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Immunodeficiency, autoimmunity, and increased risk of B cell malignancy in humans with TRAF3 mutations.
Rae, William; Sowerby, John M; Verhoeven, Dorit; Youssef, Mariam; Kotagiri, Prasanti; Savinykh, Natalia; Coomber, Eve L; Boneparth, Alexis; Chan, Angela; Gong, Chun; Jansen, Machiel H; du Long, Romy; Santilli, Giorgia; Simeoni, Ilenia; Stephens, Jonathan; Wu, Kejia; Zinicola, Marta; Allen, Hana Lango; Baxendale, Helen; Kumararatne, Dinakantha; Gkrania-Klotsas, Effrossyni; Scheffler Mendoza, Selma C; Yamazaki-Nakashimada, Marco Antonio; Ruiz, Laura Berrón; Rojas-Maruri, Cesar Mauricio; Lugo Reyes, Saul O; Lyons, Paul A; Williams, Anthony P; Hodson, Daniel J; Bishop, Gail A; Thrasher, Adrian J; Thomas, David C; Murphy, Michael P; Vyse, Timothy J; Milner, Joshua D; Kuijpers, Taco W; Smith, Kenneth G C.
Afiliação
  • Rae W; Cambridge Institute of Therapeutic Immunology and Infectious Disease, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.
  • Sowerby JM; Department of Medicine, University of Cambridge School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Verhoeven D; Cambridge Institute of Therapeutic Immunology and Infectious Disease, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.
  • Youssef M; Department of Medicine, University of Cambridge School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Kotagiri P; Emma Children's Hospital, Amsterdam University Medical Center (AUMC), University of Amsterdam, Department of Pediatric Immunology, Rheumatology and Infectious Diseases, Amsterdam, Netherlands.
  • Savinykh N; Amsterdam University Medical Center (AUMC), University of Amsterdam, Department of Experimental Immunology, Amsterdam Infection and Immunity Institute, Amsterdam, Netherlands.
  • Coomber EL; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
  • Boneparth A; Cambridge Institute of Therapeutic Immunology and Infectious Disease, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.
  • Chan A; Department of Medicine, University of Cambridge School of Clinical Medicine, University of Cambridge, Cambridge, UK.
  • Gong C; NIHR Cambridge BRC Cell Phenotyping Hub, Department of Medicine, University of Cambridge, Cambridge, UK.
  • Jansen MH; Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
  • du Long R; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
  • Santilli G; Department of Pediatrics, Columbia University Irving Medical Center, New York, NY, USA.
  • Simeoni I; Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.
  • Stephens J; Emma Children's Hospital, Amsterdam University Medical Center (AUMC), University of Amsterdam, Department of Pediatric Immunology, Rheumatology and Infectious Diseases, Amsterdam, Netherlands.
  • Wu K; Amsterdam University Medical Center (AUMC), University of Amsterdam, Department of Experimental Immunology, Amsterdam Infection and Immunity Institute, Amsterdam, Netherlands.
  • Zinicola M; Amsterdam University Center (AUMC), University of Amsterdam, Department of Pathology, Amsterdam, Netherlands.
  • Allen HL; UCL Great Ormond Street Institute of Child Health, London, UK.
  • Baxendale H; Department of Hematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
  • Kumararatne D; NIHR Bioresource-Rare Diseases, Cambridge University Hospitals, Cambridge Biomedical Campus, Cambridge, UK.
  • Gkrania-Klotsas E; Department of Hematology, University of Cambridge, Cambridge Biomedical Campus, Cambridge, UK.
  • Scheffler Mendoza SC; NIHR Bioresource-Rare Diseases, Cambridge University Hospitals, Cambridge Biomedical Campus, Cambridge, UK.
  • Yamazaki-Nakashimada MA; Department of Medical and Molecular Genetics, King's College London, London, UK.
  • Ruiz LB; UCL Great Ormond Street Institute of Child Health, London, UK.
  • Rojas-Maruri CM; NIHR Bioresource-Rare Diseases, Cambridge University Hospitals, Cambridge Biomedical Campus, Cambridge, UK.
  • Lugo Reyes SO; MRC Epidemiology Unit, University of Cambridge, Cambridge, UK.
  • Lyons PA; Cambridge Centre for Lung Infection, Royal Papworth Hospital, Cambridge, UK.
  • Williams AP; Department of Clinical Biochemistry and Immunology, Addenbrooke's Hospital, Cambridge, UK.
  • Hodson DJ; MRC Epidemiology Unit, University of Cambridge, Cambridge, UK.
  • Bishop GA; Department of Infectious Diseases, Cambridge University Hospital NHS Foundation Trust, Cambridge, UK.
  • Thrasher AJ; Clinical Immunology Service, National Institute of Pediatrics, Secretariat of Health, Mexico City, Mexico.
  • Thomas DC; Clinical Immunology Service, National Institute of Pediatrics, Secretariat of Health, Mexico City, Mexico.
  • Murphy MP; Immune Deficiencies Laboratory, National Institute of Pediatrics, Secretariat of Health, Mexico City, Mexico.
  • Vyse TJ; Pathology Department, National Institute of Pediatrics, Secretariat of Health, Mexico City, Mexico.
  • Milner JD; Immune Deficiencies Laboratory, National Institute of Pediatrics, Secretariat of Health, Mexico City, Mexico.
  • Kuijpers TW; Cambridge Institute of Therapeutic Immunology and Infectious Disease, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.
  • Smith KGC; Department of Medicine, University of Cambridge School of Clinical Medicine, University of Cambridge, Cambridge, UK.
Sci Immunol ; 7(74): eabn3800, 2022 08 12.
Article em En | MEDLINE | ID: mdl-35960817
Tumor necrosis factor receptor-associated factor 3 (TRAF3) is a central regulator of immunity. TRAF3 is often somatically mutated in B cell malignancies, but its role in human immunity is not defined. Here, in five unrelated families, we describe an immune dysregulation syndrome of recurrent bacterial infections, autoimmunity, systemic inflammation, B cell lymphoproliferation, and hypergammaglobulinemia. Affected individuals each had monoallelic mutations in TRAF3 that reduced TRAF3 expression. Immunophenotyping showed that patients' B cells were dysregulated, exhibiting increased nuclear factor-κB 2 activation, elevated mitochondrial respiration, and heightened inflammatory responses. Patients had mild CD4+ T cell lymphopenia, with a reduced proportion of naïve T cells but increased regulatory T cells and circulating T follicular helper cells. Guided by this clinical phenotype, targeted analyses demonstrated that common genetic variants, which also reduce TRAF3 expression, are associated with an increased risk of B cell malignancies, systemic lupus erythematosus, higher immunoglobulin levels, and bacterial infections in the wider population. Reduced TRAF3 conveys disease risks by driving B cell hyperactivity via intrinsic activation of multiple intracellular proinflammatory pathways and increased mitochondrial respiration, with a likely contribution from dysregulated T cell help. Thus, we define monogenic TRAF3 haploinsufficiency syndrome and demonstrate how common TRAF3 variants affect a range of human diseases.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator 3 Associado a Receptor de TNF / Neoplasias Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator 3 Associado a Receptor de TNF / Neoplasias Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article