Dysgammaglobulinemia associated with Glu349del,a hypomorphic XIAP mutation

Background: x-linked lymphoproliferative syndrome type 2 is a rare hereditary immunodeficiency caused by mutations in the xiap gene. this immunodeficiency frequently results in hemophagocytic lymphohistiocytosis,although hypogammaglobulinemia and dysgammaglobulinemia are also common. objective: we identified 17 patients from 12 japanese families with mutations in xiap. the glu349del mutation was observed in 3 patients,each from a different family. interestingly,these patients exhibited dysgammaglobulinemia but not hemophagocytic lymphohistiocytosis. we conducted an immunological study of patients carrying glu349del and other mutations to elucidate the pathogenic mechanisms of dysgammaglobulinemia in patients with mutations in the xiap gene. patients and methods: we performed an immunological study of 2 patients carrying the glu349del mutation and 8 patients with other mutations. results: flow cytometry showed that the percentage of memory b cells in patients with a mutation in xiap was lower than that observed in the healthy controls. the patients with the glu349del mutation had a lower percentage of memory b cells than those with other mutations. ig production was reduced in patients with the glu349del mutation. increased susceptibility to apoptosis was observed in the patients with other mutations. susceptibility to apoptosis was normal in patients with glu349del. microarray analysis indicated that expression of ig-related genes was reduced in patients with the glu349del mutation and that the pattern was different from that observed in the healthy controls or patients with other mutations in xiap. conclusions: patients carrying the glu349del mutation in the xiap gene may have a clinically and immunologically distinct phenotype from patients with other xiap mutations. the glu349del mutation may be associated with dysgammaglobulinemia. © 2015 esmon publicidad.