The Role of Growth Factors in the Pathogenesis of Dengue: A Scoping Review.
Victor Edgar Fiestas SolórzanoRaquel Curtinhas de LimaElzinandes Leal de AzeredoPublished in: Pathogens (Basel, Switzerland) (2022)
Growth factors (GFs) have a role in tissue repair and in the modulation of the expression of inflammatory cells in damage caused by pathogens. This study aims to systematize the evidence on the role of GFs in the pathogenesis of dengue. This scoping review considered all published peer-reviewed studies in the MEDLINE and Embase databases. Ultimately, 58 studies that analyzed GFs in dengue patients, published between 1998 and 2021, were included. DENV-2 infection and secondary infection were more frequent in the patients studied. ELISA and multiplex immunoassay (Luminex) were the most used measurement techniques. Increased levels of vascular endothelial growth factor, granulocyte-macrophage colony-stimulating factor, granulocyte colony-stimulating factor, transforming growth factor beta, and hepatocyte growth factor as well as reduced levels of platelet-derived growth factor and epidermal growth factor were observed in severe dengue in most studies. Vascular endothelial growth factor and hepatocyte growth factor were identified as biomarkers of severity. In addition, there is evidence that the dengue virus can use the growth factor pathway to facilitate its entry into the cell and promote its viral replication. The use of tyrosine kinase inhibitors is an alternative treatment for dengue that is being studied.
Keyphrases
- growth factor
- dengue virus
- zika virus
- vascular endothelial growth factor
- aedes aegypti
- end stage renal disease
- transforming growth factor
- ejection fraction
- newly diagnosed
- chronic kidney disease
- oxidative stress
- adipose tissue
- stem cells
- peritoneal dialysis
- epithelial mesenchymal transition
- sars cov
- early onset
- cell therapy
- patient reported outcomes
- randomized controlled trial
- case control
- mesenchymal stem cells
- wound healing
- high throughput
- single cell
- liver injury
- cell death
- drug induced
- multidrug resistant
- gram negative
- smoking cessation
- label free
- long non coding rna
- chronic myeloid leukemia
- recombinant human