Intrapulmonary response to Histoplasma capsulatum in gamma interferon knockout mice

R Allendoerfer, GS Deepe Jr - Infection and immunity, 1997 - Am Soc Microbiol
R Allendoerfer, GS Deepe Jr
Infection and immunity, 1997Am Soc Microbiol
We examined the immunobiological responses to Histoplasma capsulatum in lungs of
gamma interferon (IFN-gamma) knockout mice (GKO mice). Naive GKO mice succumbed by
day 9 to intranasal challenge with 2.5 x 10 (6) yeasts, whereas all wild-type (WT) mice
survived for 45 days. Compared to lungs of WT mice, the lungs of acutely infected GKO mice
exhibited dramatically elevated numbers of CFU in lungs and significantly higher levels of
tumor necrosis factor alpha (TNF-alpha) and granulocyte-macrophage colony-stimulating …
We examined the immunobiological responses to Histoplasma capsulatum in lungs of gamma interferon (IFN-gamma) knockout mice (GKO mice). Naive GKO mice succumbed by day 9 to intranasal challenge with 2.5 x 10(6) yeasts, whereas all wild-type (WT) mice survived for 45 days. Compared to lungs of WT mice, the lungs of acutely infected GKO mice exhibited dramatically elevated numbers of CFU in lungs and significantly higher levels of tumor necrosis factor alpha (TNF-alpha) and granulocyte-macrophage colony-stimulating factor (GM-CSF) but not interleukin-12 (IL-12) or IL-4. To determine if IFN-gamma is necessary in reexposure histoplasmosis, GKO and WT mice were inoculated with 10(4) yeasts intranasally and given amphotericin B for 3 weeks. Six weeks later, mice were rechallenged with 2.5 x 10(6) yeasts. All GKO mice died by day 6, whereas all WT mice survived for 45 days. Lungs of GKO mice contained substantially elevated numbers of CFU and higher TNF-alpha and GM-CSF levels but not IL-12 or IL-4. Thus, IFN-gamma is requisite for control of pulmonary histoplasmosis in naive and reexposed mice.
American Society for Microbiology