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

dc.contributor.authorMansour, Rana
dc.contributor.authorel-Hassan, Rana
dc.contributor.authorEl-Orfali, Youmna
dc.contributor.authorSaidu, Adam
dc.contributor.authorAl-Kalamouni, Habib
dc.contributor.authorChen, Qian
dc.contributor.authorBenamar, Mehdi
dc.contributor.authorDbaibo, Ghassan S.
dc.contributor.authorHanna-Wakim, Rima H.
dc.contributor.authorChatila, T. A.
dc.contributor.authorMassaad, Michel J.
dc.contributor.departmentExperimental Pathology, Microbiology, and Immunology
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.departmentPediatrics and Adolescent Medicine
dc.contributor.departmentSpecialized Clinical Programs and Services
dc.contributor.departmentDivision of Pediatric Infectious Diseases
dc.contributor.departmentCenter for Infectious Diseases Research
dc.contributor.departmentResearch Center of Excellence in Immunity and Infections
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:39:14Z
dc.date.available2025-01-24T11:39:14Z
dc.date.issued2023
dc.description.abstractBackground: 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
dc.identifier.doihttps://doi.org/10.1016/j.jaci.2023.08.005
dc.identifier.eid2-s2.0-85171381286
dc.identifier.pmid37595757
dc.identifier.urihttp://hdl.handle.net/10938/29218
dc.language.isoen
dc.publisherElsevier Inc.
dc.relation.ispartofJournal of Allergy and Clinical Immunology
dc.sourceScopus
dc.subjectCombined immunodeficiency
dc.subjectHemophagocytic lymphohistiocytosis
dc.subjectInborn errors of immunity
dc.subjectSlp76
dc.subjectStx11
dc.subjectActins
dc.subjectExtracellular signal-regulated map kinases
dc.subjectHumans
dc.subjectLymphohistiocytosis, hemophagocytic
dc.subjectMutation
dc.subjectQa-snare proteins
dc.subjectReceptors, antigen, t-cell
dc.subjectSignal transduction
dc.subjectF actin
dc.subjectMitogen activated protein kinase 1
dc.subjectT lymphocyte receptor
dc.subjectActin
dc.subjectLymphocyte antigen receptor
dc.subjectMitogen activated protein kinase
dc.subjectStx11 protein, human
dc.subjectSyntaxin
dc.subjectActin polymerization
dc.subjectAdolescent
dc.subjectArticle
dc.subjectBleeding
dc.subjectCell proliferation
dc.subjectClinical article
dc.subjectFamilial hemophagocytic lymphohistiocytosis
dc.subjectFemale
dc.subjectFlow cytometry
dc.subjectGene
dc.subjectGene deletion
dc.subjectGene expression
dc.subjectGene frequency
dc.subjectGene mutation
dc.subjectGenetic analysis
dc.subjectGenetic association
dc.subjectHemophagocytic syndrome
dc.subjectHepatosplenomegaly
dc.subjectHeterozygosity
dc.subjectHigh throughput sequencing
dc.subjectHomozygosity
dc.subjectHuman
dc.subjectHuman cell
dc.subjectHyperinflammation
dc.subjectImmunoblotting
dc.subjectImmunopathology
dc.subjectInborn error of immunity
dc.subjectJurkat cell line
dc.subjectMale
dc.subjectMissense mutation
dc.subjectPancytopenia
dc.subjectPhenotype
dc.subjectPneumonia
dc.subjectPolymerization
dc.subjectProtein expression
dc.subjectProtein function
dc.subjectProtein phosphorylation
dc.subjectSlp76 gene
dc.subjectStx11 gene
dc.subjectT lymphocyte
dc.subjectWild type
dc.subjectGenetics
dc.titleThe opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunity
dc.typeArticle

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