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A Human Dectin-2 Deficiency Associated With Invasive Aspergillosis

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...

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Detalles Bibliográficos
Autores principales: Griffiths, James S, White, P Lewis, Czubala, Magdalena A, Simonazzi, Elena, Bruno, Mariolina, Thompson, Aiysha, Rizkallah, Pierre J, Gurney, Mark, da Fonseca, Diogo M, Naglik, Julian R, Ingram, Wendy, Wilson, Keith, van de Veerdonk, Frank L, Barnes, Rosemary, Taylor, Philip R, Orr, Selinda J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8514184/
https://www.ncbi.nlm.nih.gov/pubmed/33733279
http://dx.doi.org/10.1093/infdis/jiab145
Descripción
Sumario: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.