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Munc18-2 Deficiency Causes Familial Hemophagocytic Lymphohistiocytosis Type 5 and Impairs Cytotoxic Granule Exocytosis in Patient NK Cells

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Munc18-2 Deficiency Causes Familial Hemophagocytic Lymphohistiocytosis Type 5 and Impairs Cytotoxic Granule Exocytosis in Patient NK Cells Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells Marjorie Côte, … , Alain Fischer, Geneviève de Saint Basile J Clin Invest. 2009;119(12):3765-3773. https://doi.org/10.1172/JCI40732. Research Article Immunology Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous autosomal recessive immune disorder characterized by the occurrence of uncontrolled activation of lymphocytes and macrophages infiltrating multiple organs. Disease-causing mutations in the perforin (PRF1; also known as FHL2), Munc13-4 (UNC13D; also known as FHL3), and syntaxin-11 (STX11; also known as FHL4) genes have been identified in individuals with FHL. These genes all encode proteins involved in the cytotoxic activity of lymphocytes. Here, we show that the gene encoding syntaxin-binding protein 2 (Munc18-2; official gene symbol STXBP2) is mutated in another subset of patients with FHL (designated by us as “FHL5”). Lymphoblasts isolated from these patients had strongly decreased STXBP2 protein expression, and NK cells exhibited impaired cytotoxic granule exocytosis, a defect that could be overcome by ectopic expression of wild-type STXBP2. Furthermore, we provide evidence that syntaxin-11 is the main partner of STXBP2 in lymphocytes, as its expression required the presence of STXBP2. Our work shows that STXBP2 deficiency causes FHL5. These data indicate that STXBP2 is required at a late step of the secretory pathway for the release of cytotoxic granules by binding syntaxin 11, another component of the intracellular membrane fusion machinery. Find the latest version: https://jci.me/40732/pdf Research article Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells Marjorie Côte,1,2 Mickaël M. Ménager,1,2 Agathe Burgess,1,2 Nizar Mahlaoui,3 Capucine Picard,2,4 Catherine Schaffner,1,2 Fahad Al-Manjomi,5 Musa Al-Harbi,5 Abdullah Alangari,6 Françoise Le Deist,7 Andrew R. Gennery,8 Nathalie Prince,1,2 Astrid Cariou,9 Patrick Nitschke,10 Ulrich Blank,11,12 Gehad El-Ghazali,13 Gaël Ménasché,1,2 Sylvain Latour,1,2 Alain Fischer,1,2,3 and Geneviève de Saint Basile1,2,4 1INSERM U768, Hôpital Necker-Enfants Malades, Paris, France. 2Faculté de Médecine, Université Paris Descartes, Paris, France. 3Service d’Immunologie et d’Hématologie Pédiatrique and 4Centre d’Etude des Déficits Immunitaires, Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Paris, France. 5Department of Pediatric Hematology/Oncology, Prince Sultan Hematology Oncology Center, King Fahad Medical City, Riyadh, Saudi Arabia. 6Department of Pediatrics, College of Medicine, King Saudi University and King Khalid University Hospital, Riyadh, Saudi Arabia. 7Department of Microbiology and Immunology, CHU de Sainte Justine and University of Montréal, Montreal, Quebec, Canada. 8Newcastle General Hospital, Newcastle upon Tyne, United Kingdom. 9Genomic Core Facility, IFR94, and 10Informatic Core Facility, Université Paris Descartes, Paris, France. 11INSERM U699, Faculté de Medicine Paris 7, Site Xavier Bichat, Paris, France. 12Université Paris 7, Faculté de Médecine Paris Diderot — Site Xavier Bichat, Paris, France. 13Department of Immunology, King Fahad Medical City, Riyadh, Saudi Arabia. Familial hemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous autosomal recessive immune disorder characterized by the occurrence of uncontrolled activation of lymphocytes and macrophages infiltrating multiple organs. Disease-causing mutations in the perforin (PRF1; also known as FHL2), Munc13-4 (UNC13D; also known as FHL3), and syntaxin-11 (STX11; also known as FHL4) genes have been identified in individuals with FHL. These genes all encode proteins involved in the cytotoxic activity of lymphocytes. Here, we show that the gene encoding syntaxin-binding protein 2 (Munc18-2; official gene symbol STXBP2) is mutat- ed in another subset of patients with FHL (designated by us as “FHL5”). Lymphoblasts isolated from these patients had strongly decreased STXBP2 protein expression, and NK cells exhibited impaired cytotoxic gran- ule exocytosis, a defect that could be overcome by ectopic expression of wild-type STXBP2. Furthermore, we provide evidence that syntaxin-11 is the main partner of STXBP2 in lymphocytes, as its expression required the presence of STXBP2. Our work shows that STXBP2 deficiency causes FHL5. These data indicate that STXBP2 is required at a late step of the secretory pathway for the release of cytotoxic granules by binding syntaxin 11, another component of the intracellular membrane fusion machinery. Introduction or tumorigenic cells. Once cytotoxic cells have recognized their Familial hemophagocytic lymphohistiocytosis (FHL; MIM targets and formed a conjugate, cytotoxic activity is delivered in a 267700) is a genetically heterogeneous immune disorder of auto- multi-step process. This includes the polarization of the cytotoxic somal recessive inheritance. A hallmark of this condition consists granules containing perforin and granzymes toward the immu- in the occurrence of uncontrolled proliferation and activation of nologic synapse (IS) formed with the target, docking, priming, polyclonal T/NK lymphocytes and macrophages that infiltrate and fusion of the cytotoxic granules with the plasma membrane multiple organs including liver and spleen and the CNS. It causes so that release of their content induces target cell destruction by cytopenia and hyperferritinemia and has a fatal outcome (1). apoptosis (5–7). The inability of activated cytotoxic cells to clear Disease-causing mutations in the genes encoding perforin antigen-presenting targets results in sustained immune stimu- (PRF1; FHL2) (2), Munc13-4 (UNC13D; FHL3) (3), and syntaxin-11 lation, likely accounting for the unremitting polyclonal CD8+ (STX11; FHL4) (4) have been previously identified in FHL. They T cell activation and hyperimmune reaction that characterizes account for approximately 80% of FHL cases. These genes encode FHL. Along with perforin, which is critical for granzyme delivery proteins that are involved in the cytotoxic activity of lymphocytes. to target cells, Munc13-4 is essential in priming cytotoxic gran- Lymphocyte cytotoxic activity plays a major role in the defense ules docked at the IS, whereas STX11 regulates membrane fusion against viral infection and cancer by seeking out and killing infected events. In other patients however, the underlying molecular cause remains unknown. Here, we report that biallelic mutations in the Authorship note: Marjorie Côte and Mickaël M. Ménager contributed equally to gene encoding syntaxin binding protein 2 (STXBP2) account for this work. what we believe is a new genetic form of FHL. We have identified Conflict of interest: The authors have declared that no conflict of interest exists. 2 mutations that result in an absence or markedly decreased Citation for this article: J. Clin. Invest. 119:3765–3773 (2009). doi:10.1172/JCI40732. expression of STXBP2 in leukocytes from 8 patients. Remark- The Journal of Clinical Investigation http://www.jci.org Volume 119 Number 12 December 2009 3765 research article Table 1 jects. The mutations did not show any influence Phenotypes and genotypes observed in the 9 individuals carrying STXBP2 mutations on STXBP2 steady-state mRNA levels, which was normally abundant (Figure 2, A and B). Patient Origin Age at Age at final follow-up, Mutation Sequencing of the RT-PCR products confirmed diagnosis, mo mo (treatment) the mutations and enabled characterization of F1P1 Saudi Arabian 3.5 4A 1430C>T; P477L the new splice product for the individuals with F2P1 Saudi Arabian 1.5 30A 1430C>T; P477L the IVS14-1G>C mutation. Rather than leading F2P2 Saudi Arabian 1 16A 1430C>T; P477L to a premature stop codon, this splice mutation F3P1 Saudi Arabian 1 18 (on therapy) 1430C>T; P477L resulted in exchange of the first 17 aa of exon F3P2 Saudi Arabian 2 24 (HSCT) 1430C>T; P477L 15 by 19 new aa from the intronic sequence, F4P1 Palestinian 96 162 (HSCT) IVS 14-1 in frame with the last 20 aa of the exon 15 WT F5P1 Turkish 126 168 (on therapy) IVS 14-1 sequence (Figure 1B). F5P2 Turkish Asymptomatic 32 IVS 14-1 F6P1 Iranian 150 240B IVS 14-1 Defective expression of STXBP2. We assessed the expression of STXBP2 in lymphoblasts obtained APatient is deceased; cause of death was HLH. BPatient is deceased; cause of death was from F2P1, F2P2, F5P1, and F6P1. In a protein post-HSCT (HLH). blot analysis, STXBP2 protein was not found in lymphoblasts from F2P1 (Figure 2C) or F2P2 (data not shown) but was detected in lympho- ably, the latter mutation is associated with late-onset FHL. When blasts from F5P1 and F6P1, albeit at markedly lower levels than in STXBP2 is defective, patients’ NK cells conjugate with targets and control lymphoblasts (Figure 2C). These data indicate that FHL5 is polarize their cytotoxic granule toward the IS but are unable to associated with loss-of-function mutations in the STXBP2 gene. release cytotoxic granule contents. The phenotypic expression of FHL varied considerably as a func- tion of STXBP2 mutations, as shown in Table 1. In all patients with Results the P477L transition, FHL had a very early onset and rapidly led to STXBP2 mutations cause FHL. We studied a cohort of 6 consan- death in most cases. In contrast, FHL manifestations occurred sev- guineous families in which 10 individuals had been diagnosed eral years later in all patients with the
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