Gene therapy with CCL2 (MCP-1) mutant protects CVB3-induced myocarditis by compromising Th1 polarization

Mol Immunol. 2011 Jan;48(4):706-13. doi: 10.1016/j.molimm.2010.11.018. Epub 2010 Dec 17.

Abstract

Viral myocarditis, which is most prevalently caused by Coxsackievirus B3 (CVB3) infection, affects about 5-20% of the world population and lacks efficient treatments. We previously reported that monocyte chemotactic protein-1 (MCP-1, CCL2) was significantly induced during CVB3 infection and greatly contributed to the myocardic inflammation and injury. Herein a CCL2 mutant with removed chemotactic activity was administrated and its therapeutic effect on CVB3-induced myocarditis was explored. A dominant negative CCL2 mutant, lacking the N-terminal amino acids 2-8 (CCL2(Δ2-8)), was genetically constructed and intramuscularly injected into BALB/c mice after CVB3 infection, severity of myocarditis was evaluated by weight loss, survival rate, serological indices and pathological observation. Systemic and local Th1/Th2 cytokine profiles were also assessed. Mice receiving pCCL2(Δ2-8) exhibited a profound attenuation of myocarditis compared to pcDNA3.1 or non-treated mice, as evidenced by invariant body weight, decreased serum CK-MB level, reduced myocardial inflammatory infiltration and increased survival. This effect was not attributable to the efficient viral clearance, but associated with weakened Th1 immune responses, as evidenced by significantly reduced CD4(+)IFN-γ(+) T cell frequency and Th1 cytokine level systemically and locally. Strategy of blocking in vivo CCL2 activity could effectively alleviate the severity of CVB3-induced myocarditis and may present an alternative therapeutic approach against viral myocarditis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Movement
  • Cell Polarity*
  • Chemokine CCL2 / genetics*
  • Chemokine CCL2 / metabolism
  • Chemokine CCL2 / therapeutic use*
  • Coxsackievirus Infections
  • Enterovirus / physiology
  • Genetic Therapy*
  • Humans
  • Interferon-gamma / metabolism
  • Interleukin-4 / metabolism
  • Mice
  • Mutant Proteins / administration & dosage
  • Mutant Proteins / genetics
  • Mutant Proteins / therapeutic use*
  • Myocarditis / immunology
  • Myocarditis / prevention & control*
  • Myocarditis / therapy
  • Myocarditis / virology
  • Myocardium / metabolism
  • Myocardium / pathology
  • Plasmids / administration & dosage
  • Plasmids / genetics
  • Spleen / cytology
  • Spleen / metabolism
  • Th1 Cells / cytology*
  • Th1 Cells / immunology
  • Th1 Cells / metabolism
  • Up-Regulation

Substances

  • CCL2 protein, human
  • Chemokine CCL2
  • Mutant Proteins
  • Interleukin-4
  • Interferon-gamma