Description of BCG and Tuberculosis Disease in a Cohort of 79 Patients with Chronic Granulomatous Disease.
Humans
Granulomatous Disease, Chronic
/ diagnosis
BCG Vaccine
/ adverse effects
Male
Female
Child
Tuberculosis
/ epidemiology
Child, Preschool
Infant
Adolescent
NADPH Oxidase 2
/ genetics
Cohort Studies
Mycobacterium bovis
Mexico
/ epidemiology
Antitubercular Agents
/ therapeutic use
NADPH Oxidases
/ genetics
Bacillus Calmette–Guérin
Chronic granulomatous disease
Mycobacteria
Tuberculosis
Journal
Journal of clinical immunology
ISSN: 1573-2592
Titre abrégé: J Clin Immunol
Pays: Netherlands
ID NLM: 8102137
Informations de publication
Date de publication:
05 Aug 2024
05 Aug 2024
Historique:
received:
01
05
2024
accepted:
26
07
2024
medline:
5
8
2024
pubmed:
5
8
2024
entrez:
5
8
2024
Statut:
epublish
Résumé
Chronic granulomatous disease (CGD) is an inherited immunodeficiency caused by pathogenic variants of genes encoding the enzyme complex NADPH oxidase. In countries where tuberculosis (TB) is endemic and the Bacillus Calmette-Guérin (BCG) vaccine is routinely administered, mycobacteria are major disease-causing pathogens in CGD. However, information on the clinical evolution and treatment of mycobacterial diseases in patients with CGD is limited. The present study describes the adverse reactions to BCG and TB in Mexican patients with CGD. Patients with CGD who were evaluated at the Immunodeficiency Laboratory of the National Institute of Pediatrics between 2013 and 2024 were included. Medical records were reviewed to determine the clinical course and treatment of adverse reactions to BCG and TB disease. A total of 79 patients with CGD were included in this study. Adverse reactions to BCG were reported in 55 (72%) of 76 patients who received the vaccine. Tuberculosis was diagnosed in 19 (24%) patients. Relapse was documented in three (10%) of 31 patients with BGC-osis and six (32%) of 19 patients with TB, despite antituberculosis treatment. There was no difference in the frequency of BCG and TB disease between patients with pathogenic variants of the X-linked CYBB gene versus recessive variants. This report highlights the importance of considering TB in endemic areas and BCG complications in children with CGD to enable appropriate diagnostic and therapeutic approaches to improve prognosis and reduce the risk of relapse.
Identifiants
pubmed: 39102004
doi: 10.1007/s10875-024-01778-7
pii: 10.1007/s10875-024-01778-7
doi:
Substances chimiques
BCG Vaccine
0
NADPH Oxidase 2
EC 1.6.3.-
CYBB protein, human
EC 1.6.3.-
Antitubercular Agents
0
NADPH Oxidases
EC 1.6.3.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
171Informations de copyright
© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.
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