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The present study focuses on a large family with an X-linked immunodeficiency in which there are variable clinical and laboratory phenotypes, including recurrent viral and bacterial infections, hypogammaglobulinemia, Epstein-Barr virus-driven lymphoproliferation, splenomegaly, colitis, and liver disease. Molecular and genetic analyses revealed that affected males were carriers of a hypomorphic hemizygous mutation in XIAP (XIAP(G466X)) that cosegregated with a rare polymorphism in CD40LG (CD40 ligand(G219R)). These genes are involved in the X-linked lymphoproliferative syndrome 2 and the X-linked hyper-IgM syndrome, respectively. Single expression of XIAP(G466X) or CD40L(G219R) had no or minimal effect in vivo, although in vitro, they lead to altered functional activities of their gene products, which suggests that the combination of XIAP and CD40LG mutations contributed to the expression of clinical manifestations observed in affected individuals. Our report of a primary X-linked immunodeficiency of oligogenic origin emphasizes that primary immunodeficiencies are not caused by a single defective gene, which leads to restricted manifestations, but are likely to be the result of an interplay between several genetic determinants, which leads to more variable clinical phenotypes.

Original publication

DOI

10.1182/blood-2011-01-328849

Type

Journal article

Journal

Blood

Publication Date

14/07/2011

Volume

118

Pages

252 - 261

Keywords

Adolescent, Adult, Arginine, CD40 Ligand, Child, Common Variable Immunodeficiency, Epistasis, Genetic, Family, Female, Genes, X-Linked, Glutamine, Humans, Lymphoproliferative Disorders, Male, Middle Aged, Mutation, Pedigree, Polymorphism, Single Nucleotide, X-Linked Inhibitor of Apoptosis Protein, Young Adult