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Genetic deficiency of IFNγ reveals IFNγ-independent manifestations of murine Hemophagocytic Lymphohistiocytosis

OBJECTIVE: Familial hemophagocytic lymphohistiocytosis (FHL) is a complex cytokine storm syndrome caused by genetic abnormalities rendering CD8+ T cells and NK cells incapable of cytolytic killing. Murine models of FHL have identified interferon-gamma (IFNγ) made by CD8+ T cells as a critical mediat...

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Detalhes bibliográficos
Publicado no:Arthritis Rheumatol
Main Authors: Burn, Thomas N, Weaver, Lehn, Rood, Julia E, Chu, Niansheng, Bodansky, Aaron, Kreiger, Portia A, Behrens, Edward M
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6994338/
https://ncbi.nlm.nih.gov/pubmed/31400073
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/art.41076
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