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[Cancer Research 63, 3058-3060, June 15, 2003]
© 2003 American Association for Cancer Research


Advances in Brief

Inhibition of Early Tumor Growth Requires J{alpha}18-positive (Natural Killer T) Cells1

Trina J. Stewart, Mark J. Smyth, Germain J. P. Fernando, Ian H. Frazer and Graham R. Leggatt2

Centre for Immunology and Cancer Research, University of Queensland, Princess Alexandra Hospital, Brisbane, Queensland, 4102 [T. J. S., G. J. P. F., I. H. F., G. R. L.], and Cancer Immunology Program, Peter MacCallum Cancer Institute, East Melbourne, Victoria, 8006 [M. J. S.], Australia

The role of natural killer T (NKT) cells in the immune response to tumor cells has been largely unexplored. As a model of adoptive tumor immunotherapy, cells from the draining lymph nodes of mice immunized with a tumor-specific or irrelevant antigen were transferred to naïve recipients with established tumor. Inhibition of early tumor growth (day 4) required the transfer of both CD8+ and J{alpha}18+ (NKT) cells from immunized animals without regard to immunogen. In contrast, CD8+ cells, but not J{alpha}18+ cells, were necessary for the inhibition of late tumor growth (day 8). Thus, the developing tumor changes in sensitivity to NKT-mediated events and the role for NKT cells cannot be replaced by the presence of tumor-specific cells during early tumor growth. This suggests that recruitment/activation of J{alpha}18+ NKT cells is an important consideration during the immune therapy of early stage tumors.




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Cancer Research Clinical Cancer Research
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Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
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