The Relationship of Kynurenine and Neopterin Levels and Their Association with a Selection of Other Immune Markers in Chronic Myeloid Leukaemia Patients
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
28189146
DOI
10.14712/fb2016062060235
PII: file/5825/fb2016a0029.pdf
Knihovny.cz E-resources
- MeSH
- Biomarkers blood MeSH
- C-Reactive Protein metabolism MeSH
- Leukemia, Myelogenous, Chronic, BCR-ABL Positive blood MeSH
- Adult MeSH
- Interleukin-6 blood MeSH
- Kynurenine blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Linear Models MeSH
- Young Adult MeSH
- Neopterin blood MeSH
- Leukocyte Count MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Tryptophan blood MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- C-Reactive Protein MeSH
- Interleukin-6 MeSH
- Kynurenine MeSH
- Neopterin MeSH
- Tryptophan MeSH
Among malignant diseases, chronic myeloid leukaemia (CML) is one of the best suited candidates for immunotherapy. For this purpose it is necessary to broaden the present knowledge on the immunology of this disease. As a part of such a project, the levels of kynurenine (KYN) and neopterin (NPT) were studied in 28 CML patients and in the same number of healthy subjects. At diagnosis, both KYN and NPT levels were found to be elevated in a significant portion of the patients and dependent on their leukocyte count. As in the case of KYN, increased NPT levels dropped after achieving remission. When correlating KYN and NPT levels with a selection of other markers tested, significant association was revealed only in the case of CRP and IL-6. However, there were several patients with increased KYN levels in whom NPT was not detected, and vice versa. The relapse of the disease observed in two patients was accompanied by an increased level of NPT in both cases, but by an increased level of KYN in only one of them. No significant correlation was found between KYN and NPT levels in sera taken at diagnosis. However, when the whole set of sera was taken into consideration, the association became statistically significant. Although the data obtained revealed a number of similarities between KYN and NPT production in CML patients, it also suggested a difference in the kinetics of these two biomarkers' production.
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