Fasciola hepatica - the pilot study of in vitro assessing immune response against native and recombinant antigens of the fluke

Acta Parasitol. 2013 Dec;58(4):453-62. doi: 10.2478/s11686-013-0163-5. Epub 2013 Dec 13.

Abstract

Fasciola hepatica is a liver fluke that infects 2.4 million of people and causes great economical loss in animal production. To date a 100% effective vaccine has not been developed and the disease is controlled by drug therapy. Great efforts are put into development of effective vaccine against parasite what is difficult since Fasciola spp. (like other helmints) during evolutionary process has developed sophisticated and efficient methods to evade immune response. During preliminary experiments it is convenient to use cell lines which are relatively cheap and allow for reproducible comparison of results between laboratories. We stimulated BOMA (bovine monocyte/macrophage cell line) and BOMAC (bovine macrophage cell line) with native or recombinant antigens of Fasciola hepatica and assessed IFN-γ, IL-4 and TNF-α level upon stimulation. We observed diminished secretion of proinflammatory TNF-α in LPS activated BOMA cells stimulated with Excretory/Secretory products of adult fluke (Fh-ES). We also observed greater changes in gene expression in LPS activated BOMA cells than in non activated BOMA cells upon stimulation using Fh-ES. The results show possibility of using cell lines for in vitro research of bovine immune response against liver fluke, although this model still requires validation and further characterization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Helminth / genetics
  • Antigens, Helminth / immunology*
  • Cattle
  • Cell Line
  • Fasciola hepatica / genetics
  • Fasciola hepatica / immunology*
  • Helminth Proteins / genetics
  • Helminth Proteins / immunology*
  • Interferon-gamma / metabolism
  • Interleukin-4 / metabolism
  • Macrophages / immunology
  • Monocytes / immunology
  • Pilot Projects
  • Recombinant Proteins / genetics
  • Recombinant Proteins / immunology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antigens, Helminth
  • Helminth Proteins
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Interleukin-4
  • Interferon-gamma