The Journal of Immunology · 2004 · 130 citations · 28 references
Veterinary MedicineImmunologyInfectious DiseasesHost-pathogen InteractionsParasite ImmunologyVaccinologyHost-parasite Immune InteractionsInnate Immune Responses To ParasitesParasitic Disease PathogenesisParasitic PathogenesisProtozoan ImmunologyT-cell Responses To ParasitesCellular Immune Response To ParasitesHost Immune Response To ParasitesHost Immunity To ParasitesHost-parasite ImmunityLeishmaniasis PathogenesisParasitic Infection ImmunityTh1 Immune ResponseTh1 Responses
Long-term immunity to Leishmania may require the continued presence of parasites, but previous attempts to create attenuated parasites that persist without causing disease have had limited success. Since Leishmania major mutants that lack lipophosphoglycan and other secreted phosphoglycans, termed lpg2-, persist indefinitely in infected mice without inducing any disease, we tested their ability to provide protection to virulent L. major challenge. In response to leishmanial Ag stimulation, cells from lpg2--infected mice produced minimal levels of IL-4 and IL-10, as well as very low levels of IFN-gamma. Nevertheless, when BALB/c mice infected with lpg2- parasites were challenged with virulent L. major they were protected from disease. Thus, these findings report on attenuated parasites that may be used to induce long-term protection against leishmaniasis and indicate that the immunity induced can be maintained in the absence of a strong Th1 response.
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