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PMID: 15378046 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Antimicrobial reactive oxygen and nitrogen species: concepts and controversies.

Nature reviews. Microbiology ·Vol. 2 ·No. 10 ·2004-10-00 ·Pages 820-32

Fang FC

Abstract

Phagocyte-derived reactive oxygen and nitrogen species are of crucial importance for host resistance to microbial pathogens. Decades of research have provided a detailed understanding of the regulation, generation and actions of these molecular mediators, as well as their roles in resisting infection. However, differences of opinion remain with regard to their host specificity, cell biology, sources and interactions with one another or with myeloperoxidase and granule proteases. More than a century after Metchnikoff first described phagocytosis, and more than four decades after the discovery of the burst of oxygen consumption that is associated with microbial killing, the seemingly elementary question of how phagocytes inhibit, kill and degrade microorganisms remains controversial. This review updates the reader on these concepts and the topical questions in the field.

MeSH Terms
Cytokines/biosynthesis Granulomatous Disease, Chronic/metabolism,microbiology Humans Immunity, Innate Nitric Oxide Synthase/genetics,metabolism Nitric Oxide Synthase Type II Phagocytes/immunology,metabolism,microbiology Polymorphism, Genetic Reactive Nitrogen Species/metabolism Reactive Oxygen Species/metabolism
Chemicals
Cytokines Reactive Nitrogen Species Reactive Oxygen Species NOS2 protein, human Nitric Oxide Synthase Nitric Oxide Synthase Type II
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Fang Ferric C
Department of Laboratory Medicine, University of Washington School of Medicine, 1959 North East Pacific Street, Box 357242, Seattle, Washington 98195-7242, USA. [email protected]
Article Info
Journal
Nature reviews. Microbiology
Abbr.
Nat Rev Microbiol
ISSN
1740-1526
Published
2004-10-00
Pages
820-32
Language
English
Region
England
NLM ID
101190261
Subset
IM
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