Activating PI3Kδ mutations in a cohort of 669 patients with primary immunodeficiency.

The requested reference [7aa4bad957539d6681d7ad1afad3619b075fa108] no longer exists in our database. It has been replaced by the current reference: [0dbc0b2c58f5eaa3c2b97cbd565c3a9f19911771]

Authors
Category Primary study
JournalClinical and experimental immunology
Year 2016
The gene PIK3CD codes for the catalytic subunit of phosphoinositide 3-kinase δ (PI3Kδ), and is expressed solely in leucocytes. Activating mutations of PIK3CD have been described to cause an autosomal dominant immunodeficiency that shares clinical features with common variable immunodeficiency (CVID). We screened a cohort of 669 molecularly undefined primary immunodeficiency patients for five reported mutations (four gain-of-function mutations in PIK3CD and a loss of function mutation in PIK3R1) using pyrosequencing. PIK3CD mutations were identified in three siblings diagnosed with CVID and two sporadic cases with a combined immunodeficiency (CID). The PIK3R1 mutation was not identified in the cohort. Our patients with activated PI3Kδ syndrome (APDS) showed a range of clinical and immunological findings, even within a single family, but shared a reduction in naive T cells. PIK3CD gain of function mutations are more likely to occur in patients with defective B and T cell responses and should be screened for in CVID and CID, but are less likely in patients with a pure B cell/hypogammaglobulinaemia phenotype.
Epistemonikos ID: 26eb3246cf860ac14f62d3329f489e993063d959
First added on: Dec 01, 2021