期刊
JOURNAL OF INFECTIOUS DISEASES
卷 226, 期 11, 页码 1964-1973出版社
OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jiac273
关键词
dengue; kynurenine pathway; anthranilic acid; CXCL10; CCL2
资金
- Bantuan Penyelidikan Kecil from University Malaya [BK-073]
- National Health and Medical Research Council
- Handbury Foundation
- Macquarie University
- PANDIS.org
This study found that the release of cytokines by immune cells increases as the severity of dengue infection worsens, leading to activation of the kynurenine pathway (KP). Specific biomarkers and cytokines (CXCL10, CCL2, and AA) can predict the risk of developing dengue with warning signs (DWS+). These findings suggest a potential role for these markers in the early detection and management of dengue.
Background The resolution or aggravation of dengue infection depends on the patient's immune response during the critical phase. Cytokines released by immune cells increase with the worsening severity of dengue infections. Cytokines activate the kynurenine pathway (KP) and the extent of KP activation then influences disease severity. Methods KP metabolites and cytokines in plasma samples of patients with dengue infection (dengue without warning signs [DWS-], dengue with warning signs [DWS+], or severe dengue) were analyzed. Cytokines (interferon gamma [IFN-gamma], tumor necrosis factor, interleukin 6, CXCL10/interferon-inducile protein 10 [IP-10], interleukin 18 [IL-18], CCL2/monocyte chemoattractant protein-1 [MCP-1], and CCL4/macrophage inflammatory protein-1beta [MIP-1 beta] were assessed by a Human Luminex Screening Assay, while KP metabolites (tryptophan, kynurenine, anthranilic acid [AA], picolinic acid, and quinolinic acid) were assessed by ultra-high-performance liquid chromatography and Gas Chromatography Mass Spectrophotometry [GCMS] assays. Results Patients with DWS+ had increased activation of the KP where kynurenine-tryptophan ratio, anthranilic acid, and picolinic acid were elevated. These patients also had higher levels of the cytokines IFN-gamma, CXCL10, CCL4, and IL-18 than those with DWS-. Further receiver operating characteristic analysis identified 3 prognostic biomarker candidates, CXCL10, CCL2, and AA, which predicted patients with higher risks of developing DWS+ with an accuracy of 97%. Conclusions The data suggest a unique biochemical signature in patients with DWS+. CXCL10 and CCL2 together with AA are potential prognostic biomarkers that discern patients with higher risk of developing DWS+ at earlier stages of infection. Stronger activation of the kynurenine pathway is discernible in patients with dengue with warning signs as CCL2, CCL4, CXCL10, IFN-gamma, and IL-18 are elevated, accompanied by increased kynurenine-tryptophan ratio, anthranilic acid, and picolinic acid.
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