G-CSF drives a posttraumatic immune program that protects the host from infection

J Immunol. 2014 Mar 1;192(5):2405-17. doi: 10.4049/jimmunol.1302752. Epub 2014 Jan 27.

Abstract

Traumatic injury is generally considered to have a suppressive effect on the immune system, resulting in increased susceptibility to infection. Paradoxically, we found that thermal injury to the skin induced a robust time-dependent protection of mice from a lethal Klebsiella pneumoniae pulmonary challenge. The protective response was neutrophil dependent and temporally associated with a systemic increase in neutrophils resulting from a reprioritization of hematopoiesis toward myeloid lineages. A prominent and specific activation of STAT3 in the bone marrow preceded the myeloid shift in that compartment, in association with durable increases in STAT3 activating serum cytokines G-CSF and IL-6. Neutralization of the postburn increase in serum G-CSF largely blocked STAT3 activation in marrow cells, reversing the hematopoietic changes and systemic neutrophilia. Daily administration of rG-CSF was sufficient to recapitulate the changes induced by injury including hematopoietic reprioritization and protection from pulmonary challenge with K. pneumoniae. Analysis of posttraumatic gene expression patterns in humans reveals that they are also consistent with a role for G-CSF as a switch that activates innate immune responses and suppresses adaptive immune responses. Our findings suggest that the G-CSF STAT3 axis constitutes a key protective mechanism induced by injury to reduce the risk for posttraumatic infection.

Publication types

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

MeSH terms

  • Adaptive Immunity
  • Animals
  • Bone Marrow Cells / immunology
  • Bone Marrow Cells / metabolism
  • Bone Marrow Cells / pathology
  • Burns / blood
  • Burns / complications
  • Burns / immunology*
  • Burns / pathology
  • Granulocyte Colony-Stimulating Factor / blood
  • Granulocyte Colony-Stimulating Factor / immunology*
  • Immunity, Innate
  • Interleukin-6 / blood
  • Interleukin-6 / immunology
  • Klebsiella Infections / blood
  • Klebsiella Infections / etiology
  • Klebsiella Infections / immunology*
  • Klebsiella Infections / pathology
  • Klebsiella pneumoniae / immunology*
  • Mice
  • Neutrophils / immunology
  • Neutrophils / metabolism
  • Neutrophils / pathology
  • Pneumonia, Bacterial / blood
  • Pneumonia, Bacterial / etiology
  • Pneumonia, Bacterial / immunology*
  • Pneumonia, Bacterial / pathology
  • STAT3 Transcription Factor / immunology
  • STAT3 Transcription Factor / metabolism

Substances

  • Interleukin-6
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Granulocyte Colony-Stimulating Factor