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Published on: February 15, 2011
Lack of activity of amphotericin B in systemic murine fusarial infection
E J Anaissie1, R Hachem, C Legrand
1Department of Medical Specialties, University of Texas M.D. Anderson Cancer Center, Houston 77030.
Abstract:
Systemic fusarial infections have emerged as a significant cause of mortality in cancer patients. Yet, little is known about the management of these infections. The in vivo antifungal activity of amphotericin B in CF1 mice with disseminated fusarial infections was studied. Two pathogenic strains of Fusarium solani were used. Intraperitoneal administration of amphotericin B in daily doses of 0.5, 1, and 2 mg/kg for less than or equal to 10 days did not prolong survival of treated animals. Clearance of F. solani from kidneys was similar in mice treated with 1 mg/kg per day of amphotericin B and in untreated animals. These results are in agreement with the known in vitro and in vivo resistance of Fusarium species to amphotericin B.
Insights
Systemic fusarial infections are a serious threat to cancer patients. This study found that amphotericin B did not effectively treat disseminated Fusarium infections in mice.
Area of Science:
- Mycology
- Infectious Diseases
- Cancer Research
Background:
- Systemic fusarial infections are increasingly recognized as a critical cause of mortality in immunocompromised individuals, particularly cancer patients.
- Effective management strategies for these infections remain poorly understood.
- Fusarium species exhibit known resistance to conventional antifungal therapies.
Purpose of the Study:
- To evaluate the in vivo antifungal activity of amphotericin B against disseminated fusarial infections.
- To determine the efficacy of amphotericin B in prolonging survival and clearing infection in a murine model.
Main Methods:
- CF1 mice were infected with two pathogenic strains of Fusarium solani.
- Amphotericin B was administered intraperitoneally at daily doses of 0.5, 1, and 2 mg/kg for up to 10 days.
- Survival rates and fungal burden in kidneys were assessed.
Main Results:
- Amphotericin B treatment did not significantly prolong the survival of infected mice at any tested dose.
- Clearance of Fusarium solani from the kidneys was comparable between mice treated with 1 mg/kg/day of amphotericin B and untreated control animals.
- These findings align with established in vitro and in vivo resistance of Fusarium species to amphotericin B.
Conclusions:
- Amphotericin B demonstrates limited efficacy in treating disseminated fusarial infections in this murine model.
- The study underscores the challenges in managing Fusarium infections, especially in cancer patients.
- Further research into alternative antifungal agents is warranted for Fusarium infections.
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