Natural variation of macrophage activation as disease-relevant phenotype predictive of inflammation and cancer survival

Nat Commun. 2017 Jul 24:8:16041. doi: 10.1038/ncomms16041.

Abstract

Although mouse models exist for many immune-based diseases, the clinical translation remains challenging. Most basic and translational studies utilize only a single inbred mouse strain. However, basal and diseased immune states in humans show vast inter-individual variability. Here, focusing on macrophage responses to lipopolysaccharide (LPS), we use the hybrid mouse diversity panel (HMDP) of 83 inbred strains as a surrogate for human natural immune variation. Since conventional bioinformatics fail to analyse a population spectrum, we highlight how gene signatures for LPS responsiveness can be derived based on an Interleukin-12β and arginase expression ratio. Compared to published signatures, these gene markers are more robust to identify susceptibility or resilience to several macrophage-related disorders in humans, including survival prediction across many tumours. This study highlights natural activation diversity as a disease-relevant dimension in macrophage biology, and suggests the HMDP as a viable tool to increase translatability of mouse data to clinical settings.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Genetic Predisposition to Disease
  • Genetic Variation*
  • Humans
  • Immunity, Innate / genetics
  • Inflammation
  • Lipopolysaccharides
  • Macrophage Activation / genetics*
  • Male
  • Mice
  • Models, Animal*
  • Neoplasms / immunology
  • Neoplasms / mortality
  • Phenotype

Substances

  • Lipopolysaccharides