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Synthesis, Characterization, and Application of Superparamagnetic Iron Oxide Nanoprobes for Extrapulmonary Tuberculosis Detection
Published on: February 16, 2020
Chemokine IP-10: an adjunct marker for latent tuberculosis infection in children
Jennifer Lighter1, M Rigaud, M Huie
1Saul Krugman Division of Pediatric Infectious Diseases and Immunology, New York University School of Medicine, New York, New York 10016, USA. lightj03@med.nyu.edu
Insights
Chemokine inducible protein 10 (IP-10) shows promise for diagnosing Mycobacterium tuberculosis infection in children. Combining IP-10 with interferon-gamma (IFN-γ) may improve diagnostic accuracy, particularly in young children.
Area of Science:
- Immunology
- Infectious Diseases
- Diagnostics
Background:
- Chemokine inducible protein 10 (IP-10) has been implicated in Mycobacterium tuberculosis (M. tuberculosis) infection.
- Elevated IP-10 levels are observed in plasma and at infection sites in individuals with M. tuberculosis.
Purpose of the Study:
- To assess IP-10 as a diagnostic marker for M. tuberculosis infection in children.
- To evaluate IP-10 in a low tuberculosis (TB) prevalence region.
Main Methods:
- Whole blood from 127 children was stimulated with M. tuberculosis-specific antigens to measure IP-10 levels.
- IP-10 results were analyzed against TB exposure risk, tuberculin skin test, and interferon-gamma release assay (IGRA).
Main Results:
- IP-10 reactivity correlated with M. tuberculosis exposure risk and IGRA results.
- IP-10 responses were not age-dependent and identified more positive cases in children under 5 years old compared to interferon-gamma (IFN-γ).
- IGRA demonstrated higher sensitivity than IP-10 in detecting active M. tuberculosis disease.
Conclusions:
- IP-10, when used with IFN-γ, may enhance the diagnostic performance of IGRAs for M. tuberculosis infection.
- This combination is particularly beneficial for diagnosing TB in young children.
Setting:
Recent reports indicate a role of chemokine inducible protein 10 (IP-10) in Mycobacterium tuberculosis infection substantiated by the detection of elevated levels in plasma and at infection foci in individuals infected with M. tuberculosis.
Objective:
To evaluate IP-10 as a potential marker for the diagnosis of M. tuberculosis infection in children living in a region of low tuberculosis (TB) prevalence.
Design:
IP-10 levels were obtained after whole blood stimulation with M. tuberculosis-specific antigens in 127 children. IP-10 results were evaluated upon gradations of exposure risk to M. tuberculosis and correlation with tuberculin skin test and an interferon-gamma release assay (IGRA).
Results:
IP-10 reactivity correlated well to risk of exposure to M. tuberculosis in children. There was a strong correlation between IP-10 and IGRA results. IP-10 responses, unlike interferon-gamma (IFN-gamma), were not age-dependent and detected more positive results in children aged <5 years. In the children with active disease, the IGRA was more sensitive than IP-10 at detecting M. tuberculosis infection.
Conclusion:
Our findings suggest that IP-10 in combination with IFN-gamma may enhance the diagnostic performance of IGRAs in detecting M. tuberculosis infection, especially in young children.
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