Immunopathology of Renal Tissue in Fatal Cases of Dengue in Children.
Lucca de Lima Siqueira OliveiraFelipe de Andrade Vieira AlvesKíssila RabeloLeandro Junqueira MoragasRonaldo Mohana-BorgesJorge José de CarvalhoCarlos Basílio-de-OliveiraRodrigo Basílio-de-OliveiraFernando Colonna RosmanNatália Gedeão SalomãoMarciano Viana PaesPublished in: Pathogens (Basel, Switzerland) (2022)
Dengue virus (DENV) infection represents a worldwide public health concern and can cause damage to multiple organs, including the kidney. In this work, we investigated the histopathological changes caused by dengue virus infection along with the detection of inflammatory mediators, cytokines, and cell expression patterns in the renal tissue of three fatal cases in children. Hematoxylin and Eosin staining was performed to analyze these histopathological changes. Immunohistochemistry allowed for the detection of immunological inflammatory markers in renal tissues that were quantified and further analyzed. Vascular congestion, edema and glomerular infiltrate were observed in the three cases, in addition to the thickening of the matrix area around the glomerular capillaries and mononuclear infiltrate associated with vascular congestion in the medullary region. The renal tissues exhibited collagen deposition and high expression of CD68 + Mø, CD8 + T, CD56 + cells and MMP-9, and the cytokine profile was mainly characterized by the expression of IFN-γ and TNF-α. Additionally, the expression of RANTES, VEGFR-2 and VCAM-1 were observed. The replication of DENV was evidenced by the detection of the NS3 protein. These results contributed to clarifying the main factors that may be involved in changes in the renal tissue of fatal cases of dengue in children.
Keyphrases
- dengue virus
- zika virus
- poor prognosis
- aedes aegypti
- public health
- binding protein
- loop mediated isothermal amplification
- gene expression
- rheumatoid arthritis
- long non coding rna
- induced apoptosis
- immune response
- single cell
- diabetic nephropathy
- nk cells
- cell cycle arrest
- amino acid
- high resolution
- mesenchymal stem cells
- vascular endothelial growth factor