A Human Dectin-2 Deficiency Associated with Invasive Aspergillosis

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Abstract

Immunocompromised patients are highly susceptible to invasive aspergillosis. Herein, we identified a homozygous deletion mutation (507 del C) resulting in a frameshift (N170I) and early stop codon in the fungal binding Dectin-2 receptor, in an immunocompromised patient. The mutated form of Dectin-2 was weakly expressed, did not form clusters at/near the cell surface and was functionally defective. Peripheral blood mononuclear cells from this patient were unable to mount a cytokine (tumor necrosis factor, interleukin 6) response to Aspergillus fumigatus, and this first identified Dectin-2-deficient patient died of complications of invasive aspergillosis.

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Griffiths, J. S., White, P. L., Czubala, M. A., Simonazzi, E., Bruno, M., Thompson, A., … Orr, S. J. (2021). A Human Dectin-2 Deficiency Associated with Invasive Aspergillosis. Journal of Infectious Diseases, 224(7), 1219–1224. https://doi.org/10.1093/infdis/jiab145

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