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

HJ Gober, M Kistowska, L Angman, P Jenö… - The Journal of …, 2003 - rupress.org
HJ Gober, M Kistowska, L Angman, P Jenö, L Mori, G De Libero
The Journal of experimental medicine, 2003rupress.org
T lymphocytes expressing the T cell receptor (TCR)-γδ recognize unknown antigens on
tumor cells. Here we identify metabolites of the mevalonate pathway as the tumor ligands
that activate TCR-γδ 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-γδ cells. When metabolite accumulation is
induced by overexpressing HMGR or by treatment with nitrogen-containing bisphosphonate …
T lymphocytes expressing the T cell receptor (TCR)-γδ recognize unknown antigens on tumor cells. Here we identify metabolites of the mevalonate pathway as the tumor ligands that activate TCR-γδ 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-γδ 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 TCR-γδ 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.
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