Cutting edge: cure of colitis by CD4+CD25+ regulatory T cells

J Immunol. 2003 Apr 15;170(8):3939-43. doi: 10.4049/jimmunol.170.8.3939.

Abstract

CD4(+)CD25(+) regulatory T cells have been shown to prevent T cell-mediated immune pathology; however, their ability to ameliorate established inflammation has not been tested. Using the CD4(+)CD45RB(high) T cell transfer model of inflammatory bowel disease, we show that CD4(+)CD25(+) but not CD4(+)CD25(-)CD45RB(low) T cells are able to cure intestinal inflammation. Transfer of CD4(+)CD25(+) T cells into mice with colitis led to resolution of the lamina propria infiltrate in the intestine and reappearance of normal intestinal architecture. CD4(+)CD25(+) T cells were found to proliferate in the mesenteric lymph nodes and inflamed colon. They were located between clusters of CD11c(+) cells and pathogenic T cells and found to be in contact with both cell types. These studies suggest that manipulation of CD4(+)CD25(+) T cells may be beneficial in the treatment of chronic inflammatory diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adoptive Transfer* / methods
  • Animals
  • CD11c Antigen / biosynthesis
  • CD4-Positive T-Lymphocytes / cytology
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / transplantation*
  • Cell Communication / immunology
  • Cell Division / immunology
  • Cell Movement / immunology
  • Colitis / immunology*
  • Colitis / pathology
  • Colitis / therapy*
  • Colon / cytology
  • Colon / immunology
  • Colon / metabolism
  • Colon / pathology
  • Lymph Nodes / cytology
  • Lymph Nodes / immunology
  • Lymph Nodes / metabolism
  • Mesentery
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, SCID
  • Receptors, Interleukin-2 / biosynthesis*
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocyte Subsets / metabolism
  • T-Lymphocyte Subsets / transplantation*
  • Wasting Syndrome / immunology
  • Wasting Syndrome / therapy

Substances

  • CD11c Antigen
  • Receptors, Interleukin-2