Treatment of lupus-prone mice with a dual inhibitor of TLR7 and TLR9 leads to reduction of autoantibody production and amelioration of disease symptoms. Academic Article uri icon

Overview

abstract

  • The presence of autoantibodies specific for nucleic acid-associated antigens is the hallmark of systemic lupus erythematosus (SLE). We have recently developed a specific inhibitor of TLR7 and TLR9, called immunoregulatory sequence (IRS) 954, and showed that it inhibits the induction of IFN-alpha by human plasmacytoid dendritic cells in response to DNA and RNA viruses and isolated immune complexes from lupus patients. In this study, we show that IRS 954 can prevent progression of disease when injected in the lupus prone (NZBxNZW)F1 mice. Following treatment, we observed a significant reduction of serum levels of nucleic acid-specific autoantibodies as well as decreased proteinuria, reduced glomerulonephritis, end-organ damage and increased survival. These data demonstrate that in addition to its ability to block IFN-alpha, IRS 954 can reduce symptoms in a lupus model and thus represents a promising therapeutic agent for the treatment of SLE.

publication date

  • December 1, 2007

Research

keywords

  • Autoantibodies
  • DNA
  • Immunosuppressive Agents
  • Lupus Erythematosus, Systemic
  • Membrane Glycoproteins
  • Toll-Like Receptor 7
  • Toll-Like Receptor 9

Identity

Scopus Document Identifier

  • 37549066665

Digital Object Identifier (DOI)

  • 10.1002/eji.200737815

PubMed ID

  • 18034431

Additional Document Info

volume

  • 37

issue

  • 12