Recognition of bovine respiratory syncytial virus proteins by bovine CD8+ T lymphocytes

Immunology. 2003 Feb;108(2):220-9. doi: 10.1046/j.1365-2567.2003.01566.x.


CD8+ T lymphocytes play a major role in the clearance of bovine respiratory syncytial virus (BRSV), an important respiratory pathogen of young calves that shares many of the epidemiological and pathological features of human respiratory syncytial virus (HRSV) in infants. Recombinant vaccinia virus (rVV) and recombinant fowlpox virus (rFPV), expressing individual BRSV proteins, were used to demonstrate that the F, N and M2 proteins were the major antigens recognized by bovine CD8+ T cells in major histocompatibility complex (MHC)-defined cattle. BRSV protein recognition by CD8+ T cells was analysed using cytotoxic T lymphocyte (CTL) assays or by the production of interferon-gamma (IFN-gamma) following restimulation with BRSV proteins. Strong recognition of the G protein by CD8+ T cells was observed in cattle that had been vaccinated with rVV expressing this protein and subsequently challenged with BRSV. Although there is variation in the number of expressed MHC genes in cattle with different class I haplotypes, this did not appear to influence BRSV protein recognition by CD8+ T cells. Knowledge of the antigenic specificity of BRSV-specific CD8+ T cells will facilitate the qualitative and quantitative analysis of BRSV-specific CD8+ T-cell memory in cattle and help to ensure that potential vaccines induce a qualitatively appropriate CD8+ T-cell response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation
  • Antigens, Viral / immunology
  • CD8-Positive T-Lymphocytes / immunology*
  • Cattle
  • Cytotoxicity, Immunologic
  • Epitopes, T-Lymphocyte / immunology
  • Haplotypes
  • Interferon-gamma / biosynthesis
  • Lymphocyte Activation / immunology
  • Respiratory Syncytial Virus, Bovine / immunology*
  • Viral Fusion Proteins / immunology
  • Viral Proteins / immunology*


  • Antigens, Viral
  • Epitopes, T-Lymphocyte
  • Viral Fusion Proteins
  • Viral Proteins
  • Interferon-gamma