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Human gene expression profiles of susceptibility and resistance in tuberculosis

Maertzdorf, Jeroen (författare)
Department of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany
Repsilber, Dirk, 1971- (författare)
Leibniz Institute for Farm Animal Biology, Genetics and Biometry, Dummerstorf, Germany
Parida, S K (författare)
Department of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany
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Stanley, K (författare)
Division of Molecular Biology and Human Genetics, MRC Centre for Molecular and Cellular Biology, Stellenbosch University, Cape Town, South Africa
Roberts, T (författare)
Division of Molecular Biology and Human Genetics, MRC Centre for Molecular and Cellular Biology, Stellenbosch University, Cape Town, South Africa
Black, G (författare)
Division of Molecular Biology and Human Genetics, MRC Centre for Molecular and Cellular Biology, Stellenbosch University, Cape Town, South Africa
Walzl, G (författare)
Division of Molecular Biology and Human Genetics, MRC Centre for Molecular and Cellular Biology, Stellenbosch University, Cape Town, South Africa
Kaufmann, S H E (författare)
Department of Immunology, Max Planck Institute for Infection Biology, Berlin, Germany
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 (creator_code:org_t)
2010-09-23
2011
Engelska.
Ingår i: Genes and Immunity. - London, UK : Nature Publishing Group. - 1466-4879 .- 1476-5470. ; 12:1, s. 15-22
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Tuberculosis (TB) still poses a profound burden on global health, owing to significant morbidity and mortality worldwide. Although a fully functional immune system is essential for the control of Mycobacterium tuberculosis infection, the underlying mechanisms and reasons for failure in part of the infected population remain enigmatic. Here, whole-blood microarray gene expression analyses were performed in TB patients and in latently as well as uninfected healthy controls to define biomarkers predictive of susceptibility and resistance. Fc gamma receptor 1B (FCGRIB)was identified as the most differentially expressed gene, and, in combination with four other markers, produced a high degree of accuracy in discriminating TB patients and latently infected donors. We determined differentially expressed genes unique for active disease and identified profiles that correlated with susceptibility and resistance to TB. Elevated expression of innate immune-related genes in active TB and higher expression of particular gene clusters involved in apoptosis and natural killer cell activity in latently infected donors are likely to be the major distinctive factors determining failure or success in controlling M. tuberculosis infection. The gene expression profiles defined in this study provide valuable clues for better understanding of progression from latent infection to active disease and pave the way for defining predictive correlates of protection in TB.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Bioinformatik och systembiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Bioinformatics and Systems Biology (hsv//eng)

Nyckelord

tuberculosis
microarray
biomarkers

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