Candidiasis, aspergillosis, and mucormycosis cause the majority of nosocomial fungal infections in immunocompromised patients. Using an unbiased transcriptional profiling in PBMCs exposed to the fungal species causing these infections, we found a core host response in healthy individuals that may govern effective fungal clearance: it consists of 156 transcripts, involving canonical and non-canonical immune pathways. Systematic investigation of key steps in antifungal host defense revealed fungal-specific signatures. As previously demonstrated, induced type I and Type II interferon-related pathways. In contrast, central pattern recognition receptor, reactive oxygen species production, and host glycolytic pathways were down-regulated in response to , which was associated with an ER-stress response. was identified to be uniquely regulated by and to control cytokine release in response to this fungus. In conclusion, our data reveals the transcriptional profiles induced by , and describes both the common and specific antifungal host responses that could be exploited for novel therapeutic strategies.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7817431PMC
http://dx.doi.org/10.1016/j.csbj.2020.12.036DOI Listing

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