A humanized antibody against mucormycosis targets angioinvasion and augments the host immune response
3 Οκτωβρίου, 2025Candida auris vs. Non-Candida auris Candidemia in Critically Ill Patients: Clinical Outcomes, Risk Factors, and Mortality
3 Οκτωβρίου, 2025Mucormycosis is an increasingly important, life-threatening human fungal infection caused by Mucorales, and it has limited therapeutic options, a lack of biomarkers for early diagnosis, and incompletely characterized immunopathogenesis. Mucorales possess unique virulence factors and epigenetic mechanisms that control fungal growth, pathogenicity, and resistance to antifungal agents. Furthermore, mucormycosis has distinct clinical and epidemiological features, which reflect specific underlying mechanisms of immune dysfunction. Specifically, the ability of Mucorales to induce necrotizing, angioinvasive disease in patients with certain metabolic abnormalities implies that host metabolites play a significant regulatory role in fungal pathogenicity. Furthermore, it is possible that uncharacterized, evolutionarily conserved metabolic host defense mechanisms inhibit this class of fungal pathogens. Progress in understanding the immunobiology of mucormycosis remains constrained by (a) the scarcity of human biological samples collected, (b) the lack of broadly available genetic tools and strains engineered to dissect host–Mucorales interplay, (c) the variety of fungal species that cause the disease, and (d) insufficient funding resources. Collaborative and coordinated efforts between experts in fungal biology, genetics and genomics, immunology, pathogenesis, and clinical research on mucormycosis are needed to overcome these challenges. These synergistic interactions would lead to new funding opportunities and yield novel insights into disease mechanisms, ultimately enabling the development of innovative therapies targeting Mucorales’ pathogenicity and improving clinical outcomes for this disease. (read more)
Chamilos G, Binder U, Garre V. J Fungi (Basel). 2025 Jul 22;11(8):545. doi: https://doi.org/10.3390/jof11080545