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Identification of promising plasma immune biomarkers to differentiate active pulmonary tuberculosis
- Source :
- Cytokine. 88:99-107
- Publication Year :
- 2016
- Publisher :
- Elsevier BV, 2016.
-
Abstract
- Although much research has been done related to biomarker discovery for tuberculosis infection, a set of biomarkers that can discriminate between active and latent TB diseases remains elusive. In the current study we correlate clinical aspects of TB disease with changes in the immune response as determined by biomarkers detected in plasma. Our study measured 18 molecules in human plasma in 17 patients with active disease (APTB), 14 individuals with latent tuberculosis infection (LTBI) and 16 uninfected controls (CTRL). We found that active tuberculosis patients have increased plasma levels of IL-6, IP-10, TNF-α, sCD163 and sCD14. Statistical analysis of these biomarkers indicated that simultaneous measurement of sCD14 and IL-6 was able to diagnose active tuberculosis infection with 83% accuracy. We also demonstrated that TNF-α and sCD163 were correlated with tuberculosis severity. We showed that the simultaneous detection of both plasma sCD14 and IL-6 is a promising diagnostic approach to identify APTB, and further, measurement of TNF-α and sCD163 can identify the most severe cases of tuberculosis.
- Subjects :
- Adult
Male
0301 basic medicine
Tuberculosis
Immunology
Lipopolysaccharide Receptors
Disease
Biochemistry
03 medical and health sciences
0302 clinical medicine
Immune system
Pulmonary tuberculosis
Active disease
medicine
Humans
Immunology and Allergy
Biomarker discovery
Tuberculosis, Pulmonary
Molecular Biology
Latent tuberculosis
Tetraspanin 30
business.industry
Hematology
Active tuberculosis
medicine.disease
030104 developmental biology
Cytokines
Female
business
Biomarkers
030215 immunology
Subjects
Details
- ISSN :
- 10434666
- Volume :
- 88
- Database :
- OpenAIRE
- Journal :
- Cytokine
- Accession number :
- edsair.doi.dedup.....0cf748c07fbd000154944c17512bb158
- Full Text :
- https://doi.org/10.1016/j.cyto.2016.08.030