Autor: |
V Vassia, A Iannaccone, S Marengo, A Briozzo, A Brussino, L Alessi, L Brussino, C Norbiato |
Rok vydání: |
2022 |
Předmět: |
|
Zdroj: |
Global Journal of Infectious Diseases and Clinical Research. 8:011-014 |
ISSN: |
2455-5363 |
Popis: |
Hemophagocytic Lymphohistiocytosis (HLH) is a rare and potentially life-threatening syndrome related to a dysregulation of cytolytic function of Natural Killer (NK) cells and cytotoxic T cells (CTLs), which in turns leads to an inappropriate immune stimulation and hyperinflammatory state, resulting in hypercytokinemia, accumulation of activated lymphocytes and macrophages [1,2]. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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