IL-12 induction of resistance to pulmonary blastomycosis

Abstract

Background Why severity varies in blastomycosis outbreaks remains unresolved. In experimental pulmonary blastomycosis, susceptibility varied in mouse strains. In susceptible BALB/c the response is Th-2, in immunized, resistance is associated with Th-1. Can susceptibility be redirected by IL-12? Methods, results: BALB/c bronchoalveolar and peritoneal macrophages (PM) were shown deficient in IL-12 production in response to IFN-γ + LPS. High dose IL-12 (1 μg, subcutaneously) treatment of BALB/c infected intranasally with Blastomyces resulted in enhanced survival ( P < 0.008). Since IL-12 was poorly tolerated, a new protocol for infected mice, IL-12 0.1 or 0.3 μg, every other day, resulted in minimal toxicity; almost all treated mice survived ( P < 0.002 vs. controls). When lungs of surviving mice were cultured, the 0.1 μg regimen resulted in fewer ( P < 0.02) cfu. For weeks after treatment, in vitro IFN-γ treatment enabled PM Blastomyces killing. After infection spleen cells from IL-12 treated mice produced 4-fold more IFN-γ and 3-fold less IL-10 in response to Blastomyces. IL-10 abrogated activation of macrophages by IFN-γ for enhanced Blastomyces killing. Conclusions: A proper IL-12 treatment protocol induces resistance (survival and decreased growth in lungs), low toxicity, macrophage responsiveness to IFN-γ for killing Blastomyces, up-regulation of IFN-γ and down-regulation of IL-10 production.