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Functional Defects in Type 3 Innate Lymphoid Cells and Classical Monocytes in a Patient with Hyper-IgE Syndrome

Hyper-IgE syndrome (HIES) is a very rare primary immune deficiency characterized by elevated serum IgE levels, recurrent bacterial infections, chronic dermatitis, and connective tissue abnormalities. Autosomal dominant (AD) HIES involves a mutation in signal transducer and activator of transcription...

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Detalles Bibliográficos
Autores principales:	Chang, Yuna, Kang, Sung-Yoon, Kim, Jihyun, Kang, Hye-Ryun, Kim, Hye Young
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Association of Immunologists 2017
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662784/ https://www.ncbi.nlm.nih.gov/pubmed/29093656 http://dx.doi.org/10.4110/in.2017.17.5.352

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