Hematopoietic LTβR deficiency results in skewed T cell cytokine profiles during a mucosal viral infection

J Leukoc Biol. 2016 Jul;100(1):103-10. doi: 10.1189/jlb.4MAB0715-294R. Epub 2015 Dec 10.

Abstract

The lymphotoxin signaling pathway plays an important role in the homeostasis and function of peripheral and mucosal dendritic cells, and dendritic cell-intrinsic lymphotoxin β receptor expression is required for optimal responses to opportunistic intestinal bacteria. However, it is unknown whether dendritic cell-intrinsic lymphotoxin β receptor signaling is required for responses to intestinal viral infections. We explored this question by orally administrating murine rotavirus to chimeric mice that lack lymphotoxin β receptor signaling in the myeloid compartment but retain lymphoid tissues. We found that although clearance of rotavirus was unimpaired in the lymphotoxin β receptor(-/-) → wild-type chimeric mice compared with wild-type → wild-type chimeric mice, IFN-γ-producing CD8(+) and CD4(+) T cells were significantly increased in the small intestinal lamina propria of lymphotoxin β receptor(-/-) → wild-type chimeric mice. In contrast, IL-17-producing CD4(+) T cells were reduced in lymphotoxin β receptor(-/-) → wild-type chimeric mice in the steady state, and this reduction persisted after rotavirus inoculation. In spite of this altered cytokine profile in the small intestinal lamina propria of lymphotoxin β receptor(-/-) → wild-type chimeric mice, the local production of rotavirus-specific IgA was unperturbed. Collectively, our results demonstrate that lymphotoxin β receptor signaling in radio-sensitive myeloid cells regulates the balance of IFN-γ and IL-17 cytokine production within the small intestinal lamina propria; however, these perturbations do not affect mucosal antiviral IgA responses.

Keywords: dendritic cell; rotavirus; small intestine; tumor necrosis factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Viral / blood
  • Antibodies, Viral / immunology
  • Cytokines / metabolism*
  • Dendritic Cells / immunology*
  • Immunity, Mucosal / immunology
  • Immunoglobulin A / immunology
  • Intestinal Mucosa / immunology*
  • Lymphotoxin beta Receptor / deficiency*
  • Lymphotoxin beta Receptor / immunology
  • Lymphotoxin beta Receptor / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Rotavirus / immunology*
  • Rotavirus Infections / immunology*
  • Rotavirus Infections / virology
  • T-Lymphocytes / immunology*

Substances

  • Antibodies, Viral
  • Cytokines
  • Immunoglobulin A
  • Ltbr protein, mouse
  • Lymphotoxin beta Receptor

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