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Volumn 218, Issue 5, 2013, Pages 762-771

Patients with inhibitory and neutralizing auto-antibodies to interferon-γ resemble the sporadic adult-onset phenotype of Mendelian Susceptibility to Mycobacterial Disease (MSMD) lacking Bacille Calmette-Guerin (BCG)-induced diseases

Author keywords

Autoantibodies to IFN (AutoAbs IFN ); Bacille Calmette Guerin infection (BCGitis); IL 12 23 IFN circuit; Mendelian Susceptibility to Mycobacterial Disease (MSMD); Primary immunodeficiency diseases (PIDs)

Indexed keywords

BCG VACCINE; GAMMA INTERFERON ANTIBODY; GAMMA INTERFERON RECEPTOR; GAMMA INTERFERON RECEPTOR 1; GAMMA INTERFERON RECEPTOR 2; I KAPPA B KINASE ALPHA; I KAPPA B KINASE GAMMA; INHIBITORY GAMMA INTERFERON AUTOANTIBODY; INTERFERON CONSENSUS SEQUENCE BINDING PROTEIN; INTERLEUKIN 12; INTERLEUKIN 12 RECEPTOR BETA1; INTERLEUKIN 12P40; INTERLEUKIN 23; MAJOR HISTOCOMPATIBILITY ANTIGEN CLASS 1; NEUTRALIZING GAMMA INTERFERON AUTOANTIBODY; PEPTIDES AND PROTEINS; PROTEIN CYBB; RECOMBINANT INTERFERON; STAT1 PROTEIN; UNCLASSIFIED DRUG;

EID: 84875661798     PISSN: 01712985     EISSN: 18783279     Source Type: Journal    
DOI: 10.1016/j.imbio.2012.08.281     Document Type: Article
Times cited : (36)

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