Insights on the crosstalk between dendritic cells and helper T cells in novel genetic etiology for mendelian susceptible mycobacterial disease.

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dc.catalogadorpau
dc.contributor.authorRey-Jurado, Emma
dc.contributor.authorPizarro-Ortega, Magdalena S.
dc.contributor.authorKalergis, Alexis M.
dc.contributor.otherMendelian susceptibility to mycobacterial disease (MSMD) is an inherited predisposition to infections by Bacille-Calmette Guérin (BCG) vaccine or by environmental mycobacteria. The etiology of MSMD has been associated with up to nineteen different genetic mutations in interferon (IFN)-γ-related genes.1 Although mycobacteria susceptibility-associated genetic mutations are rare in the population, their diagnosis is crucial for an efficient and timely treatment. Kong et al.2 have recently described an autosomal recessive deficiency in the signal.
dc.date.accessioned2024-03-06T14:05:53Z
dc.date.available2024-03-06T14:05:53Z
dc.date.issued2018
dc.fechaingreso.objetodigital2024-03-05
dc.fuente.origenORCID
dc.identifier.doi10.1038/s41423-018-0177-x
dc.identifier.urihttps://doi.org/10.1038/s41423-018-0177-x
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/84253
dc.information.autorucEscuela de Medicina; Kalergis Parra, Alexis Mikes; 0000-0001-7622-5263; 90610
dc.language.isoen
dc.nota.accesoContenido parcial
dc.rightsacceso restringido
dc.titleInsights on the crosstalk between dendritic cells and helper T cells in novel genetic etiology for mendelian susceptible mycobacterial disease.
dc.typeartículo
sipa.codpersvinculados90610
sipa.trazabilidadORCID;2024-01-15
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