Literature DB >> 7719350

Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production.

J D Pollock1, D A Williams, M A Gifford, L L Li, X Du, J Fisherman, S H Orkin, C M Doerschuk, M C Dinauer.   

Abstract

Chronic granulomatous disease (CGD) is a recessive disorder characterized by a defective phagocyte respiratory burst oxidase, life-threatening pyogenic infections and inflammatory granulomas. Gene targeting was used to generate mice with a null allele of the gene involved in X-linked CGD, which encodes the 91 kD subunit of the oxidase cytochrome b. Affected hemizygous male mice lacked phagocyte superoxide production, manifested an increased susceptibility to infection with Staphylococcus aureus and Aspergillus fumigatus and had an altered inflammatory response in thioglycollate peritonitis. This animal model should aid in developing new treatments for CGD and in evaluating the role of phagocyte-derived oxidants in inflammation.

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Year:  1995        PMID: 7719350     DOI: 10.1038/ng0295-202

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  391 in total

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Review 5.  Mechanisms of resistance to oxidative and nitrosative stress: implications for fungal survival in mammalian hosts.

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10.  Interaction of CarD with RNA polymerase mediates Mycobacterium tuberculosis viability, rifampin resistance, and pathogenesis.

Authors:  Leslie A Weiss; Phillip G Harrison; Bryce E Nickels; Michael S Glickman; Elizabeth A Campbell; Seth A Darst; Christina L Stallings
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