Adenovirus type 5 induces vitamin A-metabolizing enzymes in dendritic cells and enhances priming of gut-homing CD8 T cells

Mucosal Immunol. 2011 Sep;4(5):528-38. doi: 10.1038/mi.2011.1. Epub 2011 Feb 2.

Abstract

Protective immunity at the gut-associated mucosal tissue is induced primarily by oral/rectal immunization owing to the need for targeting antigen to the gut-resident dendritic cells (DCs). In this study we show that an adenovirus type 5 (Ad5)-based human immunodeficiency virus type 1 vaccine can prime a durable antigen-specific CD8 T-cell response in the gut following intramuscular (IM) immunization in mice. The ability of Ad5 to prime gut-homing CD8 T cells in vivo was associated with Ad5-induced expression of retinal dehydrogenase (RALDH) enzymes in conventional DCs. The Ad5-mediated induction of RALDH did not require signaling through Toll-like receptors, DNA-dependent activator of interferon regulatory factors and several mitogen-activated protein kinases, or replication capacity of the virus, but was dependent on nuclear factor-κB and granulocyte-macrophage colony-stimulating factor. These results provide an innate mechanism through which Ad5-stimulated DCs prime gut-homing CD8 T cells and have implications for the development of novel mucosal adjuvants for subunit vaccines administered via the IM route.

Publication types

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

MeSH terms

  • AIDS Vaccines / immunology
  • Adenoviridae / immunology*
  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • Coculture Techniques
  • Dendritic Cells / enzymology*
  • Dendritic Cells / immunology*
  • Dendritic Cells / virology
  • Female
  • Gastrointestinal Tract / immunology*
  • Gastrointestinal Tract / metabolism
  • Gene Expression Regulation / immunology
  • HIV-1 / immunology
  • Immunization
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • NF-kappa B / metabolism
  • Retinal Dehydrogenase / metabolism*
  • Signal Transduction / immunology
  • Spleen / immunology
  • TOR Serine-Threonine Kinases / metabolism
  • Tretinoin / metabolism

Substances

  • AIDS Vaccines
  • NF-kappa B
  • Tretinoin
  • Retinal Dehydrogenase
  • TOR Serine-Threonine Kinases