HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Circulating biomarkers of pulmonary and extrapulmonary tuberculosis in children.

Abstract
Tuberculosis (TB) in children is not only more likely to cause more severe disease than that seen in adults, it is also more likely to be extrapulmonary. Moreover, pediatric TB is very difficult to diagnose and suffers from a lack of understanding of host biomarkers for monitoring the progression of disease. Hence, we sought to identify the expression patterns of a variety of biomarkers in the plasma of children with pulmonary TB (PTB) and extrapulmonary TB (ETB), as well as in healthy control (HC) children. Thus, we examined a variety of circulating markers reflecting tissue inflammation, oxidative stress, innate immune activation, fibrosis, and the cytokine response. Children with active TB, compared to HC children, showed markedly elevated plasma levels of matrix metalloproteinases and their endogenous inhibitors. In addition, children with active TB had significantly elevated levels of C-reactive protein, α-2 macroglobulin, and haptoglobin, as well as hemoxygenase 1. Markers of innate immune activation (lipopolysaccharide [LPS] and lipopolysaccharide-binding protein [LBP]) were significantly lower in ETB than in PTB children. Although there were no significant differences between the two groups in their levels of cytokines (type 1 [gamma interferon (IFN-γ), tumor necrosis factor α (TNF-α), interleukin 2 (IL-2), and IL-12], type 2 [IL-4, IL-5, IL-13, and IL-33], and most type 17 [IL-17A, IL-22, IL-1β, and IL-6] and type 1 interferons [IFN-α and IFN-β]) or most of the cytokines associated with immune modulation (IL-10 and IL-20), pediatric TB was associated with elevated plasma transforming growth factor β (TGF-β), IL-21, and IL-23 levels. Thus, pediatric TB is characterized by elevated levels of a variety of biomarkers at homeostasis, suggesting that these responses may play a crucial role in disease pathogenesis.
AuthorsNathella Pavan Kumar, R Anuradha, Bruno B Andrade, N Suresh, R Ganesh, Janani Shankar, V Kumaraswami, Thomas B Nutman, Subash Babu
JournalClinical and vaccine immunology : CVI (Clin Vaccine Immunol) Vol. 20 Issue 5 Pg. 704-11 (May 2013) ISSN: 1556-679X [Electronic] United States
PMID23486418 (Publication Type: Journal Article, Research Support, N.I.H., Intramural)
Chemical References
  • Acute-Phase Proteins
  • Biomarkers
  • Carrier Proteins
  • Cytokines
  • Haptoglobins
  • Lipopolysaccharides
  • Matrix Metalloproteinase Inhibitors
  • Membrane Glycoproteins
  • Tissue Inhibitor of Metalloproteinases
  • alpha-Macroglobulins
  • lipopolysaccharide-binding protein
  • C-Reactive Protein
  • Matrix Metalloproteinases
Topics
  • Acute-Phase Proteins
  • Adolescent
  • Biomarkers (blood)
  • C-Reactive Protein (analysis)
  • Carrier Proteins (blood)
  • Child
  • Child, Preschool
  • Cytokines (blood)
  • Disease Progression
  • Female
  • Fibrosis
  • Haptoglobins (analysis)
  • Humans
  • Infant
  • Inflammation
  • Lipopolysaccharides (blood)
  • Male
  • Matrix Metalloproteinase Inhibitors (blood)
  • Matrix Metalloproteinases (blood)
  • Membrane Glycoproteins (blood)
  • Oxidative Stress
  • Tissue Inhibitor of Metalloproteinases (blood)
  • Tuberculosis (blood, diagnosis)
  • alpha-Macroglobulins (analysis)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: