Modified vaccinia virus Ankara induces Toll-like receptor-independent type I interferon responses

J Virol. 2007 Nov;81(22):12102-10. doi: 10.1128/JVI.01190-07. Epub 2007 Sep 12.

Abstract

Modified vaccinia virus Ankara (MVA) is a highly attenuated vaccinia virus strain undergoing clinical evaluation as a replication-deficient vaccine vector against various infections and tumor diseases. To analyze the basis of its high immunogenicity, we investigated the mechanism of how MVA induces type I interferon (IFN) responses. MVA stimulation of bone marrow-derived dendritic cells (DC) showed that plasmacytoid DC were main alpha IFN (IFN-alpha) producers that were triggered independently of productive infection, viral replication, or intermediate and late viral gene expression. Increased IFN-alpha levels were induced upon treatment with mildly UV-irradiated MVA, suggesting that a virus-encoded immune modulator(s) interfered with the host cytokine response. Mice devoid of Toll-like receptor 9 (TLR9), the receptor for double-stranded DNA, mounted normal IFN-alpha responses upon MVA treatment. Furthermore, mice devoid of the adaptors of TLR signaling MyD88 and TRIF and mice deficient in protein kinase R (PKR) showed IFN-alpha responses that were only slightly reduced compared to those of wild-type mice. MVA-induced IFN-alpha responses were critically dependent on autocrine/paracrine triggering of the IFN-alpha/beta receptor and were independent of IFN-beta, thus involving "one-half" of a positive-feedback loop. In conclusion, MVA-mediated type I IFN secretion was primarily triggered by non-TLR molecules, was independent of virus propagation, and critically involved IFN feedback stimulation. These data provide the basis to further improve MVA as a vaccine vector.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / genetics
  • Animals
  • Cancer Vaccines / genetics
  • Cancer Vaccines / immunology*
  • Dendritic Cells / immunology*
  • Gene Expression
  • Interferon Type I / metabolism
  • Interferon-alpha / metabolism*
  • Interferon-beta / metabolism
  • Mice
  • Mice, Knockout
  • Myeloid Differentiation Factor 88 / genetics
  • Smallpox Vaccine / genetics
  • Smallpox Vaccine / immunology*
  • Toll-Like Receptor 9 / genetics
  • Vaccinia virus / genetics
  • Vaccinia virus / immunology*
  • Vaccinia virus / physiology
  • Virus Replication

Substances

  • Adaptor Proteins, Vesicular Transport
  • Cancer Vaccines
  • Interferon Type I
  • Interferon-alpha
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • Smallpox Vaccine
  • TICAM-1 protein, mouse
  • Toll-Like Receptor 9
  • Interferon-beta