α-Galactosylceramide-activated Vα14 natural killer T cells mediate protection against murine malaria

被引:237
作者
Gonzalez-Aseguinolaza, G
de Oliveira, C
Tomaska, M
Hong, S
Bruna-Romero, O
Nakayama, T
Taniguchi, M
Bendelac, A
Van Kaer, L
Koezuka, Y
Tsuji, M
机构
[1] NYU, Sch Med, Dept Med & Mol Parasitol, New York, NY 10010 USA
[2] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Howard Hughes Med Inst, Nashville, TN 37232 USA
[3] Chiba Univ, Sch Med, Dept Mol Immunol, Chiba 260, Japan
[4] Princeton Univ, Dept Biol Mol, Princeton, NJ 08544 USA
[5] Kirin Brewery Co Ltd, Pharmaceut Res Lab, Gunma 370, Japan
关键词
D O I
10.1073/pnas.97.15.8461
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Natural killer T (NKT) cells are a unique population of lymphocytes that coexpress a semiinvariant T cell and natural killer cell receptors, which are particularly abundant in the liver. To investigate the possible effect of these cells on the development of the liver stages of malaria parasites, a glycolipid. alpha-galactosylceramide (alpha-GalCer), known to selectively activate V alpha 14 NKT cells in the context of CD1d molecules, was administered to sporozoite-inoculated mice. The administration of alpha-GalCer resulted in rapid, strong antimalaria activity, inhibiting the development of the intrahepatocytic stages of the rodent malaria parasites Plasmodium yoelii and Plasmodium berghei. The antimalaria activity mediated by alpha-GalCer is stage-specific, since the course of blood-stage-induced infection was not inhibited by administration of this glycolipid. Furthermore, it was determined that IFN-gamma is essential for the antimalaria activity mediated by the glycolipid. Taken together, our results provide the clear evidence that NKT cells can mediate protection against an intracellular microbial infection.
引用
收藏
页码:8461 / 8466
页数:6
相关论文
共 42 条
[1]   Murine natural killer cells contribute to the granulomatous reaction caused by mycobacterial cell walls [J].
Apostolou, I ;
Takahama, Y ;
Belmant, C ;
Kawano, T ;
Huerre, M ;
Marchal, G ;
Cui, J ;
Taniguchi, M ;
Nakauchi, H ;
Fournié, JJ ;
Kourilsky, P ;
Gachelin, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) :5141-5146
[2]   MOUSE NK1(+) T-CELLS [J].
BENDELAC, A .
CURRENT OPINION IN IMMUNOLOGY, 1995, 7 (03) :367-374
[3]   Mouse CD1-specific NK1 T cells: Development, specificity, and function [J].
Bendelac, A ;
Rivera, MN ;
Park, SH ;
Roark, JH .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :535-562
[4]   CD1 RECOGNITION BY MOUSE NK1(+) T-LYMPHOCYTES [J].
BENDELAC, A ;
LANTZ, O ;
QUIMBY, ME ;
YEWDELL, JW ;
BENNINK, JR ;
BRUTKIEWICZ, RR .
SCIENCE, 1995, 268 (5212) :863-865
[5]   The large difference in infectivity for mice of Plasmodium berghei and Plasmodium yoelii sporozoites cannot be correlated with their ability to enter into hepatocytes [J].
Briones, MRS ;
Tsuji, M ;
Nussenzweig, V .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1996, 77 (01) :7-17
[6]  
Burdin N, 1998, J IMMUNOL, V161, P3271
[7]  
Carnaud C, 1999, J IMMUNOL, V163, P4647
[8]   Impaired NK1(+) T cell development and early IL-4 production in CD1-deficient mice [J].
Chen, YH ;
Chiu, NM ;
Mandal, M ;
Wang, N ;
Wang, CR .
IMMUNITY, 1997, 6 (04) :459-467
[9]   Primaquine resistance in Plasmodium vivax [J].
Collins, WE ;
Jeffery, GM .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1996, 55 (03) :243-249
[10]   Requirement for V(alpha)14 NKT cells in IL-12-mediated rejection of tumors [J].
Cui, JQ ;
Shin, T ;
Kawano, T ;
Sato, H ;
Kondo, E ;
Toura, I ;
Kaneko, Y ;
Koseki, H ;
Kanno, M ;
Taniguchi, M .
SCIENCE, 1997, 278 (5343) :1623-1626