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.author | Mansour, Rana | |
| dc.contributor.author | el-Hassan, Rana | |
| dc.contributor.author | El-Orfali, Youmna | |
| dc.contributor.author | Saidu, Adam | |
| dc.contributor.author | Al-Kalamouni, Habib | |
| dc.contributor.author | Chen, Qian | |
| dc.contributor.author | Benamar, Mehdi | |
| dc.contributor.author | Dbaibo, Ghassan S. | |
| dc.contributor.author | Hanna-Wakim, Rima H. | |
| dc.contributor.author | Chatila, T. A. | |
| dc.contributor.author | Massaad, Michel J. | |
| dc.contributor.department | Experimental Pathology, Microbiology, and Immunology | |
| dc.contributor.department | Biochemistry and Molecular Genetics | |
| dc.contributor.department | Pediatrics and Adolescent Medicine | |
| dc.contributor.department | Specialized Clinical Programs and Services | |
| dc.contributor.department | Division of Pediatric Infectious Diseases | |
| dc.contributor.department | Center for Infectious Diseases Research | |
| dc.contributor.department | Research Center of Excellence in Immunity and Infections | |
| dc.contributor.faculty | Faculty of Medicine (FM) | |
| dc.contributor.institution | American University of Beirut | |
| dc.date.accessioned | 2025-01-24T11:39:14Z | |
| dc.date.available | 2025-01-24T11:39:14Z | |
| dc.date.issued | 2023 | |
| dc.description.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 | |
| dc.identifier.doi | https://doi.org/10.1016/j.jaci.2023.08.005 | |
| dc.identifier.eid | 2-s2.0-85171381286 | |
| dc.identifier.pmid | 37595757 | |
| dc.identifier.uri | http://hdl.handle.net/10938/29218 | |
| dc.language.iso | en | |
| dc.publisher | Elsevier Inc. | |
| dc.relation.ispartof | Journal of Allergy and Clinical Immunology | |
| dc.source | Scopus | |
| dc.subject | Combined immunodeficiency | |
| dc.subject | Hemophagocytic lymphohistiocytosis | |
| dc.subject | Inborn errors of immunity | |
| dc.subject | Slp76 | |
| dc.subject | Stx11 | |
| dc.subject | Actins | |
| dc.subject | Extracellular signal-regulated map kinases | |
| dc.subject | Humans | |
| dc.subject | Lymphohistiocytosis, hemophagocytic | |
| dc.subject | Mutation | |
| dc.subject | Qa-snare proteins | |
| dc.subject | Receptors, antigen, t-cell | |
| dc.subject | Signal transduction | |
| dc.subject | F actin | |
| dc.subject | Mitogen activated protein kinase 1 | |
| dc.subject | T lymphocyte receptor | |
| dc.subject | Actin | |
| dc.subject | Lymphocyte antigen receptor | |
| dc.subject | Mitogen activated protein kinase | |
| dc.subject | Stx11 protein, human | |
| dc.subject | Syntaxin | |
| dc.subject | Actin polymerization | |
| dc.subject | Adolescent | |
| dc.subject | Article | |
| dc.subject | Bleeding | |
| dc.subject | Cell proliferation | |
| dc.subject | Clinical article | |
| dc.subject | Familial hemophagocytic lymphohistiocytosis | |
| dc.subject | Female | |
| dc.subject | Flow cytometry | |
| dc.subject | Gene | |
| dc.subject | Gene deletion | |
| dc.subject | Gene expression | |
| dc.subject | Gene frequency | |
| dc.subject | Gene mutation | |
| dc.subject | Genetic analysis | |
| dc.subject | Genetic association | |
| dc.subject | Hemophagocytic syndrome | |
| dc.subject | Hepatosplenomegaly | |
| dc.subject | Heterozygosity | |
| dc.subject | High throughput sequencing | |
| dc.subject | Homozygosity | |
| dc.subject | Human | |
| dc.subject | Human cell | |
| dc.subject | Hyperinflammation | |
| dc.subject | Immunoblotting | |
| dc.subject | Immunopathology | |
| dc.subject | Inborn error of immunity | |
| dc.subject | Jurkat cell line | |
| dc.subject | Male | |
| dc.subject | Missense mutation | |
| dc.subject | Pancytopenia | |
| dc.subject | Phenotype | |
| dc.subject | Pneumonia | |
| dc.subject | Polymerization | |
| dc.subject | Protein expression | |
| dc.subject | Protein function | |
| dc.subject | Protein phosphorylation | |
| dc.subject | Slp76 gene | |
| dc.subject | Stx11 gene | |
| dc.subject | T lymphocyte | |
| dc.subject | Wild type | |
| dc.subject | Genetics | |
| dc.title | The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunity | |
| dc.type | Article |
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