Glial cells as drug targets: What does it take?

Thomas Moller*, Hendrikus W. G. M. Boddeke

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

20 Citations (Scopus)

Abstract

The last two decades have brought a significant increase in our understanding of glial biology and glial contribution to CNS disease. Yet, despite the fact that glial cells make up the majority of CNS cells, no drug specifically targeting glial cells is on the market. Given the long development times of CNS drugs, on average over 12 years, this is not completely surprising. However, there is increasing interest from academia and industry to exploit glial targets to develop drugs for the benefit of patients with currently limited or no therapeutic options. CNS drug development has a high attrition rate and has encountered many challenges. It seems unlikely that developing drugs against glial targets would be any less demanding. However, the knowledge generated in traditional CNS drug discovery teaches valuable lessons, which could enable the glial community to accelerate the cycle time from basic discovery to drug development. In this review we will discuss steps necessary to bring a "glial target idea" to a clinical development program.

Original languageEnglish
Pages (from-to)1742-1754
Number of pages13
JournalGlia
Volume64
Issue number10
DOIs
Publication statusPublished - Oct-2016

Keywords

  • drug target
  • microglia
  • target identification
  • target validation
  • screening cascade
  • assay development
  • high throughput screen
  • reproducibility
  • collaboration
  • BLOOD-BRAIN-BARRIER
  • IN-VITRO
  • ALZHEIMERS-DISEASE
  • COMPOUND QUALITY
  • PHENOTYPIC ASSAY
  • CHEMICAL PROBES
  • ANIMAL-MODELS
  • MICROGLIA
  • DISCOVERY
  • MEDICINES

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