Novel SYK variant causes enhanced SYK autophosphorylation and PI3K activation in an antibody-deficient patient
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Background
Inborn errors of immunity (IEI) affecting B-cell receptor signaling cause predominantly antibody deficiency (PAD) with varying degrees of severity. Recently, four heterozygous variants in SYK were reported to cause hypogammaglobulinemia, multiorgan inflammatory disease and diffuse large B-cell lymphoma.
Objective
We aimed to unravel the genetic and functional cause of PAD in a female (40-45 years) presenting with hypogammaglobulinemia, congenital heart disease and pulmonary hypertension requiring lung transplantation.
Methods
Patient gDNA was subjected to whole-exome and Sanger sequencing. Blood B- and T-cell subsets, as well as tonic and antigen-receptor induced expression levels of phosphorylated-SYK, phosphorylated-ribosomal S6 and phosphorylated p38 were evaluated by flow cytometry.
Results
A novel heterozygous missense SYK variant was identified, mutating a residue in the protein kinase domain (c.1769G>A; p.R590Q), which is highly conserved across vertebrates. While total B- and T-cell numbers were within the normal range, the patient had reduced unswitched and class-switched memory B-cell numbers. Resting B cells from the patient demonstrated enhanced autophosphorylation of SYK, and tonic and ligand-induced phospho-S6 levels. Spontaneous SYK autophosphorylation, S6 and p38 phosphorylation were recapitulated in a pre-clinical cell model, i.e. expression of the SYK R590Q variant in HEK293T cells.
Conclusions
We identified a novel gain-of-function variant in SYK to underlie hypogammaglobulinemia and atypical autoinflammatory disease. Flowcytometric screening for phospho-S6 in lymphocytes of IEI patients can guide genetic diagnosis of B-cell signaling abnormalities.
KEY MESSAGES
A novel monoallelic missense variant in SYK is identified in a patient with hypogammaglobulinemia and atypical autoinflammatory disease.
Increased SYK autophosphorylation and enhanced tonic PI3K and MAPK signaling are indicative of a gain-of-function effect.
Flowcytometric detection of phosphorylated S6 can provide a rapid functional evaluation of genetic variants affecting B-cell receptor signaling.
Capsule summary
Novel SYK variant enhances tonic PI3K signaling in human B cells, resulting in hypogammaglobulinemia.
