Circulatory antigen processing by mucosal dendritic cells controls CD8(+) T cell activation

Immunity. 2013 Jan 24;38(1):153-65. doi: 10.1016/j.immuni.2012.09.018. Epub 2012 Dec 13.

Abstract

Circulatory antigens transit through the small intestine via the fenestrated capillaries in the lamina propria prior to entering into the draining lymphatics. But whether or how this process controls mucosal immune responses remains unknown. Here we demonstrate that dendritic cells (DCs) of the lamina propria can sample and process both circulatory and luminal antigens. Surprisingly, antigen cross-presentation by resident CX3CR1(+) DCs induced differentiation of precursor cells into CD8(+) T cells that expressed interleukin-10 (IL-10), IL-13, and IL-9 and could migrate into adjacent compartments. We conclude that lamina propria CX3CR1(+) DCs facilitate the surveillance of circulatory antigens and act as a conduit for the processing of self- and intestinally absorbed antigens, leading to the induction of CD8(+) T cells, that partake in the control of T cell activation during mucosal immune responses.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Antigen Presentation / immunology*
  • Antigens / immunology
  • CD4-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology*
  • CX3C Chemokine Receptor 1
  • Cell Differentiation / immunology
  • Cross-Priming / immunology
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Enteritis / immunology
  • Enteritis / prevention & control
  • Epitopes, T-Lymphocyte / immunology
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / immunology*
  • Intestine, Small / immunology
  • Lymphocyte Activation / immunology*
  • Mice
  • Receptors, Chemokine / immunology
  • Receptors, Chemokine / metabolism

Substances

  • Antigens
  • CX3C Chemokine Receptor 1
  • Cx3cr1 protein, mouse
  • Epitopes, T-Lymphocyte
  • Receptors, Chemokine