## Abstract Hemophagocytic lymphohistiocytosis (HLH) is a rare and severe inflammatory disorder marked by abnormal cytotoxic T and natural killer cell activity, resulting in impaired clearance of pathogen, excessive cytokine production, and continued immune system activation. Soluble ILβ2 receptor
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?-CD25 antibody treatment in a child with hemophagocytic lymphohistiocytosis
β Scribed by Tomaske, Maren ;Amon, Oliver ;Bosk, Axel ;Handgretinger, Rupert ;Schneider, E. Marion ;Niethammer, Dietrich
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 61 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0098-1532
- DOI
- 10.1002/mpo.1294
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