A human dectin-2 deficiency associated with invasive aspergillosis

JS Griffiths, PL White, MA Czubala… - The Journal of …, 2021 - academic.oup.com
JS Griffiths, PL White, MA Czubala, E Simonazzi, M Bruno, A Thompson, PJ Rizkallah
The Journal of Infectious Diseases, 2021academic.oup.com
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 …
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.
Oxford University Press