Monocyte chemoattractant protein-1 activates a regional Th1 immunoresponse in nephritis of MRL/lpr mice

Clin Exp Rheumatol. 2005 Mar-Apr;23(2):239-42.

Abstract

Objective: Monocyte chemoattractant protein-1 (MCP-1) is upregulated and recruits and activates inflammatory cells in nephritis of MRL lpr mice. It has been shown that anti-MCP-1 gene therapy is specifically effective in nephritis, while it was apparent that an imbalance towards Th1 predominance accelerates nephritis in MRL/lpr mice. The aim of this study was to clarify whether blockade of the MCP-1 signal by anti-MCP-1 gene therapy influences the Th1/Th2 balance in MRL/lpr mice.

Method: An NH2-terminal deletion mutant of the MCP-1 gene (7ND) was injected into the skeletal muscles of MRL/Ipr mice with advanced stage nephritis to suppress MCP-1 and its receptor (CCR2) signaling pathway. We evaluated the local tissue production of cytokines in splenocytes and microdissected infiltrating cells within the glomeruli or interstitium.

Result: Although the production of cytokines in splenocytes was not influenced by anti-MCP-1 gene therapy, kidney glomeruli IL-12 mRNA production and interstitium-infiltrating cell production of IL-12 and IFN-gamma mRNA were significantly reduced.

Conclusion: The blockade of MCP-1 gene therapy does not influence helper T cell polarization, but acts directly on the regional Th1 immunoreaction in MRL/lpr mice.

MeSH terms

  • Animals
  • Chemokine CCL2 / antagonists & inhibitors
  • Chemokine CCL2 / genetics*
  • Chemokine CCL2 / metabolism
  • Disease Models, Animal
  • Gene Expression Regulation
  • Genetic Therapy* / methods
  • Humans
  • Interferon-gamma / genetics
  • Interferon-gamma / metabolism
  • Interleukin-12 / genetics
  • Interleukin-12 / metabolism
  • Kidney Glomerulus / metabolism
  • Kidney Glomerulus / pathology
  • Lupus Nephritis / genetics
  • Lupus Nephritis / metabolism
  • Lupus Nephritis / pathology
  • Lupus Nephritis / therapy*
  • Mice
  • Mice, Inbred MRL lpr
  • RNA, Messenger / biosynthesis
  • Th1 Cells / immunology
  • Th1 Cells / metabolism*
  • Th2 Cells / immunology
  • Th2 Cells / metabolism

Substances

  • Ccl2 protein, mouse
  • Chemokine CCL2
  • RNA, Messenger
  • Interleukin-12
  • Interferon-gamma