The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunity

Abstract

Background: Inborn errors of immunity are mostly monogenic. However, disease phenotype and outcome may be modified by the coexistence of a second gene defect. Objective: We sought to identify the genetic basis of the disease in a patient who experienced bleeding episodes, pancytopenia, hepatosplenomegaly, and recurrent pneumonia that resulted in death. Methods: Genetic analysis was done using next-generation sequencing. Protein expression and phosphorylation were determined by immunoblotting. T-cell proliferation and F-actin levels were studied by flow cytometry. Results: The patient harbored 2 homozygous deletions in STX11 (c.369_370del, c.374_376del; p.V124fs60∗) previously associated with familial hemophagocytic lymphohistiocytosis and a novel homozygous missense variant in SLP76 (c.767C>T; p.T256I) that resulted in an approximately 85% decrease in SLP76 levels and absent T-cell proliferation. The patient's heterozygous family members showed an approximately 50% decrease in SLP76 levels but normal immune function. SLP76-deficient J14 Jurkat cells did not express SLP76 and had decreased extracellular signal-regulated kinase signaling, basal F-actin levels, and polymerization following T-cell receptor stimulation. Reconstitution of J14 cells with T256I mutant SLP76 resulted in low protein expression and abnormal extracellular signal-regulated kinase phosphorylation and F-actin polymerization after T-cell receptor activation compared with normal expression and J14 function when wild-type SLP76 was introduced. Conclusions: The hypomorphic mutation in SLP76 tones down the hyperinflammation due to STX11 deletion, resulting in a combined immunodeficiency that overshadows the hemophagocytic lymphohistiocytosis phenotype. To our knowledge, this study represents the first report of the opposing effects of 2 gene defects on the disease in a patient with an inborn error of immunity. © 2023 American Academy of Allergy, Asthma & Immunology

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Keywords

Combined immunodeficiency, Hemophagocytic lymphohistiocytosis, Inborn errors of immunity, Slp76, Stx11, Actins, Extracellular signal-regulated map kinases, Humans, Lymphohistiocytosis, hemophagocytic, Mutation, Qa-snare proteins, Receptors, antigen, t-cell, Signal transduction, F actin, Mitogen activated protein kinase 1, T lymphocyte receptor, Actin, Lymphocyte antigen receptor, Mitogen activated protein kinase, Stx11 protein, human, Syntaxin, Actin polymerization, Adolescent, Article, Bleeding, Cell proliferation, Clinical article, Familial hemophagocytic lymphohistiocytosis, Female, Flow cytometry, Gene, Gene deletion, Gene expression, Gene frequency, Gene mutation, Genetic analysis, Genetic association, Hemophagocytic syndrome, Hepatosplenomegaly, Heterozygosity, High throughput sequencing, Homozygosity, Human, Human cell, Hyperinflammation, Immunoblotting, Immunopathology, Inborn error of immunity, Jurkat cell line, Male, Missense mutation, Pancytopenia, Phenotype, Pneumonia, Polymerization, Protein expression, Protein function, Protein phosphorylation, Slp76 gene, Stx11 gene, T lymphocyte, Wild type, Genetics

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