Uptake of antigens from modified vaccinia Ankara virus-infected leukocytes enhances the immunostimulatory capacity of dendritic cells

Cytotherapy. 2011 Jul;13(6):739-52. doi: 10.3109/14653249.2010.549123. Epub 2011 Jan 20.

Abstract

Background aims: Modified vaccinia Ankara (MVA) is a promising vaccine vector for infectious diseases and malignancies. It is fundamental to ascertain its tropism in human leukocyte populations and immunostimulatory mechanisms for application in immunotherapy.

Methods: Human peripheral blood mononuclear cells (PBMC) and leukocyte subpopulations [monocyte-derived dendritic cells (DC), monocytes and B cells] were infected with MVA in order to evaluate their infection rate, changes in surface markers, cytokine expression and apoptosis.

Results: Monocytes, DC and B cells were most susceptible to MVA infection, followed by natural killer (NK) cells. Monocytes were activated strongly, with upregulation of co-stimulatory molecules, major histocompatibility complex (MHC) molecules and chemokine (C-C motif) receptor (CCR7), while immature DC showed partial activation and B cells were inhibited. Furthermore, expression of chemokine (C-X-C motif) ligand (CXCL10), tumor necrosis factor (TNF)-α, interleukin (IL)-6 and IL-12p70 was enhanced but IL-1β and IL-10 were stable or even downregulated. MVA induced a high apoptosis rate of antigen-presenting cells (APC). Nevertheless, incubation of MVA-infected leukocytes with uninfected immature DC (iDC) led to complete maturation of the DC. Subsequently, the matured DC were able to stimulate cytomegalovirus (CMV)-immediate early protein (IE1)-specific T cells.

Conclusions: MVA induces a T-helper (Th)-1-polarizing cytokine expression in APC. Furthermore, incubation of MVA-infected leukocytes with uninfected iDC leads to complete maturation of the DC and may be the basis for cross-presentation of MVA-encoded antigens. Thus this approach seems to be an ideal model for further studies with MVA-encoded viral antigens regarding immunotherapy and vaccination strategies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigen-Presenting Cells / immunology
  • Antigen-Presenting Cells / metabolism
  • Apoptosis
  • Cell Survival
  • Cells, Cultured
  • Chemokine CXCL10 / metabolism
  • Cytokines / metabolism
  • Dendritic Cells / cytology*
  • Dendritic Cells / immunology*
  • Humans
  • Interleukin-10 / metabolism
  • Interleukin-12 / metabolism
  • Interleukin-6 / metabolism
  • Leukocytes, Mononuclear / cytology
  • Leukocytes, Mononuclear / immunology*
  • Leukocytes, Mononuclear / virology*
  • Phagocytosis / immunology
  • Receptors, CCR7 / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cell Transplantation
  • Transplantation, Homologous
  • Tumor Necrosis Factor-alpha / metabolism
  • Vaccinia virus / physiology*

Substances

  • CCR7 protein, human
  • Chemokine CXCL10
  • Cytokines
  • Interleukin-6
  • Receptors, CCR7
  • Tumor Necrosis Factor-alpha
  • Interleukin-10
  • Interleukin-12