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Hematopoietic Stem Cell Transplantation and Vasculopathy Associated With STAT3-Dominant-Negative Hyper-IgE Syndrome.
Ponsford, Mark J; Clark, James; Mock, Joel; Abinun, Mario; Carne, Emily; El-Shanawany, Tariq; Williams, Paul E; Choudhury, Anirban; Freeman, Alexandra F; Gennery, Andrew R; Jolles, Stephen.
Afiliação
  • Ponsford MJ; Immunodeficiency Centre for Wales, University Hospital for Wales, Cardiff, United Kingdom.
  • Clark J; Division of Infection, Inflammation, and Immunity, School of Medicine, Tenovus Institute, Cardiff University, Cardiff, United Kingdom.
  • Mock J; Department of Interventional Cardiology, University Hospital for Wales, Cardiff, United Kingdom.
  • Abinun M; Department of Interventional Cardiology, University Hospital for Wales, Cardiff, United Kingdom.
  • Carne E; Paediatric Haematopoietic Stem Cell Transplant Unit, Translational and Clinical Research Institute, Great North Children's Hospital, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • El-Shanawany T; Immunodeficiency Centre for Wales, University Hospital for Wales, Cardiff, United Kingdom.
  • Williams PE; Immunodeficiency Centre for Wales, University Hospital for Wales, Cardiff, United Kingdom.
  • Choudhury A; Immunodeficiency Centre for Wales, University Hospital for Wales, Cardiff, United Kingdom.
  • Freeman AF; Department of Interventional Cardiology, Morriston Hospital, Swansea Bay University Local Health Board, Swansea, United Kingdom.
  • Gennery AR; Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, United States.
  • Jolles S; Paediatric Haematopoietic Stem Cell Transplant Unit, Translational and Clinical Research Institute, Great North Children's Hospital, Newcastle University, Newcastle upon Tyne, United Kingdom.
Front Pediatr ; 8: 575, 2020.
Article em En | MEDLINE | ID: mdl-33014947
ABSTRACT
Dominant negative mutations in the transcription-factor STAT3 underlie the rare primary immunodeficiency Job's syndrome. Allogeneic Hematopoietic Stem Cell Transplantation (HSCT) has shown promise in correction of the underlying immunological defect, with one report suggesting HSCT can prevent development of wider connective tissue complications. Here, we report the case of a 26 year old male who developed an acute ST-elevation myocardial infarction due to coronary artery ectasia and thrombosis, occurring despite pediatric allogeneic HSCT for STAT3-HIES and a predicted 10-year conventional cardiovascular risk of 0.1%. Vasculopathy associated with STAT3-HIES may persist or arise following HSCT and can precipitate life-threatening complications. This has implications for counseling and vascular surveillance, and highlights the need for further studies to determine the risk, pathogenesis, and optimal management of the vasculopathy associated with STAT3-HIES.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article