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Ancliff, P.J. et al. Two novel activating mutations in the Wiskott-Aldrich syndrome protein result in congenital neutropenia. Blood 108, 2182-2189

Department of Haematology, Great Ormond Street Hospital, London, WC1N 3JH, United Kingdom.
Blood (Impact Factor: 10.43). 11/2006; 108(7):2182-9. DOI: 10.1182/blood-2006-01-010249
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ABSTRACT Severe congenital neutropenia (SCN) is characterized by neutropenia, recurrent bacterial infections, and maturation arrest in the bone marrow. Although many cases have mutations in the ELA2 gene encoding neutrophil elastase, a significant proportion remain undefined at a molecular level. A mutation (Leu270Pro) in the gene encoding the Wiskott-Aldrich syndrome protein (WASp) resulting in an X-linked SCN kindred has been reported. We therefore screened the WAS gene in 14 young SCN males with wild-type ELA2 and identified 2 with novel mutations, one who presented with myelodysplasia (Ile294Thr) and the other with classic SCN (Ser270Pro). Both patients had defects of immunologic function including a generalized reduction of lymphoid and natural killer cell numbers, reduced lymphocyte proliferation, and abrogated phagocyte activity. In vitro culture of bone marrow progenitors demonstrated a profound reduction in neutrophil production and increased levels of apoptosis, consistent with an intrinsic disturbance of normal myeloid differentiation as the cause of the neutropenia. Both mutations resulted in increased WASp activity and produced marked abnormalities of cytoskeletal structure and dynamics. Furthermore, these results also suggest a novel cause of myelodysplasia and that male children with myelodysplasia and disturbance of immunologic function should be screened for such mutations.

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    • "Autosomal recessive SCN is associated with biallelic mutations in the HAX1 gene and the G6PC3 gene44,45). Mutations in WAS are associated with X-linked inherited SCN46). Mutations in other genes (GFI1, CSF3R) are also known to be associated with SCN, demonstrating genetic heterogeneity47,48). "
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    ABSTRACT: Inherited bone marrow failure syndrome (IBMFS) encompasses a heterogeneous and complex group of genetic disorders characterized by physical malformations, insufficient blood cell production, and increased risk of malignancies. They often have substantial phenotype overlap, and therefore, genotyping is often a critical means of establishing a diagnosis. Current advances in the field of IBMFSs have identified multiple genes associated with IBMFSs and their pathways: genes involved in ribosome biogenesis, such as those associated with Diamond-Blackfan anemia and Shwachman-Diamond syndrome; genes involved in telomere maintenance, such as dyskeratosis congenita genes; genes encoding neutrophil elastase or neutrophil adhesion and mobility associated with severe congenital neutropenia; and genes involved in DNA recombination repair, such as those associated with Fanconi anemia. Early and adequate genetic diagnosis is required for proper management and follow-up in clinical practice. Recent advances using new molecular technologies, including next generation sequencing (NGS), have helped identify new candidate genes associated with the development of bone marrow failure. Targeted NGS using panels of large numbers of genes is rapidly gaining potential for use as a cost-effective diagnostic tool for the identification of mutations in newly diagnosed patients. In this review, we have described recent insights into IBMFS and how they are advancing our understanding of the disease's pathophysiology; we have also discussed the possible implications they will have in clinical practice for Korean patients.
    Korean Journal of Pediatrics 08/2014; 57(8):337-44. DOI:10.3345/kjp.2014.57.8.337
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    • "The protein encoded by the WAS gene, WASP, is a hematopoietic specific regulator of actin nucleation in response to signals arising at the cell membrane [2], [3]. In the last years several WASP mutations have been identified, resulting in a variety of clinical manifestations ranging from the relatively mild X-linked thrombocytopenia (XLT) to the classic full-blown WAS phenotype [4]–[6]. The hallmarks of classical WAS cases are represented by compromised humoral and adaptive immune responses. "
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    ABSTRACT: Wiskott-Aldrich Syndrome protein (WASP) is a key regulator of the actin cytoskeleton in hematopoietic cells. Defective expression of WASP leads to multiple abnormalities in different hematopoietic cells. Despite severe impairment of T cell function, WAS patients exhibit a high prevalence of autoimmune disorders. We attempted to induce EAE, an animal model of organ-specific autoimmunity affecting the CNS that mimics human MS, in Was(-/-) mice. We describe here that Was(-/-) mice are markedly resistant against EAE, showing lower incidence and milder score, reduced CNS inflammation and demyelination as compared to WT mice. Microglia was only poorly activated in Was(-/-) mice. Antigen-induced T-cell proliferation, Th-1 and -17 cytokine production and integrin-dependent adhesion were increased in Was(-/-) mice. However, adoptive transfer of MOG-activated T cells from Was(-/-) mice in WT mice failed to induce EAE. Was(-/-) mice were resistant against EAE also when induced by adoptive transfer of MOG-activated T cells from WT mice. Was(+/-) heterozygous mice developed an intermediate clinical phenotype between WT and Was(-/-) mice, and they displayed a mixed population of WASP-positive and -negative T cells in the periphery but not in their CNS parenchyma, where the large majority of inflammatory cells expressed WASP. In conclusion, in absence of WASP, T-cell responses against a CNS autoantigen are increased, but the ability of autoreactive T cells to induce CNS autoimmunity is impaired, most probably because of an inefficient T-cell transmigration into the CNS and defective CNS resident microglial function.
    PLoS ONE 01/2014; 9(1):e86942. DOI:10.1371/journal.pone.0086942 · 3.23 Impact Factor
    • "Several studies indicate a correlation between the clinical phenotype of WAS and the nature of the inherited mutation (Jin et al., 2004), with truncated or abolished WASp expression coinciding with the most severe cases (Ochs and Thrasher, 2006). In contrast, X-linked Neutropenia (XLN) in patients, results from constitutively active mutations in WASp, and presents with congenital neutropenia (Ancliff et al., 2006; Devriendt et al., 2001). "
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    ABSTRACT: Wiskott Aldrich syndrome (WAS) and X-linked neutropenia (XLN) are immunodeficiencies in which the functions of several haematopoietic cell lineages are perturbed due to mutations in the actin regulator WASp. From in vitro cell biology experiments and biochemical and structural approaches we know much about the functional domains of WASp, and how WASp might regulate the dynamic actin cytoskeleton downstream of activators such as Cdc42, but in vivo experiments are much more challenging. In patients there is a correlation between clinical disease and genotype, with severe reductions in WASp expression or function associating with complex multilineage immunodeficiency, whereas, specific mutations that cause constitutive activation of WASp result in congenital neutropenia. Here we take advantage of the genetic tractability and translucency of zebrafish larvae to first characterise how a null mutant in zfWASp influences the behaviour of neutrophils and macrophages in response to tissue damage and to clearance of infections. We then use this mutant background to study how leukocyte lineage-specific transgenic replacement with human WASp variants, (including normal wild type, and point mutations that either fail to bind Cdc42 or cannot be phosphorylated, and a constitutively active mutant equivalent to that seen in XLN patients), alter the capacity for generation of neutrophils, and their chemotactic response to wounds, and the phagocytic clearance capacity of macrophages. This model provides a unique insight into WASp-related immunodeficiency at both a cellular and whole organism level.
    Journal of Cell Science 07/2013; 126(18). DOI:10.1242/jcs.128728 · 5.33 Impact Factor
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