Journal Article

Mutations in Bruton’s tyrosine kinase impair IgA responses

Kosaka, Yoshiyuki, Bartol, Sophinus J. W., Grosserichter-Wagener, Christina, van der Burg, Mirjam, Mizutani, Shuki, Ohara, Osamu, Kanegane, Hirokazu, van Zelm, Menno C., Takada, Hidetoshi, Yang, Xi, Imai, Kohsuke, Morio, Tomohiro, Mitsuiki, Noriko

2015

Overview

X-linked agammaglobulinemia (XLA) is a primary immunodeficiency caused by mutations in Bruton’s tyrosine kinase (BTK), and is characterized by markedly decreased numbers of blood B cells and an absence of all immunoglobulin isotypes. We performed whole exome sequencing in a male pediatric patient with dysgammaglobulinemia with IgA deficiency. Genetic analysis revealed a BTK missense mutation (Thr316Ala). To investigate whether a BTK mutation underlay this antibody deficiency with marked decrease of IgA in this patient, we performed functional analyses of B cells and phagocytes, and molecular analyses of somatic hypermutation and class switch recombination. The BTK missense mutation resulted in B cells with reduced BTK and high IgM expression. Equal proportions of CD19 low and CD19 normal fractions were observed, and both included naïve and memory B cells. Calcium influx and phospholipase Cγ2 phosphorylation upon IgM stimulation were marginally impaired in CD19 low , but not in CD19 + B cells. Similar to XLA patients, IgA transcripts showed low SHM levels, whereas IgG transcripts were hardly affected. Our analyses suggest that the BTK mutation likely underlies the disease in this case, and that hypomorphic BTK mutations can result in normal circulating B cell numbers, but specifically impair IgA responses.

• Publisher: Springer Japan,Springer Nature B.V
• Subject: Agammaglobulinemia - genetics / Agammaglobulinemia - pathology / B-Lymphocytes - metabolism / B-Lymphocytes - pathology / Child, Preschool / Exome / Female / Genetic Diseases, X-Linked - genetics / Genetic Diseases, X-Linked - pathology / Hematology / Humans / IgA Deficiency - genetics / IgA Deficiency - pathology / Immunoglobulin A - genetics / Male / Medicine / Medicine & Public Health / Mutation, Missense / Neutrophils - metabolism / Neutrophils - pathology / Oncology / Original Article / Protein-Tyrosine Kinases - genetics / Signal Transduction