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Updated: Aug 23, 2026

Intrafemoral Injection of Human Hematopoietic Stem and Progenitor Cells into Immunocompromised Mice
Published on: December 8, 2023
Choices aplenty: antifungal prophylaxis in hematopoietic stem cell transplant recipients
N S Hamza1, M A Ghannoum, H M Lazarus
1Department of Medicine, University Hospitals of Cleveland, 11100 Euclid Ave, Wearn 341, Cleveland, OH 44106-5065, USA.
Abstract:
The incidence of invasive fungal infection (IFIs) in hematopoietic stem cell transplantation (HSCT) recipients ranges from 10 to 25% with an overall case fatality rate of up to 70-90%. Candida and Aspergillus genera remain the two most common pathogens. Although fluconazole prophylaxis in this population has been moderately effective in reducing mortality due to invasive candidiasis, this agent does not have activity against invasive aspergillosis (IA) and other mould. Several new agents such as voriconazole and caspofungin have enhanced potency and broad-spectrum antifungal activity and show promising results against yeasts and filamentous fungi when given as therapy and as chemoprophylaxis. Further, new diagnostic tools to detect circulating fungal antigens in biological fluids and PCR-based methods to detect species or genus-specific DNA or RNA have been developed. Incorporating these techniques along with clinical criteria appear to improve the accuracy of preclinical diagnosis of IFIs. Such approaches may alter the current treatment strategy from prophylaxis to pre-emptive therapy, thereby potentially decreasing cost and toxicity in high-risk patients.
Insights
Hematopoietic stem cell transplantation (HSCT) recipients face high risks of invasive fungal infections (IFIs). New antifungal agents and diagnostic tools offer improved treatment strategies and potentially reduced toxicity for these high-risk patients.
Area of Science:
- Mycology
- Hematology
- Infectious Diseases
Background:
- Invasive fungal infections (IFIs) affect 10-25% of hematopoietic stem cell transplantation (HSCT) recipients, with high fatality rates (70-90%).
- Candida and Aspergillus species are the most frequent pathogens causing IFIs in this vulnerable population.
- Current fluconazole prophylaxis is limited, lacking efficacy against invasive aspergillosis and other molds.
Purpose of the Study:
- To review advancements in antifungal therapies and diagnostics for IFIs in HSCT recipients.
- To explore the potential shift from prophylaxis to pre-emptive treatment strategies.
- To assess the impact of new approaches on patient outcomes, cost, and toxicity.
Main Methods:
- Review of current literature on IFIs in HSCT.
- Evaluation of novel antifungal agents (e.g., voriconazole, caspofungin) for therapy and chemoprophylaxis.
- Assessment of new diagnostic tools, including fungal antigen detection and PCR-based methods.
Main Results:
- Newer antifungal agents demonstrate enhanced potency and broader spectrum activity against yeasts and molds.
- Advanced diagnostic techniques improve the accuracy of preclinical IFIs diagnosis when combined with clinical criteria.
- These advancements hold promise for altering treatment paradigms in IFIs management.
Conclusions:
- Novel antifungal agents and improved diagnostics are crucial for managing IFIs in HSCT recipients.
- A transition towards pre-emptive therapy, guided by enhanced diagnostics, may reduce costs and toxicity.
- Optimizing IFI management is essential for improving survival rates in HSCT patients.
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