Journal
CELL
Volume 172, Issue 1-2, Pages 135-+Publisher
CELL PRESS
DOI: 10.1016/j.cell.2017.11.025
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Funding
- ERC [310372]
- Netherlands Organization for Scientific Research (NWO)
- NHMRC (Australia) CJ Martin Early Career Fellowship
- Netherlands Heart Foundation [2012T051]
- Romanian Ministry of European Funds (HINT) [P_37_762]
- European Union [667837]
- Ipsen Pharmaceuticals
- ERC (DEMETINL)
- IN-CONTROL CVON grant [CVON2012-03]
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Innate immune cells can develop long-term memory after stimulation by microbial products during infections or vaccinations. Here, we report that metabolic signals can induce trained immunity. Pharmacological and genetic experiments reveal that activation of the cholesterol synthesis pathway, but not the synthesis of cholesterol itself, is essential for training of myeloid cells. Rather, the metabolite mevalonate is the mediator of training via activation of IGF1-R and mTOR and subsequent histone modifications in inflammatory pathways. Statins, which block mevalonate generation, prevent trained immunity induction. Furthermore, monocytes of patients with hyper immunoglobulin D syndrome (HIDS), who are mevalonate kinase deficient and accumulate mevalonate, have a constitutive trained immunity phenotype at both immunological and epigenetic levels, which could explain the attacks of sterile inflammation that these patients experience. Unraveling the role of mevalonate in trained immunity contributes to our understanding of the pathophysiology of HIDS and identifies novel therapeutic targets for clinical conditions with excessive activation of trained immunity.
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