All three classes of CpG ODNs up-regulate IP-10 gene in pigs

Res Vet Sci. 2010 Apr;88(2):242-50. doi: 10.1016/j.rvsc.2009.10.003. Epub 2009 Nov 5.

Abstract

The analysis of CpG ODN induced innate immune responses in different animal species has shown substantial similarities and differences in levels and types of induced cytokines profile. The objectives of these studies were to identify innate immune biomarkers activated by three classes of CpG ODNs in pigs. For this purpose, we investigated the kinetics of innate immune responses in immune cells from pigs following in vitro and in vivo stimulation with CpG ODNs. The mRNA expression of cytokine and chemokine genes were assayed by SYBR green based quantitative real time PCR. A-class CpG ODN induced significant but transient levels of IFN-gamma, IL-12 (P40), IL-6, IL-4 and TNF-alpha mRNA, C-class CpG ODN induced significant level of IFN-gamma, IFN-alpha and IL-12 mRNA and the lowest level of IL-4 (Th-2 type) mRNA. A very low level of some cytokines stimulation was observed by GC ODNs. It is noteworthy, that IL-12 (P35) mRNA was significantly stimulated by B-class GpC ODN 7909. Interestingly, all classes of CpG ODNs induced significant level of IP-10 at 12h post stimulation. These in vitro and in vivo observations suggest that interferon-gamma inducible protein 10 (IP-10) may be a reliable biomarker for immune activity induced by CpG ODNs in pigs.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Chemokine CXCL10 / genetics
  • Chemokine CXCL10 / metabolism*
  • Dose-Response Relationship, Drug
  • Interleukins / genetics
  • Interleukins / metabolism
  • Leukocytes, Mononuclear / drug effects*
  • Leukocytes, Mononuclear / metabolism
  • Oligodeoxyribonucleotides / genetics
  • Oligodeoxyribonucleotides / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Swine / metabolism*
  • Up-Regulation*

Substances

  • Chemokine CXCL10
  • Interleukins
  • Oligodeoxyribonucleotides
  • RNA, Messenger