Skip to main content

Advertisement

Log in

Th1-type cytokines improve resistance to murine cysticercosis caused by Taenia crassiceps

  • ORIGINAL PAPER
  • Published:
Parasitology Research Aims and scope Submit manuscript

Abstract

Resistance and susceptibility to different parasitic diseases have been associated with the predominance of Th1- or Th2-type immune responses. In experimental murine cysticercosis a Th1 response seems to be involved in resistance, whereas Th2 activity is associated with heavy parasite intensities. To test this notion the roles of Th1- and Th2-type cytokines in infected mice were studied after treatment with anticytokine monoclonal antibodies or with recombinant murine cytokines during early stages of infection. Mice receiving anti-interleukin 10 (IL-10) carried lower parasite intensities than did control mice and developed a strong Th1-type response, whereas mice receiving anti-interferon gamma (IFN-γ) showed a dramatic increase in susceptibility. Treatment with recombinant cytokines confirmed these results; mice receiving IFN-γ and IL-2 showed low parasite numbers, whereas IL-10 induced a significant increase in parasite loads. Thus, the Th1-type immune response plays a fundamental role in protection against Taenia crassiceps cysticercosis, whereas Th2, at least through IL-10, favors parasite establishment.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Additional information

Received: 29 May 1998 / Accepted: 3 July 1998

Rights and permissions

Reprints and permissions

About this article

Cite this article

Terrazas, L., Cruz, M., Rodríguez-Sosa, M. et al. Th1-type cytokines improve resistance to murine cysticercosis caused by Taenia crassiceps . Parasitol Res 85, 135–141 (1999). https://doi.org/10.1007/s004360050522

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/s004360050522

Keywords

Navigation