Cutting edge: recombinant adenoviruses induce CD8 T cell responses to an inserted protein whose expression is limited to nonimmune cells

J Immunol. 2001 Apr 15;166(8):4809-12. doi: 10.4049/jimmunol.166.8.4809.

Abstract

CD8 T cells (T(CD8+)) play a crucial role in immunity to viruses. Current understanding of activation of naive T cells entails Ag presentation by professional APCs (pAPCs). What happens, however, when viruses evolve to avoid infecting pAPCs? We have studied the consequences of this strategy by generating recombinant adenoviruses that express influenza A virus nucleoprotein under the control of tissue-specific promoters. We show that the immunogenicity of such viruses requires their delivery to organs capable of expressing nucleoprotein. This indicates that infection of pAPCs is not required for adenoviruses to elicit a T(CD8+) response, probably due to a cross-priming via pAPCs. While this bodes well for recombinant adenoviruses as vaccines, it dims their prospects as gene therapy vectors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics*
  • Adenoviridae / immunology*
  • Animals
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / virology*
  • Cytomegalovirus / genetics
  • Cytomegalovirus / immunology
  • Cytotoxicity, Immunologic / genetics
  • Epithelial Cells / immunology
  • Epithelial Cells / virology
  • Female
  • Genetic Vectors / administration & dosage
  • Genetic Vectors / immunology
  • Histocompatibility Antigens Class II / genetics
  • Influenza A virus / genetics
  • Influenza A virus / immunology
  • Keratinocytes / immunology
  • Keratinocytes / virology
  • Lymphocyte Activation / genetics
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, SCID
  • Nucleocapsid Proteins
  • Nucleoproteins / biosynthesis
  • Nucleoproteins / genetics*
  • Nucleoproteins / immunology*
  • Organ Specificity / genetics
  • Organ Specificity / immunology
  • Promoter Regions, Genetic / immunology
  • Pulmonary Alveoli / cytology
  • Pulmonary Alveoli / immunology
  • Pulmonary Alveoli / virology
  • RNA-Binding Proteins*
  • Thymus Gland / cytology
  • Thymus Gland / immunology
  • Thymus Gland / virology
  • Viral Core Proteins / biosynthesis
  • Viral Core Proteins / genetics*
  • Viral Core Proteins / immunology*

Substances

  • Histocompatibility Antigens Class II
  • NP protein, Influenza A virus
  • Nucleocapsid Proteins
  • Nucleoproteins
  • RNA-Binding Proteins
  • Viral Core Proteins