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Published in 2020 at "European Journal of Immunology"
DOI: 10.1002/eji.201948123
Abstract: Familial hemophagocytic lymphohistiocytosis (FHL) is a hyperinflammatory syndrome affecting patients with genetic cytotoxicity defects. Perforinâdeficient (PKO) mice recapitulate the full clinical picture of FHL after infection with lymphocytic choriomeningitis virus (LCMV). Hyperactivated CD8+ T cells…
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Keywords:
dependent differences;
hemophagocytic lymphohistiocytosis;
infection;
trigger dependent ... See more keywords