Article
Quantitative defects in invariant NKT cells and TLR responses in patients with hyper-IgE syndrome.
Allergologia et immunopathologia - 1 Jan 2000
Gutierrez-Hincapié S, Muskus-López C E, Montoya C J, Trujillo-Vargas C M
Abstract excerpt
BACKGROUND: Autosomal dominant hyper-IgE syndrome (AD-HIES) is a primary immunodeficiency mainly caused by mutations in STAT3, a signalling molecule implicated in the development of appropriate immune responses. We aimed to characterise the innate immune response in AD-HIES. METHODS: The frequency of innate immune cells in peripheral blood (PB) from seven AD-HIES patients and healthy controls were determined....
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