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Published on: July 1, 2020
Vaccines for invasive fungal infections
1Division of General Internal Medicine, Los Angeles Biomedical Research Institute, Harbor-University of California Los Angeles (UCLA) Medical Center 1124 West Carson Street, Liu Vaccine Center, Torrance, CA 90502 USA.
Abstract:
Morbidity and mortality from invasive fungal infections remain unacceptably high despite availability of new antifungal agents, underscoring the need for more effective preventative strategies. Due to our enhanced understanding of the host defense and pathogenetic mechanisms that lead to invasive fungal infections, it should be feasible to develop vaccines targeting these infections. A common immunological theme across many vaccine candidates for invasive fungal infections has been the need to activate a cell-based, pro-inflammatory, Th1 or Th17 immune response to improve phagocytic killing of the fungi. Since neutralization of virulence factor functions has not been required for many active vaccines to function, the antigenic repertoire available for testing should not be limited to virulence factors. With expansion of our fundamental understanding of the immunology of fungal infections, the biggest barrier to development of fungal vaccines is the lack of available capital to translate discoveries made at the bench into biological agents used at the bedside. Continued education on the importance and feasibility of vaccination for such infections, combined with continued development of vaccine antigens and adjuvants, is necessary.
Insights
Developing vaccines for invasive fungal infections is crucial due to high mortality. Research suggests activating cell-based immune responses, not just targeting virulence factors, is key for effective fungal vaccines.
Area of Science:
- Mycology
- Immunology
- Vaccinology
Background:
- Invasive fungal infections (IFIs) cause significant morbidity and mortality, despite new antifungal drugs.
- Enhanced understanding of host defense and fungal pathogenesis provides a basis for vaccine development.
- Current vaccine strategies for IFIs focus on inducing pro-inflammatory Th1 or Th17 cell-mediated immunity.
Purpose of the Study:
- To highlight the feasibility and necessity of developing vaccines against invasive fungal infections.
- To discuss immunological themes relevant to fungal vaccine design.
- To identify barriers and future directions in fungal vaccine development.
Main Methods:
- Review of current understanding of host immune responses to fungal pathogens.
- Analysis of immunological requirements for effective antifungal immunity.
- Identification of potential antigenic targets beyond fungal virulence factors.
Main Results:
- Cell-based immune responses, particularly Th1 and Th17, are critical for fungal clearance.
- Vaccine efficacy does not necessarily depend on neutralizing virulence factors.
- The primary barrier to fungal vaccine development is a lack of funding for clinical translation.
Conclusions:
- Vaccines targeting invasive fungal infections are feasible and needed.
- Future vaccine development should consider a broader antigenic repertoire and focus on inducing robust cell-mediated immunity.
- Increased investment and continued research into vaccine antigens and adjuvants are essential for advancing fungal vaccine development.
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