Feeding by the tick, Ixodes scapularis, causes CD4(+) T cells responding to cognate antigen to develop the capacity to express IL-4

Parasite Immunol. 2007 Oct;29(10):485-99. doi: 10.1111/j.1365-3024.2007.00966.x.

Abstract

Effects of tick feeding on an early antigen-specific T cell response were studied by monitoring a clonotypic population of adoptively transferred T cell receptor (TCR) transgenic CD4 cells responding to a tick-associated antigen. When recipient mice were infested with pathogen-free Ixodes scapularis nymphs several days prior to T cell transfer and intradermal injection of soluble cognate antigen at the feeding site, the clonotypic CD4 cells gained the ability to express the Th2 effector cytokine IL-4. Notably, this effect was not only observed in BALB/c mice predisposed towards developing Th2 responses but also in B10.D2 mice predisposed towards Th1 responsiveness. Furthermore, tick feeding was able to superimpose IL-4 expression potential onto a strong Th1 response (indicated by robust IFN-gamma expression potential) elicited by immunization with a vaccinia virus expressing the cognate antigen. The magnitude to which tick feeding was able to programme IL-4 expression potential in CD4 cells was partially reduced in mice that had been previously exposed to pathogen-free tick nymphs 6 weeks earlier, as well as when the nymphs were infected with Borrelia burgdorferi. Intradermal injection of salivary gland extract programmed IL-4 expression potential similar to that of tick infestation, suggesting that IL-4 programming activity is contained within tick saliva.

Publication types

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

MeSH terms

  • Animals
  • Borrelia burgdorferi / immunology
  • Borrelia burgdorferi / physiology
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / microbiology
  • Interleukin-4 / immunology
  • Interleukin-4 / metabolism*
  • Ixodes / immunology*
  • Ixodes / microbiology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Nymph / immunology
  • Nymph / microbiology
  • Salivary Proteins and Peptides / immunology
  • Salivary Proteins and Peptides / metabolism
  • Th1 Cells / immunology
  • Th1 Cells / metabolism
  • Th2 Cells / immunology
  • Th2 Cells / metabolism
  • Tick Infestations / immunology*
  • Toll-Like Receptor 2 / metabolism
  • Vaccinia virus / immunology

Substances

  • Salivary Proteins and Peptides
  • Tlr2 protein, mouse
  • Toll-Like Receptor 2
  • Interleukin-4