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GITR intrinsically sustains early type 1 and late follicular helper CD4 T cell accumulation to control a chronic viral infection.

Abstract
CD4 T cells are critical for control of persistent infections; however, the key signals that regulate CD4 T help during chronic infection remain incompletely defined. While several studies have addressed the role of inhibitory receptors and soluble factors such as PD-1 and IL-10, significantly less work has addressed the role of T cell co-stimulatory molecules during chronic viral infection. Here we show that during a persistent infection with lymphocytic choriomeningitis virus (LCMV) clone 13, mice lacking the glucocorticoid-induced tumor necrosis factor receptor related protein (GITR) exhibit defective CD8 T cell accumulation, increased T cell exhaustion and impaired viral control. Differences in CD8 T cells and viral control between GITR+/+ and GITR-/- mice were lost when CD4 T cells were depleted. Moreover, mixed bone marrow chimeric mice, as well as transfer of LCMV epitope-specific CD4 or CD8 T cells, demonstrated that these effects of GITR are largely CD4 T cell-intrinsic. GITR is dispensable for initial CD4 T cell proliferation and differentiation, but supports the post-priming accumulation of IFNγ+IL-2+ Th1 cells, facilitating CD8 T cell expansion and early viral control. GITR-dependent phosphorylation of the p65 subunit of NF-κB as well as phosphorylation of the downstream mTORC1 target, S6 ribosomal protein, were detected at day three post-infection (p.i.), and defects in CD4 T cell accumulation in GITR-deficient T cells were apparent starting at day five p.i. Consistently, we pinpoint IL-2-dependent CD4 T cell help for CD8 T cells to between days four and eight p.i. GITR also increases the ratio of T follicular helper to T follicular regulatory cells and thereby enhances LCMV-specific IgG production. Together, these findings identify a CD4 T cell-intrinsic role for GITR in sustaining early CD8 and late humoral responses to collectively promote control of chronic LCMV clone 13 infection.
AuthorsDerek L Clouthier, Angela C Zhou, Michael E Wortzman, Olga Luft, Gary A Levy, Tania H Watts
JournalPLoS pathogens (PLoS Pathog) Vol. 11 Issue 1 Pg. e1004517 (Jan 2015) ISSN: 1553-7374 [Electronic] United States
PMID25590581 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Glucocorticoid-Induced TNFR-Related Protein
  • Tnfrsf18 protein, mouse
Topics
  • Animals
  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes (cytology, physiology)
  • Cell Differentiation (genetics)
  • Cells, Cultured
  • Chronic Disease
  • Cricetinae
  • Female
  • Glucocorticoid-Induced TNFR-Related Protein (physiology)
  • Immunity, Humoral (genetics)
  • Lymphocytic Choriomeningitis (genetics, immunology)
  • Lymphocytic choriomeningitis virus (immunology)
  • Lymphopoiesis (genetics)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • T-Lymphocytes, Helper-Inducer (physiology)
  • Virus Diseases (genetics, immunology)

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