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research article
The opposing effects of two gene defects in STX11 and SLP76 on the disease in a patient with an inborn error of immunity
Authors
Habib Al-Kalamouni
Mehdi Benamar
+9 more
T. A. Chatila
Qian Chen
Ghassan S. Dbaibo
Rana el-Hassan
Youmna El-Orfali
Rima H. Hanna-Wakim
Rana Mansour
Michel J. Massaad
Adam Saidu
Publication date
1 January 2023
Publisher
Elsevier Inc.
Doi
Cite
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 & Immunolog
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Last time updated on 30/08/2023
AUB ScholarWorks (American Univ. of Beirut)
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Last time updated on 16/04/2025