Expansion of lung Vα14 NKT cells by administration of α-galactosylceramide-pulsed dendritic cells

被引:27
作者
Akutsu, Y
Nakayama, T
Harada, M
Kawano, T
Motohashi, S
Shimizu, E
Ito, T
Kamada, N
Saito, T
Matsubara, H
Miyazawa, Y
Ochiai, T
Taniguchi, M
机构
[1] JST, CREST Project, Kawaguchi, Saitama 3320012, Japan
[2] RIKEN, Res Ctr Allergy & Immunol, Lab Immune Regulat, Tsurumi Ku, Kanagawa 2300045, Japan
[3] Chiba Univ, Grad Sch Med, Acad Dept Surg, Chuo Ku, Chiba 2608670, Japan
[4] Chiba Univ, Grad Sch Med, Dept Med Immunol, Chuo Ku, Chiba 2608670, Japan
[5] Chiba Univ, Grad Sch Med, Dept Mol Immunol, Chuo Ku, Chiba 2608670, Japan
来源
JAPANESE JOURNAL OF CANCER RESEARCH | 2002年 / 93卷 / 04期
关键词
NKT cell; dendritic cell; alpha-galactosylceramide;
D O I
10.1111/j.1349-7006.2002.tb01270.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
NKT cells, a novel murine lymphoid lineage bearing an invariant T cell receptor encoded by Valpha14 and Jalpha281 gene segments, recognize a specific ligand glycolipid, alpha-galactosylceramide (alpha-GalCer) in a CD1d-dependent manner. Recent research has revealed that activated Valpha14 NKT cells have dramatic antitumor effects against a wide variety of tumor cell lines in vivo and in vitro. Here, we demonstrate strong in vivo antitumor effects brought about by treatment with alpha-GalCer-pulsed dendritic cells in comparison with in vitro-activated Valpha14 NKT cells. Furthermore, we show a significant expansion of endogenous Valpha14 NKT cells in the lung following the administration of alpha-GalCer-pulsed dendritic cells. The feasibility of immunotherapy with alpha-GalCer-pulsed dendritic cells is discussed.
引用
收藏
页码:397 / 403
页数:7
相关论文
共 39 条
[1]  
Brandau S, 2001, INT J CANCER, V92, P697, DOI 10.1002/1097-0215(20010601)92:5<697::AID-IJC1245>3.0.CO
[2]  
2-Z
[3]   CD1d-mediated recognition of an α-galactosylceramide by natural killer T cells is highly conserved through mammalian evolution [J].
Brossay, L ;
Chioda, M ;
Burdin, N ;
Koezuka, Y ;
Casorati, G ;
Dellabona, P ;
Kronenberg, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 188 (08) :1521-1528
[4]   Antigen-presenting function of mouse CD1: one molecule with two different kinds of antigenic ligands [J].
Brossay, L ;
Burdin, N ;
Tangri, S ;
Kronenberg, M .
IMMUNOLOGICAL REVIEWS, 1998, 163 :139-150
[5]  
Burdin N, 1998, J IMMUNOL, V161, P3271
[6]   THE CELL-SURFACE OF MOUSE DENDRITIC CELLS - FACS ANALYSES OF DENDRITIC CELLS FROM DIFFERENT TISSUES INCLUDING THYMUS [J].
CROWLEY, M ;
INABA, K ;
WITMERPACK, M ;
STEINMAN, RM .
CELLULAR IMMUNOLOGY, 1989, 118 (01) :108-125
[7]   Selective expansion and partial activation of human NK cells and NK receptor-positive T cells by IL-2 and IL-15 [J].
Dunne, J ;
Lynch, S ;
O'Farrelly, C ;
Todryk, S ;
Hegarty, JE ;
Feighery, C ;
Doherty, DG .
JOURNAL OF IMMUNOLOGY, 2001, 167 (06) :3129-3138
[8]   Adoptive cellular immunotherapy for the treatment of malignant gliomas [J].
Hayes, RL ;
Arbit, E ;
Odaimi, M ;
Pannullo, S ;
Scheff, R ;
Kravchinskiy, D ;
Zaroulis, C .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2001, 39 (1-2) :31-42
[9]   The natural killer T-cell ligand α-galactosylceramide prevents autoimmune diabetes in non-obese diabetic mice [J].
Hong, S ;
Wilson, MT ;
Serizawa, I ;
Wu, L ;
Singh, N ;
Naidenko, OV ;
Miura, T ;
Haba, T ;
Scherer, DC ;
Wei, J ;
Kronenberg, M ;
Koezuka, Y ;
Van Kaer, L .
NATURE MEDICINE, 2001, 7 (09) :1052-1056
[10]   ADOPTIVE IMMUNOTHERAPY FOR HEAD AND NECK-CANCER WITH KILLER CELLS INDUCED BY STIMULATION WITH AUTOLOGOUS OR ALLOGENEIC-TUMOR CELLS AND RECOMBINANT INTERLEUKIN-2 [J].
ISHIKAWA, T ;
IKAWA, T ;
EURA, M ;
FUKIAGE, T ;
MASUYAMA, K .
ACTA OTO-LARYNGOLOGICA, 1989, 107 (5-6) :346-351