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Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.
Leiding, Jennifer W; Vogel, Tiphanie P; Santarlas, Valentine G J; Mhaskar, Rahul; Smith, Madison R; Carisey, Alexandre; Vargas-Hernández, Alexander; Silva-Carmona, Manuel; Heeg, Maximilian; Rensing-Ehl, Anne; Neven, Bénédicte; Hadjadj, Jérôme; Hambleton, Sophie; Ronan Leahy, Timothy; Meesilpavikai, Kornvalee; Cunningham-Rundles, Charlotte; Dutmer, Cullen M; Sharapova, Svetlana O; Taskinen, Mervi; Chua, Ignatius; Hague, Rosie; Klemann, Christian; Kostyuchenko, Larysa; Morio, Tomohiro; Thatayatikom, Akaluck; Ozen, Ahmet; Scherbina, Anna; Bauer, Cindy S; Flanagan, Sarah E; Gambineri, Eleonora; Giovannini-Chami, Lisa; Heimall, Jennifer; Sullivan, Kathleen E; Allenspach, Eric; Romberg, Neil; Deane, Sean G; Prince, Benjamin T; Rose, Melissa J; Bohnsack, John; Mousallem, Talal; Jesudas, Rohith; Santos Vilela, Maria Marluce Dos; O'Sullivan, Michael; Pachlopnik Schmid, Jana; Pruhová, Stepánka; Klocperk, Adam; Rees, Matthew; Su, Helen; Bahna, Sami; Baris, Safa.
Afiliación
  • Leiding JW; Division of Allergy and Immunology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore; Johns Hopkins All Children's Institute for Clinical and Translational Research, Johns Hopkins All Children's Hospital, St Petersburg. Electronic address: jleidin1@jhmi.edu.
  • Vogel TP; Department of Pediatrics, Baylor College of Medicine and William T. Shearer Center for Human Immunobiology, Texas Children's Hospital, Houston.
  • Santarlas VGJ; Lake Erie College of Osteopathic Medicine, Erie.
  • Mhaskar R; Department of Internal Medicine, Morsani College of Medicine, University of South Florida, Tampa.
  • Smith MR; Department of Pediatrics, Baylor College of Medicine and William T. Shearer Center for Human Immunobiology, Texas Children's Hospital, Houston.
  • Carisey A; Department of Cell and Molecular Biology, St Jude Children's Research Hospital, Memphis.
  • Vargas-Hernández A; Department of Pediatrics, Baylor College of Medicine and William T. Shearer Center for Human Immunobiology, Texas Children's Hospital, Houston.
  • Silva-Carmona M; Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston.
  • Heeg M; Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg.
  • Rensing-Ehl A; Institute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg.
  • Neven B; Laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM UMR 1163-Institut Imagine, Paris.
  • Hadjadj J; Laboratory of Immunogenetics of Pediatric Autoimmune Diseases, INSERM UMR 1163-Institut Imagine, Paris.
  • Hambleton S; Newcastle University Translational and Clinical Research Institute, Newcastle (United Kingdom).
  • Ronan Leahy T; Children's Health Ireland at Crumlin, Dublin.
  • Meesilpavikai K; Department of Internal Medicine, Division of Clinical Immunology and Department of Immunology, Erasmus University Medical Center, Rotterdam, Netherlands; Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Cunningham-Rundles C; Department of Medicine, Mount Sinai School of Medicine, New York.
  • Dutmer CM; Children's Hospital Colorado, University of Colorado School of Medicine, Aurora.
  • Sharapova SO; Belarusian Research Center for Pediatric Oncology, Hematology and Immunology, Minsk.
  • Taskinen M; New Children's Hospital, Pediatric Research Center, University of Helsinki and HUS Helsinki University Hospital, Helsinki, Turku and Kuopio, Finland.
  • Chua I; Department of Rheumatology, Immunology and Allergy, Christchurch Hospital, Christchurch; Clinical Immunogenomics Research Consortium of Australasia (CIRCA).
  • Hague R; Royal Hospital for Children, Glasgow.
  • Klemann C; Department of Pediatric Pneumology, Allergy and Neonatology, Hannover Medical School, Hannover.
  • Kostyuchenko L; Center of Pediatric Immunology, Western Ukrainian Specialized Children's Medical Centre, Lviv.
  • Morio T; Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo.
  • Thatayatikom A; Division of Pediatric Allergy/Immunology/Rheumatology, Shands Children's Hospital, University of Florida, Gainesville.
  • Ozen A; School of Medicine, Pediatric Allergy and Immunology, Marmara University, Istanbul.
  • Scherbina A; Dmitry Rogachev National Medical and Research Center for Pediatric Hematology, Oncology and Immunology, Moscow.
  • Bauer CS; Division of Allergy and Immunology, Phoenix Children's Hospital, Phoenix.
  • Flanagan SE; Institute of Biomedical and Clinical Science, University of Exeter Medical School, Exeter.
  • Gambineri E; Department of NEUROFARBA, Section of Children's Health, University of Florence, Anna Meyer Children's Hospital, Florence.
  • Giovannini-Chami L; Pediatric Pulmonology Department, Hôpitaux pédiatriques de Nice CHU-Lenval, Nice.
  • Heimall J; Perelman School of Medicine at University of Pennsylvania, Division of Allergy and Immunology, Children's Hospital of Philadelphia, Philadelphia.
  • Sullivan KE; Perelman School of Medicine at University of Pennsylvania, Division of Allergy and Immunology, Children's Hospital of Philadelphia, Philadelphia.
  • Allenspach E; Pediatric Immunology/Rheumatology, University of Washington, Seattle; Seattle Children's Hospital, Seattle.
  • Romberg N; Perelman School of Medicine at University of Pennsylvania, Division of Allergy and Immunology, Children's Hospital of Philadelphia, Philadelphia.
  • Deane SG; Department of Allergy, The Permanente Medical Group, Sacramento, and the Division of Rheumatology/Allergy and Clinical Immunology, University of California, Davis, School of Medicine, Sacramento.
  • Prince BT; Nationwide Children's Hospital Department of Allergy and Immunology, Columbus; College of Medicine, The Ohio State University, Columbus.
  • Rose MJ; College of Medicine, The Ohio State University, Columbus; Division of Pediatric Hematology-Oncology, Nationwide Children's Hospital, Columbus.
  • Bohnsack J; Department of Pediatrics, University of Utah, Salt Lake City.
  • Mousallem T; Duke Department of Pediatric Allergy and Immunology, Durham.
  • Jesudas R; Department of Hematology, St Jude Children's Research Hospital, Memphis.
  • Santos Vilela MMD; Pediatric Allergy and Immunology/Center of Investigation in Pediatrics, Faculty of Medical Sciences, State University of Campinas-Unicamp, São Paulo.
  • O'Sullivan M; Clinical Immunogenomics Research Consortium of Australasia (CIRCA); Immunology Department, Perth Children's Hospital, Nedlands.
  • Pachlopnik Schmid J; Division of Immunology, University Children's Hospital Zurich, Children's Research Center (CRC), Zurich.
  • Pruhová S; Department of Pediatrics, Charles University in Prague, Second Faculty of Medicine and University Hospital Motol, Prague.
  • Klocperk A; Department of Immunology, Second Faculty of Medicine and University Hospital Motol, Charles University in Prague, Prague.
  • Rees M; Department of Hematology, St Jude Children's Research Hospital, Memphis.
  • Su H; Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda.
  • Bahna S; Allergy and Immunology Section, Louisiana State University Health Sciences Center, Shreveport.
  • Baris S; School of Medicine, Pediatric Allergy and Immunology, Marmara University, Istanbul.
J Allergy Clin Immunol ; 151(4): 1081-1095, 2023 04.
Article en En | MEDLINE | ID: mdl-36228738
ABSTRACT

BACKGROUND:

In 2014, germline signal transducer and activator of transcription (STAT) 3 gain-of-function (GOF) mutations were first described to cause a novel multisystem disease of early-onset lymphoproliferation and autoimmunity.

OBJECTIVE:

This pivotal cohort study defines the scope, natural history, treatment, and overall survival of a large global cohort of patients with pathogenic STAT3 GOF variants.

METHODS:

We identified 191 patients from 33 countries with 72 unique mutations. Inclusion criteria included symptoms of immune dysregulation and a biochemically confirmed germline heterozygous GOF variant in STAT3.

RESULTS:

Overall survival was 88%, median age at onset of symptoms was 2.3 years, and median age at diagnosis was 12 years. Immune dysregulatory features were present in all patients lymphoproliferation was the most common manifestation (73%); increased frequencies of double-negative (CD4-CD8-) T cells were found in 83% of patients tested. Autoimmune cytopenias were the second most common clinical manifestation (67%), followed by growth delay, enteropathy, skin disease, pulmonary disease, endocrinopathy, arthritis, autoimmune hepatitis, neurologic disease, vasculopathy, renal disease, and malignancy. Infections were reported in 72% of the cohort. A cellular and humoral immunodeficiency was observed in 37% and 51% of patients, respectively. Clinical symptoms dramatically improved in patients treated with JAK inhibitors, while a variety of other immunomodulatory treatment modalities were less efficacious. Thus far, 23 patients have undergone bone marrow transplantation, with a 62% survival rate.

CONCLUSION:

STAT3 GOF patients present with a wide array of immune-mediated disease including lymphoproliferation, autoimmune cytopenias, and multisystem autoimmunity. Patient care tends to be siloed, without a clear treatment strategy. Thus, early identification and prompt treatment implementation are lifesaving for STAT3 GOF syndrome.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes de Inmunodeficiencia / Enfermedades del Sistema Inmune Tipo de estudio: Observational_studies / Prognostic_studies Límite: Child / Humans Idioma: En Revista: J Allergy Clin Immunol Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes de Inmunodeficiencia / Enfermedades del Sistema Inmune Tipo de estudio: Observational_studies / Prognostic_studies Límite: Child / Humans Idioma: En Revista: J Allergy Clin Immunol Año: 2023 Tipo del documento: Article