نتایج جستجو برای: chronic granulomatous disease cgd

تعداد نتایج: 1773487  

Journal: :Blood 1999
M C Dinauer L L Li H Björgvinsdóttir C Ding N Pech

Chronic granulomatous disease (CGD) is an inherited deficiency of the superoxide-generating phagocyte nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, resulting in recurrent, severe bacterial and fungal infections. The X-linked form of this disorder (X-CGD) results from mutations in the X-linked gene for gp91(phox), the larger subunit of the oxidase flavocytochrome b(558). In this s...

2005
Barbara-Ann D. Conway David P. Speert Johan Bylund Paul A. Campsall Rebecca C. Ma

Burkholderia cepacia complex is a life-threatening group of pathogens for patients with chronic granulomatous disease (CGD), whose phagocytes are unable to produce reactive oxygen species (ROS). Unlike other CGD pathogens, B. cepacia complex is particularly virulent, characteristically causing septicemia, and is the bacterial species responsible for most fatalities in these patients. We found t...

2015
Rowan Flynn Alexander Grundmann Peter Renz Walther Hänseler William S. James Sally A. Cowley Michael D. Moore

Chronic granulomatous disease (CGD) is a rare genetic disease characterized by severe and persistent childhood infections. It is caused by the lack of an antipathogen oxidative burst, normally performed by phagocytic cells to contain and clear bacterial and fungal growth. Restoration of immune function can be achieved with heterologous bone marrow transplantation; however, autologous bone marro...

Journal: :Blood 1993
C D Porter M H Parkar R J Levinsky M K Collins C Kinnon

Chronic granulomatous disease (CGD) is an inherited immunodeficiency resulting from the inability of an individual's phagocytes to produce superoxide anions because of defective NADPH oxidase. The disease may be treated by bone marrow transplantation and as such is a candidate for somatic gene therapy. Two thirds of patients have defects in an X-linked gene (X-CGD) encoding gp91-phox, the large...

Journal: :Journal of immunology 2005
Julie A Lekstrom-Himes Douglas B Kuhns W Gregory Alvord John I Gallin

The innate immune response to bacterial infections includes neutrophil chemotaxis and activation, but regulation of inflammation is less well understood. Formyl peptides, byproducts of bacterial metabolism as well as mitochondrial protein biosynthesis, induce neutrophil chemotaxis, the generation of reactive oxygen intermediates (ROI), and the production of the neutrophil chemoattractant, IL-8....

Journal: :Infection and immunity 2015
David E Greenberg Daniel E Sturdevant Kimberly R Marshall-Batty Jessica Chu Anthony M Pettinato Kimmo Virtaneva John Lane Bruce L Geller Stephen F Porcella John I Gallin Steven M Holland Kol A Zarember

Polymorphonuclear leukocytes (PMN) from patients with chronic granulomatous disease (CGD) fail to produce microbicidal concentrations of reactive oxygen species (ROS) due to mutations in NOX2. Patients with CGD suffer from severe, life-threatening infections and inflammatory complications. Granulibacter bethesdensis is an emerging Gram-negative pathogen in CGD that resists killing by PMN of CGD...

Journal: :The Journal of clinical investigation 2013
Wenli Liu Ming Yan Janyce A Sugui Hongzhen Li Chengfu Xu Jungsoo Joo Kyung J Kwon-Chung William G Coleman Griffin P Rodgers

Chronic granulomatous disease (CGD) patients have recurrent life-threatening bacterial and fungal infections. Olfactomedin 4 (OLFM4) is a neutrophil granule protein that negatively regulates host defense against bacterial infection. The goal of this study was to evaluate the impact of Olfm4 deletion on host defense against Staphylococcus aureus and Aspergillus fumigatus in a murine X-linked gp9...

Journal: :The Journal of clinical investigation 2012
Robert L Baehner Morris J Karnovsky

Pediatricians first described the clinical features of chronic granulomatous disease (CGD) in 1959. Almost a decade later, in a collaborative effort that crossed disciplines, we participated in the discoveries that defined the cellular deficiencies of CGD, specifically finding that improper degranulation of leukocytes did not explain their failure to fight pathogens, rather that the fundamental...

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