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The Journal of Immunology, Vol 156, Issue 3 1117-1125, Copyright © 1996 by American Association of Immunologists
ARTICLES |
B Liu, ER Podack, JP Allison and TR Malek
Department of Microbiology and Immunology, University of Miami School of Medicine, FL 33136, USA.
This study investigated the generation of primary tumor-specific CTL activity in vitro to several mouse tumors. We report that the development of optimal primary tumor-specific CTL to the P815 mastocytoma, the EL4 thymoma, and the Lewis lung carcinoma is dependent on tumor Ags, on enhancement of T cell costimulation by B7.1, and on exogenous T helper activity in the form of IL-2 and IL-4. A relatively low concentration of IL-2 and IL-4 was required to limit the induction of lymphokine-activated killer cells. In the case of P815, the CTL were directed toward molecularly defined tumor rejection Ags. These primary cultures yielded long term T cell lines that were heterogeneous in fine tumor Ag specificity and in cytokine production.
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