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Disruption of an anti-mycobacterial circuit between dendritic and Th cells in human SPPL2a deficiency
Human inborn errors of IFN-γ immunity underlie mycobacterial diseases. We describe patients with BCG disease who are homozygous for loss-of-function mutations of SPPL2A. This gene encodes a transmembrane protease that degrades the N-terminal fragment (NTF) of CD74 (HLA invariant chain) in antigen-pr...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130844/ https://www.ncbi.nlm.nih.gov/pubmed/30127434 http://dx.doi.org/10.1038/s41590-018-0178-z |