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PMID: 18193341 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Review

Inflammatory manifestations in chronic granulomatous disease (CGD).

Journal of clinical immunology ·Vol. 28 Suppl 1 ·2008-05-00 ·Pages S67-72

Rosenzweig SD

Abstract

Chronic granulomatous disease (CGD) is a genetically heterogeneous disease characterized by recurrent life-threatening infections with bacteria and fungi as well as dysregulated inflammatory mechanisms. CGD is caused by defects in the NADPH oxidase, the enzyme complex responsible for generation of superoxide and other reactive oxygen species (ROS) in phagocytic cells. In this review we will focus our attention on those particular inflammatory manifestations associated with CGD, their frequencies and the underlying immunologic mechanisms favoring it occurrence.

MeSH Terms
Autoimmunity/genetics Female Gene Expression Profiling Genes, X-Linked Granulomatous Disease, Chronic/genetics,immunology,physiopathology Humans Inflammation/genetics,immunology Male Mutation NADPH Oxidases/genetics,immunology Phagocytes/immunology
Chemicals
NADPH Oxidases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Rosenzweig S D
Servicio de Inmunología, Hospital Nacional de Pediatría J. P. Garrahan, Combate de los Pozos 1881, (1245) Buenos Aires, Argentina. srosenzweig@garrahan.gov.ar
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Article Info
Journal
Journal of clinical immunology
Abbr.
J Clin Immunol
ISSN
0271-9142
Published
2008-05-00
Epub
2008-00-12
Pages
S67-72
Language
English
Region
Netherlands
NLM ID
8102137
Subset
IM
Grants
FIC NIH HHS · R01TW006644 · United States
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