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The Journal of Immunology, 2002, 168: 6494-6499.
Copyright © 2002 by The American Association of Immunologists

Impaired Proliferative Response of V{alpha}24 NKT Cells from Cancer Patients Against {alpha}-Galactosylceramide1

Kazuhiko Yanagisawa*, Ken-ichiro Seino2,*,{dagger}, Yuriko Ishikawa*, Mutsumi Nozue*, Takeshi Todoroki* and Katashi Fukao*

* Department of Surgery, Institute of Clinical Medicine, University of Tsukuba, Tsukuba Science City, Ibaraki, Japan; and {dagger} Precursory Research for Embryonic Science and Technology, Kawaguchi, Saitama, Japan

Human invariant V{alpha}24+ NKT cells are a relatively new subpopulation of lymphocytes. It has been reported that V{alpha}24 NKT cells are significantly involved in some human diseases. We have evaluated the number and function of V{alpha}24 NKT cells in both healthy volunteers and cancer patients. In this study we found that V{alpha}24 NKT cells in unfractionated PBMCs obtained from cancer patients did not respond efficiently to {alpha}-galactosylceramide ({alpha}-GalCer) in vitro. Thus, their proportion after stimulation with {alpha}-GalCer was smaller than that found in healthy volunteers. However, the cancer patients’ V{alpha}24 NKT cells retained cytotoxic activity against malignant target cells, and they could efficiently proliferate to {alpha}-GalCer when fractionated by sorting. Furthermore, we found that addition of G-CSF to the culture could restore the low proliferative response of V{alpha}24 NKT cells from cancer patients. These results suggest that some functions of NKT cells in cancer patients are impaired, and this observation carries significant implications for immunotherapy-based cancer treatments.




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