Therapy with canakinumab for adult-onset Still's disease. [Применение канакинумаба при болезни Стилла взрослых]
Насонов Е. Л.
Научно-практическая ревматология
Т. 56, С. 35-40
Опубликовано: 2018
Тип ресурса: Статья
DOI:10.14412/1995-4484-2018-35-40
Аннотация:
Still's disease in children (systemic-onset juvenile idiopathic arthritis, SoJIA) and in adults (adult-onset Still's disease) are considered as non-familial systemic autoinflammatory diseases of unknown etiology driven by similar immunopathogenetic mechanisms. The adult-onset Still's disease pathogenesis is based on genetically determined innate immunity disturbances and molecular basis of immunopathogenesis consists of NLRP3 inflammasome-dependent mechanisms of inflammation characterized by hyperproduction of proinflammatory cytokines interleukin (IL) 1 and IL18. Nonsteroidal anti-inflammatory drugs, glucocorticoids, methotrexate and other disease modifying drugs are considered as «first line» medications for the treatment of adult-onset Still's disease and if they fail biologi-cals are recommended. A review of the literature data concerning anti-IL1 monoclonal antibodies administration in adult-onset Still's disease is presented, indicating good prospects for the use of canakinumab n
Ключевые слова:
Adult-onset Still's disease; Canakinumab; Interleukin 1
Язык текста: Русский
ISSN: 1995-4492
Насонов Е. Л.
Nasonov E. L.
Therapy with canakinumab for adult-onset Still's disease. [Применение канакинумаба при болезни Стилла взрослых]
Текст визуальный непосредственный
Научно-практическая ревматология
ИМА-Пресс
Т. 56 С. 35-40
2018
Статья
Adult-onset Still's disease Canakinumab Interleukin 1
Still's disease in children (systemic-onset juvenile idiopathic arthritis, SoJIA) and in adults (adult-onset Still's disease) are considered as non-familial systemic autoinflammatory diseases of unknown etiology driven by similar immunopathogenetic mechanisms. The adult-onset Still's disease pathogenesis is based on genetically determined innate immunity disturbances and molecular basis of immunopathogenesis consists of NLRP3 inflammasome-dependent mechanisms of inflammation characterized by hyperproduction of proinflammatory cytokines interleukin (IL) 1 and IL18. Nonsteroidal anti-inflammatory drugs, glucocorticoids, methotrexate and other disease modifying drugs are considered as «first line» medications for the treatment of adult-onset Still's disease and if they fail biologi-cals are recommended. A review of the literature data concerning anti-IL1 monoclonal antibodies administration in adult-onset Still's disease is presented, indicating good prospects for the use of canakinumab n