|
|
||||||||
24 NKT Cells from Cancer Patients Against
-Galactosylceramide1

* Department of Surgery, Institute of Clinical Medicine, University of Tsukuba, Tsukuba Science City, Ibaraki, Japan; and
Precursory Research for Embryonic Science and Technology, Kawaguchi, Saitama, Japan
Human invariant V
24+ NKT cells are a relatively new
subpopulation of lymphocytes. It has been reported that V
24 NKT
cells are significantly involved in some human diseases. We have
evaluated the number and function of V
24 NKT cells in both healthy
volunteers and cancer patients. In this study we found that V
24 NKT
cells in unfractionated PBMCs obtained from cancer patients did not
respond efficiently to
-galactosylceramide (
-GalCer) in vitro.
Thus, their proportion after stimulation with
-GalCer was smaller
than that found in healthy volunteers. However, the cancer patients
V
24 NKT cells retained cytotoxic activity against malignant target
cells, and they could efficiently proliferate to
-GalCer when
fractionated by sorting. Furthermore, we found that addition of G-CSF
to the culture could restore the low proliferative response of V
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.
This article has been cited by other articles:
![]() |
K. Yanagisawa, M. A. Exley, X. Jiang, N. Ohkochi, M. Taniguchi, and K.-i. Seino Hyporesponsiveness to Natural Killer T-Cell Ligand {alpha}-Galactosylceramide in Cancer-Bearing State Mediated by CD11b+ Gr-1+ Cells Producing Nitric Oxide Cancer Res., December 1, 2006; 66(23): 11441 - 11446. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Motohashi, A. Ishikawa, E. Ishikawa, M. Otsuji, T. Iizasa, H. Hanaoka, N. Shimizu, S. Horiguchi, Y. Okamoto, S.-i. Fujii, et al. A Phase I Study of In vitro Expanded Natural Killer T Cells in Patients with Advanced and Recurrent Non-Small Cell Lung Cancer Clin. Cancer Res., October 15, 2006; 12(20): 6079 - 6086. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Lizee, L. G. Radvanyi, W. W. Overwijk, and P. Hwu Improving Antitumor Immune Responses by Circumventing Immunoregulatory Cells and Mechanisms. Clin. Cancer Res., August 15, 2006; 12(16): 4794 - 4803. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. B. Atkins, D. E. Elder, R. Essner, K. T. Flaherty, T. F. Gajewski, F. G. Haluska, P. Hwu, U. Keilholz, J. M. Kirkwood, J. W. Mier, et al. Innovations and challenges in melanoma: summary statement from the first cambridge conference. Clin. Cancer Res., April 1, 2006; 12(7): 2291s - 2296s. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Crough, M. Nieda, and A. J. Nicol Granulocyte Colony-Stimulating Factor Modulates {alpha}-Galactosylceramide-Responsive Human V{alpha}24+V{beta}11+ NKT Cells J. Immunol., October 15, 2004; 173(8): 4960 - 4966. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. K. Sandberg, C. A. Stoddart, F. Brilot, K. A. Jordan, and D. F. Nixon Development of innate CD4+ {alpha}-chain variable gene segment 24 (V{alpha}24) natural killer T cells in the early human fetal thymus is regulated by IL-7 PNAS, May 4, 2004; 101(18): 7058 - 7063. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. S. Metelitsa, H.-W. Wu, H. Wang, Y. Yang, Z. Warsi, S. Asgharzadeh, S. Groshen, S. B. Wilson, and R. C. Seeger Natural Killer T Cells Infiltrate Neuroblastomas Expressing the Chemokine CCL2 J. Exp. Med., May 3, 2004; 199(9): 1213 - 1221. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. V. Dhodapkar, M. D. Geller, D. H. Chang, K. Shimizu, S.-I. Fujii, K. M. Dhodapkar, and J. Krasovsky A Reversible Defect in Natural Killer T Cell Function Characterizes the Progression of Premalignant to Malignant Multiple Myeloma J. Exp. Med., June 16, 2003; 197(12): 1667 - 1676. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |