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The effect of the host's iron status on tuberculosis.

Abstract
Several lines of evidence have suggested that iron is critical for Mycobacterium tuberculosis growth in macrophages. Macrophage iron loading in patients with African iron overload increases the risk of tuberculosis (TB) and may worsen TB outcome. Likewise, macrophage iron loading may contribute to an increased predisposition toward TB in HIV infection. Human genetic disorders or variations may increase the risk of TB or worsen its outcome through macrophage iron loading, including the haptoglobin 2-2 phenotype, NRAMP1 polymorphisms (at least in Africans and Asians), and possibly ferroportin 1 mutations, but not HFE hemochromatosis. Thus, the host's iron status may be an important yet underevaluated factor in TB prevention and therapy and in TB vaccine design.
AuthorsJohan R Boelaert, Stefaan J Vandecasteele, Rui Appelberg, Victor R Gordeuk
JournalThe Journal of infectious diseases (J Infect Dis) Vol. 195 Issue 12 Pg. 1745-53 (Jun 15 2007) ISSN: 0022-1899 [Print] United States
PMID17492589 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Review)
Chemical References
  • Antitubercular Agents
  • Cation Transport Proteins
  • Cytokines
  • Haptoglobins
  • Tuberculosis Vaccines
  • metal transporting protein 1
  • natural resistance-associated macrophage protein 1
  • Iron
Topics
  • Antitubercular Agents (pharmacology)
  • Cation Transport Proteins (genetics)
  • Cytokines (metabolism)
  • Haptoglobins (genetics)
  • Humans
  • Iron (metabolism)
  • Iron Overload (complications, genetics)
  • Macrophages (chemistry, metabolism, microbiology)
  • Mononuclear Phagocyte System (chemistry)
  • Mycobacterium tuberculosis (drug effects, growth & development, immunology)
  • Tuberculosis (drug therapy, etiology, genetics, metabolism)
  • Tuberculosis Vaccines (standards)

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