hybrids they develop into teratocarcinoma3,4. This suggests that the host reaction is important in determining the fate of a transplanted embryo. Specific embryonic and foetal antigens which are re-expressed during malignant transformation are now well established6–8, and we thought that an immunological reaction of the host against embryonic antigens in the egg-cylinder might determine whether the transplant develops as teratoma or teratocarcinoma. Splenomegaly is considered to be a sign that a host has reacted to the antigenic stimulation of a graft or tumour9,10, and we have found that although it is always present in mice with transplanted egg-cylinders, it is much more pronounced in those with teratocarcinoma. Splenectomy, however, reduced the growth of the transplanted embryos, suggesting that the immunological reaction of the host stimulates the growth of the graft.

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to which reprint requests should be sent: Wistar Institute, Philadelphia, Pennsylvania 19104.

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DAMJANOV, I., SOLTER, D. Embryo-derived teratocarcinomas elicit splenomegaly in syngeneic host. Nature 249, 569–571 (1974). https://doi.org/10.1038/249569a0

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