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Loss-of-function mutations in DOCK8 are linked to hyper-IgE syndrome. Patients typically present with recurrent sinopulmonary infections, severe cutaneous viral infections, food allergies and elevated serum IgE. Although patients may present with a spectrum of disease-related symptoms, molecular mechanisms explaining phenotypic variability in patients are poorly defined. Here we characterized a novel compound heterozygous mutation in DOCK8 in a patient diagnosed with primary combined immunodeficiency which was not typical of classical DOCK8 deficiency. In contrast to previously identified mutations in DOCK8 which result in complete loss of function, the newly identified single nucleotide insertion results in expression of a truncated DOCK8 protein. Functional evaluation of the truncated DOCK8 protein revealed its hypomorphic function. In addition we found somatic reversion of DOCK8 predominantly in T cells. The combination of somatic reversion and hypomorphic DOCK8 function explains the milder and atypical phenotype of the patient and further broadens the spectrum of DOCK8-associated disease.

Original publication

DOI

10.1016/j.clim.2015.12.003

Type

Journal article

Journal

Clin Immunol

Publication Date

02/2016

Volume

163

Pages

17 - 21

Keywords

Combined immunodeficiency, DOCK8, Hyper-IgE syndrome, Phenotypic variability, Whole exome sequencing, Bronchiectasis, Child, Female, Guanine Nucleotide Exchange Factors, Heterozygote, Humans, Immunoglobulin E, Immunoglobulin G, Immunoglobulin M, Immunologic Deficiency Syndromes, Mutation, Recurrence, Respiratory Tract Infections