Loss of the signaling adaptor TRAF1 causes CD8+ T cell dysregulation during human and murine chronic infection

J Exp Med. 2012 Jan 16;209(1):77-91. doi: 10.1084/jem.20110675. Epub 2011 Dec 19.

Abstract

The signaling adaptor TNFR-associated factor 1 (TRAF1) is specifically lost from virus-specific CD8 T cells during the chronic phase of infection with HIV in humans or lymphocytic choriomeningitis virus (LCMV) clone 13 in mice. In contrast, TRAF1 is maintained at higher levels in virus-specific T cells of HIV controllers or after acute LCMV infection. TRAF1 expression negatively correlates with programmed death 1 expression and HIV load and knockdown of TRAF1 in CD8 T cells from viral controllers results in decreased HIV suppression ex vivo. Consistent with the desensitization of the TRAF1-binding co-stimulatory receptor 4-1BB, 4-1BBL-deficient mice have defects in viral control early, but not late, in chronic infection. TGFβ induces the posttranslational loss of TRAF1, whereas IL-7 restores TRAF1 levels. A combination treatment with IL-7 and agonist anti-4-1BB antibody at 3 wk after LCMV clone 13 infection expands T cells and reduces viral load in a TRAF1-dependent manner. Moreover, transfer of TRAF1(+) but not TRAF1(-) memory T cells at the chronic stage of infection reduces viral load. These findings identify TRAF1 as a potential biomarker of HIV-specific CD8 T cell fitness during the chronic phase of disease and a target for therapy.

Publication types

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

MeSH terms

  • 4-1BB Ligand / immunology
  • 4-1BB Ligand / metabolism
  • Adoptive Transfer
  • Animals
  • Antibodies / immunology
  • Antibodies / pharmacology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • Chloroquine / pharmacology
  • Chronic Disease
  • Down-Regulation / genetics
  • Gene Expression
  • HIV Infections / genetics
  • HIV Infections / immunology*
  • Humans
  • Immunologic Memory
  • Interleukin-7 / pharmacology
  • Lymphocytic Choriomeningitis / genetics
  • Lymphocytic Choriomeningitis / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Programmed Cell Death 1 Receptor / metabolism
  • Signal Transduction / drug effects
  • TNF Receptor-Associated Factor 1 / deficiency*
  • TNF Receptor-Associated Factor 1 / genetics
  • Transforming Growth Factor beta / metabolism
  • Viral Load / immunology

Substances

  • 4-1BB Ligand
  • Antibodies
  • Interleukin-7
  • Programmed Cell Death 1 Receptor
  • TNF Receptor-Associated Factor 1
  • Transforming Growth Factor beta
  • Chloroquine