Development of protective immunity against cutaneous leishmaniasis is dependent on STAT1-mediated IFN signaling pathway

Eur J Immunol. 2003 Jul;33(7):1799-805. doi: 10.1002/eji.200323163.

Abstract

Although STAT1-dependent signaling mediates biological functions of IFN-alpha/beta and IFN-gamma, recent reports indicate that STAT1-independent IFN signaling also regulates expression of several genes. To determine the roles of STAT1-dependent and -independent IFN signaling in the regulation of immunity during cutaneous leishmaniasis, we studied the course of Leishmania major infection in resistant C57BL/6 mice lacking the STAT1 gene. While L. major-infected STAT1(+/+) mice resolved their lesions, STAT1(-/-) mice developed large lesions containing significantly more parasites. Moreover, the inability of STAT1(-/-) mice to control L. major infection was due to the lack of Th1 development associated with reduced production of IL-12, IFN-gamma and nitric oxide. Although STAT1(-/-) mice produced more IL-4 and total IgE than STAT1(+/+) mice later during infection, these differences were not significant. Nevertheless, at these time points lymph node cells from STAT1(-/-) mice produced significantly more IL-10. Finally, STAT1(-/-) mice were also susceptible to low dose L. major infection. Thesefindings demonstrate that STAT1-mediated IFN signaling is indispensable for the development of protective immunity against cutaneous L. major infection. Moreover, they also suggest that the protective role of STAT1-mediated signaling is due to its ability to induce Th1 development during infection with this parasite.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / immunology
  • DNA-Binding Proteins / metabolism*
  • Immunity / genetics
  • Interferons / immunology
  • Interferons / metabolism*
  • Leishmania major / immunology
  • Leishmaniasis, Cutaneous / immunology*
  • Mice
  • Mice, Inbred C57BL
  • Nitric Oxide / metabolism
  • STAT1 Transcription Factor
  • Signal Transduction / immunology*
  • Trans-Activators / genetics
  • Trans-Activators / immunology
  • Trans-Activators / metabolism*

Substances

  • DNA-Binding Proteins
  • STAT1 Transcription Factor
  • Stat1 protein, mouse
  • Trans-Activators
  • Nitric Oxide
  • Interferons