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Cellular and Molecular Defects Underlying Invasive Fungal Infections-Revelations from Endemic Mycoses
Pamela P Lee1, Yu-Lung Lau1,2
1LKS Faculty of Medicine, Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Abstract:
The global burden of fungal diseases has been increasing, as a result of the expanding number of susceptible individuals including people living with human immunodeficiency virus (HIV), hematopoietic stem cell or organ transplant recipients, patients with malignancies or immunological conditions receiving immunosuppressive treatment, premature neonates, and the elderly. Opportunistic fungal pathogens such as Aspergillus, Candida, Cryptococcus, Rhizopus, and Pneumocystis jiroveci are distributed worldwide and constitute the majority of invasive fungal infections (IFIs). Dimorphic fungi such as Histoplasma capsulatum, Coccidioides spp., Paracoccidioides spp., Blastomyces dermatiditis, Sporothrix schenckii, Talaromyces (Penicillium) marneffei, and Emmonsia spp. are geographically restricted to their respective habitats and cause endemic mycoses. Disseminated histoplasmosis, coccidioidomycosis, and T. marneffei infection are recognized as acquired immunodeficiency syndrome (AIDS)-defining conditions, while the rest also cause high rate of morbidities and mortalities in patients with HIV infection and other immunocompromised conditions. In the past decade, a growing number of monogenic immunodeficiency disorders causing increased susceptibility to fungal infections have been discovered. In particular, defects of the IL-12/IFN-γ pathway and T-helper 17-mediated response are associated with increased susceptibility to endemic mycoses. In this review, we put together the various forms of endemic mycoses on the map and take a journey around the world to examine how cellular and molecular defects of the immune system predispose to invasive endemic fungal infections, including primary immunodeficiencies, individuals with autoantibodies against interferon-γ, and those receiving biologic response modifiers. Though rare, these conditions provide importance insights to host defense mechanisms against endemic fungi, which can only be appreciated in unique climatic and geographical regions.
Insights
Fungal infections are rising due to more immunocompromised individuals. This review maps endemic mycoses and explores how immune defects increase susceptibility to these global fungal diseases.
Area of Science:
- Medical Mycology
- Immunology
- Infectious Diseases
Background:
- Global burden of fungal diseases is increasing.
- Expanding population of immunocompromised individuals are susceptible to fungal infections.
- Opportunistic and endemic fungal pathogens cause significant morbidity and mortality.
Purpose of the Study:
- To map endemic mycoses globally.
- To examine how cellular and molecular immune defects predispose individuals to invasive endemic fungal infections.
- To understand host defense mechanisms against endemic fungi.
Main Methods:
- Review of scientific literature on endemic mycoses and host immune responses.
- Geographical mapping of endemic fungal diseases.
- Analysis of genetic and immunological factors influencing susceptibility.
Main Results:
- Dimorphic fungi cause geographically restricted endemic mycoses.
- Specific immune defects, like those in the IL-12/IFN-γ pathway, increase susceptibility to endemic mycoses.
- Conditions like disseminated histoplasmosis are AIDS-defining.
Conclusions:
- Immune system defects significantly predispose individuals to invasive endemic fungal infections.
- Understanding these defects provides insights into host defense against fungi.
- Rare immunodeficiencies offer crucial knowledge on fighting endemic mycoses.
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