Genetic susceptibility to EBV infection: insights from inborn errors of immunity
Published 2020 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Genetic susceptibility to EBV infection: insights from inborn errors of immunity
Authors
Keywords
-
Journal
HUMAN GENETICS
Volume -, Issue -, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-03-10
DOI
10.1007/s00439-020-02145-3
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Primary immunodeficiencies reveal the molecular requirements for effective host defense against EBV infection
- (2020) Stuart G. Tangye et al. BLOOD
- The Many Faces of XMEN Disease, Report of Two Patients with Novel Mutations
- (2020) Rodrigo Hoyos-Bachiloglu et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
- (2020) Stuart G. Tangye et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Compound Heterozygous Mutations of IL2-Inducible T cell Kinase in a Swedish Patient: the Importance of Early Genetic Diagnosis
- (2019) Mingyan Fang et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Immunodeficiency and Epstein Barr virus induced lymphoproliferation caused by 4-1BB deficiency
- (2019) Mohammed Alosaimi et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- B cell–intrinsic requirement for STK4 in humoral immunity in mice and human subjects
- (2019) Imogen Moran et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Human inborn errors of the actin cytoskeleton affecting immunity: way beyond WAS and WIP
- (2019) Stuart G Tangye et al. IMMUNOLOGY AND CELL BIOLOGY
- Inherited Interleukin 2–Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma
- (2019) Leila Youssefian et al. CLINICAL INFECTIOUS DISEASES
- CARMIL2 Deficiency Presenting as Very Early Onset Inflammatory Bowel Disease
- (2019) Thomas Magg et al. INFLAMMATORY BOWEL DISEASES
- Genetic Deficiency and Biochemical Inhibition of ITK Affect Human Th17, Treg, and Innate Lymphoid Cells
- (2019) Ahmet Eken et al. JOURNAL OF CLINICAL IMMUNOLOGY
- A Novel CARMIL2 Mutation Resulting in Combined Immunodeficiency Manifesting with Dermatitis, Fungal, and Viral Skin Infections As Well as Selective Antibody Deficiency
- (2019) Faranaz Atschekzei et al. JOURNAL OF CLINICAL IMMUNOLOGY
- A Unique Presentation of Infantile-Onset Colitis and Eosinophilic Disease without Recurrent Infections Resulting from a Novel Homozygous CARMIL2 Variant
- (2019) Alina Kurolap et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype
- (2019) Eline Blommaert et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Magnesium transporter 1 (MAGT1) deficiency causes selective defects in N-linked glycosylation and expression of immune-response genes
- (2019) Mami Matsuda-Lennikov et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Compound Heterozygous DOCK8 Mutations in a Patient with B Lymphoblastic Leukemia and EBV-Associated Diffuse Large B Cell Lymphoma
- (2019) David Buchbinder et al. JOURNAL OF CLINICAL IMMUNOLOGY
- CD137 deficiency causes immune dysregulation with predisposition to lymphomagenesis
- (2019) Ido Somekh et al. BLOOD
- Signaling pathways involved in the T‐cell‐mediated immunity against Epstein‐Barr virus: Lessons from genetic diseases
- (2019) Sylvain Latour et al. IMMUNOLOGICAL REVIEWS
- Concomitant PIK3CD and TNFRSF9 deficiencies cause chronic active Epstein-Barr virus infection of T cells
- (2019) Rémy Rodriguez et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Peripheral eosinophilia in primary immunodeficiencies of actin dysregulation: A case series of Wiskott-Aldrich syndrome, CARMIL2 and DOCK8 deficiency and review of the literature
- (2019) David Kim et al. Annals of Diagnostic Pathology
- Diversity of XMEN Disease: Description of 2 Novel Variants and Analysis of the Lymphocyte Phenotype
- (2019) Elizabeth M. Klinken et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Defective glycosylation and multisystem abnormalities characterize the primary immunodeficiency XMEN disease
- (2019) Juan C. Ravell et al. JOURNAL OF CLINICAL INVESTIGATION
- Hematopoietic stem cell transplantation for cytidine triphosphate synthase 1 (CTPS1) deficiency
- (2018) Zohreh Nademi et al. BONE MARROW TRANSPLANTATION
- Activating PIK3CD mutations impair human cytotoxic lymphocyte differentiation and function and EBV immunity
- (2018) Emily S.J. Edwards et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Mutations in PI3K110δ cause impaired natural killer cell function partially rescued by rapamycin treatment
- (2018) Raquel Ruiz-García et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Novel Mutations in RASGRP1 are Associated with Immunodeficiency, Immune Dysregulation, and EBV-Induced Lymphoma
- (2018) Ido Somekh et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Interleukin-2-Inducible T-Cell Kinase Deficiency—New Patients, New Insight?
- (2018) Sujal Ghosh et al. Frontiers in Immunology
- Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from India
- (2018) Jahnavi Aluri et al. Frontiers in Immunology
- Exhaustion of the CD8+ T Cell Compartment in Patients with Mutations in Phosphoinositide 3-Kinase Delta
- (2018) Marjolein W. J. Wentink et al. Frontiers in Immunology
- Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry
- (2018) Maria Elena Maccari et al. Frontiers in Immunology
- CD70 Deficiency due to a Novel Mutation in a Patient with Severe Chronic EBV Infection Presenting As a Periodic Fever
- (2018) Roberta Caorsi et al. Frontiers in Immunology
- Inherited Immunodeficiencies With High Predisposition to Epstein–Barr Virus-Driven Lymphoproliferative Diseases
- (2018) Sylvain Latour et al. Frontiers in Immunology
- Novel CARMIL2 Mutations in Patients with Variable Clinical Dermatitis, Infections, and Combined Immunodeficiency
- (2018) Anas M. Alazami et al. Frontiers in Immunology
- Genetic Defects in Phosphoinositide 3-Kinase δ Influence CD8+ T Cell Survival, Differentiation, and Function
- (2018) Jennifer L. Cannons et al. Frontiers in Immunology
- Primary immunodeficiencies caused by mutations in actin regulatory proteins
- (2018) Erin Janssen et al. IMMUNOLOGICAL REVIEWS
- Insights into immunity from clinical and basic science studies of DOCK8 immunodeficiency syndrome
- (2018) Helen C. Su et al. IMMUNOLOGICAL REVIEWS
- Successful Bone Marrow Transplantation for XMEN: Hemorrhagic Risk Uncovered
- (2018) Dimana Dimitrova et al. JOURNAL OF CLINICAL IMMUNOLOGY
- EBV Negative Lymphoma and Autoimmune Lymphoproliferative Syndrome Like Phenotype Extend the Clinical Spectrum of Primary Immunodeficiency Caused by STK4 Deficiency
- (2018) Cyrill Schipp et al. Frontiers in Immunology
- Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study
- (2017) Tanya I. Coulter et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Dedicator of cytokinesis 8–deficient CD4 + T cells are biased to a T H 2 effector fate at the expense of T H 1 and T H 17 cells
- (2017) Stuart G. Tangye et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- RASGRP1 mutation in autoimmune lymphoproliferative syndrome-like disease
- (2017) Huawei Mao et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Persistent Impairment of T-Cell Regeneration in a Patient with Activated PI3K δ Syndrome
- (2017) Fumihiro Goto et al. JOURNAL OF CLINICAL IMMUNOLOGY
- International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity
- (2017) Capucine Picard et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Human immunity against EBV—lessons from the clinic
- (2017) Stuart G. Tangye et al. JOURNAL OF EXPERIMENTAL MEDICINE
- A human immunodeficiency syndrome caused by mutations in CARMIL2
- (2017) T. Schober et al. Nature Communications
- DOCK 8 Deficiency, EBV+ Lymphomatoid Granulomatosis, and Intrafamilial Variation in Presentation
- (2017) Victoria R. Dimitriades et al. Frontiers in Pediatrics
- Recurrent viral infections associated with a homozygous CORO1A mutation that disrupts oligomerization and cytoskeletal association
- (2016) Christina S. Yee et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Variable phenotype and discrete alterations of immune phenotypes in CTP synthase 1 deficiency: Report of 2 siblings
- (2016) Johannes Trück et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Defective Leukocyte Adhesion and Chemotaxis Contributes to Combined Immunodeficiency in Humans with Autosomal Recessive MST1 Deficiency
- (2016) Tarana Singh Dang et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Large Deletion of MAGT1 Gene in a Patient with Classic Kaposi Sarcoma, CD4 Lymphopenia, and EBV Infection
- (2016) Immacolata Brigida et al. JOURNAL OF CLINICAL IMMUNOLOGY
- CTP Synthase 1 Deficiency in Successfully Transplanted Siblings with Combined Immune Deficiency and Chronic Active EBV Infection
- (2016) Zeynep Yesim Kucuk et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Inherited CD70 deficiency in humans reveals a critical role for the CD70–CD27 pathway in immunity to Epstein-Barr virus infection
- (2016) Kazushi Izawa et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Combined immunodeficiency and Epstein-Barr virus–induced B cell malignancy in humans with inherited CD70 deficiency
- (2016) Hassan Abolhassani et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Dual T cell– and B cell–intrinsic deficiency in humans with biallelicRLTPRmutations
- (2016) Yi Wang et al. JOURNAL OF EXPERIMENTAL MEDICINE
- RASGRP1 deficiency causes immunodeficiency with impaired cytoskeletal dynamics
- (2016) Elisabeth Salzer et al. NATURE IMMUNOLOGY
- Senescence of T Lymphocytes: Implications for Enhancing Human Immunity
- (2016) Arne N. Akbar et al. TRENDS IN IMMUNOLOGY
- A potential founder variant inCARMIL2/RLTPRin three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction
- (2016) Hanne S. Sorte et al. Molecular Genetics & Genomic Medicine
- Primary immunodeficiencies and the control of Epstein-Barr virus infection
- (2015) Umaimainthan Palendira et al. Annals of the New York Academy of Sciences
- The Immunology of Epstein-Barr Virus–Induced Disease
- (2015) Graham S. Taylor et al. Annual Review of Immunology
- A case of XMEN syndrome presented with severe auto-immune disorders mimicking autoimmune lymphoproliferative disease
- (2015) Turkan Patiroglu et al. CLINICAL IMMUNOLOGY
- STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutation
- (2015) Sevil Oskay Halacli et al. CLINICAL IMMUNOLOGY
- High incidence of Epstein-Barr virus (EBV)-positive Hodgkin lymphoma and Hodgkin lymphoma-like B-cell lymphoproliferations with EBV latency profile 2 in children with interleukin-2-inducible T-cell kinase deficiency
- (2015) Kirsten Bienemann et al. HISTOPATHOLOGY
- Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency
- (2015) Omar K. Alkhairy et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- X-linked Inhibitor of Apoptosis Protein Deficiency: More than an X-linked Lymphoproliferative Syndrome
- (2015) Claire Aguilar et al. JOURNAL OF CLINICAL IMMUNOLOGY
- DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients
- (2015) Susanne E. Aydin et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Atypical Clinical Course in Pediatric Hodgkin Lymphoma
- (2015) Charlotte Alme et al. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY
- NKG2D Receptor and Its Ligands in Host Defense
- (2015) L. L. Lanier Cancer Immunology Research
- XMEN disease: a new primary immunodeficiency affecting Mg2+ regulation of immunity against Epstein-Barr virus
- (2014) F.-Y. Li et al. BLOOD
- Identification of ITK deficiency as a novel genetic cause of idiopathic CD4+ T-cell lymphopenia
- (2014) N. K. Serwas et al. BLOOD
- Exome sequencing reveals novel mutation targets in diffuse large B-cell lymphomas derived from Chinese patients
- (2014) N. F. C. C. de Miranda et al. BLOOD
- Age-Specific Prevalence of Epstein-Barr Virus Infection Among Minnesota Children: Effects of Race/Ethnicity and Family Environment
- (2014) L. M. Condon et al. CLINICAL INFECTIOUS DISEASES
- Identification of a Novel Mutation in MAGT1 and Progressive Multifocal Leucoencephalopathy in a 58-Year-Old Man with XMEN Disease
- (2014) Fatima Dhalla et al. JOURNAL OF CLINICAL IMMUNOLOGY
- First Report of the Hyper-IgM Syndrome Registry of the Latin American Society for Immunodeficiencies: Novel Mutations, Unique Infections, and Outcomes
- (2014) Otavio Cabral-Marques et al. JOURNAL OF CLINICAL IMMUNOLOGY
- XLP: Clinical Features and Molecular Etiology due to Mutations in SH2D1A Encoding SAP
- (2014) Stuart G Tangye JOURNAL OF CLINICAL IMMUNOLOGY
- Compound Heterozygous CORO1A Mutations in Siblings with a Mucocutaneous-Immunodeficiency Syndrome of Epidermodysplasia Verruciformis-HPV, Molluscum Contagiosum and Granulomatous Tuberculoid Leprosy
- (2014) Asbjorg Stray-Pedersen et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Interleukin-2-Inducible T-Cell Kinase (ITK) Deficiency - Clinical and Molecular Aspects
- (2014) Sujal Ghosh et al. JOURNAL OF CLINICAL IMMUNOLOGY
- Molecular Basis of the Dual Functions of 2B4 (CD244)
- (2014) L. K. Chlewicki et al. JOURNAL OF IMMUNOLOGY
- CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferation
- (2014) Emmanuel Martin et al. NATURE
- Lytic immune synapse function requires filamentous actin deconstruction by Coronin 1A
- (2014) E. M. Mace et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Cellular immune controls over Epstein–Barr virus infection: new lessons from the clinic and the laboratory
- (2014) Alan B. Rickinson et al. TRENDS IN IMMUNOLOGY
- X-linked inhibitor of apoptosis (XIAP) deficiency: The spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosis
- (2013) C. Speckmann et al. CLINICAL IMMUNOLOGY
- Defective actin accumulation impairs human natural killer cell function in patients with dedicator of cytokinesis 8 deficiency
- (2013) Melissa C. Mizesko et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferation
- (2013) Despina Moshous et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- Age-Specific Prevalence of Epstein–Barr Virus Infection Among Individuals Aged 6–19 Years in the United States and Factors Affecting Its Acquisition
- (2013) Henry H. Balfour et al. JOURNAL OF INFECTIOUS DISEASES
- Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiency
- (2013) Carrie L Lucas et al. NATURE IMMUNOLOGY
- Seroprevalence of Epstein-Barr Virus Infection in U.S. Children Ages 6-19, 2003-2010
- (2013) Jennifer Beam Dowd et al. PLoS One
- Phosphoinositide 3-Kinase Gene Mutation Predisposes to Respiratory Infection and Airway Damage
- (2013) I. Angulo et al. SCIENCE
- Mg2+ Regulates Cytotoxic Functions of NK and CD8 T Cells in Chronic EBV Infection Through NKG2D
- (2013) B. Chaigne-Delalande et al. SCIENCE
- Role of PI3K/Akt signaling in memory CD8 T cell differentiation
- (2013) Eui Ho Kim et al. Frontiers in Immunology
- The phenotype of human STK4 deficiency
- (2012) H. Abdollahpour et al. BLOOD
- Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27
- (2012) E. Salzer et al. HAEMATOLOGICA
- IL-2-Inducible T-Cell Kinase Deficiency with Pulmonary Manifestations due to Disseminated Epstein-Barr Virus Infection
- (2012) D. Mansouri et al. INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
- Loss-of-function mutations within the IL-2 inducible kinase ITK in patients with EBV-associated lymphoproliferative diseases
- (2012) R M Linka et al. LEUKEMIA
- Inherited MST1 Deficiency Underlies Susceptibility to EV-HPV Infections
- (2012) Amandine Crequer et al. PLoS One
- SLAM Family Receptors and SAP Adaptors in Immunity
- (2011) Jennifer L. Cannons et al. Annual Review of Immunology
- Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients
- (2011) M. Ouederni et al. BLOOD
- Surface expression patterns of negative regulatory molecules identify determinants of virus-specific CD8+ T-cell exhaustion in HIV infection
- (2011) T. Yamamoto et al. BLOOD
- MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival
- (2011) N. T. Nehme et al. BLOOD
- Recurrent deletions of the TNFSF7 and TNFSF9 genes in 19p13.3 in diffuse large B-cell and Burkitt lymphomas
- (2011) René Scholtysik et al. INTERNATIONAL JOURNAL OF CANCER
- CD27 deficiency is associated with combined immunodeficiency and persistent symptomatic EBV viremia
- (2011) Joris M. van Montfrans et al. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
- DOCK8 deficiency impairs CD8 T cell survival and function in humans and mice
- (2011) Katrina L. Randall et al. JOURNAL OF EXPERIMENTAL MEDICINE
- Second messenger role for Mg2+ revealed by human T-cell immunodeficiency
- (2011) Feng-Yen Li et al. NATURE
- Epstein-Barr Virus: An Important Vaccine Target for Cancer Prevention
- (2011) J. I. Cohen et al. Science Translational Medicine
- DNA Viruses (CMV, EBV, and the Herpesviruses)
- (2011) Martin Zamora SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE
- Molecular Pathogenesis of EBV Susceptibility in XLP as Revealed by Analysis of Female Carriers with Heterozygous Expression of SAP
- (2011) Umaimainthan Palendira et al. PLOS BIOLOGY
- X-linked lymphoproliferative syndromes: brothers or distant cousins?
- (2010) A. H. Filipovich et al. BLOOD
- Impaired Epstein-Barr virus-specific CD8+ T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family-positive B-cell targets
- (2010) A. D. Hislop et al. BLOOD
- Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)
- (2010) J. P. Schmid et al. BLOOD
- XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease
- (2010) R. A. Marsh et al. BLOOD
- X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease
- (2010) C. Booth et al. BLOOD
- Infectious Mononucleosis
- (2010) Katherine Luzuriaga et al. NEW ENGLAND JOURNAL OF MEDICINE
- Timing and tuning of CD27-CD70 interactions: the impact of signal strength in setting the balance between adaptive responses and immunopathology
- (2009) Martijn A. Nolte et al. IMMUNOLOGICAL REVIEWS
- Tec kinases regulate T-lymphocyte development and function: new insights into the roles of Itk and Rlk/Txk
- (2009) Julie A. Readinger et al. IMMUNOLOGICAL REVIEWS
- Girls homozygous for an IL-2–inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation
- (2009) Kirsten Huck et al. JOURNAL OF CLINICAL INVESTIGATION
- Differential Association of Programmed Death-1 and CD57 with Ex Vivo Survival of CD8+ T Cells in HIV Infection
- (2009) C. Petrovas et al. JOURNAL OF IMMUNOLOGY
- Phenotype and function of human T lymphocyte subsets: Consensus and issues
- (2008) Victor Appay et al. CYTOMETRY PART A
- The actin regulator coronin 1A is mutant in a thymic egress–deficient mouse strain and in a patient with severe combined immunodeficiency
- (2008) Lawrence R Shiow et al. NATURE IMMUNOLOGY
Become a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get StartedAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started