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Myeloid Cells in Alzheimer's Disease: Culprits, Victims or Innocent Bystanders?

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TRENDS IN NEUROSCIENCES
卷 38, 期 10, 页码 659-668

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ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tins.2015.08.011

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资金

  1. Emmy Noether Program of the German Research Foundation (DFG)
  2. Research Unit of the DFG [FOR1336]
  3. Hans and Ilse Breuer Foundation
  4. Federal Ministry of Education and Research (BMBF)
  5. Gemeinnutzige Hertie-Stiftung (GHST)
  6. Sobek-Stiftung
  7. Fritz Thyssen Stiftung
  8. DFG [SFB 992, SFB1160]

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Several recent genome-wide association studies (GWAS) in patients with neurodegenerative disorders have shed new light on the brain immune system, suggesting that it plays a pivotal role in disease pathogenesis. Mononuclear phagocytes are blatantly involved in Alzheimer's disease (AD) of the central nervous system (CNS), but the specific functions of resident microglia, perivascular or meningeal macrophages, and circulating myeloid cells have not yet been fully resolved. Next-generation sequencing, high-throughput immune profiling technologies, and novel genetic tools have recently revolutionized the characterization of innate immune responses during AD. These studies advocate selective and non-redundant roles for myeloid subsets, which could be a target for novel disease-modifying therapies in AD.

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