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
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