• Title of article

    Monocytes are required for optimum in vitro stimulation of bovine peripheral blood mononuclear cells by non-methylated CpG motifs

  • Author/Authors

    Pontarollo، نويسنده , , R.A. and Rankin، نويسنده , , R. and Babiuk، نويسنده , , L.A. and Godson، نويسنده , , D.L. and Griebel، نويسنده , , P.J. and Hecker، نويسنده , , R. and Krieg، نويسنده , , A.M. and van Drunen Littel-van den Hurk، نويسنده , , S.، نويسنده ,

  • Pages
    17
  • From page
    43
  • To page
    59
  • Abstract
    Bacterial DNA and synthetic oligodeoxynucleotides (ODN) containing unmethylated CpG motifs within certain flanking base pairs are recognized as a danger signal by the innate immune system of vertebrates. Using lymphocyte proliferative response (LPR) and IFN-γ secretion assays, a panel of 38 ODN was screened for immunostimulatory activity on bovine peripheral blood mononuclear cells. ODN composed of a nuclease resistant phosphorothioate backbone and a leading 5′-TCGTCGTT-3′ motif with two 5′-GTCGTT-3′ motifs were highly stimulatory in both assays. Flow cytometric analysis and cell-specific surface marker labeling determined that B-cells (surface IgM+) were the primary cell population responding in the LPR assay. Depletion of T cells (CD3+) from the PBMC population did not affect IFN-γ secretion or B-cell proliferation when cultured with CpG-ODN. However, depletion of monocytes (DH59B+) completely abrogated the ability of CpG-ODN to stimulate IFN-γ secretion, and significantly reduced the B-cell proliferative response. These data establish the identity of an optimal immunostimulatory CpG motif for cattle and demonstrate that monocytes play a pivotal role in the ability of cell populations to respond to CpG-ODN. These data provide insight for future studies investigating the mechanism of CpG-ODN bioactivity and its application in novel vaccine formulations and immunotherapy.
  • Keywords
    oligodeoxynucleotides , CpG , Monocytes , cattle , Immunostimulation
  • Journal title
    Astroparticle Physics
  • Record number

    2054849