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Título : Molecular analysis for patients with IL-12 receptor β1 deficiency.
Creador: Ramirez Alejo N
Nivel de acceso: Open access
Palabras clave : Interleucina-12 - deficiencia
Interleucina-12 - genética
Interleucina-12 - análisis
Interleucina-12 - sangre
Lupus Eritematoso Sistémico - genética
Vacuna BCG - inmunología
Interleukin-12 - deficiency
Interleukin-12 - genetics
Interleukin-12 - analysis
Interleukin-12 - blood
Lupus Erythematosus, Systemic - genetics
BCG Vaccine - immunology
Inmunodeficiencia
Interleucina-12
TB
Lupus Eritematoso Sistémico
immunodeficiency
interleukin-12 receptor β1
mycobacterial disease
systemic lupus erythematosus
Descripción : Autosomal recessive interleukin-12 receptor β1 (IL-12Rβ1) deficiency has been described as the most common cause of Mendelian susceptibility to mycobacterial disease (MSMD), characterized by clinical disease due to weakly virulent mycobacteria such as Bacille Calmette–Guérin (BCG) vaccines and environmental mycobacteria (EM) in children who are normally resistant to most infectious agents. Here, we report the cases of five patients with mycobacterial infection, including one with systemic lupus erythematosus (SLE). Blood samples from patients and healthy controls were activated in vitro with BCG, BCG+IL-12, and BCG+IFN-γ. The results showed reduced or no production of IFN-γ after IL-12 stimulation in all samples. IL-12Rβ1 expression on the cell surface was negligible or absent. Genetic analysis showed five novel mutations
Colaborador(es) u otros Autores: Blancas-Galicia L
Yamazaki-Nakashimada M
García-Rodríguez SE
Rivas-Larrauri F
Paolo-Cienfuegos DP
Alcantara-Salinas A
Espinosa-Rosales F
Santos-Argumedo L.
Fecha de publicación : 2013
Tipo de publicación: Artículo
Identificador del Recurso : 10.1111/cge.12253
Fuente: Clin Genet 86(2):161-166
URI : http://repositorio.pediatria.gob.mx:8180/handle/20.500.12103/2606
Idioma: eng
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