2020
DOI: 10.1007/s10875-020-00866-8
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Nocardiosis Associated with Primary Immunodeficiencies (Nocar-DIP): an International Retrospective Study and Literature Review

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Cited by 13 publications
(19 citation statements)
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“…A retrospective study showed that among these cases of PID complicated by invasive nocardiosis, chronic granulomatous disease (CGD) was most common (43/49, 83.8%). 17 Even in this subpopulation, the incidence of nocardiosis was low, ranging from 0.0044 to 0.0057 cases/patient year. 17 Non-CGD PID (such as IL12RB1 deficiency or idiopathic CD4 lymphopenia) was rare, but often revealed by development of nocardiosis.…”
Section: Disease Presentationmentioning
confidence: 83%
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“…A retrospective study showed that among these cases of PID complicated by invasive nocardiosis, chronic granulomatous disease (CGD) was most common (43/49, 83.8%). 17 Even in this subpopulation, the incidence of nocardiosis was low, ranging from 0.0044 to 0.0057 cases/patient year. 17 Non-CGD PID (such as IL12RB1 deficiency or idiopathic CD4 lymphopenia) was rare, but often revealed by development of nocardiosis.…”
Section: Disease Presentationmentioning
confidence: 83%
“…17 Even in this subpopulation, the incidence of nocardiosis was low, ranging from 0.0044 to 0.0057 cases/patient year. 17 Non-CGD PID (such as IL12RB1 deficiency or idiopathic CD4 lymphopenia) was rare, but often revealed by development of nocardiosis. More recently, anti-granulocyte-macrophage colony-stimulating factor (GM-CSF) autoantibodies, which reduce neutrophil and macrophage activation, phagocytosis, and bactericidal activity through the inhibition of GM-CSFinduced STAT5 phosphorylation, were identified in five out of seven patients with unexplained disseminated nocardiosis.…”
Section: Disease Presentationmentioning
confidence: 83%
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