Genetic vaccines to potentiate the effective CD103+ dendritic cell-mediated cross-priming of antitumor immunity

J Immunol. 2015 Jun 15;194(12):5937-47. doi: 10.4049/jimmunol.1500089. Epub 2015 May 13.

Abstract

The development of effective cancer vaccines remains an urgent, but as yet unmet, clinical need. This deficiency is in part due to an incomplete understanding of how to best invoke dendritic cells (DC) that are crucial for the induction of tumor-specific CD8(+) T cells capable of mediating durable protective immunity. In this regard, elevated expression of the transcription factor X box-binding protein 1 (XBP1) in DC appears to play a decisive role in promoting the ability of DC to cross-present Ags to CD8(+) T cells in the therapeutic setting. Delivery of DNA vaccines encoding XBP1 and tumor Ag to skin DC resulted in increased IFN-α production by plasmacytoid DC (pDC) from skin/tumor draining lymph nodes and the cross-priming of Ag-specific CD8(+) T cell responses associated with therapeutic benefit. Antitumor protection was dependent on cross-presenting Batf3(+) DC, pDC, and CD8(+) T cells. CD103(+) DC from the skin/tumor draining lymph nodes of the immunized mice appeared responsible for activation of Ag-specific naive CD8(+) T cells, but were dependent on pDC for optimal effectiveness. Similarly, human XBP1 improved the capacity of human blood- and skin-derived DC to activate human T cells. These data support an important intrinsic role for XBP1 in DC for effective cross-priming and orchestration of Batf3(+) DC-pDC interactions, thereby enabling effective vaccine induction of protective antitumor immunity.

Publication types

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

MeSH terms

  • Animals
  • Antigen Presentation
  • Antigens, CD / metabolism
  • Antigens, Neoplasm / genetics
  • Antigens, Neoplasm / immunology
  • Basic-Leucine Zipper Transcription Factors / metabolism
  • Bone Marrow / immunology
  • Bone Marrow / pathology
  • Cancer Vaccines / genetics
  • Cancer Vaccines / immunology*
  • Cross-Priming / immunology*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / immunology
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism
  • Disease Models, Animal
  • Female
  • HSP72 Heat-Shock Proteins / genetics
  • HSP72 Heat-Shock Proteins / immunology
  • Humans
  • Integrin alpha Chains / metabolism
  • Interferon-alpha / biosynthesis
  • Intramolecular Oxidoreductases / genetics
  • Intramolecular Oxidoreductases / immunology
  • Lung Neoplasms / immunology
  • Lung Neoplasms / secondary
  • Lymphocyte Activation
  • Melanoma, Experimental
  • Mice
  • Mice, Knockout
  • Neoplasms / immunology*
  • Neoplasms / mortality
  • Neoplasms / pathology
  • Neoplasms / therapy
  • Phenotype
  • Rats
  • Regulatory Factor X Transcription Factors
  • Repressor Proteins / metabolism
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • Toll-Like Receptor 3 / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / immunology
  • Vaccines, DNA / immunology*
  • X-Box Binding Protein 1

Substances

  • Antigens, CD
  • Antigens, Neoplasm
  • Basic-Leucine Zipper Transcription Factors
  • Cancer Vaccines
  • DNA-Binding Proteins
  • HSP72 Heat-Shock Proteins
  • Integrin alpha Chains
  • Interferon-alpha
  • Regulatory Factor X Transcription Factors
  • Repressor Proteins
  • SNFT protein, mouse
  • Toll-Like Receptor 3
  • Transcription Factors
  • Vaccines, DNA
  • X-Box Binding Protein 1
  • XBP1 protein, human
  • Xbp1 protein, mouse
  • Xbp1 protein, rat
  • alpha E integrins
  • Intramolecular Oxidoreductases
  • dopachrome isomerase