Iron, Infections, and Anemia of Inflammation
Abstract
Iron is essential to all microorganisms. To obtain iron from the very low concentrations present in their environment, microorganisms have developed sophisticated mechanisms such as the siderophore system. As a primitive defense mechanism, humans have developed mechanisms to withhold iron from microorganisms. Iron-binding proteins such as transferrin, ferritin, and lactoferrin have a central role in human ferrokinetics. These iron-binding proteins also participate in the process of decreasing iron availability for the microorganisms. They do so by decreasing iron reutilization. Anemia of inflammation (previously called anemia of chronic disease) is seen in the setting of infectious, inflammatory, and neoplastic diseases. It results, in part, from changes in the intracellular metabolism of iron. Alterations of iron physiology seen in many clinical circumstances make excess iron available to microorganisms, thus enhancing their pathogenicity. Understanding the molecular basis of iron withholding by the human host, both in the absence of and during infection, and that of iron acquisition by microorganisms may provide us with new and innovative antimicrobial agents and vaccines.
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Bacteria and fungi solved problems of iron solubility and toxicity by creating and excreting siderophores, which have extremely tight binding constants (Kf > 10^30) and can solubilise and sequester iron.
“Consequently, and because these reflect fundamental physicochemical properties of such ions, the problems of both solubility and toxicity were faced by bacteria (and indeed fungi [166-169]) long ago in evolution, and were solved by their creation and excretion of (mainly ferric-)iron chelators known as siderophores [170-189] (and for haemophores see [190]). These typically have extremely tight b”
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- Authors
- Jurado, R. L.
- Affiliations
- Emory University (US)
- Corresponding author
- Jurado, Rafael L.
- Venue
- Clinical Infectious Diseases
- Publisher
- Oxford University Press (OUP)
- Published
- 1997-10
- Volume
- 25
- Issue
- 4
- Pages
- 888-895
- ISSN
- 1058-4838 (ISSN-L)
- 1537-6591
- OpenAlex
- W2091260254
- Cited by
- 358
- References
- 100
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 8 · 2023: 6 · 2022: 12 · 2021: 2 · 2020: 13 · 2019: 3 · 2018: 9 · 2017: 7 · 2016: 11 · 2015: 10 · 2014: 8 · 2013: 8 · 2012: 22
- FWCI
- 5.39
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Infectious Diseases (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Health Sciences › Medicine › Hematology › Erythropoietin and Anemia Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hemoglobin structure and function
- Keywords
- iron acquisition, siderophores, iron-binding proteins, transferrin, ferritin, lactoferrin, anemia of chronic disease, iron metabolism, host defense against infection, microbial pathogenicity, antimicrobial agents, vaccines
- MeSH terms
- Anemia, Bacteria, Bacterial Infections, Blood Transfusion, Carrier Proteins, Conalbumin, Deferoxamine, Ferritins, Hemochromatosis, Hemolysis, Humans, Inflammation, Iron, Lactoferrin, Transferrin, Diabetic Ketoacidosis, Iron-Binding Proteins, Transferrin-Binding Proteins
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