Immunological Aspects of Cancer 1978
DOI: 10.1007/978-94-010-9418-4_14
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Experimental non-specific immunotherapy

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Cited by 3 publications
(3 citation statements)
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“…Much research and discussion has centered around the therapy of experimental and human cancers using agents whose traditional biologic function is modification of RES activity (Gutterman et al, 1978;Bast and Bast, 1976;Sadler and Castro, 1978). The rationale for evaluation of RES stimulants as anti-tumor agents has often been based on the premise that they activate cells of the host defense systems to become potentially cytotoxic for malignant cells (Levy and Wheelock, 1974;Schultz et al, 1976).…”
Section: Discussionmentioning
confidence: 99%
“…Much research and discussion has centered around the therapy of experimental and human cancers using agents whose traditional biologic function is modification of RES activity (Gutterman et al, 1978;Bast and Bast, 1976;Sadler and Castro, 1978). The rationale for evaluation of RES stimulants as anti-tumor agents has often been based on the premise that they activate cells of the host defense systems to become potentially cytotoxic for malignant cells (Levy and Wheelock, 1974;Schultz et al, 1976).…”
Section: Discussionmentioning
confidence: 99%
“…Accordingly, live, attenuated, or killed facultative intracellular pathogens, known to augment immunity to infectious agents, were among the earliest factors introduced in cancer immunotherapy. Such microbial agents, particularly BCG and CP, are capable of inducing anti-tumor activity in defined animal models and in some solid human tumors (Laucius et al, 1974;Scott, 1974;Sadler and Castro, 1978;Herberman, 1980;Woodruff, 1980;Morales and Ersil, 1982). Such treatments may also be effective in autochthonous tumors without detectable immunogenicity, suggesting that nonspecific mechanisms, as mediated by activated MP, NK and/or LAK cells, are dominant (Laucius et al, 1974;Scott, 1974;Sadler and Castro, 1978;Oldham, 1987).…”
mentioning
confidence: 97%
“…Such microbial agents, particularly BCG and CP, are capable of inducing anti-tumor activity in defined animal models and in some solid human tumors (Laucius et al, 1974;Scott, 1974;Sadler and Castro, 1978;Herberman, 1980;Woodruff, 1980;Morales and Ersil, 1982). Such treatments may also be effective in autochthonous tumors without detectable immunogenicity, suggesting that nonspecific mechanisms, as mediated by activated MP, NK and/or LAK cells, are dominant (Laucius et al, 1974;Scott, 1974;Sadler and Castro, 1978;Oldham, 1987). The present work is a further attempt to analyze the complex processes involved in the interaction of tumor and host in vivo, utilizing the operationally simple and reproducible DA rat D-12 ascites tumor model (Keller, 1976(Keller, , 1977(Keller, , 1980.…”
mentioning
confidence: 97%