Differential mTOR and ERK pathway utilization by effector CD4 T cells suggests combinatorial drug therapy of arthritis

Clin Immunol. 2012 Feb;142(2):127-38. doi: 10.1016/j.clim.2011.09.008. Epub 2011 Oct 1.

Abstract

The signaling pathways utilized by naïve and experienced effector CD4 T cells during activation and proliferation were evaluated. While inhibition of either mTOR or MAPK alone was able to inhibit naïve T cell proliferation, both mTOR and MAPK (ERK) pathway inhibition was required to efficiently block experienced, effector CD4 T cell proliferation. This was demonstrated both in vitro, and in vivo by treating mice with collagen-induced arthritis using mTOR and/or ERK inhibitors. The combination of mTOR and ERK inhibition prevented or treated disease more efficiently than either agent alone. These data illustrate the different requirements of naïve and experienced effector CD4 T cells in the use of the mTOR and MAPK pathways in proliferation, and suggest that therapies targeting both the mTOR and MAPK pathways may be more effective than targeting either pathway alone in the treatment of CD4 T cell-mediated autoimmunity.

Publication types

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

MeSH terms

  • Animals
  • Arthritis, Experimental / immunology
  • Arthritis, Experimental / therapy*
  • Benzamides / pharmacology
  • Benzopyrans / pharmacology
  • Cell Proliferation / drug effects*
  • Chromones / pharmacology
  • Diphenylamine / analogs & derivatives
  • Diphenylamine / pharmacology
  • Drug Therapy, Combination
  • Female
  • Humans
  • Lymphocyte Activation / immunology
  • MAP Kinase Signaling System* / drug effects
  • MAP Kinase Signaling System* / immunology
  • Mice
  • Mice, Inbred BALB C
  • Monosaccharides / pharmacology
  • Morpholines / pharmacology
  • Sirolimus / pharmacology
  • T-Lymphocytes, Helper-Inducer* / immunology
  • T-Lymphocytes, Helper-Inducer* / metabolism
  • TOR Serine-Threonine Kinases* / antagonists & inhibitors
  • TOR Serine-Threonine Kinases* / immunology

Substances

  • Benzamides
  • Benzopyrans
  • Chromones
  • Monosaccharides
  • Morpholines
  • SL0101
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • mirdametinib
  • Diphenylamine
  • mTOR protein, mouse
  • TOR Serine-Threonine Kinases
  • Sirolimus