Human T cell receptor γδ cells recognize endogenous mevalonate metabolites in tumor cells

被引:711
作者
Gober, HJ
Kistowska, M
Angman, L
Jenö, P
Mori, L
De Libero, G
机构
[1] Univ Basel Hosp, Dept Res, CH-4031 Basel, Switzerland
[2] Univ Basel, Bioctr, Dept Biochem, CH-4056 Basel, Switzerland
关键词
antigen recognition; tumor antigen; HMGR; IPP; bisphosphonate drugs;
D O I
10.1084/jem.20021500
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T lymphocytes expressing the T cell receptor (TCR)-gammadelta recognize unknown antigens on tumor cells. Here we identify metabolites of the mevalonate pathway as the tumor ligands that activate TCR-gammadelta cells. In tumor cells, blockade of hydroxy-methylglutaryl-CoA reductase (HMGR), the rate limiting enzyme of the mevalonate pathway, prevents both accumulation of mevalonate metabolites and recognition by TCR-gammadelta cells. When metabolite accumulation is induced by overexpressing HMGR, or by treatment with nitrogen-containing bisphosphonate drugs, tumor cells derived from many tissues acquire the capacity to stimulate the same TCP-gammadelta population. Accumulation of mevalonate metabolites in tumor cells is a powerful danger signal that activates the immune response and may represent a novel target of tumor immunotherapy.
引用
收藏
页码:163 / 168
页数:6
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